JP6831633B2 - Solid electrolyte membrane and all-solid-state lithium-ion battery - Google Patents

Description

The present invention relates to a solid electrolyte membrane and an all-solid-state lithium-ion battery.

Lithium-ion batteries are generally used as a power source for small portable devices such as mobile phones and laptop computers. Recently, in addition to small portable devices, lithium-ion batteries have begun to be used as power sources for electric vehicles and electric power storage.

Currently commercially available lithium ion batteries use an electrolytic solution containing a flammable organic solvent. On the other hand, a lithium-ion battery (hereinafter, also referred to as an all-solid-state lithium-ion battery) in which the electrolyte is changed to a solid electrolyte and the battery is completely solidified does not use a flammable organic solvent in the battery, and thus is a safety device. It is considered that the manufacturing cost and productivity are excellent.

In such an all-solid-state lithium-ion battery, a solid electrolyte sheet mainly containing a solid electrolyte material is used as the solid electrolyte layer. Examples of such a solid electrolyte sheet are described in Patent Documents 1 and 2 below.

Patent Document 1 (Japanese Unexamined Patent Publication No. 4-133209) describes a solid electrolyte sheet containing a mixture of a lithium ion conductive solid electrolyte and a thermoplastic polymer resin.

Patent Document 2 (Japanese Unexamined Patent Publication No. 2008-124011) describes the production of a crystalline solid electrolyte sheet in which a glass-like lithium ion conductive solid electrolyte is formed into a sheet and then heat-treated, or is formed into a sheet and then heat-treated. The method is described.

Japanese Unexamined Patent Publication No. 4-133209 Japanese Unexamined Patent Publication No. 2008-124011

However, since the binder resin such as the thermoplastic polymer resin has almost no ionic conductivity, if the binder resin is present between the solid electrolyte materials, the ionic conduction between the solid electrolyte materials is hindered. Therefore, the solid electrolyte sheet as described in Patent Document 1 has low lithium ion conductivity, and is not yet satisfactory as a solid electrolyte sheet for an all-solid-state lithium ion battery.
Further, according to the study by the present inventors, it has become clear that the battery characteristics of the obtained all-solid-state lithium-ion battery are not yet satisfactory for the solid electrolyte sheet as described in Patent Document 2. It was.

The present invention has been made in view of the above circumstances, and provides a solid electrolyte membrane capable of realizing an all-solid-state lithium-ion battery having excellent battery characteristics, and an all-solid-state lithium-ion battery having excellent battery characteristics.

The present inventors have diligently studied to achieve the above-mentioned problems. As a result, they have found that an all-solid-state lithium-ion battery having excellent battery characteristics can be obtained by highly controlling the uniformity of the thickness of the solid electrolyte membrane, and have reached the present invention.

That is, according to the present invention.
A solid electrolyte membrane containing a sulfide-based inorganic solid electrolyte material having lithium ion conductivity as a main component.
The standard deviation of the thickness of the solid electrolyte membrane is 5.0 μm or less.
Ri average thickness 60.4 [mu] m or more 180μm der less of said solid electrolyte membrane,
It is a pressure-molded body of the sulfide-based inorganic solid electrolyte material in the form of particles.
Provided is a solid electrolyte membrane in which the content of the binder resin in the solid electrolyte membrane is less than 0.5% by mass when the total content of the solid electrolyte membrane is 100% by mass .

Further, according to the present invention
An all-solid-state lithium-ion battery in which a positive electrode layer, a solid electrolyte layer, and a negative electrode layer are laminated in this order.
An all-solid-state lithium ion battery in which the solid electrolyte layer is formed of the solid electrolyte membrane is provided.

According to the present invention, it is possible to provide a solid electrolyte membrane capable of realizing an all-solid-state lithium-ion battery having excellent battery characteristics, and an all-solid-state lithium-ion battery having excellent battery characteristics.

It is a process sectional view schematically showing an example of the manufacturing process of the solid electrolyte membrane of the embodiment which concerns on this invention. It is a process sectional view schematically showing an example of the manufacturing process of the solid electrolyte membrane of the embodiment which concerns on this invention. It is a process sectional view schematically showing an example of the manufacturing process of the solid electrolyte membrane of the embodiment which concerns on this invention. It is a process sectional view schematically showing an example of the manufacturing process of the solid electrolyte membrane of the embodiment which concerns on this invention. It is sectional drawing which shows typically an example of the structure of the all-solid-state lithium ion battery of embodiment which concerns on this invention.

Hereinafter, embodiments of the present invention will be described with reference to the drawings. In all drawings, similar components are designated by a common reference numeral, and description thereof will be omitted as appropriate. Moreover, the figure is a schematic view and does not match the actual dimensional ratio. Unless otherwise specified, "A to B" in the numerical range represent A or more and B or less.

[Solid electrolyte membrane]
First, the solid electrolyte membrane according to the present embodiment will be described.
The solid electrolyte membrane according to the present embodiment contains an inorganic solid electrolyte material having lithium ion conductivity as a main component. The standard deviation of the thickness of the solid electrolyte membrane is 5.0 μm or less, preferably 4.0 μm or less, more preferably 3.5 μm or less, and particularly preferably 3.0 μm or less.
When the standard deviation of the thickness of the solid electrolyte membrane according to the present embodiment is not more than the above upper limit value, the battery characteristics of the obtained all-solid-state lithium ion battery can be improved.
The standard deviation of the thickness of the solid electrolyte membrane according to the present embodiment is not particularly limited, but is, for example, 0.1 μm or more.
In the present embodiment, the battery characteristics of the all-solid-state lithium-ion battery refer to, for example, discharge capacity density, output characteristics, cycle characteristics, and the like.

According to the study by the present inventors, by highly controlling the uniformity of the thickness of the solid electrolyte membrane, that is, by setting the standard deviation of the thickness of the solid electrolyte membrane to the above upper limit or less, all the battery characteristics are excellent. They have found that a solid-state lithium-ion battery can be obtained, and have reached the present invention.
The reason why an all-solid-state lithium-ion battery having excellent battery characteristics can be obtained by using the solid electrolyte membrane according to the present embodiment is not clear, but the following reasons can be considered.
First, if the thickness of the solid electrolyte film varies, the lithium ions between the electrodes move preferentially at the thin part of the solid electrolyte film, so that the electrodes expand and contract non-uniformly in the plane, and the solid electrolyte film is affected. There is a distribution of stress. As a result, it is considered that cracks are likely to occur in the solid electrolyte membrane. When this crack occurs, the positive electrode and the negative electrode come into contact with each other to cause a short circuit or the like, and the battery characteristics of the obtained all-solid-state lithium-ion battery deteriorate.
On the other hand, the solid electrolyte membrane according to the present embodiment has a standard deviation of thickness of not more than the above upper limit value and is excellent in thickness uniformity. Therefore, it is considered that the expansion and contraction of the electrode occurs uniformly in the plane, the distribution of stress on the solid electrolyte membrane is relaxed, and cracks are less likely to occur in the solid electrolyte membrane. For the above reasons, it is considered that the use of the solid electrolyte membrane according to the present embodiment can suppress deterioration of the battery characteristics of the obtained all-solid-state lithium-ion battery.
From the above, according to the solid electrolyte membrane according to the present embodiment, an all-solid-state lithium-ion battery having excellent battery characteristics can be realized.

