JP6492741B2 - Nonaqueous secondary battery functional layer binder composition, nonaqueous secondary battery functional layer slurry composition, nonaqueous secondary battery functional layer, nonaqueous secondary battery and method for producing the same - Google Patents

Description

  The present invention relates to a binder composition for a non-aqueous secondary battery functional layer, a slurry composition for a non-aqueous secondary battery functional layer, a non-aqueous secondary battery functional layer and a non-aqueous secondary battery, and a non-aqueous secondary battery. It is related with the manufacturing method.

  Non-aqueous secondary batteries such as lithium ion secondary batteries (hereinafter sometimes simply referred to as “secondary batteries”) have the characteristics of being small and light, having high energy density, and capable of repeated charge and discharge. Yes, it is used for a wide range of purposes. The non-aqueous secondary battery generally includes a battery member such as a positive electrode, a negative electrode, and a separator that separates the positive electrode and the negative electrode and prevents a short circuit between the positive electrode and the negative electrode.

  Here, in recent years, in secondary batteries, battery members having a functional layer that imparts desired performance (for example, heat resistance and strength) to the battery members are used. Specifically, for example, a separator in which a functional layer is formed on a separator base material, or an electrode in which a functional layer is formed on an electrode base material in which an electrode mixture layer is provided on a current collector It is used as a battery member. In addition, as a functional layer that can improve the heat resistance and strength of the battery member, a functional layer made of a porous film layer formed by binding non-conductive particles with a binder (binder) is used.

In recent years, functional layers have been actively improved for the purpose of further improving the performance of secondary batteries (see, for example, Patent Document 1).
Specifically, for example, in Patent Document 1, as a functional layer capable of suppressing the occurrence of powder falling, non-conductive particles made of an inorganic filler, a styrene resin having a glass transition temperature of 20 ° C. or higher, and a glass transition temperature of 15 ° C. A functional layer composed of a porous film layer formed by applying a slurry composition containing a binder composed of the following polymer and an organic solvent capable of uniformly dissolving a styrene resin to a substrate and then drying is proposed. Yes. And in the functional layer formed using the slurry composition of this patent document 1, when apply | coating and drying a slurry composition, the styrene resin melt | dissolved in the organic solvent raise | generates migration, and it is on the surface layer of a functional layer. Since it is unevenly distributed, occurrence of powder falling is prevented.

International Publication No. 2010/024328

  However, the functional layer described in Patent Document 1 has low ion conductivity because the styrene resin is dissolved in an organic solvent and is unevenly distributed on the surface layer by migration when the functional layer is formed. Therefore, in the secondary battery including the functional layer described in Patent Document 1, there is a possibility that the internal resistance increases and the battery characteristics (life characteristics and rate characteristics) are deteriorated.

  In recent years, secondary batteries have been required to have further improved performance, and the functional layer binder exhibits high adhesion not only before being immersed in the electrolytic solution but also after being immersed in the electrolytic solution. In addition, it has been required to improve the adhesive strength (peel strength) of the functional layer after immersion in the electrolyte and the battery characteristics of the secondary battery.

Therefore, the present invention is a non-aqueous system that can increase the peel strength of the functional layer after being immersed in the electrolyte while suppressing the increase in internal resistance when used for forming the functional layer and exhibiting high adhesion even in the electrolyte. It aims at providing the binder composition for secondary battery functional layers.
Another object of the present invention is to provide a slurry composition for a non-aqueous secondary battery functional layer that can form a functional layer having high peel strength even after immersion in an electrolyte while suppressing an increase in internal resistance. .
Furthermore, an object of the present invention is to provide a functional layer for a non-aqueous secondary battery that has a high peel strength even after being immersed in an electrolytic solution and can exhibit excellent battery characteristics in the non-aqueous secondary battery.
And an object of this invention is to provide the non-aqueous secondary battery excellent in a battery characteristic, and its manufacturing method.

  The present inventor has intensively studied for the purpose of solving the above problems. The inventor then comprises non-conductive particles, a water-insoluble particulate polymer having a predetermined glass transition temperature and electrolyte swelling degree, an adhesive polymer having a predetermined glass transition temperature, water, The present inventors have found that a functional layer having a high peel strength can be formed even after immersion in an electrolytic solution while suppressing an increase in internal resistance by forming a functional layer using a slurry composition containing the present invention.

That is, the present invention aims to advantageously solve the above-mentioned problems, and the binder composition for a non-aqueous secondary battery functional layer of the present invention comprises a water-insoluble particulate polymer and an adhesive polymer. And a water-containing binder composition for a secondary battery functional layer, wherein the water-insoluble particulate polymer has a glass transition temperature of 50 ° C. or more and an electrolyte swelling degree of more than 1 time. The adhesive polymer has a glass transition temperature of 20 ° C. or lower. Thus, a water-insoluble particulate polymer having a glass transition temperature of 50 ° C. or higher and an electrolyte swelling degree of more than 1 time and less than 3 times, and an adhesive weight having a glass transition temperature of 20 ° C. or less. When the coalescence is contained, the peel strength after immersion of the functional layer in the electrolytic solution can be increased when used for forming the functional layer. Further, if the degree of swelling of the electrolyte solution of the water-insoluble particulate polymer is more than 1 time, and a water-based composition containing a water-insoluble particulate polymer and an adhesive polymer is used, a binder composition is used. It is possible to suppress an increase in internal resistance by suppressing a decrease in ion conductivity of the formed functional layer. Therefore, the rate characteristic of a secondary battery provided with a functional layer formed using the binder composition can be improved.
In the present invention, the polymer being “water-insoluble” means that at 25 ° C., when 0.5 g of the polymer is dissolved in 100 g of water, the insoluble content becomes 90% by mass or more. Say. In the present invention, the “glass transition temperature” and “electrolyte swelling degree” of the polymer can be measured using the measuring methods described in the examples of the present specification.

Here, in the binder composition for a non-aqueous secondary battery functional layer of the present invention, the volume average particle diameter of the water-insoluble particulate polymer is preferably 50 nm or more and 400 nm or less. If the volume average particle diameter of the water-insoluble particulate polymer is 50 nm or more, the dispersion stability of the water-insoluble particulate polymer is improved, and the secondary battery having a functional layer formed using the binder composition Life characteristics can be improved. Moreover, if the volume average particle diameter of the water-insoluble particulate polymer is 400 nm or less, the peel strength of the functional layer formed using the binder composition after immersion in the electrolyte can be further increased.
In the present invention, the “volume average particle diameter” of the polymer can be measured using the measuring method described in the examples of the present specification.

  In the binder composition for a non-aqueous secondary battery functional layer of the present invention, the content of the water-insoluble particulate polymer is 1 part by mass or more and 20 parts by mass or less per 100 parts by mass of the adhesive polymer. It is preferable. When the content of the water-insoluble particulate polymer is 1 part by mass or more and 20 parts by mass or less per 100 parts by mass of the adhesive polymer, the peel before the electrolyte solution is immersed in the functional layer when used for forming the functional layer. Both the strength and the peel strength after immersion of the functional layer in the electrolytic solution can be improved in a well-balanced manner.

Furthermore, in the binder composition for a non-aqueous secondary battery functional layer of the present invention, the water-insoluble particulate polymer preferably contains 70% by mass to 99% by mass of an aromatic monovinyl monomer unit. If a water-insoluble particulate polymer containing an aromatic monovinyl monomer unit in a proportion of 70% by mass or more is used, the peel strength after immersion of the electrolyte in the functional layer formed using the binder composition is further increased. Can do. Moreover, if a water-insoluble particulate polymer containing an aromatic monovinyl monomer unit in a proportion of 99% by mass or less is used, the dispersion stability of the water-insoluble particulate polymer is improved, and a binder composition is obtained. The lifetime characteristic of a secondary battery provided with the functional layer formed using can be improved.
In the present invention, the polymer "contains a monomer unit" means "a monomer-derived structural unit is contained in a polymer obtained using the monomer". To do.

  In the binder composition for a non-aqueous secondary battery functional layer of the present invention, the adhesive polymer swelling degree of the adhesive polymer is preferably more than 1 time and less than 3 times. If the degree of swelling of the electrolytic solution of the adhesive polymer is more than 1 time and less than 3 times, the peel strength of the functional layer before immersion in the electrolytic solution can be sufficiently increased. In addition, if the swelling degree of the electrolyte solution of the adhesive polymer is more than 1 time, the decrease in ionic conductivity of the functional layer formed using the binder composition is suppressed, and the increase in internal resistance is suppressed. Can do. Therefore, the rate characteristic of a secondary battery provided with a functional layer formed using the binder composition can be improved.

In the binder composition for a non-aqueous secondary battery functional layer of the present invention, the adhesive polymer contains 35% by mass or more of a (meth) acrylic acid alkyl ester monomer unit, and an aromatic monovinyl monomer unit. It is preferable that 10 mass% or more and 55 mass% or less are included. If the adhesive polymer containing the (meth) acrylic acid alkyl ester monomer unit and the aromatic monovinyl monomer unit in the above proportion is used, the peel strength of the functional layer before immersion in the electrolyte can be sufficiently increased. In addition, the life characteristics of the secondary battery including the functional layer formed using the binder composition can be improved.
In the present invention, “(meth) acryl” means acryl and / or methacryl.

  Moreover, this invention aims at solving the said subject advantageously, The slurry composition for non-aqueous secondary battery functional layers of this invention is the binder composition for non-aqueous secondary battery functional layers mentioned above. It contains any of the objects and non-conductive particles. Thus, when the binder composition for a non-aqueous secondary battery functional layer described above is used, the peel strength after immersion of the functional layer formed using the slurry composition can be increased, and the functional layer It is possible to suppress an increase in internal resistance by suppressing a decrease in ion conductivity. Accordingly, it is possible to improve the rate characteristics of the secondary battery including the functional layer formed using the slurry composition.

  Furthermore, this invention aims at solving the said subject advantageously, The functional layer for non-aqueous secondary batteries of this invention is formed from the slurry composition for non-aqueous secondary battery functional layers mentioned above. It is characterized by being made. Thus, if the slurry composition for a non-aqueous secondary battery functional layer described above is used, a functional layer that has high peel strength even after immersion in an electrolyte and can exhibit excellent battery characteristics in a non-aqueous secondary battery. can get.

  And this invention aims at solving the said subject advantageously, The non-aqueous secondary battery of this invention is equipped with the functional layer for non-aqueous secondary batteries mentioned above, It is characterized by the above-mentioned. Thus, if the functional layer for non-aqueous secondary batteries described above is used, a secondary battery having excellent battery characteristics can be obtained.

  Moreover, this invention aims at solving the said subject advantageously, The manufacturing method of the non-aqueous secondary battery of this invention is the process of heat-pressing the functional layer for non-aqueous secondary batteries mentioned above. It is characterized by including. Thus, if the non-aqueous secondary battery mentioned above is manufactured through the process of heat-pressing the functional layer for non-aqueous secondary batteries mentioned above, the secondary battery which has the outstanding battery characteristic will be obtained efficiently.

According to the present invention, when used for the formation of a functional layer, a non-aqueous system capable of increasing the peel strength after immersion of the functional layer by exhibiting high adhesiveness even in the electrolytic solution while suppressing an increase in internal resistance. A binder composition for a secondary battery functional layer can be provided.
Moreover, according to this invention, the slurry composition for non-aqueous secondary battery functional layers which can form a functional layer with high peel strength even after electrolyte immersion, suppressing the increase in internal resistance can be provided. .
Furthermore, according to the present invention, it is possible to provide a functional layer for a non-aqueous secondary battery that has a high peel strength even after being immersed in an electrolytic solution and can exhibit excellent battery characteristics in the non-aqueous secondary battery.
And according to this invention, the non-aqueous secondary battery excellent in a battery characteristic and its manufacturing method can be provided.

