COMPOSITION FOR ELECTROCHEMICAL DEVICE FUNCTIONAL LAYER, FUNCTIONAL LAYER FOR ELECTROCHEMICAL DEVICE, AND ELECTROCHEMICAL DEVICE

TECHNICAL FIELD

The present disclosure relates to a composition for an electrochemical device functional layer, a functional layer for an electrochemical device, and an electrochemical device.

BACKGROUND

Electrochemical devices such as lithium ion secondary batteries and electric double-layer capacitors have characteristics such as compact size, light weight, high energy-density, and the ability to be repeatedly charged and discharged, and are used in a wide variety of applications.

A lithium ion secondary battery, for example, normally includes battery members such as a positive electrode, a negative electrode, and a separator that isolates the positive electrode and the negative electrode from each other and prevents short-circuiting between the positive and negative electrodes.

Studies have been made to further improve separators in recent years with the aim of providing lithium secondary batteries with even higher performance.

As one specific example, Patent Literature (PTL) 1 proposes a separator in which a heat-resistant layer containing non-conductive particles and a binder is formed on a separator substrate and in which an adhesive layer containing a specific particulate polymer is further provided on the heat-resistant layer. PTL 1 reports that by using this separator having an adhesive layer on a heat-resistant layer, the separator and an electrode are well adhered, and battery characteristics of a secondary battery are improved.

CITATION LIST
Patent Literature

PTL 1: WO2013/151144A1

SUMMARY
Technical Problem

However, in production of the conventional separator described above that includes a heat-resistant layer and an adhesive layer, it is necessary to implement formation of the heat-resistant layer on the separator substrate and formation of the adhesive layer on the heat-resistant layer sequentially, resulting in a complicated production process.

One strategy that may be considered in response to this problem is forming a single layer that can simultaneously display both heat resistance and adhesiveness (hereinafter, such a layer is referred to as a “functional layer”) on a separator substrate, instead of a heat-resistant layer and an adhesive layer that are each formed individually, so as to simplify the production process of a separator and increase productivity.

The inventors decided to focus on the fact that an obtained functional layer can be caused to display heat resistance and adhesiveness simultaneously by using a composition containing a component that contributes to heat resistance and a component that contributes to adhesiveness. However, studies carried out by the inventors revealed that when a functional layer is formed using a composition in which a component that contributes to heat resistance and a component that contributes to adhesiveness are simply mixed, constituent components of the functional layer become detached therefrom (hereinafter, referred to as “dusting”). It also became clear that it is difficult to form a functional layer that can ensure sufficient heat resistance while also displaying excellent adhesiveness because there is a trade-off relationship between heat resistance and adhesiveness.

Accordingly, an object of the present disclosure is to provide a technique that enables efficient formation of a functional layer for an electrochemical device in which dusting is inhibited and that can ensure sufficient heat resistance while also displaying excellent adhesiveness.

Solution to Problem

The inventors conducted diligent studies to achieve the object set forth above. The inventors discovered that by using a composition containing a binder, inorganic particles, and a particulate polymer having a specific average circularity and a specific volume-average particle diameter, it is possible to efficiently form a functional layer in which dusting is inhibited and that can ensure sufficient heat resistance while also displaying excellent adhesiveness. In this manner, the inventors completed the present disclosure.

Specifically, the present disclosure aims to advantageously solve the problem set forth above, and a presently disclosed composition for an electrochemical device functional layer comprises a particulate polymer, a binder, and inorganic particles, wherein the particulate polymer has an average circularity of not less than 0.90 and less than 0.99, and the particulate polymer has a volume-average particle diameter of not less than 1.0 μm and not more than 10.0 μm. When a particulate polymer having a specific average circularity and a specific volume-average particle diameter is used in combination with a binder and inorganic particles in this manner, it is possible to efficiently form a functional layer for an electrochemical device in which dusting is inhibited and that can ensure sufficient heat resistance while also displaying excellent adhesiveness.

Note that the “average circularity” and the “volume-average particle diameter” referred to in the present disclosure can be measured by methods described in the EXAMPLES section of the present specification.

In the presently disclosed composition for an electrochemical device functional layer, the particulate polymer preferably has a particle diameter distribution of not less than 1.10 and not more than 1.50. When the particle diameter distribution of the particulate polymer is within the range set forth above, a functional layer for an electrochemical device formed using the composition for an electrochemical device functional layer can be caused to comply with changes of an electrochemical device. Moreover, unevenness of the functional layer for an electrochemical device after members are adhered to each other through the functional layer for an electrochemical device can be inhibited, and electrochemical characteristics of an electrochemical device can be improved.

Note that the “particle diameter distribution” referred to in the present disclosure can be measured using a method described in the EXAMPLES section of the present specification.

In the presently disclosed composition for an electrochemical device functional layer, a mixing ratio of the inorganic particles and the particulate polymer, as a volume ratio, is preferably 95:5 to 55:45. When the mixing ratio of the inorganic particles and the particulate polymer, as a volume ratio, is within the range set forth above, a better balance of heat resistance and adhesiveness can be obtained in a functional layer for an electrochemical device that is formed using the composition for an electrochemical device functional layer.

In the presently disclosed composition for an electrochemical device functional layer, the particulate polymer preferably has a glass-transition temperature of not lower than 10° C. and not higher than 90° C. When the glass-transition temperature of the particulate polymer is within the range set forth above, good adhesiveness can be ensured in a functional layer for an electrochemical device that is formed using the composition for an electrochemical device functional layer while also inhibiting blocking of the functional layer for an electrochemical device.

Note that the “glass-transition temperature” referred to in the present disclosure can be measured using a method described in the EXAMPLES section of the present specification.

In the presently disclosed composition for an electrochemical device functional layer, the particulate polymer preferably includes an aromatic vinyl monomer unit. The inclusion of an aromatic vinyl monomer unit in the particulate polymer can improve close adherence to a substrate of a functional layer for an electrochemical device that is formed using the composition for an electrochemical device functional layer. Moreover, the amount of the particulate polymer that elutes into electrolyte solution can be reduced, and thus an electrochemical device can be provided with excellent output characteristics.

Note that when a polymer is said to “include a monomer unit” in the present disclosure, this means that “a structural unit derived from the monomer is included in the polymer obtained using the monomer”.

Moreover, the present disclosure aims to advantageously solve the problem set forth above, and a presently disclosed functional layer for an electrochemical device is formed using any one of the compositions for an electrochemical device functional layer set forth above. By using the presently disclosed composition for an electrochemical device functional layer in this manner, it is possible to provide a functional layer for an electrochemical device in which dusting is inhibited and that can ensure sufficient heat resistance while also displaying excellent adhesiveness.

Furthermore, the present disclosure aims to advantageously solve the problem set forth above, and a presently disclosed electrochemical device comprises the functional layer for an electrochemical device set forth above. The inclusion of the presently disclosed functional layer for an electrochemical device in this manner makes it possible to provide an electrochemical device that can display excellent electrochemical characteristics.

Advantageous Effect

According to the present disclosure, it is possible to provide a composition for an electrochemical device functional layer with which it is possible to efficiently form a functional layer for an electrochemical device in which dusting is inhibited and that can ensure sufficient heat resistance while also displaying excellent adhesiveness.

Moreover, according to the present disclosure, it is possible to provide a functional layer for an electrochemical device in which dusting is inhibited and that can ensure sufficient heat resistance while also displaying excellent adhesiveness.

Furthermore, according to the present disclosure, it is possible to provide an electrochemical device that can display excellent electrochemical characteristics.

DETAILED DESCRIPTION

The following provides a detailed description of embodiments of the present disclosure.

The presently disclosed composition for an electrochemical device functional layer (hereinafter, also referred to simply as a “composition for a functional layer”) is used as a material in formation of the presently disclosed functional layer for an electrochemical device (hereinafter, also referred to simply as a “functional layer”). Moreover, the presently disclosed functional layer for an electrochemical device is formed using the presently disclosed composition for an electrochemical device functional layer. Furthermore, the presently disclosed electrochemical device is an electrochemical device that includes at least the presently disclosed functional layer for an electrochemical device.

(Composition for Electrochemical Device Functional Layer)

The presently disclosed composition for an electrochemical device functional layer contains a specific particulate polymer, a binder, and inorganic particles, and can optionally further contain other components. By using the presently disclosed composition for a functional layer, it is possible to form a functional layer for an electrochemical device in which dusting is inhibited and that can ensure sufficient heat resistance while also displaying excellent adhesiveness.

The particulate polymer contained in the composition for a functional layer is a polymer that, as described in detail below, has a specific average circularity and a specific volume-average particle diameter, and has a particulate form in the composition for a functional layer. It should be noted that the particulate polymer may have a particulate form or may have any other form after members have been adhered to each other through a functional layer formed using the composition for a functional layer. The particulate polymer may be a crystalline macromolecule polymer, an amorphous macromolecule polymer, or a mixture thereof.

«Average Circularity of Particulate Polymer»

The average circularity of the particulate polymer is required to be 0.90 or more, and is preferably 0.94 or more. Moreover, the average circularity of the particulate polymer is required to be less than 0.99, and is preferably 0.98 or less. When the average circularity of the particulate polymer is not less than any of the lower limits set forth above, dusting can be inhibited in a functional layer formed using the composition for a functional layer because the number of adhesion points between the particulate polymer and the inorganic particles increases. On the other hand, when the average circularity of the particulate polymer is not more than any of the upper limits set forth above, dusting can be inhibited because the state of the particulate polymer in a functional layer stabilizes.

«Volume-Average Particle Diameter of Particulate Polymer»

The volume-average particle diameter of the particulate polymer is required to be 1.0 μm or more, and is preferably 1.5 μm or more, more preferably 2.0 μm or more, even more preferably 3.0 μm or more, and most preferably more than 5.0 μm. Moreover, the volume-average particle diameter of the particulate polymer is required to be 10.0 μm or less, and is preferably 9.0 μm or less, and more preferably 8.0 μm or less. When the volume-average particle diameter of the particulate polymer is not less than any of the lower limits set forth above, better adhesiveness can be obtained because the particulate polymer tends to protrude relative to the inorganic particles at a thickness direction surface of a functional layer formed using the composition for a functional layer. Moreover, the heat resistance of a functional layer formed using the composition for a functional layer improves. On the other hand, when the volume-average particle diameter of the particulate polymer is not more than any of the upper limits set forth above, detachment of the particulate polymer during application of the composition for a functional layer onto a substrate can be inhibited, and a uniform functional layer can be formed. Moreover, as a result of the number of particles of the particulate polymer per unit area of a functional layer increasing, the number of adhesion points between the functional layer and an adherend increases, and adhesive strength increases. Although it is not clear why the heat resistance of a functional layer improves as described above, the reason for this is presumed to be as follows. In order to increase the heat resistance of a functional layer, it is necessary for inorganic particles to constitute a high proportion in the functional layer. It is thought that as a result of the particulate polymer protruding relative to the inorganic particles at a thickness direction surface of a functional layer, the proportion constituted by the inorganic particles in an inorganic particle layer included in the functional layer appears to be higher, and thus heat resistance increases. Moreover, heat shrinkage of the functional layer is thought to be inhibited through the presence of the inorganic particles around the particulate polymer in the inorganic particle layer. It is also presumed that through the volume-average particle diameter of the particulate polymer being not more than any of the upper limits set forth above, heat shrinkage of the functional layer can be inhibited well because the inorganic particles can be present around the particulate polymer in a good balance in the inorganic particle layer. Note that the inorganic particle layer mentioned above is described in detail further below.

The volume-average particle diameter of the particulate polymer can be adjusted through the type and/or amount of a metal hydroxide used in production of the particulate polymer. This metal hydroxide is described in detail further below.

«Particle Diameter Distribution of Particulate Polymer»

The particle diameter distribution of the particulate polymer is preferably 1.10 or more, and more preferably 1.20 or more, and is preferably 1.50 or less, and more preferably 1.40 or less. When the particle diameter distribution of the particulate polymer is not less than any of the lower limits set forth above, it is possible to form a functional layer that can comply with expansion and contraction of an electrode, and particularly of a negative electrode. On the other hand, when the particle diameter distribution of the particulate polymer is not more than any of the upper limits set forth above, electrochemical characteristics of an electrochemical device improve because it is possible to reduce unevenness of thickness of a functional layer after adhesion of members to each other through the functional layer. Moreover, dusting can be inhibited well.

«Glass-Transition Temperature of Particulate Polymer»

The glass-transition temperature (Tg) of the particulate polymer is preferably 10° C. or higher, more preferably 20° C. or higher, and even more preferably 30° C. or higher, and is preferably 90° C. or lower, more preferably 80° C. or lower, and even more preferably 70° C. or lower. When the glass-transition temperature of the particulate polymer is not lower than any of the lower limits set forth above, blocking of a functional layer can be inhibited during storage or the like of an electrochemical device that includes the functional layer, for example. On the other hand, when the glass-transition temperature of the particulate polymer is not higher than any of the upper limits set forth above, good adhesiveness of a functional layer can be obtained even when members are pressed and adhered to each other through the functional layer.

«Melting Point of Particulate Polymer»

The melting point (Tm) of the particulate polymer is preferably 50° C. or higher, and more preferably 100° C. or higher. When the melting point of the particulate polymer is not lower than any of the lower limits set forth above, good adhesiveness of a functional layer can be ensured even in a case in which the particulate polymer includes a crystalline macromolecule polymer.