The solid electrolyte membrane according to the present embodiment is used, for example, in the solid electrolyte layer constituting the all-solid-state lithium ion battery.
An example of an all-solid-state lithium-ion battery to which the solid electrolyte membrane according to the present embodiment is applied includes a battery in which a positive electrode layer, a solid electrolyte layer, and a negative electrode layer are laminated in this order. In this case, the solid electrolyte layer is composed of the solid electrolyte membrane.

The average thickness of the solid electrolyte membrane according to the present embodiment is preferably 10 μm or more and 500 μm or less, more preferably 20 μm or more and 200 μm or less, and further preferably 30 μm or more and 180 μm or less. When the average thickness of the solid electrolyte membrane is at least the above lower limit value, the lack of the inorganic solid electrolyte material and the cracking on the surface of the solid electrolyte membrane can be further suppressed. Further, when the average thickness of the solid electrolyte membrane is not more than the upper limit value, the impedance of the solid electrolyte membrane can be further lowered. As a result, the battery characteristics of the obtained all-solid-state lithium-ion battery can be further improved.

The solid electrolyte membrane according to the present embodiment is preferably a pressure-molded body of a particulate inorganic solid electrolyte material. That is, it is preferable to pressurize the particulate inorganic solid electrolyte material to form a solid electrolyte film having a certain strength due to the anchor effect between the inorganic solid electrolyte materials.
By forming the pressure-molded body, the inorganic solid electrolyte materials are bonded to each other, and the strength of the obtained solid electrolyte membrane is further increased. As a result, the lack of the inorganic solid electrolyte material and the cracking on the surface of the inorganic solid electrolyte material can be further suppressed.

The content of the inorganic solid electrolyte material in the solid electrolyte membrane according to the present embodiment is preferably 98% by mass or more, more preferably 99% by mass or more, still more preferably, when the whole solid electrolyte membrane is 100% by mass. Is 100% by mass. As a result, the contact property between the inorganic solid electrolyte materials can be improved, and the interfacial contact resistance of the solid electrolyte membrane can be reduced. As a result, the lithium ion conductivity of the solid electrolyte membrane can be further improved. Then, by using such a solid electrolyte membrane having excellent lithium ion conductivity, the battery characteristics of the obtained all-solid-state lithium ion battery can be further improved.

The solid electrolyte membrane according to the present embodiment has a lithium ion conductivity of preferably 0.5 × 10 ^-3 S · cm ^-1 or more, more preferably 0.8 × 10 ^-3 , in a state where no electrolytic solution is used. It is S · cm ^-1 or more, more preferably 1.0 × 10 ^-3 S · cm ^-1 or more, and particularly preferably 1.2 × 10 ^-3 S · cm ^-1 or more.
When the lithium ion conductivity of the solid electrolyte membrane according to the present embodiment is at least the above lower limit value, an all-solid-state lithium ion battery having further excellent battery characteristics can be obtained.
Here, the lithium ion conductivity is the lithium ion conductivity by the AC impedance method under the measurement conditions of 27.0 ° C., an applied voltage of 10 mV, and a measurement frequency range of 0.1 Hz to 7 MHz.

The inorganic solid electrolyte material is not particularly limited as long as it has ionic conductivity and insulating properties, but a material generally used for an all-solid-state lithium ion battery can be used. For example, a sulfide-based inorganic solid electrolyte material, an oxide-based inorganic solid electrolyte material, and other lithium-based inorganic solid electrolyte materials can be mentioned. Among these, a sulfide-based inorganic solid electrolyte material is preferable. As a result, the interfacial resistance between the inorganic solid electrolyte materials is further reduced, and a solid electrolyte membrane having more excellent lithium ion conductivity can be obtained.

Examples of the sulfide-based inorganic solid electrolyte material include Li ₂ S-P ₂ S ₅ material, Li ₂ S-SiS ₂ material, Li ₂ S-GeS ₂ material, Li ₂ S-Al ₂ S ₃ material, and Li ₂ S-SiS ₂ -Li ₃ PO ₄ material, Li ₂ S-P ₂ S _5- GeS ₂ material, Li ₂ S-Li ₂ O-P ₂ S _5- SiS ₂ material, Li ₂ S-GeS _2- P ₂ Examples thereof include S _5- SiS ₂ material, Li ₂ S-SnS _2- P ₂ S _5- SiS ₂ material and the like. Among these, the Li ₂ SP ₂ S ₅ material is preferable because it has excellent lithium ion conductivity and the manufacturing method is simple.
These may be used individually by 1 type, or may be used in combination of 2 or more type. Among these, the Li ₂ SP ₂ S ₅ material is preferable because it has excellent lithium ion conductivity and stability that does not cause decomposition in a wide voltage range. Here, for example, the Li ₂ SP ₂ S ₅ material means a material obtained by mixing and pulverizing a mixture containing at least Li ₂ S (lithium sulfide) and P ₂ S ₅ by mechanochemical treatment or the like. To do.

Examples of the oxide-based inorganic solid electrolyte material include NASICON type materials such as LiTi ₂ (PO ₄ ) ₃ , LiZr ₂ (PO ₄ ) ₃ , LiGe ₂ (PO ₄ ) ₃ , and (La _{0.5 + x} Li _{0.5). -3x} ) Perovskite type such as TiO ₃ can be mentioned.
Examples of other lithium-based inorganic solid electrolyte materials include LiPON, LiNbO ₃ , LiTaO ₃ , Li ₃ PO ₄ , LiPO _4-x N _x (x is 0 <x ≦ 1), LiN, LiI, and LISION. Be done. Further, glass ceramics obtained by precipitating crystals of these inorganic solid electrolytes can also be used as the inorganic solid electrolyte material.

Examples of the shape of the inorganic solid electrolyte material include particulate matter. The particulate inorganic solid electrolyte material of the present embodiment is not particularly limited, but the average particle size d ₅₀ in the weight-based particle size distribution measured by the laser diffraction / scattering particle size distribution measurement method is preferably 1 μm or more and 40 μm or less, more preferably. It is 2 μm or more and 30 μm or less, more preferably 3 μm or more and 20 μm or less.
By setting the average particle size d ₅₀ of the inorganic solid electrolyte material within the above range, good handleability can be maintained and the lithium ion conductivity of the solid electrolyte membrane can be further improved.