Hereinafter, embodiments of the present invention will be described in detail.
Here, the non-aqueous secondary battery functional layer binder composition of the present invention (hereinafter sometimes abbreviated as “binder composition”) is a non-aqueous secondary battery functional layer slurry composition (hereinafter “ It may be abbreviated as “slurry composition”.). And the slurry composition for non-aqueous secondary battery functional layers of this invention is prepared using the binder composition for non-aqueous secondary battery functional layers of this invention, and nonelectroconductive particle. Moreover, the functional layer for non-aqueous secondary batteries of this invention is formed using the slurry composition for non-aqueous secondary battery functional layers of this invention. In addition, the non-aqueous secondary battery of the present invention can be manufactured using, for example, the non-aqueous secondary battery manufacturing method of the present invention, and the non-aqueous secondary battery of the present invention is formed on the surface of at least one battery member. Functional layer.

(Binder composition for non-aqueous secondary battery functional layer)
The binder composition for a non-aqueous secondary battery functional layer of the present invention is a water-based composition containing a water-insoluble particulate polymer, an adhesive polymer, and water, and optionally further containing other components. is there. The binder composition for a non-aqueous secondary battery functional layer of the present invention, as a water-insoluble particulate polymer, has a glass transition temperature of 50 ° C. or higher and an electrolyte swelling degree of more than 1 and less than 3 times. And a polymer having a glass transition temperature of 20 ° C. or lower is used as the adhesive polymer.
And if a functional layer is formed using the slurry composition for non-aqueous secondary battery functional layers prepared using the binder composition for a non-aqueous secondary battery functional layer of the present invention, after the electrolyte solution is immersed in the functional layer The peel strength of the non-aqueous secondary battery including the functional layer can be suppressed by suppressing the ion conductivity of the functional layer from being lowered. Therefore, if the binder composition for a non-aqueous secondary battery functional layer of the present invention is used, battery characteristics (for example, life characteristics and rate characteristics) of the secondary battery can be improved.

Here, the reason why the above-described effect is obtained by using the binder composition of the present invention is not clear, but is presumed to be as follows.
That is, a water-insoluble particulate polymer having a glass transition temperature of 50 ° C. or more and an electrolyte solution swelling degree of more than 1 time and less than 3 times exhibits high adhesiveness in the electrolyte solution. If the binder composition of the present invention containing a water-soluble particulate polymer is used, the peel strength after immersion of the functional layer in the electrolytic solution can be increased. Therefore, if the binder composition of the present invention is used, for example, it is possible to prevent the functional layer from being peeled off during aging after the secondary battery is assembled and the interelectrode distance is increased, and the rate characteristics of the secondary battery are deteriorated. can do.
In addition, a water-insoluble particulate polymer having a glass transition temperature of 50 ° C. or higher usually does not exhibit a large adhesive force before being immersed in an electrolytic solution, but an adhesive polymer having a glass transition temperature of 20 ° C. or lower. Exhibits sufficient adhesion even before immersion in the electrolyte. Therefore, if the binder composition of the present invention containing an adhesive polymer is used, the functional layer is satisfactorily formed by binding non-conductive particles and water-insoluble particulate polymer mainly by the adhesive polymer. In addition, the peel strength of the functional layer before immersion in the electrolyte can be ensured.
Furthermore, since the binder composition of the present invention is a water-based composition containing a water-insoluble particulate polymer, the particulate polymer ensures the porosity of the functional layer and decreases the ionic conductivity. It is possible to suppress the increase in internal resistance of the secondary battery using the functional layer. Therefore, if the binder composition of the present invention is used, a secondary battery excellent in rate characteristics and life characteristics can be obtained.

<Water-insoluble particulate polymer>
The water-insoluble particulate polymer needs to have a glass transition temperature of 50 ° C. or higher and an electrolyte swelling degree of more than 1 time and less than 3 times. And a water-insoluble particulate polymer exhibits the outstanding adhesive force mainly in electrolyte solution.
In addition, the water-insoluble particulate polymer exists in a particulate state in water, and usually maintains the particulate state even in a functional layer formed using a binder composition.

[Glass-transition temperature]
Here, the glass transition temperature of the water-insoluble particulate polymer needs to be 50 ° C. or higher, preferably 75 ° C. or higher, and more preferably 90 ° C. or higher. If the glass transition temperature is too low, sufficient adhesive strength cannot be exhibited in the electrolytic solution, and the peel strength after the functional layer is immersed in the electrolytic solution cannot be increased. In addition, the glass transition temperature of a water-insoluble particulate polymer is 120 degrees C or less normally.

[Electrolytic solution swelling]
Further, the degree of swelling of the electrolyte solution of the water-insoluble particulate polymer needs to be more than 1 time and less than 3 times, preferably 1.2 times or more, and more preferably 1.5 times or more. More preferably, it is 2.5 times or less, and more preferably 2.0 times or less. When the degree of swelling of the electrolytic solution is more than 1 time and less than 3 times, sufficient adhesive strength can be exhibited in the electrolytic solution, and the peel strength after immersion of the functional layer in the electrolytic solution can be sufficiently increased. In addition, if the electrolyte swelling degree of the water-insoluble particulate polymer is too low, the ionic conductivity of the functional layer is lowered and the internal resistance of the secondary battery using the functional layer is increased, and the rate characteristics of the secondary battery are increased. May not be sufficiently improved.

  Even if the degree of swelling of the electrolyte is more than 1 and less than 3 times, the water-insoluble particulate polymer moves the molecular chain of the polymer when swollen in the electrolyte when the glass transition temperature is low. It becomes easy, strength falls, and sufficient adhesive force cannot be exhibited in electrolyte solution. Therefore, the water-insoluble particulate polymer needs to have both a predetermined glass transition temperature and a predetermined degree of electrolyte solution swelling.

[Volume average particle diameter]
Further, the volume average particle diameter of the water-insoluble particulate polymer is preferably 50 nm or more, more preferably 80 nm or more, further preferably 100 nm or more, and particularly preferably 130 nm or more. 400 nm or less, more preferably 350 nm or less, still more preferably 300 nm or less, and particularly preferably 200 nm or less. If the volume average particle diameter is 50 nm or more, the dispersion stability can be improved, and for example, the aggregation of the water-insoluble particulate polymer can be suppressed even when subjected to a high shearing force. The lifetime characteristic of a secondary battery provided with the functional layer formed using the composition can be improved. Moreover, if the volume average particle diameter is 400 nm or less, a high adhesive force can be exhibited in the electrolytic solution, and the peel strength after immersion of the functional layer in the electrolytic solution can be further increased.

[composition]
The water-insoluble particulate polymer is not particularly limited as long as it is a water-insoluble polymer having the above-described glass transition temperature and electrolyte solution swelling degree, and any polymer can be used. Among these, from the viewpoint of improving dispersion stability and adhesion in the electrolyte, it is preferable to use a polymer containing an aromatic monovinyl monomer unit as the water-insoluble particulate polymer. It is more preferable to use a copolymer containing a monomer unit and an acidic group-containing monomer unit and / or a crosslinkable monomer unit.

[[Aromatic monovinyl monomer unit]]
Here, examples of the aromatic monovinyl monomer that can form an aromatic monovinyl monomer unit include styrene, styrenesulfonic acid and salts thereof (for example, sodium styrenesulfonate), α-methylstyrene, vinyltoluene, 4 -(Tert-butoxy) styrene etc. are mentioned. Among these, styrene is preferable. These can be used alone or in combination of two or more.

  The content ratio of the aromatic monovinyl monomer unit in the water-insoluble particulate polymer is preferably 70% by mass or more, more preferably 80% by mass or more, and further preferably 94% by mass or more. Yes, preferably 99% by mass or less, more preferably 98% by mass or less, and still more preferably 97% by mass or less. If the content ratio of the aromatic monovinyl monomer unit is 70% by mass or more, the adhesion in the electrolytic solution is further improved, and the peel strength after immersion of the functional layer formed using the binder composition is further increased. Can be increased. On the other hand, when the content ratio of the aromatic monovinyl monomer unit is 99% by mass or less, the dispersion stability is further improved. For example, the water-insoluble particulate polymer is aggregated even when subjected to a high shearing force. Can be sufficiently suppressed, and the life characteristics of the secondary battery can be further improved.

[[Acid group-containing monomer unit]]
Examples of the acidic group-containing monomer that can form an acidic group-containing monomer unit include a carboxylic acid group-containing monomer, a sulfonic acid group-containing monomer, and a phosphoric acid group-containing monomer. it can. These can be used alone or in combination of two or more.

Examples of the carboxylic acid group-containing monomer include ethylenically unsaturated monocarboxylic acid and derivatives thereof, ethylenically unsaturated dicarboxylic acid and acid anhydrides thereof, and derivatives thereof.
Examples of the ethylenically unsaturated monocarboxylic acid include acrylic acid, methacrylic acid, crotonic acid and the like. Examples of the ethylenically unsaturated monocarboxylic acid derivatives include 2-ethylacrylic acid, isocrotonic acid, α-acetoxyacrylic acid, β-trans-aryloxyacrylic acid, α-chloro-β-E-methoxyacrylic. Examples include acid and β-diaminoacrylic acid.
Examples of the ethylenically unsaturated dicarboxylic acid include maleic acid, fumaric acid, itaconic acid, mesaconic acid and the like. Examples of acid anhydrides of ethylenically unsaturated dicarboxylic acids include maleic anhydride, acrylic anhydride, methyl maleic anhydride, dimethyl maleic anhydride, and the like. In addition, examples of ethylenically unsaturated dicarboxylic acid derivatives include methylmaleic acid, dimethylmaleic acid, phenylmaleic acid, chloromaleic acid, dichloromaleic acid, fluoromaleic acid, diphenyl maleate, nonyl maleate, decyl maleate , Dodecyl maleate, octadecyl maleate, fluoroalkyl maleate and the like.

Examples of the sulfonic acid group-containing monomer include vinyl sulfonic acid, methyl vinyl sulfonic acid, (meth) allyl sulfonic acid, (meth) acrylic acid-2-ethyl sulfonate, 2-acrylamido-2-methylpropane sulfonic acid, 3 -Allyloxy-2-hydroxypropane sulfonic acid etc. are mentioned.
In the present invention, “(meth) allyl” means allyl and / or methallyl.

Examples of phosphoric acid group-containing monomers include 2- (meth) acryloyloxyethyl phosphate, methyl-2- (meth) acryloyloxyethyl phosphate, ethyl- (meth) acryloyloxyethyl phosphate, and the like.
In the present invention, “(meth) acryloyl” means acryloyl and / or methacryloyl.

  Among these, as the acidic group-containing monomer, a carboxylic acid group-containing monomer is preferable, fumaric acid, itaconic acid, acrylic acid, and methacrylic acid are more preferable, and methacrylic acid is further preferable.

  The content ratio of the acidic group-containing monomer unit in the water-insoluble particulate polymer is preferably 0.1% by mass or more, more preferably 1.0% by mass or more, and further preferably 1.5% by mass. It is above, Preferably it is 10 mass% or less, More preferably, it is 5.0 mass% or less, More preferably, it is 2.5 mass% or less. When the content ratio of the acidic group-containing monomer unit is 0.1% by mass or more, the dispersion stability is further improved. For example, the water-insoluble particulate polymer aggregates even when subjected to a high shearing force. Can be sufficiently suppressed, and the life characteristics of the secondary battery can be further improved. Moreover, if the content ratio of the acidic group-containing monomer unit is 10% by mass or less, the adhesiveness in the electrolytic solution is further improved, and the peel strength after immersion of the functional layer formed using the binder composition in the electrolytic solution Can be further increased.