Note that in a case in which the particulate polymer has both a glass-transition temperature and a melting point, the melting point of the particulate polymer is preferably not lower than any of the lower limits set forth above from a viewpoint of further improving adhesiveness of a functional layer.

«Degree of Swelling in Electrolyte Solution of Particulate Polymer»

The degree of swelling in electrolyte solution of the particulate polymer is preferably a factor of 1.0 or more, more preferably a factor of 1.2 or more, and even more preferably a factor of 1.3 or more, and is preferably a factor of 15 or less, more preferably a factor of 10 or less, even more preferably a factor of 7 or less, and particularly preferably a factor of 5 or less. When the degree of swelling in electrolyte solution of the particulate polymer is not less than any of the lower limits set forth above, a functional layer can be provided with strong adhesive strength in electrolyte solution. On the other hand, when the degree of swelling in electrolyte solution of the particulate polymer is not more than any of the upper limits set forth above, electrochemical characteristics of an electrochemical device that includes a functional layer can be improved because resistance of the functional layer in electrolyte solution decreases.

The “degree of swelling in electrolyte solution” referred to in the present disclosure can be measured by a method described in the EXAMPLES section of the present specification.

«Chemical Composition of Particulate Polymer»

The particulate polymer can be a known polymer that can be used as a binder in formation of a functional layer, for example, without any specific limitations so long as at least the average circularity and volume-average particle diameter thereof are within any of the ranges set forth above.

Examples of monomer units that may be included in the particulate polymer include an aromatic vinyl monomer unit, a (meth)acrylic acid ester monomer unit, a fluorine atom-containing monomer unit, and so forth. Note that in the present disclosure, “(meth)acryl” is used to indicate “acryl” and/or “methacryl”. The particulate polymer preferably includes an aromatic vinyl monomer unit from a viewpoint of increasing close adherence of a functional layer and a substrate.

—Aromatic Vinyl Monomer Unit—

Examples of aromatic vinyl monomers that can form an aromatic vinyl monomer unit include, but are not specifically limited to, styrene, α-methylstyrene, styrene sulfonic acid, butoxystyrene, and vinylnaphthalene, of which, styrene is preferable.

One of these aromatic vinyl monomers may be used individually, or two or more of these aromatic vinyl monomers may be used in combination in a freely selected ratio.

The proportional content of an aromatic vinyl monomer unit in the particulate polymer when all monomer units in the particulate polymer are taken to be 100 mass % is preferably 30 mass % or more, and more preferably 60 mass % or more, and is preferably 95 mass % or less, more preferably 90 mass % or less, and even more preferably 89.9 mass % or less. When the proportional content of an aromatic vinyl monomer unit is not less than any of the lower limits set forth above, elasticity of the particulate polymer improves, strength of an obtained functional layer is ensured, and close adherence of the functional layer and a substrate can be increased. On the other hand, when the proportional content of an aromatic vinyl monomer unit is not more than any of the upper limits set forth above, flexibility of the particulate polymer increases, and film forming properties during drying of the composition for a functional layer improve. Consequently, close adherence of a functional layer and a substrate can be increased.

Note that the “proportional content” of each “monomer unit” referred to the present disclosure can be measured by a nuclear magnetic resonance (NMR) method such as ¹H-NMR.

—(Meth)Acrylic Acid Ester Monomer Unit—

Examples of (meth)acrylic acid ester monomers that can form a (meth)acrylic acid ester monomer unit include acrylic acid alkyl esters such as methyl acrylate, ethyl acrylate, n-propyl acrylate, isopropyl acrylate, butyl acrylate (n-butyl acrylate, t-butyl acrylate, etc.), pentyl acrylate, hexyl acrylate, heptyl acrylate, octyl acrylate (2-ethylhexyl acrylate, etc.), nonyl acrylate, decyl acrylate, lauryl acrylate, n-tetradecyl acrylate, and stearyl acrylate; and methacrylic acid alkyl esters such as methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, isopropyl methacrylate, butyl methacrylate (n-butyl methacrylate, t-butyl methacrylate, etc.), pentyl methacrylate, hexyl methacrylate, heptyl methacrylate, octyl methacrylate (2-ethylhexyl methacrylate, etc.), nonyl methacrylate, decyl methacrylate, lauryl methacrylate, n-tetradecyl methacrylate, and stearyl methacrylate. Of these (meth)acrylic acid ester monomers, n-butyl acrylate, 2-ethylhexyl acrylate, and methyl methacrylate are preferable, and 2-ethylhexyl acrylate is more preferable.

One of these (meth)acrylic acid ester monomers may be used individually, or two or more of these (meth)acrylic acid ester monomers may be used in combination in a freely selected ratio.

The proportional content of a (meth)acrylic acid ester monomer unit in the particulate polymer when all repeating units of the particulate polymer are taken to be 100 mass % is preferably 10 mass % or more, and is preferably 80 mass % or less, more preferably 75 mass % or less, and even more preferably 64.9 mass % or less. When the proportional content of a (meth)acrylic acid ester monomer unit is not less than the lower limit set forth above, excessive lowering of the glass transition of the particulate polymer can be avoided, and blocking resistance of an obtained functional layer can be improved. On the other hand, when the proportional content of a (meth)acrylic acid ester monomer unit is not more than any of the upper limits set forth above, good close adherence of a functional layer and a substrate can be achieved.

—Fluorine Atom-Containing Monomer Unit—

Examples of fluorine atom-containing monomers that can form a fluorine atom-containing monomer unit include, but are not specifically limited to, vinylidene fluoride, tetrafluoroethylene, hexafluoropropylene, chlorotrifluoroethylene, vinyl fluoride, and perfluoroalkyl vinyl ethers. Of these fluorine atom-containing monomers, vinylidene fluoride is preferable.

One of these fluorine atom-containing monomers may be used individually, or two or more of these fluorine atom-containing monomers may be used in combination in a freely selected ratio.

In a case in which the particulate polymer includes a fluorine atom-containing monomer unit, the particulate polymer is preferably a fluorine atom-containing polymer obtained using vinylidene fluoride as a fluorine atom-containing monomer from a viewpoint that better adhesiveness of a functional layer can be ensured. In particular, the fluorine atom-containing polymer is preferably (i) a homopolymer of vinylidene fluoride, (ii) a copolymer of vinylidene fluoride and another fluorine atom-containing monomer that is copolymerizable with vinylidene fluoride, or (iii) a copolymer of vinylidene fluoride, another fluorine atom-containing monomer that is copolymerizable with vinylidene fluoride, and a monomer that is copolymerizable with vinylidene fluoride and the other fluorine atom-containing monomer. Of fluorine atom-containing polymers, polyvinylidene fluoride (PVdF), polytetrafluoroethylene (PTFE), vinylidene fluoride-hexafluoropropylene copolymer (PVdF-HFP), polyvinyl fluoride, and a copolymer of tetrafluoroethylene and a perfluoroalkyl vinyl ether are preferable.

The particulate polymer may further include a cross-linkable monomer unit in addition to the monomer units described above. A cross-linkable monomer unit is a monomer that can form a cross-linked structure during polymerization or after polymerization through heating or irradiation with energy rays.

—Cross-Linkable Monomer Unit—

Examples of monomers that can form a cross-linkable monomer unit include polyfunctional monomers that include at least two groups displaying polymerization reactivity in the monomer. Examples of such polyfunctional monomers include divinyl compounds such as allyl methacrylate and divinylbenzene; di(meth)acrylic acid ester compounds such as diethylene glycol dimethacrylate, ethylene glycol dimethacrylate, diethylene glycol diacrylate, and 1,3-butylene glycol diacrylate; tri(meth)acrylic acid ester compounds such as trimethylolpropane trimethacrylate and trimethylolpropane triacrylate; and epoxy group-containing ethylenically unsaturated monomers such as allyl glycidyl ether and glycidyl methacrylate. Of these monomers, ethylene glycol dimethacrylate is preferable.

One of these cross-linkable monomers may be used individually, or two or more of these cross-linkable monomers may be used in combination in a freely selected ratio.

The proportional content of a cross-linkable monomer unit in the particulate polymer when the amount of all monomer units in the particulate polymer is taken to be 100 mass % is preferably 0.02 mass % or more, and more preferably 0.1 mass % or more, and is preferably 2 mass % or less, more preferably 1.5 mass % or less, and even more preferably 1 mass % or less. When the proportional content of a cross-linkable monomer unit is within any of the ranges set forth above, elution of the particulate polymer into electrolyte solution can be sufficiently inhibited.

—Other Monomer Units—

The particulate polymer may include other monomer units besides an aromatic vinyl monomer unit, a (meth)acrylic acid ester monomer unit, a fluorine atom-containing monomer unit, and a cross-linkable monomer unit. Examples of such other monomer units include, but are not specifically limited to, a nitrile group-containing monomer unit and an acid group-containing monomer unit, which is described further below in the “Binder” section.

—Nitrile Group-Containing Monomer Unit—

Examples of nitrile group-containing monomers that can form a nitrile group-containing monomer unit include α,β-ethylenically unsaturated nitrile monomers. Specifically, any α,β-ethylenically unsaturated compound that includes a nitrile group can be used as an α,β-ethylenically unsaturated nitrile monomer without any specific limitations. Examples include acrylonitrile; α-halogenoacrylonitriles such as α-chloroacrylonitrile and α-bromoacrylonitrile; and α-alkylacrylonitriles such as methacrylonitrile and α-ethylacrylonitrile.

One of these nitrile group-containing monomers may be used individually, or two or more of these nitrile group-containing monomers may be used in combination in a freely selected ratio.

The proportional content of a nitrile group-containing monomer unit in the particulate polymer when all repeating units in the particulate polymer are taken to be 100 mass % is preferably 3 mass % or more, more preferably 4 mass % or more, and even more preferably 6 mass % or more, and is preferably 30 mass % or less, more preferably 27 mass % or less, and even more preferably 25 mass % or less. When the proportional content of a nitrile group-containing monomer unit is not less than any of the lower limits set forth above, binding strength of the particulate polymer can be improved, and peel strength of a functional layer can be increased. On the other hand, when the proportional content of a nitrile group-containing monomer unit is not more than any of the upper limits set forth above, flexibility of the particulate polymer can be increased.

The proportional content of other monomer units in the particulate polymer, with the exception of a nitrile group-containing monomer unit, is preferably 0 mass % or more, and is preferably 10 mass % or less, more preferably 7 mass % or less, and even more preferably 5 mass % or less. When the proportional content of other monomer units is 10 mass % or less, reduction of stability of the composition for a functional layer can be inhibited.

The proportional content of the particulate polymer in the composition for a functional layer is preferably not less than 1 mass % and not more than 12 mass % relative to the total amount (100 mass %) of the particulate polymer, the binder, and the inorganic particles.

[Production of Particulate Polymer]

The particulate polymer can be produced through polymerization of a monomer composition that contains the monomers set forth above, carried out in an aqueous solvent such as water, for example. The proportion constituted by each monomer in the monomer composition is normally the same as the proportion constituted by each monomer unit in the particulate polymer.

The method of polymerization is not specifically limited and may, for example, be a method such as suspension polymerization, emulsion polymerization and aggregation, or pulverization. Of these methods, suspension polymerization or emulsion polymerization and aggregation is preferable from a viewpoint of ease of adjusting the particulate polymer to the specific average circularity prescribed in the present disclosure, and suspension polymerization is more preferable. The polymerization reaction may, for example, be a reaction such as radical polymerization or living radical polymerization.

[Other Compounding Agents]

Other compounding agents such as chain transfer agents, polymerization modifiers, polymerization reaction-delaying agents, reactive fluidizers, fillers, flame retardants, antioxidants, and colorants can be compounded in any amounts in the monomer composition used in production of the particulate polymer.

The following describes a method of producing the particulate polymer by suspension polymerization as one example.

[Production of Particulate Polymer by Suspension Polymerization]

(1) Production of Monomer Composition

First, monomers for forming the target particulate polymer and other compounding agents that are added as necessary are mixed in order to produce a monomer composition.

(2) Formation of Droplets

Next, the monomer composition is dispersed in water, a polymerization initiator is added, and then droplets of the monomer composition are formed. No specific limitations are placed on the method by which the droplets are formed. For example, the droplets can be formed through shear stirring of water containing the monomer composition using a disperser such as an emulsifying/dispersing device.

The polymerization initiator that is used may be an oil-soluble polymerization initiator such as t-butyl peroxy-2-ethylhexanoate or azobisisobutyronitrile, for example. Note that the polymerization initiator may be added after dispersion of the monomer composition in water but before formation of droplets, or may be added to the monomer composition before dispersion thereof in water.

Formation of the droplets of the monomer composition is preferably performed after a dispersion stabilizer has been added to the water from a viewpoint of stabilizing droplets of the monomer composition formed in the water. The dispersion stabilizer may be a metal hydroxide such as magnesium hydroxide, or may be sodium dodecylbenzenesulfonate, or the like, for example.

(3) Polymerization

Once droplets of the monomer composition have been formed, the water containing the formed droplets is heated to initiate polymerization and thereby form the particulate polymer in the water. The reaction temperature during polymerization is preferably not lower than 50° C. and not higher than 95° C. Moreover, the reaction time during polymerization is preferably not less than 1 hour and not more than 10 hours, and is preferably 8 hours or less, and more preferably 6 hours or less.