The planar shape of the solid electrolyte membrane is not particularly limited and can be appropriately selected according to the shape of the electrode layer or the current collector layer, but can be, for example, a rectangle.

Further, the solid electrolyte film according to the present embodiment may contain a binder resin, but the content of the binder resin is preferably less than 0.5% by mass when the whole solid electrolyte film is 100% by mass. It is more preferably 0.1% by mass or less, further preferably 0.05% by mass or less, and even more preferably 0.01% by mass or less. Further, it is more preferable that the solid electrolyte membrane according to the present embodiment is substantially free of the binder resin, and most preferably no binder resin is contained.
As a result, the contact property between the inorganic solid electrolyte materials can be improved, and the interfacial contact resistance of the solid electrolyte membrane can be reduced. As a result, the lithium ion conductivity of the solid electrolyte membrane can be further improved. Then, by using such a solid electrolyte membrane having excellent lithium ion conductivity, the battery characteristics of the obtained all-solid-state lithium ion battery can be improved.
In addition, "substantially free of binder resin" means that the binder resin may be contained to the extent that the effect of the present invention is not impaired. When the adhesive resin layer is provided between the solid electrolyte layer and the positive electrode layer or the negative electrode layer, the adhesive resin derived from the adhesive resin layer existing near the interface between the solid electrolyte layer and the adhesive resin layer is ". It is removed from the "binder resin in the solid electrolyte membrane".

The binder resin refers to a binder generally used in lithium ion batteries for binding inorganic solid electrolyte materials, for example, polyvinyl alcohol, polyacrylic acid, carboxymethyl cellulose, and polytetrafluoro. Examples thereof include ethylene, polyvinylidene fluoride, styrene-butadiene rubber, and polyimide.

[Manufacturing method of solid electrolyte membrane]
Next, a method for producing the solid electrolyte membrane according to the present embodiment will be described.
1 to 4 are process cross-sectional views schematically showing an example of a manufacturing process of the solid electrolyte membrane 100 according to the embodiment of the present invention.
The method for producing the solid electrolyte membrane 100 according to the present embodiment preferably includes the following steps (A), (B) and (C).
(A) Step of filling the voids of the porous body 103 with the particulate inorganic solid electrolyte material 101 (B) The inorganic solid electrolyte material 101 filled in the voids of the porous body 103 is placed on the cavity surface 107 of the mold 105 or as a base material. A step of depositing the inorganic solid electrolyte material 101 in a film shape on the cavity surface 107 of the mold or on the surface of the base material by sieving it off on the surface (C) A step of pressurizing the inorganic solid electrolyte material 101 deposited in the film shape.

Conventionally, the solid electrolyte membrane has been produced by directly supplying the inorganic solid electrolyte material on the cavity surface of the die or the surface of the base material and then pressing the inorganic solid electrolyte membrane at high pressure. However, according to the studies by the present inventors, it has been clarified that the solid electrolyte membrane produced by such a method has a non-uniform thickness.
Based on the above findings, the present inventors have diligently studied a method for producing the solid electrolyte membrane 100 in order to provide the solid electrolyte membrane 100 having excellent thickness uniformity. As a result, by sieving the inorganic solid electrolyte material 101 filled in the voids of the porous body 103 onto the cavity surface 107 of the mold or the surface of the base material, the uniformity of the thickness is excellent, and the standard deviation of the thickness is the upper limit. It has been found that a solid electrolyte membrane 100 having a standard deviation of 100 or less can be obtained.
Although it is not clear why the solid electrolyte membrane 100 having the standard deviation of the thickness equal to or less than the above upper limit can be obtained by using the method for producing the solid electrolyte membrane 100 of the present embodiment, the present inventors have made it a particulate inorganic substance. It is presumed that this is because the solid electrolyte material 101 is sifted off little by little while passing through the opening of the porous body 103, so that it can be deposited in a film shape with a uniform thickness on the cavity surface 107 of the mold or on the surface of the base material. doing.
Hereinafter, each step will be described in detail.

First, (A) the particulate inorganic solid electrolyte material 101 is filled in the voids of the porous body 103. The method of filling the voids of the porous body 103 with the particulate inorganic solid electrolyte material 101 is not particularly limited. For example, the particulate inorganic solid electrolyte material 101 is filled in the voids of the porous body 103 in the air or in an inert atmosphere. Is directly supplied, or the particulate inorganic solid electrolyte material 101 is dispersed in a solvent to form a slurry, and then the slurry is applied onto the porous body 103 to allow the slurry to permeate into the voids, and then the solvent is applied. Examples include a method of drying.

As a method of directly supplying the particulate inorganic solid electrolyte material 101 into the voids of the porous body 103 in the air or in an inert atmosphere, the inorganic solid electrolyte material 101 is powder-coated on the porous body 103, and the squeegee 109 is used. A method of filling the voids with the inorganic solid electrolyte material 101 while removing the excess inorganic solid electrolyte material 101 on the porous body 103 can be mentioned.
As a method for applying the slurry, generally known methods such as a doctor blade coating method, a dip coating method, a spray coating method, and a bar coater coating method can be used.
By these methods, the voids of the porous body 103 can be continuously filled with the inorganic solid electrolyte material 101.
Here, in the porous body 103, from the viewpoint of sieving the inorganic solid electrolyte material 101 filled in the voids of the porous body 103 only at a desired position, the voids in the portion where the particulate inorganic solid electrolyte material 101 is not desired to be filled are provided. Is preferably embedded in advance with a resin or the like so that the particulate inorganic solid electrolyte material 101 is not filled. By doing so, in the step (B), the inorganic solid electrolyte material 101 can be sieved off only at a desired position, so that the solid electrolyte membrane 100 having a desired size can be obtained more easily.

Subsequently, if necessary, by applying pressure, the voids are filled with the inorganic solid electrolyte material 101 that adheres to the surface of the porous body 103 without being filled in the voids. The method of pressurizing the porous body 103 is not particularly limited, and for example, a roll press or the like can be used. As a result, pressurization can be performed continuously, and productivity can be improved.

Further, as shown in FIG. 2, it is preferable that a space portion 115 for accommodating the inorganic solid electrolyte material 101 is provided on one surface of the porous body 103. In this case, in the step (A), the space 115 is also filled with the inorganic solid electrolyte material 101. As a result, the space portion 115 can also be filled with the inorganic solid electrolyte material 101, so that the loading amount of the inorganic solid electrolyte material 101 can be increased.
The space portion 115 is not particularly limited as long as it has a structure capable of filling the inorganic solid electrolyte material 101, but is formed, for example, by providing a support 113 on one surface of the porous body 103 via a spacer 111. Structure can be mentioned. In this case, the portion surrounded by the porous body 103, the support 113, and the spacer 111 becomes the space portion 115.