[[Crosslinkable monomer unit]]
As the crosslinkable monomer capable of forming a crosslinkable monomer unit, a monomer capable of forming a crosslinked structure upon polymerization can be used. Specifically, a monofunctional monomer having a thermally crosslinkable crosslinkable group and one ethylenically unsaturated bond per molecule, and a polyfunctional having two or more ethylenically unsaturated bonds per molecule Ionic monomers. Examples of the thermally crosslinkable group contained in the monofunctional monomer include an epoxy group, an N-methylolamide group, an oxetanyl group, an oxazoline group, and combinations thereof. By including a crosslinkable monomer unit, the degree of swelling of the electrolyte solution of the water-insoluble particulate polymer is moderately increased while enhancing the anti-powder resistance of the functional layer formed using the binder composition. It can be.

The crosslinkable monomer may be hydrophobic or hydrophilic.
In the present invention, that the crosslinkable monomer is “hydrophobic” means that the crosslinkable monomer does not contain a hydrophilic group, and the crosslinkable monomer is “hydrophilic”. The term “crosslinkable monomer” includes a hydrophilic group. Here, the “hydrophilic group” in the crosslinkable monomer means a carboxylic acid group, a hydroxyl group, a sulfonic acid group, a phosphoric acid group, an epoxy group, a thiol group, an aldehyde group, an amide group, an oxetanyl group, or an oxazoline group.

Hydrophobic crosslinkable monomers include allyl (meth) acrylate, ethylene di (meth) acrylate, diethylene glycol di (meth) acrylate, triethylene glycol di (meth) acrylate, tetraethylene glycol di (meth) acrylate, trimethylol Polyfunctional (meth) acrylates such as propane-tri (meth) acrylate; polyfunctional allyl / vinyl ethers such as dipropylene glycol diallyl ether, polyglycol diallyl ether, triethylene glycol divinyl ether, hydroquinone diallyl ether, tetraallyloxyethane And divinylbenzene and the like.
Examples of the hydrophilic crosslinkable monomer include vinyl glycidyl ether, allyl glycidyl ether, N-methylol acrylamide, acrylamide, and allyl methacrylamide.
In addition, these can be used individually by 1 type or in combination of 2 or more types.

  Among these, ethylene dimethacrylate is preferable from the viewpoint of enhancing the powder resistance of the functional layer formed using the binder composition.

  The content of the crosslinkable monomer unit in the water-insoluble particulate polymer is preferably 0.1% by mass or more, more preferably 1.0% by mass or more, and further preferably 1.5% by mass or more. Preferably, it is 10 mass% or less, More preferably, it is 5.0 mass% or less, More preferably, it is 2.5 mass% or less. If the content ratio of the crosslinkable monomer unit is 0.1% by mass or more, the degree of swelling of the electrolyte solution of the water-insoluble particulate polymer is set to an appropriate level, and the adhesion in the electrolyte solution is further increased. Can be increased. Moreover, if the content rate of a crosslinkable monomer unit shall be 10 mass% or less, the powder-proofing property of the functional layer formed using the binder composition can be improved.

[[Other monomer units]]
The water-insoluble particulate polymer may contain other monomer units in addition to the monomer units described above. The other monomer units are not particularly limited, and examples thereof include (meth) acrylic acid alkyl ester monomer units.

Here, as the (meth) acrylic acid alkyl ester monomer that can form a (meth) acrylic acid alkyl ester monomer unit, methyl acrylate, ethyl acrylate, n-propyl acrylate, isopropyl acrylate, n-butyl acrylate, t-butyl acrylate, isobutyl acrylate, n-pentyl acrylate, isopentyl acrylate, hexyl acrylate, heptyl acrylate, octyl acrylate, 2-ethylhexyl acrylate, nonyl acrylate, decyl acrylate, lauryl acrylate, n-tetradecyl acrylate, stearyl acrylate, etc. Acrylic acid alkyl ester; methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, isopropyl methacrylate Rate, n-butyl methacrylate, t-butyl methacrylate, isobutyl methacrylate, n-pentyl methacrylate, isopentyl methacrylate, hexyl methacrylate, heptyl methacrylate, octyl methacrylate, 2-ethylhexyl methacrylate, nonyl methacrylate, decyl methacrylate, lauryl methacrylate, n-tetra And methacrylic acid alkyl esters such as decyl methacrylate, stearyl methacrylate, and glycidyl methacrylate;
Among these, 2-ethylhexyl acrylate, ethyl acrylate, butyl acrylate, and methyl methacrylate are preferable, and 2-ethylhexyl acrylate is more preferable.

  The content ratio of other monomer units in the water-insoluble particulate polymer is preferably 30% by mass or less, more preferably 10% by mass or less. More preferably, no monomer unit is contained. If the content ratio of other monomer units is 30% by mass or less, the adhesiveness in the electrolytic solution can be further improved.

[Method for preparing water-insoluble particulate polymer]
And a water-insoluble particulate polymer can be prepared by polymerizing the monomer composition containing the monomer mentioned above, for example.
Here, the content ratio of each monomer in the monomer composition is usually the same as the content ratio of the monomer unit in the desired water-insoluble particulate polymer.
The polymerization mode of the water-insoluble particulate polymer is not particularly limited, and any method such as a solution polymerization method, a suspension polymerization method, a bulk polymerization method, and an emulsion polymerization method may be used. As the polymerization reaction, addition polymerization such as ionic polymerization, radical polymerization, and living radical polymerization can be used. And generally used emulsifiers, dispersants, polymerization initiators, polymerization aids and the like used for the polymerization can be used, and the amount used is also generally used.

<Adhesive polymer>
The adhesive polymer needs to have a glass transition temperature of 20 ° C. or lower. And an adhesive polymer exhibits the outstanding adhesive force even before immersion of electrolyte solution.
From the standpoint of ensuring the porosity of the functional layer and suppressing the decrease in ionic conductivity, and suppressing the increase in internal resistance of the secondary battery using the functional layer, the adhesive polymer is It is preferable that it exists in a particulate state, and it is more preferable that the particulate state is maintained even in a functional layer formed using the binder composition. That is, the binder composition preferably contains an adhesive particulate polymer.

[Glass-transition temperature]
Here, the glass transition temperature of the adhesive polymer needs to be 20 ° C. or lower, preferably 0 ° C. or lower, and more preferably −10 ° C. or lower. If the glass transition temperature is too high, sufficient adhesive force cannot be exhibited before immersion in the electrolytic solution, and it becomes difficult to form the functional layer and to ensure the peel strength of the functional layer before immersion in the electrolytic solution. In addition, the glass transition temperature of an adhesive polymer is -60 degreeC or more normally.

[Electrolytic solution swelling]
Moreover, the electrolyte solution swelling degree of the adhesive polymer is preferably more than 1 time, more preferably 1.2 times or more, further preferably 1.5 times or more, and less than 3 times. Preferably, it is 2.5 times or less, more preferably 2.0 times or less. If the degree of swelling of the electrolytic solution is more than 1 and less than 3 times, sufficient functional strength can be exerted before immersion in the electrolytic solution to form the functional layer well, and before the functional layer is immersed in the electrolytic solution The peel strength can be sufficiently increased.
If the swelling degree of the electrolyte solution of the adhesive polymer is too low, the ionic conductivity of the functional layer is lowered, the internal resistance of the secondary battery using the functional layer is increased, and the secondary battery has sufficient rate characteristics. There is a possibility that it cannot be improved.

[Volume average particle diameter]
Furthermore, the volume average particle diameter of the adhesive polymer is preferably 50 nm or more, more preferably 100 nm or more, further preferably 150 nm or more, preferably 500 nm or less, and preferably 300 nm or less. More preferably, it is more preferably 250 nm or less. If the volume average particle diameter is 50 nm or more, the dispersion stability is improved, and for example, the adhesive polymer can be prevented from aggregating even when subjected to a high shearing force. The lifetime characteristic of a secondary battery provided with the functional layer formed using can be improved. Further, when the volume average particle diameter is 500 nm or less, a high adhesive force can be exhibited before immersion in the electrolytic solution, and the peel strength of the functional layer before immersion in the electrolytic solution can be further increased.

[composition]
In addition, as an adhesive polymer, if it is a polymer which has the glass transition temperature mentioned above, it will not specifically limit, An arbitrary polymer can be used. Among them, from the viewpoint of improving dispersion stability and adhesion before immersion in the electrolyte, the adhesive polymer includes a (meth) acrylic acid alkyl ester monomer unit and an aromatic monovinyl monomer unit. It is preferable to use a copolymer, and it is more preferable to use a random copolymer containing a (meth) acrylic acid alkyl ester monomer unit and an aromatic monovinyl monomer unit.

[[(Meth) acrylic acid alkyl ester monomer unit]]
Here, as the (meth) acrylic acid alkyl ester monomer that can form the (meth) acrylic acid alkyl ester monomer unit, in the above-described water-insoluble particulate polymer, The same thing as the (meth) acrylic-acid alkylester monomer which can form a (meth) acrylic-acid alkylester monomer unit is mentioned.
Among these, 2-ethylhexyl acrylate, ethyl acrylate, butyl acrylate, and methyl methacrylate are preferable, and 2-ethylhexyl acrylate is more preferable.

  The content ratio of the (meth) acrylic acid alkyl ester monomer unit in the adhesive polymer is preferably 35% by mass or more, more preferably 45% by mass or more, and further preferably 55% by mass or more. Is 80% by mass or less, more preferably 75% by mass or less, and still more preferably 70% by mass or less. If the content ratio of the (meth) acrylic acid alkyl ester monomer unit is 35% by mass or more, the adhesion before immersion in the electrolytic solution is further improved, and the functional layer formed using the binder composition is immersed in the electrolytic solution. The previous peel strength can be further increased. On the other hand, when the content ratio of the (meth) acrylic acid alkyl ester monomer unit is 80% by mass or less, the life characteristics of the secondary battery including the functional layer formed using the binder composition can be improved.

[[Aromatic monovinyl monomer unit]]
The aromatic monovinyl monomer that can form an aromatic monovinyl monomer unit includes an aromatic monovinyl monomer that can form an aromatic monovinyl monomer unit in the water-insoluble particulate polymer described above. The same thing is mentioned.
Among them, styrene is preferable as the aromatic monovinyl monomer.

  The content of the aromatic monovinyl monomer unit in the adhesive polymer is preferably 10% by mass or more, more preferably 20% by mass or more, and further preferably 27% by mass or more, preferably Is 55% by mass or less, more preferably 45% by mass or less, and still more preferably 35% by mass or less. When the content ratio of the aromatic monovinyl monomer unit is 10% by mass or more, the life characteristics of the secondary battery including the functional layer formed using the binder composition can be improved. On the other hand, if the content ratio of the aromatic monovinyl monomer unit is 55% by mass or less, the adhesiveness before immersion in the electrolytic solution is further improved, and the functional layer formed using the binder composition before immersion in the electrolytic solution. Peel strength can be further increased.

[[Other monomer units]]
The adhesive polymer may contain other monomer units in addition to the monomer units described above. The other monomer units are not particularly limited, and examples thereof include acidic group-containing monomer units and crosslinkable monomer units.
Other monomer units, such as acidic group-containing monomer units and crosslinkable monomer units, are units other than the above-mentioned (meth) acrylic acid alkyl ester monomer units and aromatic monovinyl monomer units. It is a unit of mass. Accordingly, the acidic group-containing monomer that can form an acidic group-containing monomer unit and the crosslinkable monomer that can form a crosslinkable monomer unit include the above-mentioned (meth) acrylic acid alkyl ester monomers. And aromatic monovinyl monomers (such as styrene sulfonic acid and its salts) are not included.

-Acid group-containing monomer unit-
Here, as the acidic group-containing monomer that can form an acidic group-containing monomer unit, the acidic group-containing monomer that can form an acidic group-containing monomer unit in the water-insoluble particulate polymer described above. The same thing is mentioned.
Especially, as an acidic group containing monomer, a carboxylic acid group containing monomer is preferable, fumaric acid, itaconic acid, acrylic acid, and methacrylic acid are more preferable, and acrylic acid is still more preferable.