(4) Washing, Filtration, Dehydration, and Drying Steps

Once polymerization has ended, the water containing the particulate polymer can be subjected to washing, filtration, and drying by standard methods to obtain the particulate polymer.

The binder contained in the composition for a functional layer is used in order to inhibit components contained in a functional layer formed using the presently disclosed composition for a functional layer, such as the particulate polymer, from detaching from the functional layer.

The binder is not specifically limited and may be a known polymer that is water-insoluble and can be dispersed in a dispersion medium such as water. For example, the binder may be a binding resin such as a thermoplastic elastomer. The thermoplastic elastomer is preferably a conjugated diene polymer or an acrylic polymer, and is more preferably an acrylic polymer.

The term “conjugated diene polymer” refers to a polymer that includes a conjugated diene monomer unit. Specific examples of conjugated diene polymers include, but are not specifically limited to, copolymers including an aromatic vinyl monomer unit and an aliphatic conjugated diene monomer unit, such as styrene-butadiene copolymer (SBR), butadiene rubber (BR), acrylic rubber (NBR) (copolymer including an acrylonitrile unit and a butadiene unit), and hydrogenated products thereof.

The term “acrylic polymer” refers to a polymer that includes a (meth)acrylic acid ester monomer unit.

One of these binders may be used individually, or two or more of these binders may be used in combination in a freely selected ratio.

Examples of acrylic polymers that can preferably be used as the binder include, but are not specifically limited to, polymers that include a (meth)acrylic acid ester monomer unit and a cross-linkable monomer unit such as previously described and an acid group-containing monomer unit such as described below.

—Acid Group-Containing Monomer Unit—

Examples of acid group-containing monomers that can form an acid group-containing monomer unit include carboxy group-containing monomers, sulfo group-containing monomers, phosphate group-containing monomers, and hydroxy group-containing monomers.

Moreover, examples of carboxy group-containing monomers include monocarboxylic acids and dicarboxylic acids. Examples of monocarboxylic acids include acrylic acid, methacrylic acid, and crotonic acid. Examples of dicarboxylic acids include maleic acid, fumaric acid, and itaconic acid.

Examples of sulfo group-containing monomers include vinyl sulfonic acid, methyl vinyl sulfonic acid, (meth)allyl sulfonic acid, (meth)acrylic acid 2-sulfoethyl, 2-acrylamido-2-methylpropane sulfonic acid, and 3-allyloxy-2-hydroxypropane sulfonic acid.

Note that in the present specification, “(meth)allyl” is used to indicate “allyl” and/or “methallyl”, whereas “(meth)acryl” is used to indicate “acryl” and/or “methacryl”.

Examples of phosphate group-containing monomers include 2-(meth)acryloyloxyethyl phosphate, methyl-2-(meth)acryloyloxyethyl phosphate, and ethyl-(meth)acryloyloxyethyl phosphate. Note that in the present specification, “(meth)acryloyl” is used to indicate “acryloyl” and/or “methacryloyl”.

Examples of hydroxy group-containing monomers include 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, 2-hydroxyethyl methacrylate, and 2-hydroxypropyl methacrylate.

One of these acid group-containing monomers may be used individually, or two or more of these acid group-containing monomers may be used in combination in a freely selected ratio.

The proportion constituted by a (meth)acrylic acid ester monomer unit in the acrylic polymer is preferably 50 mass % or more, more preferably 55 mass % or more, and even more preferably 58 mass % or more, and is preferably 98 mass % or less, more preferably 97 mass % or less, and even more preferably 96 mass % or less. When the proportion constituted by a (meth)acrylic acid ester monomer unit is not less than any of the lower limits set forth above, peel strength of a functional layer can be further increased. Moreover, when the proportion constituted by a (meth)acrylic acid ester monomer unit is not more than any of the upper limits set forth above, electrochemical characteristics of an electrochemical device that includes a functional layer can be further enhanced.

The proportion constituted by a cross-linkable monomer unit in the acrylic polymer is preferably 0.1 mass % or more, and more preferably 1.0 mass % or more, and is preferably 3.0 mass % or less, and more preferably 2.5 mass % or less. When the proportion constituted by a cross-linkable monomer unit is not less than any of the lower limits set forth above, electrochemical characteristics of an electrochemical device that includes a functional layer can be further enhanced. Moreover, when the proportion constituted by a cross-linkable monomer unit is not more than any of the upper limits set forth above, peel strength of a functional layer can be even further increased.

The proportion constituted by an acid group-containing monomer unit in the acrylic polymer is preferably 0.1 mass % or more, more preferably 0.3 mass % or more, and even more preferably 0.5 mass % or more, and is preferably 20 mass % or less, more preferably 10 mass % or less, and even more preferably 5 mass % or less. When the proportion constituted by an acid group-containing monomer unit is not less than any of the lower limits set forth above, dispersibility of the binder in the composition for a functional layer and in a functional layer can be increased, and electrochemical characteristics of an electrochemical device that includes the functional layer can be sufficiently enhanced. Moreover, when the proportion constituted by an acid group-containing monomer unit is not more than any of the upper limits set forth above, residual water content of a functional layer can be reduced, and electrochemical characteristics of an electrochemical device can be sufficiently enhanced.

The acrylic polymer may include other monomer units. Examples of other monomers that can form other monomer units that can be included in the acrylic polymer include aliphatic conjugated diene monomers such as 1,3-butadiene, 2-methyl-1,3-butadiene, 2,3-dimethyl-1,3-butadiene, and 2-chloro-1,3-butadiene; aromatic vinyl monomers and nitrile group-containing monomers described in the “Chemical composition of particulate polymer” section; olefin monomers such as ethylene and propylene; halogen atom-containing monomers such as vinyl chloride and vinylidene chloride; vinyl ester monomers such as vinyl acetate, vinyl propionate, vinyl butyrate, and vinyl benzoate; vinyl ether monomers such as methyl vinyl ether, ethyl vinyl ether, and butyl vinyl ether; vinyl ketone monomers such as methyl vinyl ketone, ethyl vinyl ketone, butyl vinyl ketone, hexyl vinyl ketone, and isopropenyl vinyl ketone; and heterocycle-containing vinyl compound monomers such as N-vinylpyrrolidone, vinylpyridine, and vinylimidazole. Of these other monomers, acrylonitrile is preferable.

One of these other monomers may be used individually, or two or more of these other monomers may be used in combination in a freely selected ratio. The proportional content of other monomer units in the acrylic polymer may be adjusted as appropriate.

«Glass-Transition Temperature of Binder»

The glass-transition temperature (Tg) of the binder is preferably −100° C. or higher, more preferably −90° C. or higher, and even more preferably −80° C. or higher, and is preferably lower than 30° C., more preferably 20° C. or lower, and even more preferably 15° C. or lower. When the glass-transition temperature of the binder is not lower than any of the lower limits set forth above, adhesiveness and strength of the binder can be increased. On the other hand, when the glass-transition temperature of the binder is not higher than any of the upper limits set forth above, flexibility of a functional layer can be further increased.

«Volume-Average Particle Diameter of Binder»

The volume-average particle diameter of the binder is preferably 0.1 μm or more, and is preferably 0.4 μm or less. When the volume-average particle diameter of the binder is not less than the lower limit set forth above, reduction of ion conductivity in a functional layer can be further inhibited, and electrochemical characteristics (particularly output characteristics) of an electrochemical device can be improved. On the other hand, when the volume-average particle diameter of the binder is not more than the upper limit set forth above, peel strength of a functional layer can be sufficiently increased.

The volume-average particle diameter of the binder can be measured by a method described in the EXAMPLES section of the present specification.

[Content of Binder]

The content of the binder in a functional layer per 100 parts by mass, in total, of the inorganic particles and the particulate polymer is preferably 0.1 parts by mass or more, more preferably 0.2 parts by mass or more, and even more preferably 0.5 parts by mass or more, and is preferably 20 parts by mass or less, more preferably 15 parts by mass or less, and even more preferably 10 parts by mass or less. When the content of the binder in a functional layer is not less than any of the lower limits set forth above, detachment of the particulate polymer from the functional layer can be sufficiently prevented, and peel strength of the functional layer can be sufficiently increased. On the other hand, when the content of the binder in a functional layer is not more than any of the upper limits set forth above, reduction of ion conductivity of the functional layer can be inhibited, and deterioration of electrochemical characteristics of an electrochemical device can be inhibited.

The binder can be produced through polymerization of a monomer composition that contains the monomers set forth above, carried out in an aqueous solvent such as water, for example, but is not specifically limited to being produced in this manner. The proportion constituted by each monomer in the monomer composition is normally the same as the proportion constituted by each monomer unit in the binder.

The polymerization method and the polymerization reaction are not specifically limited, and any of the polymerization methods and polymerization reactions given as examples in relation to the polymerization method of the particulate polymer described above can be used, for example.

The form of the binder may be a particulate form or a non-particulate form, but is preferably a particulate form from a viewpoint of good inhibition of detachment of components contained in a functional layer.

The inorganic particles contained in the composition for a functional layer can normally increase the heat resistance of a functional layer. The material of the inorganic particles is preferably an electrochemically stable material that is stably present in the environment of use of an electrochemical device. Examples of preferable materials of the inorganic particles from such viewpoints include particles of oxides such as aluminum oxide (alumina), hydrous aluminum oxide (boehmite (AlOOH)), gibbsite (Al(OH)₃), silicon oxide, magnesium oxide (magnesia), magnesium hydroxide, calcium oxide, titanium oxide (titania), barium titanate (BaTiO₃), zirconium oxide (ZrO), and alumina-silica complex oxide; particles of nitrides such as aluminum nitride and boron nitride; particles of covalently bonded crystals such as silicon and diamond; particles of sparingly soluble ionic crystals such as barium sulfate, calcium fluoride, and barium fluoride; and fine particles of clays such as talc and montmorillonite. Of these materials, aluminum oxide, hydrous aluminum oxide (boehmite), titanium oxide, and barium sulfate are more preferable, and aluminum oxide is even more preferable. These particles may be subjected to element substitution, surface treatment, solid solution treatment, or the like as necessary.

One of these types of inorganic particles may be used individually, or two or more of these types of inorganic particles may be used in combination in a freely selected ratio.

<Volume-Average Particle Diameter of Inorganic Particles>

The volume-average particle diameter (D50) of the inorganic particles is preferably 0.1 μm or more, more preferably 0.2 μm or more, and even more preferably 0.3 μm or more, and is preferably 1 μm or less, more preferably 0.9 μm or less, and even more preferably 0.8 μm or less. When the volume-average particle diameter of the inorganic particles is not less than any of the lower limits set forth above, the inorganic particles are densely packed in a functional layer. Consequently, reduction of ion conductivity of the functional layer can be inhibited, and electrochemical characteristics (particularly output characteristics) of an electrochemical device can be improved. Moreover, when the volume-average particle diameter of the inorganic particles is not more than any of the upper limits set forth above, a functional layer can be caused to display excellent heat resistance even when the thickness thereof is reduced, and thus the capacity of an electrochemical device can be increased.

The mixing ratio of the inorganic particles and the particulate polymer in the composition for a functional layer, as a volume ratio (inorganic particles:particulate polymer), is preferably 95:5 to 55:45, more preferably 80:20 to 55:45, even more preferably 75:25 to 60:40, and particularly preferably 70:30 to 65:35. When the mixing ratio of the inorganic particles and the particulate polymer, as a volume ratio, is within any of the ranges set forth above, a better balance of heat resistance and adhesiveness of a functional layer is obtained.

Moreover, the mixing ratio of the inorganic particles and the particulate polymer in the composition for a functional layer, as a mass ratio (inorganic particles:particulate polymer), is preferably 49:51 to 99:1, more preferably 58:42 to 94:6, and even more preferably 64:39 to 91:9. When the mixing ratio of the inorganic particles and the particulate polymer, as a mass ratio, is within any of the ranges set forth above, a better balance of heat resistance and adhesiveness of a functional layer is obtained.

The composition for a functional layer may contain any other components besides the components described above. These other components are not specifically limited so long as they do not affect electrochemical reactions in an electrochemical device, and examples thereof include known additives such as dispersants, viscosity modifiers, and wetting agents. One of these other components may be used individually, or two or more of these other components may be used in combination.

No specific limitations are placed on the method by which the composition for a functional layer is produced. For example, the composition for a functional layer can be produced by mixing the above-described particulate polymer, binder, inorganic particles, water serving as a dispersion medium, and other components that are used as necessary. Note that in a case in which the particulate polymer or the binder is produced through polymerization of a monomer composition in an aqueous solvent, the particulate polymer or binder may be mixed with other components while still in the state of a water dispersion. Moreover, in a case in which the particulate polymer or the binder is mixed in the state of a water dispersion, water in the water dispersion may be used as the dispersion medium.

Although no specific limitations are placed on the mixing method of these components, the mixing is preferably performed using a disperser as a mixing device in order to efficiently disperse the components. The disperser is preferably a device that can homogeneously disperse and mix the components. Examples of dispersers that can be used include a ball mill, a sand mill, a pigment disperser, a grinding machine, an ultrasonic disperser, a homogenizer, and a planetary mixer.

(Functional Layer for Electrochemical Device)

The functional layer for an electrochemical device can be formed on a suitable substrate, for example, using the composition for a functional layer set forth above. The functional layer contains at least the above-described particulate polymer, binder, inorganic particles, and other components that are used as necessary. Note that since components contained in the functional layer are components that were contained in the composition for a functional layer set forth above, the preferred ratio of these components in the functional layer is also the same as the preferred ratio of the components in the composition for a functional layer.