The spacer 111 is not particularly limited, and examples thereof include masking tape. The support 113 is not particularly limited, and examples thereof include a resin plate such as a polyethylene terephthalate (PET) plate, a metal plate, and the like. A transparent resin plate is preferable from the viewpoint that the inside can be confirmed.

The size of the space portion 115 is not particularly limited, and is appropriately set according to the filling amount of the inorganic solid electrolyte material 101 and the desired thickness of the solid electrolyte membrane 100. The size of the space portion 115 can be adjusted by, for example, the thickness of the spacer 111.

Here, the porous body 103 is capable of filling the voids with the inorganic solid electrolyte material 101.
The shape of the porous body 103 is not particularly limited, but is preferably a sheet shape from the viewpoint of ease of handling.

Examples of the form of the porous body 103 include one or more selected from woven fabrics, non-woven fabrics, mesh cloths, porous films, expanding sheets, punching sheets and the like. Among these, mesh cloth is preferable from the viewpoint of excellent filling property of the inorganic solid electrolyte material 101 and excellent performance of sieving the inorganic solid electrolyte material 101.

The materials constituting the porous body 103 include polyesters such as nylon and polyethylene terephthalate (PET), polyethylene, polypropylene, polytetrafluoroethylene (PTFE), ethylene-tetrafluoroethylene copolymer, polyvinylidene chloride, and polyvinylidene chloride. Resin materials such as vinylidene, polyvinylidene chloride, polyurethane, vinylon, polybenzimidazole, polyimide, polyphenylene sulfide, polyether ether ketone, cellulose, acrylic resin; natural fibers such as hemp, wood pulp, cotton linter; iron, aluminum, Metallic materials such as titanium, nickel and stainless steel; one or more selected from inorganic materials such as glass and carbon.
Among these, resin materials and natural fibers are preferable, resin materials are more preferable, and nylon is particularly preferable, from the viewpoint of excellent flexibility. The opening of the porous body 103 having excellent flexibility changes slightly when vibration is applied. Therefore, by using the porous body 103 having excellent flexibility, the inorganic solid electrolyte material 101 can be more easily dropped while suppressing the occurrence of clogging, and the inorganic solid electrolyte material 101 can be made more uniform. It becomes possible to deposit in.

The porosity of the porous body 103 is preferably 10% or more and 90% or less, more preferably 25% or more and 70% or less, and particularly preferably 30% or more and 55% or less. When the porosity is at least the above lower limit value, the amount of the inorganic solid electrolyte material 101 that can be filled in the voids can be increased, so that the productivity of the solid electrolyte membrane 100 can be improved.
Further, when the porosity is not more than the above upper limit value, the performance of sieving the inorganic solid electrolyte material 101 can be improved, so that the thickness of the obtained solid electrolyte membrane 100 can be made more uniform.
Here, the porosity in the present embodiment differs depending on the form of the porous body 103. For example, a mesh cloth having a regular shape with monotonous voids, an expanding sheet, a punching sheet, or the like means an aperture ratio.
The aperture ratio of the porous body 103 can be calculated according to the following formula for each difference in form. For example, in the case of a punched plate such as a punching sheet, a common name is given according to the difference in the shape and arrangement of holes, and calculation formulas are provided for each. For example, 60 ° staggered type: opening ratio (%) = 90.6 × D ² / P ² , square staggered type: opening ratio (%) = 157 × D ² / P ² , parallel type: opening ratio (%) ) = 78.5 × D ² / P ² , oval hole zigzag type: aperture ratio (%) = {(2 × W × L) − (0.43 × W ² )} × 100 / (2 × SP ×) LP), Oval hole parallel type: Opening ratio (%) = {(2 x W x L)-(0.43 x W ² )} x 100 / (2 x SP x LP), Square hole staggered type: Opening Rate (%) = W ² x 100 / (SP ₁ x SP ₂ ), Square hole parallel type: Aperture ratio (%) = W ² x 100 / (SP ₁ x SP ₂ ), Hexagonal 60 ° zigzag type: Opening Rate (%) = W ² x 100 / P ² , long square hole staggered type: aperture ratio (%) = (W x L x 100) / (SP x LP), long square hole parallel type: opening ratio (%) = (W x L x 100) / (SP x LP), in the above formula, D is the diameter of the round hole, P is the distance between the centers of the round hole or hexagonal hole, and W is the oblong hole, square hole, hexagonal hole. Alternatively, the length of the oblong hole in the shorter direction, L is the length of the oblong hole or oblong hole in the longer direction, SP is the distance between the centers in the shorter direction of the oblong hole or oblong hole, and LP is the oblong hole or oblong angle. The distance between centers in the longer direction of the hole, SP ₁ indicates the distance between centers in the shorter direction of the square hole, and SP ₂ indicates the distance between centers in the longer direction of the square hole.
In the case of a plate that has been stretched after making staggered cuts such as an expanding sheet, the aperture ratio (%) = [{SWO × (LWO + B)} / (SW × LW)] × 100 is provided. Here, SWO is the length of the opening in the short direction, LWO is the length of the opening in the long direction, SW is the distance between the centers in the short direction of the mesh, LW is the distance between the centers in the long direction of the mesh, and B is the length of the bond. Is.
Further, in the mesh cloth, the aperture ratio (%) = {A / (A + d)} ² × 100 is provided. Here, A is a mesh opening (mm) and can be calculated by A = (25.4 / M) −d. M is a mesh and d is a wire diameter (mm).
Further, in the case of a woven fabric, a non-woven fabric, or a porous membrane in which the voids have a three-dimensionally complicated shape, the porosity means the ratio of the total volume of the voids to the total volume of the porous body 103. That is, the porosity is represented by (volume of constituent material in 1-porous body 103 / volume of porous body 103) × 100 (%).

The opening of the porous body 103 is preferably 40 μm or more and 300 μm or less, and more preferably 50 μm or more and 150 μm or less. When the opening is at least the above lower limit value, the amount of the inorganic solid electrolyte material 101 that can be filled in the voids can be increased, so that the productivity of the solid electrolyte membrane 100 can be improved.
Further, when the opening is not more than the above upper limit value, the performance of sieving the inorganic solid electrolyte material 101 can be improved, so that the thickness of the obtained solid electrolyte membrane 100 can be made more uniform.