  The content ratio of the acidic group-containing monomer unit in the adhesive polymer is preferably 1% by mass or more, more preferably 2% by mass or more, still more preferably 3% by mass or more, and preferably 10% by mass. Hereinafter, it is more preferably 6% by mass or less, still more preferably 5% by mass or less. When the content ratio of the acidic group-containing monomer unit is 1% by mass or more, the dispersion stability is improved, for example, the aggregation of the adhesive polymer is suppressed even when subjected to a high shearing force. In addition, the life characteristics of the secondary battery can be further improved. Moreover, if the content rate of an acidic group containing monomer unit shall be 10 mass% or less, the adhesiveness before immersion to electrolyte solution will further be improved, and before the electrolyte solution immersion of the functional layer formed using the binder composition Peel strength can be further increased.

-Crosslinkable monomer unit-
The crosslinkable monomer that can form a crosslinkable monomer unit is the same as the crosslinkable monomer that can form a crosslinkable monomer unit in the water-insoluble particulate polymer described above. Can be mentioned.
Among these, as the crosslinkable monomer, it is preferable to use a hydrophilic crosslinkable monomer and a hydrophobic crosslinkable monomer in combination, and it is more preferable to use allyl glycidyl ether and allyl methacrylate in combination.

  The content of the crosslinkable monomer unit in the adhesive polymer is preferably 0.2% by mass or more, more preferably 0.5% by mass or more, and still more preferably 0.8% by mass or more. Preferably it is 5 mass% or less, More preferably, it is 2 mass% or less. When the content ratio of the crosslinkable monomer unit is 0.2% by mass or more and 5% by mass or less, the adhesiveness before immersion in the electrolytic solution is further improved, and the electrolytic solution of the functional layer formed using the binder composition The peel strength before immersion can be further increased.

[Method for Preparing Adhesive Polymer]
And an adhesive polymer can be prepared by superposing | polymerizing the monomer composition containing the monomer mentioned above, for example.
Here, the content ratio of each monomer in the monomer composition is usually the same as the content ratio of the monomer unit in the desired adhesive polymer.
The polymerization mode of the adhesive polymer is not particularly limited, and any method such as a solution polymerization method, a suspension polymerization method, a bulk polymerization method, and an emulsion polymerization method may be used. As the polymerization reaction, addition polymerization such as ionic polymerization, radical polymerization, and living radical polymerization can be used. And generally used emulsifiers, dispersants, polymerization initiators, polymerization aids and the like used for the polymerization can be used, and the amount used is also generally used.
Here, when preparing an adhesive polymer made of a random copolymer, the polymerization is started not in the form of an oligomer obtained by polymerizing the monomer in the monomer composition to some extent but in the monomer state. Thus, the generation of the block copolymer and the graft copolymer may be suppressed.

<Other ingredients>
In addition, the binder composition may contain other arbitrary components in addition to the components described above. The optional component is not particularly limited as long as it does not have an excessively unfavorable influence on the battery reaction in the secondary battery using the functional layer. Further, the kind of the arbitrary component may be one kind or two or more kinds.
Examples of the optional component include known additives used for forming a functional layer, such as a wetting agent, a leveling agent, an electrolytic solution decomposition inhibitor, and a water-soluble polymer.

<Preparation of binder composition for non-aqueous secondary battery functional layer>
The binder composition of the present invention can be prepared by dispersing the above-described components in water as a dispersion medium. Specifically, by mixing the above-described components and water using a mixer such as a ball mill, sand mill, bead mill, pigment disperser, crushed grinder, ultrasonic disperser, homogenizer, planetary mixer, fill mix, etc. A binder composition can be prepared.
In addition, when the water-insoluble particulate polymer or adhesive polymer is prepared by polymerizing the monomer composition in an aqueous solvent, it can be mixed with other components as it is in the state of an aqueous dispersion. it can. Moreover, when mixing a water-insoluble particulate polymer and adhesive polymer in the state of an aqueous dispersion, you may use the water in an aqueous dispersion as a dispersion medium.

[Blending ratio of water-insoluble particulate polymer and adhesive polymer]
Here, in preparing the binder composition, the mixing ratio of the water-insoluble particulate polymer and the adhesive polymer is such that the content of the water-insoluble particulate polymer is 1 part by mass per 100 parts by mass of the adhesive polymer. It is preferable that the amount is 20 parts by mass or less. The content of the water-insoluble particulate polymer in the binder composition is more preferably 1.5 parts by mass or more, and 2.0 parts by mass or more per 100 parts by mass of the adhesive polymer. Is more preferably 3.0 parts by mass or more, more preferably 15 parts by mass or less, still more preferably 12 parts by mass or less, and particularly preferably 9.0 parts by mass or less. preferable. If the amount of the water-insoluble particulate polymer is 1 part by mass or more per 100 parts by mass of the adhesive polymer, the adhesive strength in the electrolyte is sufficiently improved, and the peel strength of the functional layer after immersion in the electrolyte is increased. It can be raised enough. On the other hand, if the amount of the water-insoluble particulate polymer is 20 parts by mass or less per 100 parts by mass of the adhesive polymer, the adhesive force before immersion in the electrolyte is sufficiently improved, and the functional layer before immersion in the electrolyte The peel strength can be sufficiently increased. In addition, the water-insoluble particulate polymer usually does not develop a large adhesive force before being immersed in the electrolytic solution, but the amount of the water-insoluble particulate polymer is 20 parts by mass per 100 parts by mass of the adhesive polymer. If it is as follows, the anti-powder resistance of the functional layer can be improved, and the non-water-soluble particulate polymer can be prevented from falling off from the functional layer before being immersed in the electrolytic solution. The peel strength after immersion can be sufficiently increased.

(Slurry composition for non-aqueous secondary battery functional layer)
The slurry composition for a non-aqueous secondary battery functional layer of the present invention comprises an aqueous system containing the above-mentioned binder composition for a non-aqueous secondary battery functional layer and non-conductive particles, and optionally further containing other components. It is a slurry composition. That is, the slurry composition for a non-aqueous secondary battery functional layer of the present invention includes non-conductive particles, a water-insoluble particulate polymer, an adhesive polymer, and water, and optionally further contains other components. contains.
And if a functional layer is formed using the slurry composition for non-aqueous secondary battery functional layers of this invention, while the peel strength after electrolyte solution immersion of a functional layer can be raised, the ion conductivity of a functional layer Can be suppressed, and an increase in the internal resistance of the secondary battery can be suppressed. Therefore, if the functional layer formed using the slurry composition for a non-aqueous secondary battery functional layer of the present invention is used, the rate characteristics of the secondary battery can be improved.

<Non-conductive particles>
Here, the non-conductive particles are particles that do not dissolve in water and the non-aqueous electrolyte solution of the secondary battery, and maintain the shape thereof. And since a nonelectroconductive particle is electrochemically stable, it exists stably in a functional layer under the use environment of a secondary battery.

As the nonconductive particles, for example, various inorganic fine particles and organic fine particles can be used.
Specifically, as the non-conductive particles, both inorganic fine particles and organic fine particles other than the above-described water-insoluble particulate polymer and adhesive polymer can be used. Usually, inorganic fine particles are used. It is done. Especially, as a material of nonelectroconductive particle, the material which exists stably in the use environment of a non-aqueous secondary battery and is electrochemically stable is preferable. From this point of view, preferable examples of the non-conductive particle material include aluminum oxide (alumina), hydrated aluminum oxide (boehmite), silicon oxide, magnesium oxide (magnesia), calcium oxide, titanium oxide (titania). Oxide particles such as BaTiO ₃ , ZrO, alumina-silica composite oxide; nitride particles such as aluminum nitride and boron nitride; covalently bonded crystal particles such as silicon and diamond; barium sulfate, calcium fluoride, barium fluoride Insoluble ion crystal particles such as; clay fine particles such as talc and montmorillonite; In addition, these particles may be subjected to element substitution, surface treatment, solid solution, and the like as necessary.
In addition, the nonelectroconductive particle mentioned above may be used individually by 1 type, and may be used in combination of 2 or more types.

<Combination ratio of binder composition for non-aqueous secondary battery functional layer>
Here, the mixing ratio of the non-conductive particles and the binder composition for the non-aqueous secondary battery functional layer in the slurry composition for the non-aqueous secondary battery functional layer is not particularly limited. The total content of the water-soluble particulate polymer and the adhesive polymer is preferably 1 part by mass or more, more preferably 1.5 parts by mass or more, and further preferably 2 parts by mass, per 100 parts by mass of the non-conductive particles. It is above, Preferably it is 10 mass parts or less, More preferably, it is 8 mass parts or less, More preferably, it is 5 mass parts or less. If the total of the content of the water-insoluble particulate polymer and the content of the adhesive polymer is 1 part by mass or more per 100 parts by mass of the non-conductive particles, before and after the immersion in the electrolyte solution Both adhesivenesses can be sufficiently secured, and both the peel strength before immersion of the functional layer in the electrolytic solution and the peel strength after immersion of the functional layer in the electrolytic solution can be sufficiently increased. Further, if the total content of the water-insoluble particulate polymer and the content of the adhesive polymer is 10 parts by mass or less per 100 parts by mass of the non-conductive particles, the internal resistance of the secondary battery is increased. It can suppress and can improve the rate characteristic and lifetime characteristic of a secondary battery.

<Other ingredients>
In addition, the slurry composition may contain other arbitrary components in addition to the components described above. The optional component is not particularly limited as long as it does not have an excessively unfavorable influence on the battery reaction in the secondary battery using the functional layer. Further, the kind of the arbitrary component may be one kind or two or more kinds.
As said arbitrary component, the thing similar to the other component which can be mix | blended with the binder composition mentioned above is mentioned.

<Preparation of slurry composition for non-aqueous secondary battery functional layer>
The method for preparing the slurry composition is not particularly limited, but usually, the binder composition described above, non-conductive particles, and optional components used as necessary, in the presence of water as a dispersion medium. It is obtained by mixing with. In addition, the water used as the dispersion medium may include the water contained in the binder composition.

  Here, although the mixing method of the component mentioned above is not restrict | limited in particular, In order to disperse | distribute each component efficiently, it is preferable to mix using a disperser as a mixing apparatus. The disperser is preferably an apparatus capable of uniformly dispersing and mixing the above components. Examples include a ball mill, a sand mill, a pigment disperser, a crusher, an ultrasonic disperser, a homogenizer, and a planetary mixer. Among them, a high dispersion apparatus such as a bead mill, a roll mill, or a fill mix is particularly preferable because a high dispersion share can be added.

(Functional layer for non-aqueous secondary batteries)
The functional layer for a non-aqueous secondary battery of the present invention is formed from the above-described slurry composition for a non-aqueous secondary battery functional layer. For example, the above-described slurry composition is applied to the surface of an appropriate substrate. And after forming a coating film, it can form by drying the formed coating film.
And since the non-aqueous secondary battery functional layer of the present invention is formed using the slurry composition for non-aqueous secondary battery functional layer described above, the peel strength is high even after the electrolyte is immersed, Excellent battery characteristics can be exhibited in the non-aqueous secondary battery. In particular, the functional layer for a non-aqueous secondary battery of the present invention is formed using an aqueous slurry composition containing a water-insoluble particulate polymer, and the particulate polymer is present in the layer. Therefore, compared with a functional layer formed by using a solvent-based slurry composition obtained by dissolving a polymer in an organic solvent, the polymer is easily formed into a film in the layer, and has high porosity and excellent ionic conductivity. ing. Therefore, if the functional layer of the present invention is used, a nonaqueous secondary battery excellent in battery characteristics such as rate characteristics can be obtained.