Examples of methods by which the functional layer may be formed on the substrate using the composition for a functional layer include, but are not specifically limited to:

(1) a method in which the composition for a functional layer is applied onto the surface of the substrate and is then dried;

(2) a method in which the substrate is immersed in the composition for a functional layer and is then dried; and

(3) a method in which the composition for a functional layer is applied onto a releasable substrate and is dried to form a functional layer that is then transferred onto the surface of the substrate.

Note that the functional layer may be formed on only one side of the substrate or may be formed on both sides of the substrate.

Of these methods, method (1) is preferable in terms of ease of control of thickness of the functional layer. Method (1) may, for example, include a step of applying the composition for a functional layer onto the substrate (application step) and a step of drying the composition for a functional layer that has been applied onto the substrate to form the functional layer (functional layer formation step).

[Application Step]

Examples of methods by which the composition for a functional layer can be applied onto the substrate in the application step include, but are not specifically limited to, doctor blading, reverse roll coating, direct roll coating, gravure coating, extrusion coating, and brush coating.

[Functional Layer Formation Step]

The composition for a functional layer on the substrate may be dried by any commonly known method in the functional layer formation step, without any specific limitations. For example, the drying method may be drying by warm, hot, or low-humidity air; drying in a vacuum; or drying by irradiation with infrared light, electron beams, or the like. Although no specific limitations are placed on the drying conditions, the drying temperature is preferably 50° C. to 150° C., and the drying time is preferably 1 minute to 30 minutes.

The functional layer formed on the substrate can suitably be used as a single layer that simultaneously displays the function of a heat-resistant layer that increases heat resistance of the substrate and the function of an adhesive layer that strongly adheres members together.

The substrate including the functional layer formed using the composition for a functional layer as described above (hereinafter, also referred to as a “functional layer-equipped substrate”) is highly producible because it can be produced with shortened workload and time compared to a conventional substrate that includes a heat-resistant layer and an adhesive layer.

In the functional layer formed using the composition for a functional layer, a plurality of inorganic particles are normally disposed in a stacked manner in a thickness direction of the functional layer. The thickness of a layer (hereinafter, also referred to as an “inorganic particle layer”) where the inorganic particles are stacked in a thickness direction of the functional layer is preferably 0.5 μm or more, more preferably 0.8 μm or more, and even more preferably 1 μm or more, and is preferably 6 μm or less, more preferably 5 μm or less, and even more preferably 4 μm or less. When the thickness of the inorganic particle layer is not less than any of the lower limits set forth above, the functional layer has extremely good heat resistance. On the other hand, when the thickness of the inorganic particle layer is not more than any of the upper limits set forth above, ion diffusivity of the functional layer can be ensured, and electrochemical characteristics (output characteristics) of an electrochemical device can be sufficiently enhanced.

[Ratio of Volume-Average Particle Diameter of Particulate Polymer Relative to Thickness of Inorganic Particle Layer]

The ratio of the volume-average particle diameter of the particulate polymer relative to the thickness of the inorganic particle layer (volume-average particle diameter of particulate polymer/thickness of inorganic particle layer) is preferably 0.75 or more, more preferably 1.0 or more, and even more preferably 1.5 or more, and is preferably 5.0 or less, and more preferably 3.0 or less. When the ratio of the volume-average particle diameter of the particulate polymer relative to the thickness of the inorganic particle layer is not less than any of the lower limits set forth above, the particulate polymer has an even higher tendency to protrude relative to the surface of the inorganic particles at a thickness direction surface of the functional layer, and thus even better adhesiveness can be displayed. Moreover, when the ratio of the volume-average particle diameter of the particulate polymer relative to the thickness of the inorganic particle layer is not less than any of the lower limits set forth above, detachment of the particulate polymer during application of the composition for a functional layer onto the substrate can be further inhibited, and an even more uniform functional layer can be formed.

[Maximum Thickness of Functional Layer]

The maximum thickness of the functional layer formed on the substrate is preferably 1.0 μm or more, more preferably 1.5 μm or more, even more preferably 2.0 μm or more, particularly preferably 2.5 μm or more, and most preferably 5.0 μm or more, and is preferably 10.0 μm or less, more preferably 9.0 μm or less, and even more preferably 8.0 μm or less. In other words, in the formed functional layer, it is preferable that the previously described inorganic particle layer and the particulate polymer do not overlap in a thickness direction of the functional layer and that the thickness of the functional layer is equal to the volume-average particle diameter of the particulate polymer contained in the functional layer. Moreover, when the maximum thickness of the functional layer is not less than any of the lower limits set forth above, the functional layer has extremely good heat resistance. On the other hand, when the maximum thickness of the functional layer is not more than any of the upper limits set forth above, ion diffusivity of the functional layer can be ensured, and electrochemical characteristics (output characteristics) of an electrochemical device can be more sufficiently enhanced.

The “maximum thickness of the functional layer” referred to in the present specification can be measured using a field emission scanning electron microscope (FE-SEM), for example.

(Electrochemical Device)

The presently disclosed electrochemical device including a functional layer includes at least the presently disclosed functional layer, and, accordingly, may include any constituent elements other than the presently disclosed functional layer so long as they do not cause significant loss of the effects disclosed herein.

The presently disclosed electrochemical device may be a lithium ion secondary battery or an electric double-layer capacitor, for example, but is not specifically limited thereto, and is preferably a lithium ion secondary battery.

The following describes a lithium ion secondary battery as one example of the presently disclosed electrochemical device. A lithium ion secondary battery according to the present disclosure includes the presently disclosed functional layer set forth above. More specifically, the lithium ion secondary battery includes a positive electrode, a negative electrode, a separator having the presently disclosed functional layer formed on a separator substrate (functional layer-equipped separator), and an electrolyte solution. Note that the functional layer may be formed on only one side of the separator substrate or may be formed on both sides of the separator substrate.

In the lithium ion secondary battery according to the present disclosure, the functional layer causes strong adhesion of the positive electrode and the separator substrate and/or of the negative electrode and the separator substrate in the electrolyte solution. Consequently, widening of the distance between electrode plates of the electrodes associated with repeated charging and discharging is inhibited, and good battery characteristics such as cycle characteristics are obtained. Moreover, the functional layer improves the heat resistance of the separator substrate in the lithium ion secondary battery.

Furthermore, the time required to produce the separator can be shortened and the lithium ion secondary battery can be produced with high productivity compared to a situation in which a conventional separator including a heat-resistant layer and an adhesive layer is used.

Note that the positive electrode, negative electrode, and electrolyte solution mentioned above can be any known positive electrode, negative electrode, and electrolyte solution that are used in lithium ion secondary batteries.

Specifically, the electrodes (positive electrode and negative electrode) can each be an electrode that is obtained by forming an electrode mixed material layer on a current collector. The current collector may be formed of a metal material such as iron, copper, aluminum, nickel, stainless steel, titanium, tantalum, gold, or platinum. Of these metal materials, a current collector formed of copper is preferable as a current collector for the negative electrode. Moreover, a current collector formed of aluminum is preferable as a current collector for the positive electrode. The electrode mixed material layer can be a layer including an electrode active material and a binder.

The functional layer-equipped separator can be produced by, for example, forming a functional layer on a separator substrate using any of the methods of forming a functional layer previously described in the “Functional layer for electrochemical device” section.

The separator substrate is not specifically limited and can be any of those described in JP2012-204303A, for example. Of these separator substrates, a microporous membrane formed of polyolefinic resin (polyethylene, polypropylene, polybutene, or polyvinyl chloride) is preferred since such a membrane can reduce the total thickness of the functional layer-equipped separator, which increases the ratio of electrode active material in the lithium ion secondary battery, and consequently increases the volumetric capacity.

The electrolyte solution is normally an organic electrolyte solution obtained by dissolving a supporting electrolyte in an organic solvent. The supporting electrolyte may, for example, be a lithium salt in the case of a lithium ion secondary battery. Examples of lithium salts that can be used include LiPF₆, LiAsF₆, LiBF₄, LiSbF₆, LiAlCl₄, LiClO₄, CF₃SO₃Li, C₄F₉SO₃Li, CF₃COOLi, (CF₃CO)₂NLi, (CF₃SO₂)₂NLi, and (C₂F₅SO₂)NLi. Of these lithium salts, LiPF₆, LiClO₄, and CF₃SO₃Li are preferable in terms of readily dissolving in solvents and displaying a high degree of dissociation. One electrolyte may be used individually, or two or more electrolytes may be used in combination. In general, lithium ion conductivity tends to increase when a supporting electrolyte having a high degree of dissociation is used. Therefore, lithium ion conductivity can be adjusted through the type of supporting electrolyte that is used.

The organic solvent used in the electrolyte solution is not specifically limited so long as the supporting electrolyte can dissolve therein. Examples of organic solvents that can suitably be used in a lithium ion secondary battery, for example, include carbonates such as dimethyl carbonate (DMC), ethylene carbonate (EC), diethyl carbonate (DEC), propylene carbonate (PC), butylene carbonate (BC), methyl ethyl carbonate (ethyl methyl carbonate (EMC)), and vinylene carbonate; esters such as γ-butyrolactone and methyl formate; ethers such as 1,2-dimethoxyethane and tetrahydrofuran; and sulfur-containing compounds such as sulfolane and dimethyl sulfoxide.

Furthermore, a mixture of these organic solvents may be used. Of these organic solvents, carbonates are preferable due to having high permittivity and a wide stable potential region. In general, lithium ion conductivity tends to increase when an organic solvent having a low viscosity is used. Therefore, lithium ion conductivity can be adjusted through the type of organic solvent that is used.

The concentration of the electrolyte in the electrolyte solution may be adjusted as appropriate. Furthermore, known additives may be added to the electrolyte solution.

The lithium ion secondary battery that is an example of the presently disclosed electrochemical device can be produced by, for example, overlapping the previously described positive electrode and negative electrode with the functional layer-equipped separator in-between, performing rolling, folding, or the like of the resultant laminate as necessary, placing the laminate in a battery container, injecting the electrolyte solution into the battery container, and sealing the battery container. In order to prevent pressure increase inside the battery and occurrence of overcharging or overdischarging, an expanded metal, an overcurrent preventing device such as a fuse or a PTC device, or a lead plate may be placed in the battery container as necessary. The shape of the battery may be a coin type, a button type, a sheet type, a cylinder type, a prismatic type, a flat type, or the like.

EXAMPLES

The following provides a more specific description of the present disclosure based on examples. However, the present disclosure is not limited to the following examples. In the following description, “%” and “parts” used in expressing quantities are by mass, unless otherwise specified.

Moreover, in the case of a polymer that is produced through copolymerization of a plurality of types of monomers, the proportion constituted in the polymer by a structural unit formed through polymerization of a given monomer is normally, unless otherwise specified, the same as the ratio (charging ratio) of the given monomer among all monomers used in polymerization for forming the polymer.

In the examples and comparative examples, methods described below were used for measurement of glass-transition temperature, volume-average particle diameter, particle diameter distribution, degree of swelling in electrolyte solution, average circularity, thickness of an inorganic particle layer, and mixing ratio of inorganic particles and a particulate polymer.

Moreover, methods described below were used for measurement and evaluation of process adhesiveness, blocking resistance of a functional layer, heat resistance of a functional layer, electrolyte solution injectability, cycle characteristics of a secondary battery, output characteristics of a secondary battery, and dusting resistance of a functional layer.

<Glass-Transition Temperature>

Particulate polymers and binders produced in the examples and comparative examples were each used as a measurement sample. After weighing 10 mg of the measurement sample into an aluminum pan, a differential scanning calorimeter (EXSTAR DSC6220 produced by SIT NanoTechnology Inc.) was used to perform measurement under conditions prescribed by JIS Z 8703 with a measurement temperature range of −100° C. to 500° C. and a heating rate of 10° C./min, and using an empty aluminum pan as a reference so as to obtain a differential scanning calorimetry (DSC) curve. In the heating process, an intersection point of a baseline directly before a heat absorption peak on the DSC curve at which a derivative signal (DDSC) reached 0.05 mW/min/mg or more and a tangent to the DSC curve at a first inflection point to appear after the heat absorption peak was determined as the glass-transition temperature (° C.).

<Volume-Average Particle Diameter>

«Volume-Average Particle Diameter and Particle Diameter Distribution of Particulate Polymer»

A particulate polymer produced in each example or comparative example was used as a measurement sample. An amount equivalent to 0.1 g of the measurement sample was weighed and taken into a beaker, and then 0.1 mL of alkylbenzenesulfonic acid aqueous solution (DRIWEL produced by FUJIFILM Corporation) was added as a dispersant. In addition, 10 mL to 30 mL of a diluent (ISOTON II produced by Beckman Coulter, Inc.) was added into the beaker, and 3 minutes of dispersing was performed using a 20 W (watt) ultrasonic disperser. A particle diameter meter (Multisizer produced by Beckman Coulter, Inc.) was subsequently used to measure the volume-average particle diameter (Dv) of the measurement sample under conditions of an aperture diameter of 20 μm, a medium of ISOTON II, and a measured particle count of 100,000 particles. The number-average particle diameter (Dn) of the particulate polymer was also measured, and the particle diameter distribution (Dv/Dn) of the particulate polymer was calculated.