The air permeability of the porous body 103 is preferably 1 cm ³ / cm ² / sec or more and 30 cm ³ / cm ² / sec or less, and more preferably 2 cm ³ / cm ² / sec or more and 20 cm ³ / cm ² / sec or less. When the air permeability is equal to or higher than the above lower limit value, the amount of the inorganic solid electrolyte material 101 that can be filled in the voids can be increased, so that the productivity of the solid electrolyte membrane 100 can be improved. Further, when the air permeability is not more than the above upper limit value, the performance of sieving the inorganic solid electrolyte material 101 can be improved, so that the thickness of the obtained solid electrolyte membrane 100 can be made more uniform.
Here, the air permeability of the porous body 103 can be measured according to JIS L1096-A (Frazier method).

The thickness of the porous body 103 is preferably 10 μm or more and 300 μm or less, and more preferably 20 μm or more and 200 μm or less. When the thickness of the porous body 103 is at least the above lower limit value, the amount of the inorganic solid electrolyte material 101 that can be filled in the voids can be increased, so that the productivity of the solid electrolyte membrane 100 can be improved.
Further, when the thickness of the porous body 103 is not more than the above upper limit value, the unfilled region of the inorganic solid electrolyte material 101 can be reduced, and the performance of sieving the inorganic solid electrolyte material 101 can be improved. The thickness of the solid electrolyte membrane 100 to be obtained can be made even more uniform.

Next, (B) the inorganic solid electrolyte material 101 filled in the voids of the porous body 103 is sieved onto the cavity surface 107 of the mold 105 or the surface of the base material, thereby forming the cavity surface 107 of the mold or the base material. The inorganic solid electrolyte material 101 is deposited on the surface in the form of a film. Here, the inorganic solid electrolyte material 101 filled in the voids of the porous body 103 is sieved onto the cavity surface 107 of the mold 105 or the surface of the base material until a desired thickness is obtained.
Since the inorganic solid electrolyte material 101 is sieved off little by little by the opening of the porous body 103, it can be deposited in a film shape with a uniform thickness on the cavity surface 107 of the mold or on the surface of the base material.

As a method of sieving the inorganic solid electrolyte material 101 onto the cavity surface 107 of the mold 105 or the surface of the base material, for example, the inorganic solid electrolyte material filled in the voids of the porous body 103 by vibrating the porous body 103. Examples thereof include a method of sieving the 101 onto the cavity surface 107 of the mold 105 or the surface of the base material.

Further, as shown in FIG. 2, when the space portion 115 for accommodating the inorganic solid electrolyte material 101 is provided on one surface of the porous body 103, the voids of the porous body 103 and the inorganic solid electrolyte material filled in the space portion 115 are provided. By sieving the 101 onto the cavity surface 107 of the mold 105 or the surface of the base material, the inorganic solid electrolyte material 101 is deposited in a film form on the cavity surface 107 of the mold 105 or on the surface of the base material. As a result, the inorganic solid electrolyte material 101 can be continuously screened off, so that the productivity of the solid electrolyte membrane 100 can be further improved.

Further, as shown in FIG. 3, in the step (B), the inorganic solid electrolyte material 101 deposited in the form of a film is vibrated to cause the particulate inorganic solid electrolyte material 101 to flow, and the inorganic material deposited in the form of a film. It is preferable to further include a step of densifying the solid electrolyte material 101. The thickness of the solid electrolyte membrane 100 thus obtained can be made even more uniform. Examples of the method of vibrating include vibration with a small amplitude such as ultrasonic vibration and light impact by a hammer.

Examples of the base material include a positive electrode layer, a negative electrode layer, a metal foil, a plastic film, carbon and the like.

Next, as shown in FIG. 4, (C) the inorganic solid electrolyte material 101 deposited in the form of a film is pressurized. As a result, the solid electrolyte membrane 100 has a certain strength due to the anchor effect between the inorganic solid electrolyte materials 101. Here, when the particulate inorganic solid electrolyte material 101 is deposited on the surface of the base material, the base material may be pressurized in a laminated state, or the base material may be peeled off and then pressurized.
When pressure is applied, the inorganic solid electrolyte materials 101 are bonded to each other, and the strength of the obtained solid electrolyte membrane 100 is further increased. As a result, the lack of the inorganic solid electrolyte material 101 and the cracking on the surface of the inorganic solid electrolyte material 101 can be further suppressed.
The method of pressurizing the inorganic solid electrolyte material 101 is not particularly limited. For example, when the inorganic solid electrolyte material 101 is deposited on the cavity surface 107 of the mold 105, it is pressed by a mold and a stamp, and is inorganic in the form of particles. When the solid electrolyte material 101 is deposited on the surface of the base material, a press using a die and a pressing die, a roll press, a flat plate press, or the like can be used.
The pressure for pressurizing the inorganic solid electrolyte material 101 is, for example, 10 MPa or more and 500 MPa or less.

Further, if necessary, the inorganic solid electrolyte material 101 deposited in the form of a film may be pressurized and heated. When the heating and pressurizing is performed, the inorganic solid electrolyte materials 101 are fused and bonded to each other, and the strength of the obtained solid electrolyte membrane 100 is further increased. As a result, the lack of the inorganic solid electrolyte material 101 and the cracking on the surface of the inorganic solid electrolyte material 101 can be further suppressed.
The temperature for heating the inorganic solid electrolyte material 101 is, for example, 40 ° C. or higher and 500 ° C. or lower.

[All-solid-state lithium-ion battery]
Next, the all-solid-state lithium-ion battery 200 according to the present embodiment will be described. FIG. 5 is a cross-sectional view schematically showing an example of the structure of the all-solid-state lithium-ion battery according to the embodiment of the present invention. The all-solid-state lithium-ion battery 200 according to the present embodiment is a lithium-ion secondary battery, but may be a lithium-ion primary battery.

In the all-solid-state lithium-ion battery 200 according to the present embodiment, the positive electrode layer 210, the solid electrolyte layer 220, and the negative electrode layer 230 are laminated in this order. The solid electrolyte layer 220 is composed of the solid electrolyte membrane 100 according to the present embodiment.
Further, the all-solid-state lithium ion battery 200 according to the embodiment is a bipolar lithium ion battery by stacking two or more unit cells composed of a positive electrode layer 210, a solid electrolyte layer 220, and a negative electrode layer 230. It can also be.
The shape of the all-solid-state lithium-ion battery 200 is not particularly limited, and examples thereof include a cylindrical type, a coin type, a square type, a film type, and any other shape.

The all-solid-state lithium-ion battery 200 according to the present embodiment is manufactured according to a generally known method. For example, it is produced by forming a stack of a positive electrode layer 210, a solid electrolyte layer 220, and a negative electrode layer 230 into a cylindrical shape, a coin shape, a square shape, a film shape, or any other shape.