<Base material>
Here, there is no restriction | limiting in the base material which apply | coats a slurry composition, for example, forms the coating film of a slurry composition on the surface of a mold release base material, dries the coating film, forms a functional layer, The release substrate may be peeled off. Thus, the functional layer peeled off from the release substrate can be used as a self-supporting film for forming a battery member of a secondary battery. Specifically, the functional layer peeled off from the release substrate may be laminated on the separator substrate to form a separator having the functional layer, or the functional layer peeled off from the release substrate may be used as the electrode substrate. An electrode provided with a functional layer may be formed by stacking on the substrate.
However, from the viewpoint of improving the production efficiency of the battery member by omitting the step of peeling off the functional layer, it is preferable to use a separator substrate or an electrode substrate as the substrate. The functional layer provided on the separator substrate and the electrode substrate can be suitably used as a protective layer (heat resistant layer) for improving the heat resistance and strength of the separator and the electrode.

[Separator substrate]
Here, although it does not specifically limit as a separator base material, Known separator base materials, such as an organic separator base material, are mentioned. The organic separator base material is a porous member made of an organic material. Examples of the organic separator base material include microporous films or nonwoven fabrics including polyolefin resins such as polyethylene and polypropylene, aromatic polyamide resins, and the like. From the viewpoint of excellent strength, a polyethylene microporous film or nonwoven fabric is preferred. In addition, the thickness of an organic separator base material can be made into arbitrary thickness, Usually, 0.5 micrometer or more, Preferably it is 5 micrometers or more, Usually, 40 micrometers or less, Preferably it is 30 micrometers or less, More preferably, it is 20 micrometers or less.

[Electrode substrate]
Although it does not specifically limit as an electrode base material (a positive electrode base material and a negative electrode base material), The electrode base material with which the electrode compound-material layer was formed on the electrical power collector is mentioned.
Here, the current collector, the electrode active material in the electrode mixture layer (positive electrode active material, negative electrode active material) and the binder for electrode mixture layer (binder for positive electrode mixture layer, binder for negative electrode mixture layer) As a method for forming the electrode mixture layer on the current collector and the current collector, known methods can be used, and examples thereof include those described in JP2013-145663A.

<Method for forming functional layer for non-aqueous secondary battery>
Examples of the method for forming a functional layer on a substrate such as the separator substrate and electrode substrate described above include the following methods.
1) A method in which the slurry composition is applied to the surface of a separator substrate or an electrode substrate (in the case of an electrode substrate, the surface on the electrode mixture layer side, the same shall apply hereinafter) and then dried;
2) A method of drying a separator substrate or an electrode substrate after immersing them in a slurry composition;
3) A method in which the slurry composition is applied onto a release substrate and dried to produce a functional layer, and the obtained functional layer is transferred to the surface of a separator substrate or an electrode substrate;
Among these, the method 1) is particularly preferable because the thickness of the functional layer can be easily controlled. Specifically, the method 1) includes a step of applying the slurry composition onto the substrate (application step), and a step of forming the functional layer by drying the slurry composition applied onto the substrate (functional layer). Forming step).

[Coating process]
In the coating process, the method of coating the slurry composition on the substrate is not particularly limited, and examples thereof include a doctor blade method, a reverse roll method, a direct roll method, a gravure method, an extrusion method, and a brush coating method. Is mentioned.

[Functional layer formation process]
In the functional layer forming step, the method for drying the slurry composition on the substrate is not particularly limited, and a known method can be used. For example, drying with hot air, hot air, low-humidity air, vacuum drying, infrared ray And a drying method by irradiation with electron beam or the like. The drying conditions are not particularly limited, but the drying temperature is preferably 50 to 150 ° C., and the drying time is preferably 5 to 30 minutes.

(Battery member having a functional layer)
The battery member (separator and electrode) provided with the functional layer of the present invention is not limited to the separator base or electrode base and the functional layer of the present invention as long as the effects of the present invention are not significantly impaired. You may provide components other than a functional layer. For example, you may have another functional layer between the separator base material or the electrode base material, and the functional layer of this invention as needed. In this case, the functional layer of the present invention is indirectly provided on the surface of the separator substrate or the electrode substrate. Moreover, the battery member provided with the functional layer of the present invention may have another functional layer on the surface of the functional layer of the present invention.

Here, the other functional layer is not particularly limited as long as it does not correspond to the functional layer of the present invention, and an adhesive layer provided on the functional layer of the present invention and used for bonding battery members to each other. Is mentioned.
In addition, when providing an adhesive layer as another functional layer on the functional layer of the present invention, in particular, when providing an adhesive layer that exhibits excellent adhesive force in the electrolyte as the other functional layer, the function of the present invention. If the peel strength of the layer in the electrolyte is not sufficiently high, even if the adhesive strength of the other functional layer (adhesive layer) is excellent, peeling may occur in the functional layer portion of the present invention, and the battery characteristics may deteriorate. There is. However, since the functional layer of the present invention also has high peel strength in the electrolytic solution, if the functional layer of the present invention is used, an adhesive layer that exhibits excellent adhesive force in the electrolytic solution is further laminated to form a battery member. Even if it is a case where it uses for adhesion | attachment of each other, a battery member can be adhere | attached favorably by making the adhesive layer exhibit expected performance. Incidentally, the adhesive layer exhibiting excellent adhesive force in the electrolytic solution is not particularly limited, and the core portion made of a polymer having an electrolytic solution swelling degree of 5 times or more and 30 times or less, and the electrolytic solution swelling degree is Examples include an adhesive layer formed using a polymer having a core-shell structure having a shell portion made of a polymer that is greater than 1 time and less than 4 times, such as an adhesive layer described in JP-A-2015-28842.

  The thickness of the functional layer of the present invention is preferably 0.01 μm or more, more preferably 0.1 μm or more, still more preferably 1 μm or more, preferably 20 μm or less, more preferably 10 μm or less, and even more preferably 5 μm or less. It is. When the thickness of the functional layer is 0.01 μm or more, the strength of the functional layer can be sufficiently ensured, and when it is 20 μm or less, the diffusibility of the electrolytic solution is secured, and the secondary using the functional layer The rate characteristics of the battery can be improved.

(Non-aqueous secondary battery)
The non-aqueous secondary battery of the present invention includes the above-described functional layer for a non-aqueous secondary battery of the present invention. More specifically, the non-aqueous secondary battery of the present invention includes a positive electrode, a negative electrode, a separator, and an electrolyte solution, and the functional layer for the non-aqueous secondary battery described above is a battery member of the positive electrode, the negative electrode, and the separator. Included in at least one. And since the non-aqueous secondary battery of this invention is equipped with the functional layer obtained from the slurry composition of this invention, it exhibits the outstanding battery characteristic.

<Positive electrode, negative electrode and separator>
At least one of the positive electrode, the negative electrode, and the separator used for the secondary battery of the present invention includes the functional layer of the present invention. Specifically, as a positive electrode and a negative electrode having a functional layer, an electrode in which the functional layer of the present invention is provided on an electrode substrate formed by forming an electrode mixture layer on a current collector can be used. . Moreover, as a separator which has a functional layer, the separator which provides the functional layer of this invention on a separator base material can be used. In addition, as an electrode base material and a separator base material, the thing similar to what was mentioned by the term of the "functional layer for non-aqueous secondary batteries" can be used.
Moreover, as a positive electrode, a negative electrode, and a separator which do not have a functional layer, it does not specifically limit, The electrode which consists of an electrode base material mentioned above, and the separator which consists of a separator base material mentioned above can be used.

<Electrolyte>
As the electrolytic solution, an organic electrolytic solution in which a supporting electrolyte is dissolved in an organic solvent is usually used. As the supporting electrolyte, for example, a lithium salt is used in a lithium ion secondary battery. Examples of the lithium salt include LiPF ₆ , LiAsF ₆ , LiBF ₄ , LiSbF ₆ , LiAlCl ₄ , LiClO ₄ , CF ₃ SO ₃ Li, C ₄ F ₉ SO ₃ Li, CF ₃ COOLi, (CF ₃ CO) ₂ NLi , (CF ₃ SO ₂ ) ₂ NLi, (C ₂ F ₅ SO ₂ ) NLi, and the like. Among these, LiPF ₆ , LiClO ₄ , and CF ₃ SO ₃ Li are preferable because they are easily dissolved in a solvent and exhibit a high degree of dissociation. In addition, electrolyte may be used individually by 1 type and may be used in combination of 2 or more types. Usually, the lithium ion conductivity tends to increase as the supporting electrolyte having a higher degree of dissociation is used, so that the lithium ion conductivity can be adjusted depending on the type of the supporting electrolyte.

The organic solvent used in the electrolytic solution is not particularly limited as long as it can dissolve the supporting electrolyte. For example, in a lithium ion secondary battery, dimethyl carbonate (DMC), ethylene carbonate (EC), diethyl carbonate (DEC). Carbonates such as propylene carbonate (PC), butylene carbonate (BC), and methyl ethyl carbonate (MEC); esters such as γ-butyrolactone and methyl formate; ethers such as 1,2-dimethoxyethane and tetrahydrofuran; sulfolane, Sulfur-containing compounds such as dimethyl sulfoxide; are preferably used. Moreover, you may use the liquid mixture of these solvents. Among these, carbonates are preferable because they have a high dielectric constant and a wide stable potential region. Usually, the lower the viscosity of the solvent used, the higher the lithium ion conductivity tends to be, so the lithium ion conductivity can be adjusted depending on the type of solvent.
The concentration of the electrolyte in the electrolytic solution can be adjusted as appropriate. Moreover, you may add a known additive to electrolyte solution.

(Method for producing non-aqueous secondary battery)
In the non-aqueous secondary battery of the present invention described above, for example, a positive electrode and a negative electrode are overlapped via a separator, and this is placed in a battery container by winding or folding as necessary. It can manufacture by inject | pouring and sealing, Preferably it manufactures using the manufacturing method of the non-aqueous secondary battery of this invention demonstrated in detail below. Of the positive electrode, the negative electrode, and the separator, at least one member is a member with a functional layer. In addition, an expanded metal, an overcurrent prevention element such as a fuse or a PTC element, a lead plate, or the like may be placed in the battery container to prevent an increase in pressure inside the battery or overcharge / discharge. The shape of the battery may be any of a coin shape, a button shape, a sheet shape, a cylindrical shape, a square shape, a flat shape, and the like.

Here, in the manufacturing method of the non-aqueous secondary battery of the present invention, the non-aqueous secondary battery is manufactured through the step of heat-pressing the above-described functional layer for the non-aqueous secondary battery of the present invention. Specifically, in the production method of the present invention, for example, a step (battery member preparation step) of preparing a battery member (positive electrode, negative electrode and separator) at least one having the functional layer of the present invention, and a prepared positive electrode And a negative electrode are stacked with a separator interposed between them and wound or bent as necessary to form a laminated body (laminated body forming process), and the laminated body is put into a battery container, and an electrolytic solution is put into the battery container. A non-aqueous secondary battery is manufactured by carrying out a step of filling and sealing (sealing step) and a step of heating and pressing the functional layer of the present invention together with the laminate (heat pressing step).
And in the manufacturing method of this invention, since the functional layer of this invention is heat-pressed, the peel strength in the electrolyte solution of a functional layer is further raised and the secondary battery which has the outstanding battery characteristic is manufactured efficiently. can do.

In the production method of the present invention, the hot pressing step may be performed before the enclosing step, but from the viewpoint of suppressing the occurrence of misalignment of the stacked battery members during the hot pressing, the hot pressing step Is preferably carried out after the encapsulation step.
Moreover, it is preferable to perform a heat press process in the state which contacted the functional layer and electrolyte solution (for example, in electrolyte solution). If the pressing is performed in a state where the functional layer and the electrolytic solution are in contact with each other and the water-insoluble particulate polymer or the like is swollen in the electrolytic solution, the peel strength of the functional layer in the electrolytic solution can be further increased.