«Volume-Average Particle Diameter of Binder»

The volume-average particle diameter of a binder produced in each example was measured by laser diffraction. Specifically, a produced water dispersion (adjusted to a solid content concentration of 0.1 mass %) containing the binder was used as a sample. In a particle diameter distribution (by volume) measured using a laser diffraction particle diameter distribution analyzer (LS-230 produced by Beckman Coulter, Inc.), the particle diameter D50 at which cumulative volume calculated from a small diameter end of the distribution reached 50% was taken to be the volume-average particle diameter.

A water dispersion containing a particulate polymer produced in each example or comparative example was loaded into a petri dish made of polytetrafluoroethylene and was dried under conditions of 48 hours at 25° C. to produce a powder. Approximately 0.2 g of the obtained powder was pressed at 200° C. and 5 MPa for 2 minutes to obtain a film. The obtained film was cut to a 1 cm square to obtain a test specimen. The mass W0 of this test specimen was measured.

The test specimen described above was then immersed in electrolyte solution at 60° C. for 72 hours. Thereafter, the test specimen was removed from the electrolyte solution, electrolyte solution on the surface of the test specimen was wiped off, and the mass W1 of the test specimen after immersion was measured.

The measured masses W0 and W1 were used to calculate the degree of swelling in electrolyte solution S (factor) by S=W1/W0.

Note that the electrolyte solution was a solution obtained by dissolving LiPF₆with a concentration of 1 mol/L as a supporting electrolyte in a mixed solvent of ethylene carbonate (EC), diethyl carbonate (DEC), and vinylene carbonate (VC) (volume ratio: EC/DEC/VC=68.5/30/1.5).

A particulate polymer produced in each example or comparative example was used as a measurement sample. A vessel was charged with 10 mL of deionized water in advance, 0.02 g of a surfactant (alkylbenzenesulfonic acid) was then added thereto as a dispersant, 0.02 g of the measurement sample was further added, and 3 minutes of dispersing treatment was performed at 60 W (watt) using an ultrasonic disperser. The measurement sample concentration during measurement was adjusted to 3,000 particles/4 to 10,000 particles/4, and measurement was performed for 1,000 to 10,000 particles of the measurement sample having a circle-equivalent diameter of 0.4 μm or more using a flow particle image analyzer (FPIA-3000 produced by Sysmex Corporation). Note that the circularity is expressed by the following formula (I), and the average circularity is obtained by taking the average thereof.

Circularity=Perimeter of circle of equivalent area to projected area of particulate polymer/Perimeter of projected image of particulate polymer (I)

A cross-section of a functional layer-equipped separator was observed using a field emission scanning electron microscope (FE-SEM), and the thickness of an inorganic particle layer was calculated from an obtained image. Note that the thickness of the inorganic particle layer was taken to be the distance in a vertical direction from a surface of the separator at a side where the functional layer was formed to inorganic particles forming a surface of the functional layer.

A mixing ratio (volume ratio) of inorganic particles (alumina) and a particulate polymer was determined from the charged amounts of the inorganic particles (alumina) and the particulate polymer in production of a slurry composition. Note that the density of alumina was taken to be 4 g/cm³in this calculation.

A positive electrode and a functional layer-equipped separator produced in each example or comparative example were each cut out as 10 mm in width and 50 mm in length. The positive electrode and the functional layer-equipped separator were stacked and were pressed by roll pressing under conditions of a temperature of 70° C., a load of 10 kN/m, and a pressing speed of 30 m/min to obtain a joined product in which the positive electrode and the functional layer-equipped separator were joined.

The obtained joined product was placed with a surface at the current collector-side of the positive electrode facing downward, and cellophane tape was affixed to the surface of the positive electrode. Tape prescribed by JIS Z1522 was used as the cellophane tape. The cellophane tape was secured to a horizontal test stage in advance. Thereafter, the stress when the functional layer-equipped separator was peeled off by pulling one end of the functional layer-equipped separator vertically upward at a pulling speed of 50 mm/min was measured.

The same operations as when using the positive electrode were performed for a negative electrode produced in each example or comparative example in order to measure the stress.

The measurement of stress described above was performed 3 times for a joined product of a positive electrode and a functional layer-equipped separator and 3 times for a joined product of a negative electrode and a functional layer-equipped separator (i.e., 6 times in total), an average value of the stresses was determined, and the obtained average value was taken to be the peel strength (N/m).

The calculated peel strength was used to evaluate the process adhesiveness of the electrodes and the functional layer-equipped separator by the following standard. A larger peel strength indicates higher process adhesiveness (adhesiveness of battery members in a production process of a battery).

A: Peel strength of 3 N/m or more

B: Peel strength of not less than 2 N/m and less than 3 N/m

C: Peel strength of not less than 1 N/m and less than 2 N/m

D: Peel strength of less than 1 N/m

Two pieces having a size of 4 cm in width by 4 cm in length were cut out from a functional layer-equipped separator produced in each example or comparative example to obtain test specimens. The two obtained test specimens were overlapped with the functional layer-sides thereof facing each other and were then pressed at a temperature of 40° C. and a pressure of 5 MPa for 2 minutes to obtain a pressed product. One end of the pressed product that had been obtained was fixed in place, the stress when the other end of the pressed product was pulled vertically upward at a pulling speed of 50 mm/min to cause peeling was measured, and the obtained stress was taken to be the blocking strength. The blocking strength was evaluated by the following standard. A smaller blocking strength indicates that the functional layer inhibits blocking well, and thus indicates that the functional layer has high blocking resistance.

A: Blocking strength of less than 4 N/m

B: Blocking strength of not less than 4 N/m and less than 6 N/m

C: Blocking strength of not less than 6 N/m and less than 8 N/m

D: Blocking strength of not less than 8 N/m and less than 10 N/m

E: Blocking strength of 10 N/m or more

A square of 12 cm in width by 12 cm in length was cut out from a functional layer-equipped separator produced in each example or comparative example. A square having a side length of 10 cm was then drawn in an inner part of the obtained square piece to obtain a test specimen. The test specimen was placed in a 150° C. thermostatic tank and was left in the thermostatic tank for 1 hour. Thereafter, the area change of the square drawn in the inner part of the test specimen (={(area of square before being left—area of square after being left)/area of square before being left}×100%) was determined as the heat shrinkage rate and was evaluated by the following standard. A smaller heat shrinkage rate indicates that the functional layer-equipped separator has better heat resistance.

A: Heat shrinkage rate of less than 3%

B: Heat shrinkage rate of not less than 3% and less than 5%

C: Heat shrinkage rate of not less than 5% and less than 10%

D: Heat shrinkage rate of 10% or more

Electrolyte solution was injected into a pre-electrolyte solution injection lithium ion secondary battery produced in each example or comparative example. The inside of the lithium ion secondary battery was depressurized to −100 kPa, and this state was maintained for 1 minute. Thereafter, heat sealing was performed. Once 10 minutes had passed, an electrode (positive electrode) was dismantled and the impregnation state of electrolyte solution in the electrode was visually checked. An evaluation was made by the following standard. A larger section impregnated with electrolyte solution in the electrode indicates higher electrolyte solution injectability.

A: Electrolyte solution impregnates entire face of electrode

B: Section of less than 1 cm²remains unimpregnated with electrolyte solution in electrode (excluding when the entire face is impregnated)

C: Section of 1 cm²or more remains unimpregnated with electrolyte solution in electrode

A lithium ion secondary battery produced in each example or comparative example was left at rest at a temperature of 25° C. for 5 hours.

Next, the lithium ion secondary battery was charged to a cell voltage of 3.65 V by a 0.2 C constant-current method at a temperature of 25° C., and was then subjected to 12 hours of aging at a temperature of 60° C. The lithium ion secondary battery was subsequently discharged to a cell voltage of 3.00 V by a 0.2 C constant-current method at a temperature of 25° C. Thereafter, CC-CV charging (upper limit cell voltage 4.20 V) was performed by a 0.2 C constant-current method and CC discharging to 3.00 V was performed by a 0.2 C constant-current method. This charging and discharging at 0.2 C was repeated 3 times.

Thereafter, the lithium ion secondary battery was subjected to 100 cycles of a charge/discharge operation with a cell voltage of 4.20 V to 3.00 V and a charge/discharge rate of 1.0 C in an environment having a temperature of 25° C. The discharge capacity of the 1s^tcycle was defined as X1 and the discharge capacity of the 100^thcycle was defined as X2.

A capacity maintenance rate ΔC′ (=(X2/X1)×100(%)) was determined using the discharge capacity X1 and the discharge capacity X2 and was evaluated by the following standard. A larger value for the capacity maintenance rate ΔC′ indicates that the secondary battery has better cycle characteristics.

A: Capacity maintenance rate ΔC′ of 93% or more

B: Capacity maintenance rate ΔC′ of not less than 90% and less than 93%

C: Capacity maintenance rate ΔC′ of not less than 87% and less than 90%

D: Capacity maintenance rate ΔC′ of less than 87%

A lithium ion secondary battery produced in each example or comparative example was constant-current constant-voltage (CCCV) charged to 4.3 V in an atmosphere having a temperature of 25° C. for cell preparation. The prepared cell was discharged to 3.0 V by 0.2 C and 1.5 C constant-current methods to determine electric capacities for these methods. A discharge capacity maintenance rate expressed by the ratio of the electric capacities (=(electric capacity at 1.5 C/electric capacity at 0.2 C)×100(%)) was determined. This measurement was performed for five lithium ion secondary battery cells. An average value for the discharge capacity maintenance rates of these cells was determined and was evaluated by the following standard. A larger average value for the discharge capacity maintenance rates indicates that the secondary battery has better output characteristics.

A: Discharge capacity maintenance rate average value of 90% or more

B: Discharge capacity maintenance rate average value of not less than 85% and less than 90%

C: Discharge capacity maintenance rate average value of not less than 75% and less than 85%

D: Discharge capacity maintenance rate average value of less than 75%

A functional layer-equipped separator produced in each example or comparative example was cut out as 5 cm×5 cm, and the mass (a) of the obtained functional layer-equipped separator piece was measured. Next, the functional layer-equipped separator piece was placed inside a 500 mL glass bottle, and a shaking machine was used to perform 3 hours of shaking at a rotation speed of 300 rpm. The mass (b) of the functional layer-equipped separator piece after this shaking was measured, and a dusting rate was calculated in accordance with the following formula (II).

Dusting rate (mass %)=[(a−b)/a]×100 (II)

Dusting resistance of the functional layer was evaluated by the following standard. A smaller value for the dusting rate indicates that constituent components of the functional layer, such as a particulate polymer, do not detach from the functional layer and that the functional layer has better dusting resistance.

A: Dusting rate of less than 1 mass %

B: Dusting rate of not less than 1 mass % and less than 3 mass %

C: Dusting rate of not less than 3 mass % and less than 5 mass %

D: Dusting rate of 5 mass % or more

Example 1
<Production of Particulate Polymer (A)>
[Production of Monomer Composition (A)]

A monomer composition (A) was produced by mixing 81.9 parts of styrene as an aromatic vinyl monomer, 18 parts of 2-ethylhexyl acrylate as a (meth)acrylic acid ester monomer, and 0.1 parts of ethylene glycol dimethacrylate as a cross-linkable monomer.

[Production of Metal Hydroxide]

A colloidal dispersion liquid (A) containing magnesium hydroxide as a metal hydroxide was produced through gradual addition under stirring of an aqueous solution (A2) of 5.6 parts of sodium hydroxide dissolved in 50 parts of deionized water to an aqueous solution (A1) of 8 parts of magnesium chloride dissolved in 200 parts of deionized water.

[Suspension Polymerization]

A particulate polymer (A) was produced by suspension polymerization. Specifically, the monomer composition (A) obtained as described above was added to the colloidal dispersion liquid (A) containing magnesium hydroxide, further stirring thereof was performed, and then 2.0 parts of t-butyl peroxy-2-ethylhexanoate (PERBUTYL® O (PERBUTYL is a registered trademark in Japan, other countries, or both) produced by NOF Corporation) was added as a polymerization initiator to obtain a mixed liquid. The obtained mixed liquid was subjected to 1 minute of high-shear stirring at a rotation speed of 15,000 rpm using an inline emulsifying/dispersing device (CAVITRON produced by Pacific Machinery & Engineering Co., Ltd.) to form droplets of the monomer composition (A) in the colloidal dispersion liquid (A) containing magnesium hydroxide.

The magnesium hydroxide-containing colloidal dispersion liquid (A) in which droplets of the monomer composition (A) had been formed was loaded into a reactor, was heated to 90° C., and a polymerization reaction was performed for 5 hours to yield a water dispersion containing a particulate polymer (A).

The water dispersion containing the particulate polymer (A) was used to measure the volume-average particle diameter, particle diameter distribution, and degree of swelling in electrolyte solution of the particulate polymer (A). The results are shown in Table 1.

Sulfuric acid was added dropwise to the water dispersion containing the particulate polymer (A) under stirring at room temperature (25° C.), and acid washing was performed until the pH reached 6.5 or lower. Next, separation was performed by filtration, 500 parts of deionized water was added to the obtained solid content to once again form a slurry, and water washing treatment (washing, filtration, and dehydration) was repeated a number of times. Separation was subsequently performed by filtration, and the obtained solid content was loaded into a vessel of a dryer and was dried at 40° C. for 48 hours to obtain dried particulate polymer (A).

The glass-transition temperature and average circularity of the obtained particulate polymer (A) were measured. The results are shown in Table 1.