The positive electrode layer 210 is not particularly limited, and a positive electrode generally used for an all-solid-state lithium ion battery can be used. The positive electrode layer 210 is not particularly limited, but can be manufactured according to a generally known method. For example, it can be obtained by forming a positive electrode active material layer containing a positive electrode active material on a current collector such as aluminum foil.
The thickness and density of the positive electrode layer 210 are appropriately determined according to the intended use of the battery and the like, and are not particularly limited, and can be set according to generally known information.

The positive electrode active material layer contains a positive electrode active material as an essential component.
The positive electrode active material is not particularly limited, and a generally known positive electrode active material that can be used for the positive electrode layer of the all-solid-state lithium ion battery can be used. For example, lithium cobalt oxide (LiCoO ₂ ), lithium nickel oxide (LiNiO ₂ ), lithium manganese oxide (LiMn ₂ O ₄ ), solid solution oxide (Li ₂ MnO _3- LiMO ₂ (M = Co, Ni, etc.)). ), Lithium-manganese-nickel oxide (LiNi _1/3 Mn _1/3 Co _1/3 O ₂ ), olivine-type lithium phosphorus oxide (LiFePO ₄ ) and other compound oxides; polyaniline, polypyrrole, etc. with high conductivity _{molecule; Li 2 S, CuS, Li} -CuS _{compounds, TiS 2, FeS, MoS 2} , Li-MoS compounds, Li-TiS compound, sulfide-based positive active such as Li-V-S compound Substances; materials using sulfur as an active material, such as acetylene black impregnated with sulfur, porous carbon impregnated with sulfur, and a mixed powder of sulfur and carbon, can be used. These positive electrode active materials may be used alone or in combination of two or more.
Among these, a sulfide-based positive electrode active material is preferable from the viewpoint of having a higher discharge capacity density and being superior in cycle characteristics, and Li-Mo-S compound, Li-Ti-S compound, Li-VS. More preferably, one or more selected from the compounds.

Here, the Li-Mo-S compound contains Li, Mo, and S as constituent elements, and is usually obtained by mixing and pulverizing molybdenum sulfide and lithium sulfide, which are raw materials, by mechanochemical treatment or the like. be able to.
Further, the Li-Ti-S compound contains Li, Ti, and S as constituent elements, and is usually obtained by mixing and pulverizing titanium sulfide and lithium sulfide, which are raw materials, by mechanochemical treatment or the like. Can be done.
The Li-VS compound contains Li, V, and S as constituent elements, and can be obtained by mixing and pulverizing vanadium sulfide and lithium sulfide, which are usually raw materials, by mechanochemical treatment or the like. ..

The positive electrode active material layer is not particularly limited, but may contain one or more kinds of materials selected from, for example, a solid electrolyte material, a binder, a conductive auxiliary agent, and the like as components other than the positive electrode active material.
The blending ratio of various materials in the positive electrode active material layer is appropriately determined according to the intended use of the battery and the like, and is not particularly limited, and can be set according to generally known information.

The negative electrode layer 230 is not particularly limited, and those generally used for all-solid-state lithium ion batteries can be used. The negative electrode layer 230 is not particularly limited, but can be manufactured according to a generally known method. For example, it can be obtained by forming a negative electrode active material layer containing a negative electrode active material on a current collector such as copper.
The thickness and density of the negative electrode active material layer are appropriately determined according to the intended use of the battery and the like, and are not particularly limited, and can be set according to generally known information.

The negative electrode active material layer contains a negative electrode active material as an essential component.
The negative electrode active material is not particularly limited, and a generally known negative electrode active material that can be used for the negative electrode layer of the all-solid-state lithium ion battery can be used. For example, carbonaceous materials such as natural graphite, artificial graphite, resin charcoal, carbon fiber, activated charcoal, hard carbon, soft carbon; tin, tin alloy, silicon, silicon alloy, gallium, gallium alloy, indium, indium alloy, aluminum, aluminum. Metal-based materials mainly composed of alloys and the like; conductive polymers such as polyacene, polyacetylene and polypyrrole; metallic lithium; lithium titanium composite oxides (for example, Li ₄ Ti ₅ O ₁₂ ) and the like can be mentioned. These negative electrode active materials may be used alone or in combination of two or more.

The negative electrode active material layer is not particularly limited, but may contain one or more materials selected from, for example, a solid electrolyte material, a binder, a conductive auxiliary agent, and the like as components other than the negative electrode active material.
The blending ratio of various materials in the negative electrode active material layer is appropriately determined according to the intended use of the battery and the like, and is not particularly limited, and can be set according to generally known information.

Although the embodiments of the present invention have been described above, these are examples of the present invention, and various configurations other than the above can be adopted.
The present invention is not limited to the above-described embodiment, and modifications, improvements, and the like within the range in which the object of the present invention can be achieved are included in the present invention.

Hereinafter, the present invention will be described with reference to Examples and Comparative Examples, but the present invention is not limited thereto.

[1] Measurement method First, the measurement methods in the following Examples and Comparative Examples will be described.

(1) ICP luminescence spectroscopic analysis Using an ICP luminescence spectroscopic analyzer (manufactured by Seiko Instruments Co., Ltd., SPS3000), measurement was performed by ICP luminescence spectroscopic analysis to determine the mass% of each element in the positive electrode active material. The molar ratio of each element was calculated based on the value of.

(2) Particle Size Distribution The particle size distribution of the inorganic solid electrolyte material used in Examples and Comparative Examples was measured by a laser diffraction method using a laser diffraction scattering type particle size distribution measuring device (Mastersizer 3000 manufactured by Malvern). From the measurement results, the inorganic solid electrolyte material, the particle diameter at 50% cumulative time in a cumulative distribution of weight (D _50, average particle size) was determined.

(3) Measurement of Lithium Ion Conductivity The solid electrolyte membranes obtained in Examples and Comparative Examples were measured for lithium ion conductivity by the AC impedance method.
The lithium ion conductivity was measured using a potentiostat / galvanostat SP-300 manufactured by Hokuto Denko. The measurement conditions were an applied voltage of 10 mV, a measurement temperature of 27.0 ° C., a measurement frequency range of 0.1 Hz to 7 MHz, and an electrode made of a carbon plate.

(4) Using a standard deviation micrometer (Mitutoyo Coulan and Proof Micrometer 290-230, spindle diameter φ6.35 mm, measuring force 5-10 N), the thickness of the obtained solid electrolyte membrane was determined at 5 points. The measurements were taken to determine the (arithmetic) mean and standard deviation of the thickness.
Here, the thickness of the solid electrolyte membrane was measured at four points at the corners of the solid electrolyte membrane (size: 25 mm × 25 mm) obtained in Examples and Comparative Examples, and at one point in the center, for a total of five points.