Here, when performing the heat press process of the manufacturing method of this invention before an enclosure process, the temperature at the time of heat-pressing a functional layer exceeds the glass transition temperature (Tg) of a water-insoluble particulate polymer. It is good also as temperature. If heat-pressing is performed at a temperature exceeding the glass transition temperature (Tg) of the water-insoluble particulate polymer, the water-insoluble particulate polymer can exhibit a certain degree of adhesive force even before being immersed in the electrolyte, and the functional layer Can be formed satisfactorily. From the viewpoint of suppressing the water-insoluble particulate polymer from fluidizing and forming into a film in the functional layer, and suppressing the deterioration of the battery characteristics of the secondary battery, the heating press process is included in the encapsulation process. When performing before, it is preferable to make temperature at the time of carrying out the heat press of a functional layer below 30 degreeC higher than the glass transition temperature (Tg) of a water-insoluble particulate polymer (Tg + 30 degreeC).
On the other hand, when the heating press step of the production method of the present invention is performed after the encapsulation step, the temperature when the functional layer is hot pressed is 40 ° C. lower than the glass transition temperature (Tg) of the water-insoluble particulate polymer. It is preferable to set the temperature (Tg-40 ° C) or higher, more preferably 35 ° C lower than Tg (Tg-35 ° C) or higher, and 30 ° C lower than Tg (Tg-30 ° C) or higher. Is more preferable. Moreover, when performing a heat press process after an enclosure process, in the heat press process, the temperature at the time of carrying out the heat press of a functional layer shall be below the glass transition temperature (Tg) of a water-insoluble particulate polymer. Preferably, the temperature is 5 ° C. lower than Tg (Tg−5 ° C.) or lower, and more preferably 10 ° C. lower than Tg (Tg−10 ° C.) or lower. When the hot pressing process is performed after the sealing process, if the temperature at which the functional layer is hot pressed is set to 40 ° C. or lower than Tg, high adhesion to the water-insoluble particulate polymer is exhibited in the electrolytic solution. The peel strength of the functional layer can be further increased. In addition, when the heating press process is performed after the encapsulation process, if the temperature at which the functional layer is heated and pressed is Tg or less, the deterioration of the substrate can be prevented, and water-insoluble particles can be prevented during the heating press. It is possible to suppress the fluidized polymer from fluidizing and forming into a film in the functional layer, and to suppress the deterioration of the battery characteristics of the secondary battery.
In addition, the pressure at the time of carrying out the heat press of the functional layer in a heat press process is not specifically limited, For example, it can be 0.7 MPa or more and 5 MPa or less.

EXAMPLES Hereinafter, although this invention is demonstrated concretely based on an Example, this invention is not limited to these Examples. In the following description, “%” and “part” representing amounts are based on mass unless otherwise specified.
In addition, in a polymer produced by copolymerizing a plurality of types of monomers, the proportion of the structural unit formed by polymerizing a certain monomer in the polymer is usually that unless otherwise specified. This coincides with the ratio (preparation ratio) of the certain monomer in the total monomers used for polymerization of the polymer.
In Examples and Comparative Examples, polymer electrolyte swelling degree, glass transition temperature and volume average particle diameter, stability of slurry composition for non-aqueous secondary battery functional layer under high shear, for non-aqueous secondary battery The peel strength of the functional layer before immersion in the electrolyte solution, the peel strength after immersion of the electrolyte solution, and the rate characteristics and life characteristics of the secondary battery were measured and evaluated by the following methods.

<Electrolytic solution swelling>
The aqueous dispersion of the polymer is applied to an electrolytic copper foil (NC-WS (registered trademark) manufactured by Furukawa Electric) using a table coater, 20 minutes at 50 ° C, 20 minutes at 120 ° C, with a hot air dryer. The film was dried to produce a 1 cm × 1 cm film (thickness: 500 μm), and the weight M0 was measured. Thereafter, the obtained film was immersed in a nonaqueous electrolytic solution at 60 ° C. for 72 hours. Here, as the non-aqueous electrolyte, a mixed solvent of ethylene carbonate (EC), diethyl carbonate (DEC), and vinylene carbonate (VC) (volume mixing ratio: EC / DEC / VC = 68.5 / 30 / In 1.5), LiPF ₆ dissolved in a mixed solvent at a concentration of 1 mol / L was used as a supporting electrolyte. Thereafter, the non-aqueous electrolyte solution on the surface of the film after immersion was wiped off, and the weight M1 was measured. And according to the following formula, electrolyte solution swelling degree was computed.
Electrolyte swelling degree = M1 / M0
<Glass transition temperature>
The aqueous dispersion containing the polymer was dried for 3 days in an environment of 50% humidity and 23 to 25 ° C. to obtain a film having a thickness of 1 ± 0.3 mm. The film was dried in a 120 ° C. hot air oven for 1 hour. Then, using the dried film as a sample, a differential scanning calorimeter (DSC6220SII, manufactured by Nanotechnology Co., Ltd.) is used at a measurement temperature of −100 ° C. to 180 ° C. and a temperature increase rate of 5 ° C./min according to JIS K7121. The glass transition temperature (° C) was measured.
<Volume average particle diameter>
An aqueous dispersion containing a polymer is diluted with ion-exchanged water to prepare a measurement sample having a solid content concentration of 2% by mass, and a laser diffraction / light scattering type particle size distribution analyzer (LS230, manufactured by Beckman Coulter, Inc.) is used. The volume average particle diameter (D50) of the particulate polymer was measured.
<Stability under high shear>
The slurry composition was applied onto a separator substrate (made of polyethylene) using a gravure roll (number of lines: 95) under the conditions of a conveyance speed of 50 m / min and a gravure rotation ratio of 100%. Cut out and the coating amount Q0 (mg / cm ² ) per unit area was calculated. Further, the coating amount Q1 (mg / cm ² ) was similarly calculated 1 hour after the start of coating. Then, a coating amount change rate ΔQ (%) was calculated using an equation of ΔQ = (| Q0−Q1 |) / Q0 × 100 (%), and evaluated according to the following criteria. The smaller the coating amount change rate ΔQ, the smaller the change in the coating amount and the higher the stability of the slurry composition under high shear.
A: Application rate change rate ΔQ is less than 5% B: Application rate change rate ΔQ is 5% or more and less than 10% C: Application rate change rate ΔQ is 10% or more and less than 20% D: Application rate change rate ΔQ is 20% or more <Peel strength before immersion in electrolyte>
An organic separator substrate made of a polyethylene porous substrate (manufactured by Celgard, thickness 16 μm) was prepared. The slurry composition was applied to one side of the prepared organic separator substrate and dried at 60 ° C. for 10 minutes to obtain a separator with a functional layer (porous membrane layer) having a thickness of 18 μm. And it cut out into the rectangle of length 100mm and width 10mm, and it was set as the test piece. Moreover, the cellophane tape was fixed to the test stand beforehand. As this cellophane tape, the one specified in JIS Z1522 was used.
And the test piece cut out from the separator was affixed on the cellophane tape with the functional layer (porous membrane layer) facing down. Thereafter, the stress was measured when one end of the separator was pulled in the vertical direction at a pulling speed of 100 mm / min and peeled off. The measurement was performed three times, the average value of the measured stress was determined, and this was defined as the peel strength before immersion of the functional layer in the electrolyte solution. And it evaluated on the following reference | standard.
A: Peel strength is 50 N / m or more B: Peel strength is 35 N / m or more and less than 50 N / m C: Peel strength is 20 N / m or more and less than 35 N / m D: Peel strength is less than 20 N / m <After electrolytic solution immersion Peel strength>
Two organic separator substrates made of a polyethylene porous substrate (manufactured by Celgard, thickness 16 μm) were prepared. The slurry composition was applied to one surface of one organic separator substrate, and the other organic separator substrate was stacked on the coated surface. And it was made to dry for 10 minutes at 60 degreeC, and the laminated body (laminated body of an organic separator base material, a functional layer, and an organic separator base material) with a thickness of 34 micrometers was obtained. Thereafter, the laminate was cut into a rectangle having a length of 100 mm and a width of 10 mm to obtain a test piece.
The obtained test piece was immersed in a non-aqueous electrolyte at a temperature of 60 ° C. for 3 days. Here, as the non-aqueous electrolyte, a mixed solvent of ethylene carbonate (EC), diethyl carbonate (DEC), and vinylene carbonate (VC) (volume mixing ratio: EC / DEC / VC = 68.5 / 30 / In 1.5), LiPF ₆ dissolved in a mixed solvent at a concentration of 1 mol / L was used as a supporting electrolyte.
Thereafter, the test piece immersed in the electrolytic solution was pressed under conditions of 1 MPa and 80 ° C. for 2 minutes, one organic separator substrate was fixed, and one end of the other organic separator substrate was pulled vertically upward at a speed of 50 mm / min. The stress when it was pulled and peeled off was measured. The measurement was performed three times, the average value of the measured stress was determined, and this was taken as the peel strength after the functional layer was immersed in the electrolytic solution. And it evaluated on the following reference | standard.
A: Peel strength is 9.0 N / m or more B: Peel strength is 8.0 N / m or more and less than 9.0 N / m C: Peel strength is 6.0 N / m or more and less than 8.0 N / m D: Peel strength is <6.0 N / m <Rate characteristics>
The produced secondary battery was allowed to stand for 12 hours in an environment at 60 ° C. in a 20% charged state, and then charged at 4.35 V and 0.1 C in an environment at 25 ° C., 2.75 V and 0.1 C. The initial capacity C0 was measured by performing a charge / discharge operation. Thereafter, in a 25 ° C. environment, 4.35 V, 0.1 C charge, 2.75 V, and 2 C discharge were performed, and the capacity C1 was measured. Then, ΔC = {(C0−C1) / C0} × 100 (%) was calculated and evaluated according to the following criteria. It shows that it is excellent in a rate characteristic, so that (DELTA) C is large.
A: ΔC is 90% or more B: ΔC is 85% or more and less than 90% C: ΔC is 80% or more and less than 85% D: ΔC is less than 80% <lifetime characteristics>
The produced secondary battery was left in a 20% charged state at 60 ° C. for 12 hours, and then charged at 4.35 V and 0.1 C in an environment at 25 ° C., 2.75 V and 0.1 C. The charging / discharging operation was performed by discharging. Thereafter, the battery was charged at 4.35 V and 0.1 C, and allowed to stand at 60 ° C. for 168 hours (7 days). Thereafter, the cell voltage V2 (V) was measured at 25 ° C. The voltage drop ΔV (mV) was calculated using the equation: ΔV = {4.35−V2} × 1000 and evaluated as follows. It shows that it is excellent in the lifetime characteristic (self-discharge characteristic), so that this value is small.
A: Voltage drop ΔV is 200 mV or less B: Voltage drop ΔV is more than 200 mV and 400 mV or less C: Voltage drop ΔV is more than 400 mV and 600 mV or less D: Voltage drop ΔV is more than 600 mV