A reactor including a stirrer was charged with 70 parts of deionized water, 0.15 parts of sodium lauryl sulfate (EMAL® 2F (EMAL is a registered trademark in Japan, other countries, or both) produced by Kao Corporation) as an emulsifier, and 0.5 parts of ammonium persulfate as a polymerization initiator, the gas phase was purged with nitrogen gas, and heating was performed to 60° C.

Meanwhile, a monomer composition (α) was produced in a separate vessel by mixing 50 parts of deionized water, 0.5 parts of sodium dodecylbenzenesulfonate as a dispersion stabilizer, 94 parts of n-butyl acrylate as a (meth)acrylic acid ester monomer, 2 parts of methacrylic acid as an acid group-containing monomer, 2 parts of acrylonitrile as a nitrile group-containing monomer, and 1 part of allyl methacrylate and 1 part of allyl glycidyl ether as cross-linkable monomers.

The obtained monomer composition (α) was continuously added to the aforementioned reactor including a stirrer over 4 hours to carry out polymerization. The reaction was carried out at 60° C. during this addition. Once the addition was complete, a further 3 hours of stirring was performed at 70° C., and then the reaction was ended to yield a water dispersion containing a particulate binder (α) as an acrylic polymer. The obtained particulate binder (α) had a volume-average particle diameter of 0.25 μm and a glass-transition temperature of −40° C.

After adding 0.5 parts of polyacrylic acid as a dispersant to 100 parts of alumina (AKP3000 produced by Sumitomo Chemical Co., Ltd.; volume-average particle diameter: 0.7 μm) as inorganic particles, 6 parts in terms of solid content of the water dispersion containing the binder (α) and 1.5 parts of carboxymethyl cellulose as a thickener were further added, the solid content concentration was adjusted to 55% through addition of deionized water, and mixing was performed using a ball mill to obtain a pre-mixing slurry.

A mixed liquid obtained by adding 0.2 parts of sodium dodecylbenzenesulfonate (NEOPELEX G-15 produced by Kao Corporation) as a surfactant to 100 parts of the particulate polymer (A) and performing mixing such that the solid content concentration was 40% was added to the pre-mixing slurry obtained as described above. Deionized water was added to adjust the solid content concentration to 40% and thereby yield a slurry composition (composition for a functional layer) in which the mixing ratio of the inorganic particles (alumina) and the particulate polymer (A) was a mixing ratio shown in Table 1.

A microporous membrane made of polyethylene (thickness: 12 μm) was prepared as a separator substrate. The slurry composition obtained as described above was then applied onto one side of the separator substrate by bar coating.

Next, the separator substrate onto which the slurry composition had been applied was dried at 50° C. for 1 minute to form a functional layer. The same operations were performed with respect to the other side of the separator substrate so as to produce a functional layer-equipped separator that included functional layers at both sides of the separator substrate. Note that the thickness of an inorganic particle layer in each of the functional layers was set as 2.0 μm.

A slurry composition for a positive electrode was produced by mixing 100 parts of LiCoO₂(volume-average particle diameter: 12 μm) as a positive electrode active material, 2 parts of acetylene black (HS-100 produced by Denka Company Limited) as a conductive material, 2 parts in terms of solid content of polyvinylidene fluoride (#7208 produced by Kureha Corporation) as a binder for a positive electrode mixed material layer, and N-methylpyrrolidone as a solvent such that the total solid content concentration was 70%, and then mixing these materials in a planetary mixer.

The slurry composition for a positive electrode was applied onto aluminum foil of 20 μm in thickness serving as a current collector by a comma coater such as to have a thickness after drying of approximately 150 μm. The applied slurry composition was dried by conveying the aluminum foil inside a 60° C. oven for 2 minutes at a speed of 0.5 m/min. Thereafter, 2 minutes of heat treatment was performed at 120° C. to obtain a pre-pressing positive electrode web. The pre-pressing positive electrode web was rolled by roll pressing to obtain a post-pressing positive electrode including a positive electrode mixed material layer (thickness: 60 μm).

A 5 MPa pressure-resistant vessel equipped with a stirrer was charged with 33 parts of 1,3-butadiene, 3.5 parts of itaconic acid, 63.5 parts of styrene, 0.4 parts of sodium dodecylbenzenesulfonate as an emulsifier, 150 parts of deionized water, and 0.5 parts of potassium persulfate as a polymerization initiator. These materials were sufficiently stirred and were then heated to 50° C. to initiate polymerization. The reaction was quenched by cooling at the point at which the polymerization conversion rate reached 96% to yield a mixture containing a binder (SBR) for a negative electrode mixed material layer. The mixture containing the binder for a negative electrode mixed material layer was adjusted to pH 8 through addition of 5% sodium hydroxide aqueous solution and was then subjected to thermal-vacuum distillation to remove unreacted monomer. Thereafter, the mixture was cooled to 30° C. or lower to yield a water dispersion containing the target binder for a negative electrode mixed material layer.

After blending 80 parts of artificial graphite (volume-average particle diameter: 15.6 μm) as a negative electrode active material (1) and 16 parts of a silicon-based active material SiOx (volume-average particle diameter: 4.9 μm) as a negative electrode active material (2), mixing 2.5 parts in terms of solid content of a 2% aqueous solution of carboxymethyl cellulose sodium salt (MAC350HC produced by Nippon Paper Industries Co., Ltd.) as a viscosity modifier and deionized water therewith, and adjusting the solid content concentration to 68%, a further 60 minutes of mixing was performed at 25° C. The solid content concentration was further adjusted to 62% with deionized water, and a further 15 minutes of mixing was performed at 25° C. to obtain a mixed liquid. Deionized water and 1.5 parts in terms of solid content of the water dispersion containing the binder for a negative electrode mixed material layer were added to the mixed liquid, the final solid content concentration was adjusted to 52%, and a further 10 minutes of mixing was performed to obtain a mixed liquid. This mixed liquid was subjected to a defoaming process under reduced pressure to yield a slurry composition for a negative electrode having good fluidity.

The slurry composition for a negative electrode was applied onto copper foil of 20 μm in thickness serving as a current collector by a comma coater such as to have a thickness after drying of approximately 150 μm. The applied slurry composition was dried by conveying the copper foil inside a 60° C. oven for 2 minutes at a speed of 0.5 m/min. Thereafter, 2 minutes of heat treatment was performed at 120° C. to obtain a pre-pressing negative electrode web. The pre-pressing negative electrode web was rolled by roll pressing to obtain a post-pressing negative electrode including a negative electrode mixed material layer (thickness: 80 μm).

The functional layer-equipped separator, positive electrode, and negative electrode obtained as described above were used to evaluate process adhesiveness, blocking resistance of a functional layer, heat resistance of a functional layer, and dusting resistance of a functional layer. The results are shown in Table 1.

The post-pressing positive electrode produced as described above was cut out as a rectangle of 49 cm×5 cm and was placed with the surface at the positive electrode mixed material layer-side thereof facing upward. The functional layer-equipped separator was cut out as 120 cm×5.5 cm and was arranged on the positive electrode mixed material layer such that the positive electrode was positioned at one side of the functional layer-equipped separator in a longitudinal direction. In addition, the post-pressing negative electrode produced as described above was cut out as a rectangle of 50 cm×5.2 cm and was arranged on the functional layer-equipped separator such that a surface at the negative electrode mixed material layer-side thereof faced toward the functional layer-equipped separator and such that the negative electrode was positioned at the other side of the functional layer-equipped separator in the longitudinal direction. The resultant laminate was wound by a winding machine to obtain a roll. This roll was pressed at 70° C. and 1 MPa to obtain a flattened roll, the flattened roll was packed into an aluminum packing case serving as a battery case, and electrolyte solution (solvent: ethylene carbonate/diethyl carbonate/vinylene carbonate (volume ratio)=68.5/30/1.5; electrolyte: LiPF₆of 1 M in concentration) was injected such that no air remained. An opening of the aluminum packing case was heat sealed at a temperature of 150° C. to close the aluminum packing case and thereby produce a wound lithium ion secondary battery having a capacity of 800 mAh.

The obtained lithium ion secondary battery was used to evaluate electrolyte solution injectability of the secondary battery, and cycle characteristics and output characteristics of the secondary battery. The results are shown in Table 1.

Example 2

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that a particulate polymer (B) produced as described below was used instead of the particulate polymer (A) in production of the slurry composition. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 1.

The particulate polymer (B) was produced by performing the same operations as in Example 1 with the exception that a colloidal dispersion liquid

(B) containing magnesium hydroxide was used instead of the colloidal dispersion liquid (A) containing magnesium hydroxide as a metal hydroxide in production of the particulate polymer.

Note that the colloidal dispersion liquid (B) containing magnesium hydroxide was produced through gradual addition under stirring of an aqueous solution (B2) of 7.0 parts of sodium hydroxide dissolved in 50 parts of deionized water to an aqueous solution (B1) of 10.0 parts of magnesium chloride dissolved in 200 parts of deionized water.

Example 3

A particulate polymer (C) produced as described below was used instead of the particulate polymer (A) in production of the slurry composition. Moreover, the amount of sodium dodecylbenzenesulfonate used as an emulsifier was adjusted to an amount such as to be 0.2 parts per 100 parts, in total, of the particulate polymer and alumina. With the exception of the above, a functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 1.

The particulate polymer (C) was obtained by performing the same operations as in Example 1 with the exception that 0.3 parts of sodium dodecylbenzenesulfonate was used instead of the colloidal dispersion liquid (A) containing magnesium hydroxide as a metal hydroxide in production of the particulate polymer.

Example 4

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that a particulate polymer (D) produced as described below was used instead of the particulate polymer (A) in production of the slurry composition. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 1.

The particulate polymer (D) was produced by performing the same operations as in Example 1 with the exception that a colloidal dispersion liquid (D) containing magnesium hydroxide was used instead of the colloidal dispersion liquid (A) containing magnesium hydroxide as a metal hydroxide in production of the particulate polymer.

Note that the colloidal dispersion liquid (D) containing magnesium hydroxide was produced through gradual addition under stirring of an aqueous solution (D2) of 4.2 parts of sodium hydroxide dissolved in 50 parts of deionized water to an aqueous solution (D1) of 6.0 parts of magnesium chloride dissolved in 200 parts of deionized water.

Example 5

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that a particulate polymer (E) produced by emulsion polymerization and aggregation as described below was used instead of the particulate polymer (A) in production of the slurry composition. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 1.

(1) Production of Resin Fine Particles

A monomer composition (E) was produced by mixing 81.9 parts of styrene as an aromatic vinyl monomer, 18 parts of 2-ethylhexyl acrylate as a (meth)acrylic acid ester monomer, and 0.1 parts of ethylene glycol dimethacrylate as a cross-linkable monomer in a flask.

Meanwhile, a surfactant solution was produced in a separable flask by dissolving 0.7 parts of sodium dodecylbenzenesulfonate as an anionic surfactant in 373 parts of deionized water.

The monomer composition (E) obtained as described above was added to the surfactant solution and was dispersed using an emulsifying/dispersing device (CLEARMIX produced by M Technique Co., Ltd.) to produce an emulsified dispersion liquid of the monomer composition (E).

After adding 400 parts of deionized water to the emulsified dispersion liquid that was obtained, 1.9 parts of n-octyl mercaptan as a molecular weight modifier and an aqueous solution containing 2.1 parts of potassium persulfate as a polymerization initiator (aqueous solution of 2.1 parts of potassium persulfate dissolved in 39.6 parts of deionized water) were further added, and polymerization was performed for 3 hours at 80° C. (first stage polymerization).

Next, an aqueous solution containing 3.2 parts of potassium persulfate as a polymerization initiator (aqueous solution of 3.2 parts of potassium persulfate dissolved in 61.3 parts of deionized water) was added, and then 81.1 parts of styrene as an aromatic vinyl monomer, 12.0 parts of methacrylic acid and 36.8 parts of n-butyl acrylate as (meth)acrylic acid ester monomer , and 2.1 parts of n-octyl mercaptan as a molecular weight modifier were added dropwise. After this dropwise addition, the temperature (80° C.) was maintained for 2 hours to perform polymerization (second stage polymerization).

After polymerization, the reaction liquid was water cooled to yield a dispersion liquid containing resin fine particles.

(2) Production of Resin Particles

A flask was charged with 150 parts in terms of solid content of the dispersion liquid containing the resin fine particles obtained as described above and 645 parts of deionized water and then stirring thereof was performed. The resultant dispersion liquid was adjusted to a temperature of 30° C. and was subsequently adjusted to pH 10 through addition of sodium hydroxide aqueous solution (concentration: 5 mol/L).

Next, an aqueous solution of 32 parts of magnesium chloride hexahydrate dissolved in 32 parts of deionized water was added to the dispersion liquid over 10 minutes at 30° C. under stirring. Thereafter, the dispersion liquid was heated to 90° C. over 60 minutes, and then aggregation of resin fine particles through salting-out and fusion through heating were performed while continuing the stirring and heating so as to form resin particles.

The particle diameters of the resin particles were measured by a particle diameter meter (Multisizer produced by Beckman Coulter, Inc.) while continuing the stirring and heating until the volume-average particle diameter of the formed resin particles reached 3 μm, at which point, an aqueous solution of 8.8 parts of sodium chloride dissolved in 57.7 parts of deionized water was added, and the salting-out and fusing were ended. Heating and stirring were continued at 90° C. for 3 hours so as to perform control of the particle shape and yield a dispersion liquid containing a particulate polymer (E).