(5) Evaluation of battery characteristics Conductive copper foil Conductive tape (8313 0.03 manufactured by Teraoka Seisakusho, external dimensions: 25.0 mm x 25.0 mm, thickness: 30 μm, electrolytic copper foil: 0.009 mm, conductive acrylic adhesive Layer: 0.021 mm, graphite (CGC-20, 8 mg manufactured by Nippon Graphite Industry Co., Ltd.) attached to the adhesive layer surface, negative electrode active material layer (indium foil, manufactured by Niraco Co., Ltd., 23.0 mm x 23.0 mm, average thickness) : 20 μm), solid electrolyte membranes obtained in Examples and Comparative Examples, positive electrode active material layer (Li ₁₄ MoS ₉ : Ketjen Black (KB): Li ₁₁ P ₃ S ₁₂ = 1: 0.5: 1.2 (Mass ratio), average thickness: 30 μm), conductive copper foil conductive tape (Teraoka Seisakusho 8313 0.03, external dimensions: 25.0 mm × 25.0 mm, thickness: 30 μm, electrolytic copper foil: 0.009 mm, conductive A acrylic pressure-sensitive adhesive layer: 0.021 mm, and Ketjen Black (325 mesh manufactured by Lion, 0.1 mg) was laminated on the surface of the pressure-sensitive adhesive layer in this order. Next, the obtained laminate was pressurized at 320 MPa to prepare a first unit cell. Here, a second unit cell having the same configuration as the first unit cell was produced by the same method as for producing the first unit cell.
Next, an adhesive resin layer having a circular through hole with a diameter of 15 mm formed in the center (manufactured by Nitto Denko Co., Ltd., ultra-thin double-sided tape No. 5600, layer composition: acrylic adhesive layer / PET film base material / acrylic adhesive A laminate was prepared by laminating the obtained first unit cell and second unit cell via an agent layer, total thickness: 5 μm, outer dimensions: 25.0 mm × 25.0 mm), and the obtained laminate was obtained. Was pressurized at 80 MPa. Next, the obtained laminate was vacuum-laminated with an aluminum laminate film to obtain a bipolar all-solid-state lithium-ion battery.
Next, the obtained all-solid-state lithium-ion battery was charged to a charge termination potential of 4.5 V at a current density of 65 μA / cm ² at 25 ° C., and then discharged at a current density of 65 μA / cm ^2. Charging and discharging were performed 35 times or more under the condition of discharging to 2.0 V.
Here, the 20th discharge capacity when the first discharge capacity is 100% is defined as the discharge capacity change rate [%], the discharge capacity change rate of 100% is ⊚, and the discharge capacity change rate is 80% or more. Those with less than 100% were evaluated as ◯, and those with a discharge capacity change rate of less than 80% were evaluated as x.

[2] Materials Next, the materials used in the following Examples and Comparative Examples will be described.

(1) Positive electrode active material (Li ₁₄ MoS ₉ )
In an argon atmosphere, weigh and add MoS ₂ (4.7 mmol manufactured by Wako Pure Chemical Industries, Ltd.) and Li ₂ S (32.5 mmol manufactured by Sigma-Aldrich Japan Co., Ltd.) to a pot made of Al ₂ O ₃ . , Further, a ZrO ₂ ball was put in, and the Al ₂ O ₃ pot was sealed.
Next, the pot made of Al ₂ O ₃ was placed on a ball mill turntable and treated at 120 rpm for 4 days to obtain a mixture.
The obtained Li-Mo-S compound was pulverized in a mortar and classified by a sieve having a mesh size of 43 μm to obtain a Li-Mo-S compound.
The molar ratio of the Li content to the Mo content (Li / Mo) was 14, and the molar ratio of the S content to the Mo content (S / Mo) was 9.

(2) Sulfide-based Inorganic Solid Electrolyte Material The Li ₂ SP ₂ S ₅ material, which is the sulfide-based inorganic solid electrolyte material used in Examples and Comparative Examples, was prepared by the following procedure.
As raw materials, Li ₂ S (manufactured by Sigma-Aldrich Japan, purity 99.9%) and P ₂ S ₅ (reagent manufactured by Kanto Chemical Co., Inc.) were used. Li ₃ N was prepared by the following procedure.
First, in a glove box with a nitrogen atmosphere, a stainless steel swordsman was used for Li foil (manufactured by Honjo Metal Co., Ltd., purity 99.8%, thickness 0.5 mm) to make many holes of φ1 mm or less. The Li foil began to turn black-purple from the hole portion, and when left as it was at room temperature for 24 hours, all the Li foil changed to black-purple Li ₃ N. Li ₃ N was pulverized in an agate mortar and then sieved with a stainless steel sieve, and a powder of 75 μm or less was recovered and used as a raw material for an inorganic solid electrolyte material.
Next, each raw material was precisely weighed in an argon glove box so that Li ₂ S: P ₂ S ₅ : Li ₃ N = 67.5: 22.5: 10.0 (mol%), and these powders were added. It was mixed in an agate mortar for 20 minutes. Next, 2 g of the mixed powder was weighed and mixed and pulverized with 500 g of zirconia balls having a diameter of 10 mm on a planetary ball mill (Fritsch, P-7) at 100 rpm for 1 hour. Then, it was mixed and pulverized at 400 rpm for 15 hours. The powder after mixing and pulverization was placed in a carbon boat and heat-treated in an argon air stream at 300 ° C. for 2 hours to obtain a Li ₂ SP ₂ S ₅ material having a Li ₁₁ P ₃ S ₁₂ composition. The average particle size D ₅₀ was 12 μm.

_Further, by a method according to the manufacturing method of the Li ₁₁ P _{3 S 12} composition of _Li 2 _S-P 2 _{S 5 material,} to obtain a _Li 2 _S-P 2 _{S 5} material Li ₉ P _{3 S 12} composition. The average particle size D ₅₀ was 10 μm.
_Further, by a method according to the manufacturing method of the Li ₁₁ P _{3 S 12} composition of _Li 2 _S-P 2 _{S 5 material,} to obtain a _Li 2 _S-P 2 _{S 5} material Li ₇ P _{3 S 11} composition. The average particle size D ₅₀ was 9 μm.

(3) Porous body As the porous body, nylon mesh cloth (13XX-100 manufactured by Sanjiro Tanaka Shoten Co., Ltd., thickness 105 μm, porosity 36%, opening 100 μm) was used.