Example 1
<Preparation of water-insoluble particulate polymer>
In a reactor equipped with a stirrer, 150 parts of ion-exchanged water, 0.1 part of sodium lauryl sulfate (product name “Emar 2F”, manufactured by Kao Chemical Co., Ltd.) as an emulsifier, and ammonium persulfate as a polymerization initiator 0.3 parts were respectively supplied, the gas phase part was replaced with nitrogen gas, and the temperature was raised to 80 ° C.
On the other hand, in a separate container, 40 parts of ion exchange water, 0.2 part of sodium dodecylbenzenesulfonate as a dispersant, 96 parts of styrene as an aromatic monovinyl monomer, and methacrylic acid as an acidic group-containing monomer. 2 parts of acid and 2 parts of ethylene dimethacrylate as a crosslinkable monomer were mixed to obtain a monomer composition. And the obtained monomer composition was continuously added to the said reactor over 3 hours, and superposition | polymerization was performed. In addition, reaction was performed at 80 degreeC during addition of a monomer composition. After completion of the addition, the reaction was terminated by further stirring at 80 ° C. for 2 hours to obtain an aqueous dispersion of a water-insoluble particulate polymer.
And about the obtained water-insoluble particulate polymer, electrolyte solution swelling degree, glass transition temperature, and volume average particle diameter were measured. The results are shown in Table 1.
<Preparation of adhesive polymer>
In a reactor equipped with a stirrer, 90 parts of ion-exchanged water and 0.5 part of ammonium persulfate as a polymerization initiator were supplied, the gas phase part was replaced with nitrogen gas, and the temperature was raised to 80 ° C. .
On the other hand, in a separate container, 40 parts of ion-exchanged water, 0.8 part of sodium dodecylbenzenesulfonate as an emulsifier, and 65.1 parts of 2-ethylhexyl acrylate as a (meth) acrylic acid alkyl ester monomer, aroma 30 parts of styrene as an aromatic monovinyl monomer, 3 parts of acrylic acid as an acidic group-containing monomer, 1.7 parts of allyl glycidyl ether as a crosslinkable monomer and 0.2 part of allyl methacrylate A mass composition was obtained. And the obtained monomer composition was continuously added to the said reactor over 4 hours, and superposition | polymerization was performed. In addition, reaction was performed at 80 degreeC during addition of a monomer composition. After completion of the addition, the reaction was further terminated by stirring at 80 ° C. for 3 hours to obtain an aqueous dispersion of a particulate adhesive polymer.
And about the obtained adhesive polymer, electrolyte solution swelling degree, glass transition temperature, and volume average particle diameter were measured. The results are shown in Table 1.
<Preparation of binder composition for non-aqueous secondary battery functional layer>
The aqueous dispersion of the water-insoluble particulate polymer and the aqueous dispersion of the adhesive polymer were mixed in an amount of 5 parts of water-insoluble particulate polymer per 100 parts of the adhesive polymer (in terms of solid content) ( Solid content conversion) and stirred at 25 ° C. for 30 minutes to obtain a binder composition.
<Preparation of slurry composition for non-aqueous secondary battery functional layer>
Boehmite filler (BMM-W, manufactured by Kawai Lime Industry Co., Ltd.) as non-conductive particles and a total amount (in terms of solid content) of the water-insoluble particulate polymer and adhesive polymer is 3 parts. A binder composition, 1.0 part of carboxymethyl cellulose (Daicel 1220) as a thickener, 0.2 part of a polyethylene glycol type surfactant (San Nopco SN wet 366), and ion-exchanged water are mixed together to form a slurry composition. I got a thing.
And about the obtained slurry composition, stability under high shear was evaluated. Moreover, the peel strength before electrolyte solution immersion of the functional layer and the peel strength after electrolyte solution immersion were evaluated using the obtained slurry composition. The results are shown in Table 1.
<Preparation of other functional layer compositions>
-Preparation of organic particles having a core-shell structure-
In a 5 MPa pressure vessel with a stirrer, 75 parts of methyl methacrylate as a (meth) acrylic acid ester monomer, 4 parts of methacrylic acid as an acid group-containing monomer, 1 part of ethylene glycol dimethacrylate; 1 part of sodium dodecylbenzenesulfonate as an emulsifier; 150 parts of ion-exchanged water and 0.5 part of potassium persulfate as a polymerization initiator were added and sufficiently stirred. Then, it heated to 60 degreeC and superposition | polymerization was started. Polymerization was continued until the polymerization conversion rate reached 96% to obtain an aqueous dispersion containing a particulate polymer constituting the core portion.
To this aqueous dispersion, a mixture of 19 parts of styrene as an aromatic monovinyl monomer and 1 part of methacrylic acid as an acid group-containing monomer was continuously added to form a shell part, and heated to 70 ° C. Polymerization was continued. When the polymerization conversion rate reached 96%, the reaction was stopped by cooling to prepare an aqueous dispersion containing organic particles having a core-shell structure in which the outer surface of the core part was partially covered with the shell part.
In addition, the volume average particle diameter of the obtained organic particles was 0.45 μm.
-Preparation of binder-
In a reactor equipped with a stirrer, 70 parts of ion-exchanged water, 0.15 part of sodium lauryl sulfate (product name “Emar 2F”, manufactured by Kao Chemical Co., Ltd.) as an emulsifier, and ammonium persulfate 0 as a polymerization initiator .5 parts were respectively supplied, the gas phase part was replaced with nitrogen gas, and the temperature was raised to 60 ° C.
On the other hand, in a separate container, 50 parts of ion exchange water, 0.5 part of sodium dodecylbenzenesulfonate as a dispersant, 94 parts of butyl acrylate, 2 parts of acrylonitrile, 2 parts of methacrylic acid, 1 part of N-methylolacrylamide 1 part of acrylamide was mixed to obtain a monomer composition. This monomer composition was continuously added to the reactor over 4 hours for polymerization. During the addition of the monomer composition, the reaction was performed at 60 ° C. After completion of the addition, the reaction was further terminated by stirring at 70 ° C. for 3 hours to prepare an aqueous dispersion containing a particulate binder (acrylic polymer).
The obtained binder had a glass transition temperature of −40 ° C.
-Preparation of composition-
The aqueous dispersion containing the organic particles having the core-shell structure is 100 parts in terms of solid content, and the aqueous dispersion containing the binder is 15 parts in terms of solid content, ethylene oxide-propylene oxide as a wetting agent. Copolymer (solid content concentration 70% by mass, polymerization ratio: 5/5 (mass ratio)) is mixed with 1.9 parts in terms of solid content, and ion exchange water is further added so that the solid content concentration becomes 15% by mass. By mixing, a slurry-like composition was prepared.
<Preparation of separator for non-aqueous secondary battery including functional layer>
An organic separator substrate made of a polyethylene porous substrate (manufactured by Celgard, thickness 16 μm) was prepared. The slurry composition for non-aqueous secondary battery functional layers was applied to one side of the prepared organic separator substrate, and dried at 60 ° C. for 10 minutes. As a result, a separator having a functional layer (porous membrane layer) having a thickness of 18 μm was obtained.
To the separator provided with the functional layer (porous membrane layer), other functional layer compositions were applied on both sides to a thickness of 1 μm and dried at 60 ° C. for 10 minutes. Thereby, a separator having a thickness of 20 μm provided with a functional layer (porous membrane layer) and other functional layers (adhesive layer) was obtained.
<Preparation of positive electrode for non-aqueous secondary battery>
100 parts of LiCoO ₂ (volume average particle diameter: 12 μm) as the positive electrode active material, ₂ parts of acetylene black (“HS-100” manufactured by Denki Kagaku Kogyo Co., Ltd.) as the conductive material, binder for the positive electrode mixture layer As a solid content, 2 parts of polyvinylidene fluoride (manufactured by Kureha Co., Ltd., # 7208) and N-methylpyrrolidone as a solvent were mixed to give a total solid content concentration of 70%. These were mixed by a planetary mixer to prepare a positive electrode slurry composition.
The positive electrode slurry composition obtained as described above was applied onto a 20 μm-thick aluminum foil as a current collector with a comma coater so that the film thickness after drying was about 150 μm and dried. I let you. This drying was performed by transporting the aluminum foil in an oven at 60 ° C. at a speed of 0.5 m / min for 2 minutes. Thereafter, heat treatment was performed at 120 ° C. for 2 minutes to obtain a positive electrode raw material. The positive electrode raw material before pressing was rolled with a roll press to obtain a positive electrode after pressing with a positive electrode mixture layer thickness of 80 μm.
<Preparation of negative electrode for non-aqueous secondary battery>
In a 5 MPa pressure vessel with a stirrer, 33 parts of 1,3-butadiene, 3.5 parts of itaconic acid, 63.5 parts of styrene, 0.4 part of sodium dodecylbenzenesulfonate as an emulsifier, 150 parts of ion-exchanged water and a polymerization initiator After adding 0.5 parts of potassium persulfate as a mixture and sufficiently stirring, the mixture was heated to 50 ° C. to initiate polymerization. When the polymerization conversion rate reached 96%, the reaction was stopped by cooling to obtain a mixture containing a particulate binder (SBR) for the negative electrode mixture layer. A 5% aqueous sodium hydroxide solution was added to the mixture containing the particulate binder and the pH was adjusted to 8, and then the unreacted monomer was removed by heating under reduced pressure. Then, it cooled to 30 degrees C or less, and obtained the water dispersion liquid containing a desired particulate-form binder.
Next, 100 parts of artificial graphite (volume average particle diameter: 15.6 μm) as a negative electrode active material and a 2% aqueous solution of carboxymethylcellulose sodium salt (manufactured by Nippon Paper Industries Co., Ltd., “MAC350HC”) as a thickener 1 part and ion-exchanged water were mixed to adjust the solid content concentration to 68%, and then mixed at 25 ° C. for 60 minutes. Subsequently, it adjusted with ion-exchange water so that solid content concentration might be 62%, and also mixed for 15 minutes at 25 degreeC. After that, 1.5 parts of the aqueous dispersion containing the particulate binder described above and ion-exchanged water are added to the obtained mixed liquid and adjusted so that the final solid content concentration is 52%. And mixed for another 10 minutes. This was defoamed under reduced pressure to obtain a negative electrode slurry composition having good fluidity.
Then, the negative electrode slurry composition obtained as described above was applied on a copper foil having a thickness of 20 μm, which is a current collector, with a comma coater so that the film thickness after drying was about 150 μm. , Dried. This drying was performed by conveying the copper foil in an oven at 60 ° C. at a speed of 0.5 m / min for 2 minutes. Thereafter, heat treatment was performed at 120 ° C. for 2 minutes to obtain a negative electrode raw material before pressing. The negative electrode raw material before pressing was rolled with a roll press to obtain a negative electrode after pressing with a negative electrode mixture layer thickness of 80 μm.
<Manufacture of non-aqueous secondary batteries>
The pressed positive electrode obtained above was cut out to 49 cm × 5 cm and placed so that the surface of the positive electrode mixture layer side was on the upper side, and a separator for a non-aqueous secondary battery cut out to 120 cm × 5.5 cm ( The separator provided with the functional layer and other functional layers) was disposed so that the positive electrode was located on the left side in the longitudinal direction of the separator. Further, the pressed negative electrode obtained above was cut out into 50 cm × 5.2 cm, and this was cut on the separator so that the surface on the negative electrode mixture layer side faced the separator, and the negative electrode was on the right side in the longitudinal direction of the separator. It arranged so that it may be located in. This was wound by a winding machine around the middle in the longitudinal direction of the separator to obtain a wound body (laminate). The wound body was pressed at 60 ° C. and 0.5 MPa to form a flat body, and then wrapped with an aluminum packaging exterior as a battery exterior. Electrolyte (solvent: EC / DEC / VC (volume mixing ratio) = 68 5/30 / 1.5, electrolyte: LiPF ₆ ) with a concentration of 1M was injected so that no air remained. Furthermore, in order to seal the opening of the aluminum packaging material exterior, heat sealing at 150 ° C. was performed to close the aluminum packaging material exterior. Thereafter, the wound body enclosed in the aluminum packaging material exterior is pressed together with the aluminum packaging material exterior at a temperature of 80 ° C. and a pressure of 1 MPa for 2 minutes to produce a wound lithium ion secondary battery with a discharge capacity of 1000 mAh as a non-aqueous secondary battery. did.
And the rate characteristic and lifetime characteristic were evaluated about the obtained secondary battery. The results are shown in Table 1.