The dispersion liquid containing the particulate polymer (E) was subjected to dehydration and water washing using deionized water, and was then dried at a pressure of 30 torr and a temperature of 50° C. for 1 day using a vacuum dryer to obtain the particulate polymer (E).

Example 6

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that a particulate polymer (F) produced by pulverization as described below was used instead of the particulate polymer (A) in production of the slurry composition. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 1.

Mixing of 81.9 parts of styrene as an aromatic vinyl monomer, 18 parts of 2-ethylhexyl acrylate as a (meth)acrylic acid ester monomer, and 0.1 parts of ethylene glycol dimethacrylate as a cross-linkable monomer was performed in toluene. Next, 0.5 parts of azobisisobutyronitrile (AIBN) was added as a polymerization initiator, and a reaction was carried out at 70° C. for 10 hours. After the reaction, precipitate formation was performed in methanol, and then vacuum drying was performed to yield a polymer (F). Next, the obtained polymer (F) was pulverized using a jet mill. The obtained pulverized product was then classified by an air flow distributor (100 ATP produced by Hosokawa Micron Corporation).

Thereafter, the pulverized product that had been classified was subjected to heat spheroidization treatment to obtain a particulate polymer (F). The heat spheroidization treatment was performed in an atmosphere having a temperature of 270° C. using a heat spheroidization device (SFS3 produced by Nippon Pneumatic Mfg. Co., Ltd.).

Example 7

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that a particulate polymer (G) produced as described below was used instead of the particulate polymer (A) in production of the slurry composition. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 1.

The particulate polymer (G) was produced by performing the same operations as in Example 1 with the exception that a monomer composition (G) was used instead of the monomer composition (A) in production of the particulate polymer.

The monomer composition (G) was produced by mixing 20.9 parts of n-butyl acrylate as a (meth)acrylic acid ester monomer, 20 parts of acrylonitrile as a nitrile group-containing monomer, 59 parts of methyl methacrylate as a (meth)acrylic acid ester monomer, and 0.1 parts of ethylene glycol dimethacrylate as a cross-linkable monomer.

Example 8

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that a particulate polymer (H) produced as described below was used instead of the particulate polymer (A) in production of the slurry composition. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 2.

The particulate polymer (H) was produced by performing the same operations as in Example 1 with the exception that a monomer composition (H) was used instead of the monomer composition (A) in production of the particulate polymer, and the obtained particulate polymer was further subjected to fine powder and coarse powder cutting treatment.

Specifically, the monomer composition (H) was produced by mixing 60 parts of styrene as an aromatic vinyl monomer, 39.9 parts of 2-ethylhexyl acrylate as a (meth)acrylic acid ester monomer, and 0.1 parts of ethylene glycol dimethacrylate as a cross-linkable monomer.

A particulate polymer obtained using the monomer composition (H) was subjected to fine powder and coarse powder cutting treatment using a classifier (Alpine produced by Hosokawa Micron Corporation) to obtain a particulate polymer (H).

Example 9

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that a particulate polymer (I) produced as described below was used instead of the particulate polymer (A) in production of the slurry composition. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 2.

The particulate polymer (I) was obtained by performing the same operations as in Example 1 with the exception that the time for which high-shear stirring was performed in suspension polymerization was changed to 10 seconds.

Example 10

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that in production of the slurry composition, the mixing ratio of alumina and the particulate polymer (A) in the slurry composition was adjusted such that the volume ratio (alumina:particulate polymer (A)) was 80:20. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 2.

Example 11

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that in production of the slurry composition, the mixing ratio of alumina and the particulate polymer (A) in the slurry composition was adjusted such that the volume ratio (alumina:particulate polymer (A)) was 55:45. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 2.

Example 12

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that a particulate polymer (J) produced as described below was used instead of the particulate polymer (A) in production of the slurry composition. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 2.

The particulate polymer (J) was produced by performing the same operations as in Example 1 with the exception that a monomer composition (J) was used instead of the monomer composition (A) in production of the particulate polymer.

The monomer composition (J) was produced by mixing 35 parts of styrene as an aromatic vinyl monomer, 64.9 parts of 2-ethylhexyl acrylate as a (meth)acrylic acid ester monomer, and 0.1 parts of ethylene glycol dimethacrylate as a cross-linkable monomer.

Example 13

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that a particulate polymer (K) produced as described below was used instead of the particulate polymer (A) in production of the slurry composition. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 2.

The particulate polymer (K) was produced by performing the same operations as in Example 1 with the exception that a monomer composition (K) was used instead of the monomer composition (A) in production of the particulate polymer.

The monomer composition (K) was produced by mixing 89.9 parts of styrene as an aromatic vinyl monomer, 10 parts of 2-ethylhexyl acrylate as a (meth)acrylic acid ester monomer, and 0.1 parts of ethylene glycol dimethacrylate as a cross-linkable monomer.

Example 14

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that a water dispersion containing a binder (β) that was produced as described below was used instead of the water dispersion containing the binder (α) in production of the slurry composition. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 2.

A reactor including a stirrer was charged with 70 parts of deionized water, 0.15 parts of polyoxyethylene lauryl ether (EMULGEN® 120 (EMULGEN is a registered trademark in Japan, other countries, or both) produced by Kao Corporation) as an emulsifier, and 0.5 parts of ammonium persulfate as a polymerization initiator, the gas phase was purged with nitrogen gas, and heating was performed to 60° C.

Meanwhile, a monomer composition (β) was produced in a separate vessel by mixing 50 parts of deionized water, 0.5 parts of polyoxyethylene lauryl ether (EMULGEN® 120 produced by Kao Corporation) as an emulsifier, 70 parts of 2-ethylhexyl acrylate as a (meth)acrylic acid alkyl ester monomer, 25 parts of styrene as an aromatic vinyl monomer, 1.7 parts of allyl glycidyl ether and 0.3 parts of allyl methacrylate as cross-linkable monomers, and 3 parts of acrylic acid as an acid group-containing monomer.

The obtained monomer composition (β) was continuously added to the aforementioned reactor including a stirrer over 4 hours to carry out polymerization. The reaction was carried out at 70° C. during this addition. Once the addition was complete, a further 3 hours of stirring was performed at 80° C., and then the reaction was ended to yield a water dispersion containing a particulate binder (β). The obtained particulate binder (β) had a volume-average particle diameter of 0.3 μm and a glass-transition temperature of −35° C.

Example 15

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that a water dispersion containing a binder (γ) that was produced as described below was used instead of the water dispersion containing the binder (α) in production of the slurry composition. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 2.

A mixture containing 33 parts of 1,3-butadiene as an aliphatic conjugated diene monomer, 62 parts of styrene as an aromatic vinyl monomer, 4 parts of itaconic acid as a carboxy group-containing monomer, 0.3 parts of t-dodecyl mercaptan as a chain transfer agent, and 0.3 parts of sodium lauryl sulfate as an emulsifier was loaded into a vessel A. A polymerization reaction was initiated by initiating addition of the mixture in the vessel A into a pressure-resistant vessel B, and, simultaneously thereto, initiating addition of 1 part of potassium persulfate as a polymerization initiator into the pressure-resistant vessel B. A reaction temperature of 75° C. was maintained.

Once 4 hours had passed from the start of polymerization (i.e., once 70% of the mixture had been added into the pressure-resistant vessel B), 1 part of 2-hydroxyethyl acrylate (acrylic acid-2-hydroxyethyl) as a hydroxy group-containing monomer was added into the pressure-resistant vessel B over 1 hour and 30 minutes.

Addition of the total amount of the above-described monomers was completed 5 hours and 30 minutes after the start of polymerization. Heating was subsequently performed to 85° C., and a reaction was carried out for 6 hours.

The reaction was quenched by cooling at the point at which the polymerization conversion rate reached 97% to yield a mixture containing a particulate polymer (γ1). The obtained mixture was adjusted to pH 8 through addition of 5% sodium hydroxide aqueous solution. Unreacted monomer was subsequently removed through thermal-vacuum distillation. Cooling was then performed to yield a water dispersion (solid content concentration: 40%) containing a styrene-butadiene copolymer (SBR) as a particulate binder (γ). The obtained particulate binder (γ) had a volume-average particle diameter of 0.18 μm and a glass-transition temperature of 15° C.

Comparative Example 1

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that a particulate polymer (V) produced by seeded polymerization as described below was used instead of the particulate polymer (A) in production of the slurry composition. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 3.

A monomer composition (V1) containing 79.9 parts of styrene as an aromatic vinyl monomer, 18 parts of 2-ethylhexyl acrylate as a (meth)acrylic acid ester monomer, 2 parts of methacrylic acid as an acid group-containing monomer, and 0.1 parts of ethylene glycol dimethacrylate as a di(meth)acrylic acid ester monomer, and also 1 part of sodium dodecylbenzenesulfonate as an emulsifier, 150 parts of deionized water, and 0.5 parts of potassium persulfate as a polymerization initiator were loaded into a 5 MPa pressure-resistant vessel equipped with a stirrer, were sufficiently stirred, and were then heated to 60° C. to initiate polymerization.

The reaction was quenched by cooling at the point at which the polymerization conversion rate reached 96% to yield a water dispersion containing seed particles (Vs1). Note that the seed particles (Vs1) had a volume-average particle diameter of 500 nm.

A monomer composition (V2) containing 2077.4 parts of styrene as an aromatic vinyl monomer, 494 parts of 2-ethylhexyl acrylate as a (meth)acrylic acid ester monomer, 52 parts of methacrylic acid as an acid group-containing monomer, and 2.6 parts of ethylene glycol dimethacrylate as a di(meth)acrylic acid ester monomer was further added to the water dispersion containing the seed particles (Vs1). These materials were sufficiently stirred and were then heated to 60° C. to initiate polymerization.

The reaction was quenched by cooling at the point at which the polymerization conversion rate reached 96% to yield a water dispersion containing seed particles (Vs2). Note that the seed particles (Vs2) had a volume-average particle diameter of 1.5 μm.

In addition, 559.3 parts of styrene as an aromatic vinyl monomer, 133 parts of 2-ethylhexyl acrylate as a (meth)acrylic acid ester monomer, 14 parts of methacrylic acid as an acid group-containing monomer, and 0.7 parts of ethylene glycol dimethacrylate as a di(meth)acrylic acid ester monomer were added to the water dispersion containing the seed particles (Vs2). These materials were sufficiently stirred and were then heated to 60° C. to initiate polymerization.

The reaction was quenched by cooling at the point at which the polymerization conversion rate reached 96% to yield a water dispersion containing a particulate polymer (V).

Comparative Example 2

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that a particulate polymer (W) produced by seeded polymerization as described below was used instead of the particulate polymer (A) in production of the slurry composition. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 3.

A monomer composition (W1) containing 75 parts of styrene as an aromatic vinyl monomer, 20 parts of n-butyl acrylate as a (meth)acrylic acid alkyl ester monomer, 4 parts of methacrylic acid as an acid group-containing monomer, and 1 part of ethylene glycol dimethacrylate as a di(meth)acrylic acid ester monomer, and also 1.2 parts of sodium dodecylbenzenesulfonate as an emulsifier, 150 parts of deionized water, and 0.5 parts of potassium persulfate as a polymerization initiator were loaded into a 5 MPa pressure-resistant vessel equipped with a stirrer, were sufficiently stirred, and were then heated to 60° C. to initiate polymerization.

The reaction was quenched by cooling at the point at which the polymerization conversion rate reached 96% to yield a water dispersion containing seed particles (Ws1).

A monomer composition (W2) containing 75,000 parts of styrene as an aromatic vinyl monomer, 20,000 parts of n-butyl acrylate as a (meth)acrylic acid ester monomer, 4,000 parts of methacrylic acid as an acid group-containing monomer, and 1,000 parts of ethylene glycol dimethacrylate as a di(meth)acrylic acid ester monomer was further added to the water dispersion containing the seed particles (Ws1). These materials were sufficiently stirred and were then heated to 60° C. to initiate polymerization.

The reaction was quenched by cooling at the point at which the polymerization conversion rate reached 96% to yield a water dispersion containing a particulate polymer (W).

Comparative Example 3

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that a particulate polymer (X) produced as described below was used instead of the particulate polymer (A) in production of the slurry composition. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 3.

The particulate polymer (E) produced in Example 5 was coarsely pulverized. The obtained coarsely pulverized product was then finely pulverized with a pulverizing air pressure of 500 kPa and a rotor speed of 7,000 rpm using a jet mill (200AFG produced by Hosokawa Micron Corporation) to obtain a particulate polymer (X).

Comparative Example 4

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that a particulate polymer (Y) produced as described below was used instead of the particulate polymer (A) in production of the slurry composition. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 3.

The particulate polymer (Y) was obtained by performing the same operations as in Example 1 with the exception that a colloidal dispersion liquid (Y) containing magnesium hydroxide that was produced as described below was used instead of the colloidal dispersion liquid (A) containing magnesium hydroxide that was used in Example 1 in production of the particulate polymer.

[Production of Colloidal Dispersion Liquid (Y) Containing Magnesium Hydroxide]

The colloidal dispersion liquid (Y) containing magnesium hydroxide was produced through gradual addition under stirring of an aqueous solution (Y2) of 2.8 parts of sodium hydroxide dissolved in 50 parts of deionized water to an aqueous solution (Y1) of 4.0 parts of magnesium chloride dissolved in 200 parts of deionized water.

Comparative Example 5

A functional layer-equipped separator, a positive electrode, and a negative electrode were produced, and a lithium ion secondary battery was obtained in the same way as in Example 1 with the exception that a particulate polymer (Z) produced as described below was used instead of the particulate polymer (A) in production of the slurry composition. Various measurements and evaluations were performed in the same way as in Example 1. The results are shown in Table 3.

A monomer composition (Z1) containing 79.9 parts of styrene as an aromatic vinyl monomer, 18 parts of 2-ethylhexyl acrylate as a (meth)acrylic acid ester monomer, 2 parts of methacrylic acid as an acid group-containing monomer, and 0.1 parts of ethylene glycol dimethacrylate as a cross-linkable monomer, and also 1 part of sodium dodecylbenzenesulfonate as an emulsifier, 150 parts of deionized water, and 0.5 parts of potassium persulfate as a polymerization initiator were loaded into a 5 MPa pressure-resistant vessel equipped with a stirrer, were sufficiently stirred, and were then heated to 60° C. to initiate polymerization.

The reaction was quenched by cooling at the point at which the polymerization conversion rate reached 96% to yield a water dispersion containing a particulate polymer (Z).

TABLE 1

Example 1
Example 2
Example 3
Example 4
Example 5
Example 6
Example 7

Composition
Particulate
Glass-transition temperature [° C.]
66
66
66
66
66
66
60

for
polymer
Chemical composition
ST/
ST/
ST/
ST/
ST/
ST/
BA/AN/

electro-

2EHA/
2EHA/
2EHA/
2EHA/
2EHA/
2EHA/
MMA/

chemical

EDMA
EDMA
EDMA
EDMA
EDMA
EDMA
EDMA

device

Chemical composition
81.9/
81.9/
81.9/
81.9/
81.9/
81.9/
20.9/20/

functional

ratio [mass %]
18/0.1
18/0.1
18/0.1
18/0.1
18/0.1
18/0.1
59/0.1

layer

Volume-average particle
6.0
3.0
1.5
9.0
3.2
5.0
4.0

diameter [μm]

Degree of swelling in electrolyte
2
2
2
2
2
2
14

solution [factor]

Average circularity
0.98
0.98
0.98
0.98
0.97
0.94
0.98

Particle diameter distribution
1.20
1.20
1.20
1.20
1.15
1.20
1.20

Production method of particulate
Suspen-
Suspen-
Suspen-
Suspen-
Emulsion
Pulveri-
Suspen-

polymer
sion
sion
sion
sion
polymeri-
zation
sion

polymeri-
polymeri-
polymeri-
polymeri-
zation and

polymeri-

zation
zation
zation
zation
aggregation

zation

Volume ratio of inorganic particles
70:30
70:30
70:30
70:30
70:30
70:30
70:30

and particulate polymer

[inorganic particles:particulate polymer]

Surfactant [parts by mass]
0.2
0.2
0.2
0.2
0.2
0.2
0.2

Binder
Chemical composition
BA/AN/
BA/AN/
BA/AN/
BA/AN/
BA/AN/
BA/AN/
BA/AN/

AMA/
AMA/
AMA/
AMA/
AMA/
AMA/
AMA/

MAA/
MAA/
MAA/
MAA/
MAA/
MAA/
MAA/

AGE
AGE
AGE
AGE
AGE
AGE
AGE

Form
Parti-
Parti-
Parti-
Parti-
Parti-
Parti-
Parti-

culate
culate
culate
culate
culate
culate
culate

Additive amount [parts by mass
5.4
5.4
5.4
5.4
5.4
5.4
5.4

per 100 parts by mass, in total,

of inorganic particles and particulate

polymer]

Inorganic
Type
Alumina
Alumina
Alumina
Alumina
Alumina
Alumina
Alumina

particles
Volume-average particle
0.7
0.7
0.7
0.7
0.7
0.7
0.7

diameter [μm]

Thickness of inorganic particle layer [μm]
2
2
2
2
2
2
2

Evaluation
Process adhesiveness
A
B
B
B
A
B
A

Blocking resistance of
A
A
A
A
A
A
A

functional layer

Heat resistance of functional
A
B
B
A
A
A
A

layer

Electrolyte solution injectability
A
A
A
A
A
A
A

Cycle characteristics of
A
A
A
A
B
A
A

secondary battery

Output characteristics of
A
A
A
A
A
A
B

secondary battery

Dusting resistance of functional layer
A
A
A
B
A
A
A

TABLE 2

Example 8
Example 9
Example 10
Example 11

Composition
Particulate
Glass-transition temperature [° C.]
66
66
66
66

for
polymer
Chemical composition
ST/
ST/
ST/
ST/

electro-

2EHA/
2EHA/
2EHA/
2EHA/

chemical

EDMA
EDMA
EDMA
EDMA

device

Chemical composition ratio [mass %]
60/
60/
81.9/
81.9/

functional

39.9/0.1
39.9/0.1
18/0.1
18/0.1

layer

Volume-average particle diameter [μm]
6.0
6.0
6.0
6.0

Degree of swelling in electrolyte
2
2
2
2

solution [factor]

Average circularity
0.98
0.98
0.98
0.98

Particle diameter distribution
1.05
1.5
1.20
1.20

Production method of particulate
Suspension
Suspension
Suspension
Suspension

polymer
polymerization
polymerization
polymerization
polymerization

Volume ratio of inorganic particles
70:30
70:30
80:20
55:45

and particulate polymer

[inorganic particles:particulate polymer]

Surfactant [parts by mass]
0.2
0.2
0.2
0.2

Binder
Chemical composition
BA/AN/
BA/AN/
BA/AN/
BA/AN/

AMA/
AMA/
AMA/
AMA/

MAA/
MAA/
MAA/
MAA/

AGE
AGE
AGE
AGE

Form
Particulate
Particulate
Particulate
Particulate

Additive amount [parts by mass
5.4
5.4
5.4
5.4

per 100 parts by mass, in total,

of inorganic particles and particulate

polymer]

Inorganic
Type
Alumina
Alumina
Alumina
Alumina

particles
Volume-average particle diameter [μm]
0.7
0.7
0.7
0.7

Thickness of inorganic particle layer [μm]
2
2
2
2

Evaluation
Process adhesiveness
A
A
B
A

Blocking resistance of functional layer
A
A
A
B

Heat resistance of functional layer
A
A
A
B

Electrolyte solution injectability
B
A
A
A

Cycle characteristics of secondary battery
B
B
A
A

Output characteristics of secondary battery
A
A
A
A

Dusting resistance of functional layer
A
B
A
A

Example 12
Example 13
Example 14
Example 15

Composition
Particulate
Glass-transition temperature [° C.]
10
75
66
66

for
polymer
Chemical composition
ST/
ST/
ST/
ST/

electro-

2EHA/
2EHA/
2EHA/
2EHA/

chemical

EDMA
EDMA
EDMA
EDMA

device

Chemical composition ratio [mass %]
35/
89.9/
81.9/
81.9/

functional

64.9/0.1
10/0.1
18/0.1
18/0.1

layer

Volume-average particle diameter [μm]
4.0
4.0
6.0
6.0

Degree of swelling in electrolyte
2
2
2
2

solution [factor]

Average circularity
0.98
0.98
0.98
0.98

Particle diameter distribution
1.20
1.20
1.20
1.20

Production method of particulate
Suspension
Suspension
Suspension
Suspension

polymer
polymerization
polymerization
polymerization
polymerization

Volume ratio of inorganic particles
70:30
70:30
70:30
70:30

and particulate polymer

[inorganic particles:particulate polymer]

Surfactant [parts by mass]
0.2
0.2
0.2
0.2

Binder
Chemical composition
BA/AN/
BA/AN/
2EHA/ST/
SBR

AMA/
AMA/
AGE/

MAA/
MAA/
AMA/

AGE
AGE
AA

Form
Partculate
Partculate
Partculate
Partculate

Additive amount [parts by mass
5.4
5.4
5.4
5.4

per 100 parts by mass, in total,

of inorganic particles and particulate

polymer]

Inorganic
Type
Alumina
Alumina
Alumina
Alumina

particles
Volume-average particle diameter [μm]
0.7
0.7
0.7
0.7

Thickness of inorganic particle layer [μm]
2
2
2
2

Evaluation
Process adhesiveness
A
B
A
A

Blocking resistance of functional layer
C
A
A
A

Heat resistance of functional layer
A
A
A
A

Electrolyte solution injectability
A
A
A
A

Cycle characteristics of secondary battery
A
A
A
A

Output characteristics of secondary battery
A
A
A
A

Dusting resistance of functional layer
A
A
A
A

TABLE 3

Comparative
Comparative
Comparative

Example 1
Example 2
Example 3

Composition
Particulate
Glass-transition temperature [° C.]
66
60
66

for
polymer
Chemical composition
ST/2EHA/
ST/BA/MAA/
ST/2EHA/EDMA

electro-

MAA/EDMA
EDMA

chemical

Chemical composition ratio [mass %]
79.9/18.2/0.1
75/20/4/1
81.9/18/0.1

device

Volume-average particle diameter [μm]
6.0
5.0
6.0

functional

Degree of swelling in electrolyte
2
2
2

layer

solution [factor]

Average circularity
0.99
0.99
0.89

Particle diameter distribution
1.10
1.10
1.20

Production method of particulate
Seeded
Seeded
Pulverization

polymer
polymeriztion
polymerization

Volume ratio of inorganic particles

and particulate polymer
70:30
70:30
70:30

[inorganic particles:particulate polymer]

Surfactant [parts by mass]
0.2
0.2
0.2

Binder
Chemical composition
BA/AN/AMA/
BA/AN/AMA/
BA/AN/AMA/

MAA/AGE
MAA/AGE
MAA/AGE

Form
Particulate
Particulate
Particulate

Additive amount [parts by mass
5.4
5.4
5.4

per 100 parts by mass, in total,

of inorganic particles and particulate

polymer]

Inorganic
Type
Alumina
Alumina
Alumina

particles
Volume-average particle diameter [μm]
0.7
0.7
0.7

Thickness of inorganic particle layer [μm]
2
2
2

Evaluation
Process adhesiveness
A
A
A

Blocking resistance of functional layer
A
A
A

Heat resistance of functional layer
A
A
B

Electrolyte solution injectability
A
A
A

Cycle characteristics of secondary battery
B
B
A

Output characteristics of secondary battery
A
A
A

Dusting resistance of functional layer
C
D
C

Comparative
Comparative

Example 4
Example 5

Composition
Particulate
Glass-transition temperature [° C.]
66
66

for
polymer
Chemical composition
ST/2EHA/EDMA
ST/2EHA/MAA/EDMA

electro-

Chemical composition ratio [mass %]
81.9/18/0.1
79.9/18/2/0.1

chemical

Volume-average particle diameter [μm]
12.0
0.6

device

Degree of swelling in electrolyte
2
2

functional

solution [factor]

layer

Average circularity
0.98
0.99

Particle diameter distribution
1.30
1.1

Production method of particulate
Suspension polymerization
Emulsion polymerization

polymer

Volume ratio of inorganic particles
70:30
70:30

and particulate polymer

[inorganic particles:particulate polymer]

Surfactant [parts by mass]
0.2
0.2

Binder
Chemical composition
BA/AN/AMA/MAA/AGE
BA/AN/AMA/MAA/AGE

Form
Particulate
Particulate

Additive amount [parts by mass
5.4
5.4

per 100 parts by mass, in total,

of inorganic particles and particulate

polymer]

Inorganic
Type
Alumina
Alumina

particles
Volume-average particle diameter [μm]
0.7
0.7

Thickness of inorganic particle layer [μm]
2
2

Evaluation
Process adhesiveness
D
D

Blocking resistance of functional layer
A
A

Heat resistance of functional layer
A
D

Electrolyte solution injectability
A
B

Cycle characteristics of secondary battery
A
A

Output characteristics of secondary battery
A
B

Dusting resistance of functional layer
D
A

In Tables 1 to 3:

“ST” indicates styrene;

“2EHA” indicates 2-ethylhexyl acrylate;

“EDMA” indicates ethylene glycol dimethacrylate;

“BA” indicates n-butyl acrylate;

“AN” indicates acrylonitrile;

“MAA” indicates methacrylic acid;

“MMA” indicates methyl methacrylate;

“AGE” indicates allyl glycidyl ether;

“AMA” indicates allyl methacrylate;

“AA” indicates acrylic acid; and

“SBR” indicates styrene-butadiene copolymer.

It can be seen from Tables 1 to 3 that in Examples 1 to 15 in which the used slurry composition (composition for a functional layer) contained a binder, inorganic particles, and a particulate polymer having an average circularity of not less than 0.90 and less than 0.99 and a volume-average particle diameter of not less than 1.0 μm and not more than 10.0 μm, it was possible to form a functional layer in which dusting was inhibited and that could ensure high heat resistance while also strongly adhering a separator and an electrode together in electrolyte solution. It can also be seen that a secondary battery having good electrochemical characteristics was obtained using this functional layer.

INDUSTRIAL APPLICABILITY

Furthermore, according to the present disclosure, it is possible to provide an electrochemical device that can display excellent electrochemical characteristics.

COMPOSITION FOR ELECTROCHEMICAL DEVICE FUNCTIONAL LAYER, FUNCTIONAL LAYER FOR ELECTROCHEMICAL DEVICE, AND ELECTROCHEMICAL DEVICE

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