(Examples 2 to 4)
At the time of preparing the binder composition for the non-aqueous secondary battery functional layer, the mixing ratio of the water dispersion of the water-insoluble particulate polymer and the water dispersion of the adhesive polymer was changed, and 100 parts of the adhesive polymer was obtained. In the same manner as in Example 1 except that the amount of the water-insoluble particulate polymer (in terms of solid content) (in terms of solid content) was as shown in Table 1, a water-insoluble particulate polymer, An adhesive polymer, a binder composition, a slurry composition, other functional layer compositions, a separator, a positive electrode, a negative electrode, and a secondary battery were prepared and evaluated in the same manner as in Example 1. The results are shown in Table 1.

(Example 5)
When preparing the water-insoluble particulate polymer, the amount of styrene as the aromatic monovinyl monomer was changed to 70 parts, and 26 parts of 2-ethylhexyl acrylate as a (meth) acrylic acid alkyl ester monomer was further added. In the same manner as in Example 1 except that the monomer composition was obtained, a water-insoluble particulate polymer, an adhesive polymer, a binder composition, a slurry composition, other functional layer compositions, a separator A positive electrode, a negative electrode, and a secondary battery were prepared and evaluated in the same manner as in Example 1. The results are shown in Table 1.

(Example 6)
The water-insoluble particulate polymer, adhesiveness was the same as in Example 1 except that the amount of ammonium persulfate as a polymerization initiator was changed to 0.4 part during the preparation of the water-insoluble particulate polymer. A polymer, a binder composition, a slurry composition, other functional layer compositions, a separator, a positive electrode, a negative electrode, and a secondary battery were prepared and evaluated in the same manner as in Example 1. The results are shown in Table 1.

(Example 7)
The water-insoluble particulate polymer, adhesiveness was the same as in Example 1 except that the amount of ammonium persulfate as a polymerization initiator was changed to 0.2 parts when preparing the water-insoluble particulate polymer. A polymer, a binder composition, a slurry composition, other functional layer compositions, a separator, a positive electrode, a negative electrode, and a secondary battery were prepared and evaluated in the same manner as in Example 1. The results are shown in Table 1.

(Examples 8 to 9)
When preparing the adhesive polymer, the amount of 2-ethylhexyl acrylate as the (meth) acrylic acid alkyl ester monomer and the amount of styrene as the aromatic monovinyl monomer were changed as shown in Table 1 A water-insoluble particulate polymer, an adhesive polymer, a binder composition, a slurry composition, other functional layer compositions, a separator, a positive electrode, and a negative electrode in the same manner as in Example 1 except that a body composition was obtained. A secondary battery was prepared and evaluated in the same manner as in Example 1. The results are shown in Table 1.

(Examples 10 to 11)
When preparing the slurry composition for the non-aqueous secondary battery functional layer, the blending amount of the binder composition is changed, and the total amount (in terms of solid content) of the water-insoluble particulate polymer and the adhesive polymer is shown in Table 1. In the same manner as in Example 1 except that the amount was changed, the water-insoluble particulate polymer, adhesive polymer, binder composition, slurry composition, other functional layer composition, separator, positive electrode, negative electrode A secondary battery was prepared and evaluated in the same manner as in Example 1. The results are shown in Table 1.

(Comparative Example 1)
When preparing water-insoluble particulate polymer, styrene as an aromatic monovinyl monomer and ethylene dimethacrylate as a crosslinkable monomer are not used, but butyl acrylate as a (meth) acrylic acid alkyl ester monomer In the same manner as in Example 1, except that 96 parts and 2 parts of N-methylolacrylamide as a crosslinkable monomer were further added to obtain a monomer composition, a water-insoluble particulate polymer, adhesive weight A coalescence, a binder composition, a slurry composition, other functional layer compositions, a separator, a positive electrode, a negative electrode, and a secondary battery were prepared and evaluated in the same manner as in Example 1. The results are shown in Table 1.

(Comparative Example 2)
When preparing the water-insoluble particulate polymer, the amount of styrene as the aromatic monovinyl monomer was changed to 55 parts, and 41 parts of 2-ethylhexyl acrylate as a (meth) acrylic acid alkyl ester monomer was further added. In the same manner as in Example 1 except that the monomer composition was obtained, a water-insoluble particulate polymer, an adhesive polymer, a binder composition, a slurry composition, other functional layer compositions, a separator A positive electrode, a negative electrode, and a secondary battery were prepared and evaluated in the same manner as in Example 1. The results are shown in Table 1.

(Comparative Example 3)
When preparing the water-insoluble particulate polymer, the amount of styrene as the aromatic monovinyl monomer was changed to 57.5 parts, and the amount of methacrylic acid as the acidic group-containing monomer was changed to 0.5 parts. In the same manner as in Example 1, except that 40 parts of methyl methacrylate as a (meth) acrylic acid alkyl ester monomer was further added to obtain a monomer composition, a water-insoluble particulate polymer, adhesive A functional polymer, a binder composition, a slurry composition, other functional layer compositions, a separator, a positive electrode, a negative electrode, and a secondary battery were prepared and evaluated in the same manner as in Example 1. The results are shown in Table 1.

(Comparative Example 4)
When preparing a slurry composition for a non-aqueous secondary battery functional layer, 100 parts of boehmite filler (BMM-W, manufactured by Kawai Lime Industry Co., Ltd.) as non-conductive particles without using a thickener or the like and water-insoluble A binder composition in which the total amount of the particulate polymer and the adhesive polymer (in terms of solid content) is 3 parts and N-methylpyrrolidone are mixed, and then water is removed to form a water-insoluble particulate form. A water-insoluble particulate polymer, an adhesive polymer, a binder composition, a slurry composition, and other functions in the same manner as in Example 1 except that a slurry composition in which the polymer was dissolved in N-methylpyrrolidone was obtained. A layer composition, a separator, a positive electrode, a negative electrode, and a secondary battery were prepared and evaluated in the same manner as in Example 1. The results are shown in Table 1.

In Table 1 shown below,
“St” represents styrene, “MAA” represents methacrylic acid,
“2-EHA” represents 2-ethylhexyl acrylate, “BA” represents butyl acrylate,
“MMA” indicates methyl methacrylate;
“EDMA” refers to ethylene dimethacrylate,
“NMA” indicates N-methylolacrylamide,
“AA” indicates acrylic acid;
“AGE” refers to allyl glycidyl ether;
“AMA” indicates allyl methacrylate,
“NMP” refers to N-methylpyrrolidone.

From Table 1, a water-insoluble particulate polymer having a glass transition temperature of 50 ° C. or higher and an electrolyte solution swelling degree of more than 1 and less than 3 times, and an adhesive weight having a glass transition temperature of 20 ° C. or less. In Examples 1 to 11 using the union, it can be seen that a secondary battery having high peel strength before and after immersion of the functional layer in the electrolyte solution and excellent in battery characteristics can be obtained. Further, from Table 1, Comparative Example 1 using a water-insoluble particulate polymer having a low glass transition temperature and a large degree of electrolyte swelling, Comparison using a water-insoluble particulate polymer having a low glass transition temperature In Example 2 and Comparative Example 3 using a water-insoluble particulate polymer having a high degree of electrolyte swelling, the peel strength of the functional layer after immersion in the electrolyte is low, and the rate characteristics of the secondary battery may be reduced. I understand. Furthermore, from Table 1, in Comparative Example 4 in which a polymer having a glass transition temperature of 50 ° C. or higher and an electrolyte swelling degree of more than 1 time and less than 3 times was dissolved in N-methylpyrrolidone, It can be seen that the polymer becomes a film in the layer, the internal resistance increases, and the rate characteristics and life characteristics of the secondary battery are degraded.
In addition, from Examples 1 to 4, by adjusting the blending ratio of the water-insoluble particulate polymer and the adhesive polymer, the peel strength of the functional layer before immersion in the electrolyte and the peel strength after immersion of the electrolyte are obtained. It can be seen that the balance can be improved.
Furthermore, from Example 1 and Example 5, by adjusting the composition of the water-insoluble particulate polymer, it is possible to increase the peel strength after immersion of the functional layer in the electrolyte and improve the rate characteristics of the secondary battery. I understand. Moreover, it turns out that the secondary battery which is excellent in a battery characteristic is obtained by performing the heat press of a functional layer in the electrolyte solution at the temperature below the glass transition temperature of a water-insoluble particulate polymer.
Moreover, from Example 1 and Examples 6-7, by adjusting the particle diameter of the water-insoluble particulate polymer, the stability of the slurry composition, the peel strength after immersion of the functional layer in the electrolyte solution, and two It can be seen that the life characteristics of the secondary battery can be improved in a well-balanced manner.
Furthermore, it can be seen from Example 1 and Examples 8 to 9 that by adjusting the composition of the adhesive polymer, the peel strength of the functional layer before immersion in the electrolyte and the life characteristics of the secondary battery can be improved.
And from Example 1 and Examples 10-11, by adjusting the compounding quantity of a binder composition, the peel strength before and behind the electrolyte solution of a functional layer and the battery characteristic of a secondary battery can be improved with good balance. I understand.

According to the present invention, when used for the formation of a functional layer, a non-aqueous system capable of increasing the peel strength after immersion of the functional layer by exhibiting high adhesiveness even in the electrolytic solution while suppressing an increase in internal resistance. A binder composition for a secondary battery functional layer can be provided.
Moreover, according to this invention, the slurry composition for non-aqueous secondary battery functional layers which can form a functional layer with high peel strength even after electrolyte immersion, suppressing the increase in internal resistance can be provided. .
Furthermore, according to the present invention, it is possible to provide a functional layer for a non-aqueous secondary battery that has a high peel strength even after being immersed in an electrolytic solution and can exhibit excellent battery characteristics in the non-aqueous secondary battery.
And according to this invention, the non-aqueous secondary battery excellent in a battery characteristic and its manufacturing method can be provided.

Claims (9)

A binder composition for a non-aqueous secondary battery functional layer containing a water-insoluble particulate polymer, an adhesive polymer, and water,
The water-insoluble particulate polymer has a glass transition temperature of 50 ° C. or higher and an electrolyte swelling degree of more than 1 time and less than 3 times,
The adhesive polymer state, and are the glass transition temperature of 20 ° C. or less,
The binder composition for a nonaqueous secondary battery functional layer , wherein the content of the water-insoluble particulate polymer is 1 part by mass or more and 20 parts by mass or less per 100 parts by mass of the adhesive polymer .   The binder composition for a non-aqueous secondary battery functional layer according to claim 1, wherein the water-insoluble particulate polymer has a volume average particle diameter of 50 nm or more and 400 nm or less. The water-insoluble particulate polymer is an aromatic monovinyl the monomer unit not less than 70 wt% containing 99 wt% or less, a non-aqueous secondary battery functional layer binder composition according to claim 1 or 2. The binder composition for a non-aqueous secondary battery functional layer according to any one of claims 1 to 3 , wherein the degree of swelling of the electrolytic solution of the adhesive polymer is more than 1 time and less than 3 times. The adhesive polymer, (meth) comprises more than 35 wt% acrylic acid alkyl ester monomer unit, an aromatic monovinyl monomer units containing 10 wt% or more 55 wt% or less, any claim 1-4 A binder composition for a non-aqueous secondary battery functional layer according to claim 1. The slurry composition for non-aqueous secondary battery functional layers containing the binder composition for non-aqueous secondary battery functional layers in any one of Claims 1-5, and a nonelectroconductive particle. The functional layer for non-aqueous secondary batteries formed from the slurry composition for non-aqueous secondary battery functional layers according to claim 6 . A nonaqueous secondary battery comprising the functional layer for a nonaqueous secondary battery according to claim 7 . Comprising the step of heat-pressing a non-aqueous secondary battery functional layer according to claim 7, the manufacturing method of the nonaqueous secondary battery of claim 8.