<Example 1>
A polyethylene terephthalate (PET) plate was prepared by attaching a polyethylene terephthalate (PET) plate to one surface of a nylon mesh cloth via a spacer having a thickness of 75 μm (masking tape having a thickness of 60 μm and baseless double-sided tape having a thickness of 15 μm). The nylon mesh cloth was filled with a resin at openings other than 25 mm × 25 mm so that the powder could pass through only 25 mm × 25 mm.
Next, a particulate inorganic solid electrolyte material (Li ₁₁ P ₃ ) was used in the space provided between the nylon mesh cloth and the PET plate (the space secured by the spacer) and the opening (void) of the nylon mesh cloth using a squeegee. S ₁₂ ) was filled.
Next, the nylon mesh cloth filled with the particulate inorganic solid electrolyte material is inverted and placed on the press die, and the PET plate is beaten with a wooden mallet and vibrated to be inorganic on the cavity surface of the press die. By sieving 90 mg of the solid electrolyte material, the inorganic solid electrolyte material was deposited in a film form on the cavity surface of the press die. Here, the inorganic solid electrolyte material was deposited in a film shape with a uniform thickness in the cavity (25 mm × 25 mm) of the press die.
Next, after the stamp is placed in the press die, each side surface of the press die is hit with a titanium hammer to vibrate the particulate inorganic solid electrolyte material in the press die to form a film-like inorganic substance. The solid electrolyte material was densified.
Then, a solid electrolyte membrane was obtained by pressing at 320 MPa using a hydraulic flat plate press. Each evaluation was performed on the obtained solid electrolyte membrane. The results obtained are shown in Table 1.

<Examples 2 to 8>
The solid electrolyte membranes were prepared in the same manner as in Example 1 except that the types of the inorganic solid electrolyte materials were set to the inorganic solid electrolyte materials shown in Table 1 and the amount of the inorganic solid electrolyte materials to be sieved was set to the values shown in Table 1. Then, each evaluation was performed individually. The results obtained are shown in Table 1.
Ta.

<Comparative example 1>
90 mg of a particulate inorganic solid electrolyte material (Li ₁₁ P ₃ S ₁₂ ) was powder coated into the cavity (25 mm × 25 mm) of the press die using a squeegee.
Next, after the stamp is placed in the press die, each side surface of the press die is hit with a titanium hammer to vibrate the particulate inorganic solid electrolyte material in the press die, and the inorganic solid electrolyte material is applied. Was densified.
Then, a solid electrolyte membrane was obtained by pressing at 320 MPa using a hydraulic flat plate press. Each evaluation was performed on the obtained solid electrolyte membrane. The results obtained are shown in Table 1.

<Comparative Examples 2 and 3>
Solid electrolyte membranes were prepared in the same manner as in Comparative Example 1 except that the type of the inorganic solid electrolyte material was the inorganic solid electrolyte material shown in Table 1, and each evaluation was performed. The results obtained are shown in Table 1.

The all-solid-state lithium-ion battery using the solid-state electrolyte film obtained in the examples was superior in battery characteristics to the all-solid-state lithium-ion battery using the solid-state electrolyte film obtained in the comparative example.
From the above, it was confirmed that according to the solid electrolyte membrane according to the present embodiment, an all-solid-state lithium-ion battery having excellent battery characteristics can be obtained.
Hereinafter, an example of the reference form will be added.
1. 1.
A solid electrolyte membrane containing an inorganic solid electrolyte material having lithium ion conductivity as a main component.
A solid electrolyte membrane having a standard deviation of the thickness of the solid electrolyte membrane of 5.0 μm or less.
2. 2.
1. 1. In the solid electrolyte membrane described in
A solid electrolyte membrane having an average thickness of 10 μm or more and 500 μm or less.
3. 3.
1. 1. Or 2. In the solid electrolyte membrane described in
A solid electrolyte membrane which is a pressure-molded body of a particulate inorganic solid electrolyte material.
4.
3. 3. In the solid electrolyte membrane described in
A solid electrolyte membrane having an average particle diameter d ₅₀ of 1 μm or more and 40 μm or less of the particulate inorganic solid electrolyte material in a weight-based particle size distribution measured by a laser diffraction / scattering particle size distribution measurement method .
5.
1. 1. To 4. In the solid electrolyte membrane according to any one,
A solid electrolyte membrane in which the content of the binder resin in the solid electrolyte membrane is less than 0.5% by mass when the total content of the solid electrolyte membrane is 100% by mass.
6.
1. 1. To 5. In the solid electrolyte membrane according to any one,
A solid electrolyte membrane in which the content of the inorganic solid electrolyte material in the solid electrolyte membrane is 98% by mass or more, assuming that the entire solid electrolyte membrane is 100% by mass.
7.
1. 1. To 6. In the solid electrolyte membrane according to any one,
A solid electrolyte membrane having a lithium ion conductivity of 0.5 × 10 ^-3 S · cm ^-1 or more by the AC impedance method under measurement conditions of 27.0 ° C., an applied voltage of 10 mV, and a measurement frequency range of 0.1 Hz to 7 MHz .
8.
1. 1. To 7. In the solid electrolyte membrane according to any one,
A solid electrolyte membrane in which the inorganic solid electrolyte material contains a sulfide-based inorganic solid electrolyte material.
9.
1. 1. ~ 8. In the solid electrolyte membrane according to any one,
A solid electrolyte membrane used for the solid electrolyte layer constituting an all-solid-state lithium-ion battery.
10.
An all-solid-state lithium-ion battery in which a positive electrode layer, a solid electrolyte layer, and a negative electrode layer are laminated in this order.
The solid electrolyte layer is 1. ~ 9. An all-solid-state lithium-ion battery composed of the solid electrolyte membrane according to any one of them.

100 Solid electrolyte film 101 Inorganic solid electrolyte material 103 Porous 105 Mold 107 Surface 109 Squeegee 111 Spacer 113 Support 115 Space 200 All-solid-state lithium-ion battery 210 Positive electrode layer 220 Negative electrode layer 230 Solid electrolyte layer

Claims (6)

A solid electrolyte membrane containing a sulfide-based inorganic solid electrolyte material having lithium ion conductivity as a main component.
The standard deviation of the thickness of the solid electrolyte membrane is 5.0 μm or less.
Ri average thickness 60.4 [mu] m or more 180μm der less of said solid electrolyte membrane,
It is a pressure molded body of the sulfide-based inorganic solid electrolyte material in the form of particles.
A solid electrolyte membrane in which the content of the binder resin in the solid electrolyte membrane is less than 0.5% by mass when the total content of the solid electrolyte membrane is 100% by mass . In the solid electrolyte membrane according to claim 1 ,
A solid electrolyte membrane having an average particle diameter d ₅₀ of 1 μm or more and 40 μm or less of the particulate sulfide-based inorganic solid electrolyte material in a weight-based particle size distribution measured by a laser diffraction / scattering particle size distribution measurement method. In the solid electrolyte membrane according to claim 1 or 2 .
A solid electrolyte membrane in which the content of the sulfide-based inorganic solid electrolyte material in the solid electrolyte membrane is 98% by mass or more when the total content of the solid electrolyte membrane is 100% by mass. In the solid electrolyte membrane according to any one of claims 1 to 3 ,
A solid electrolyte membrane having a lithium ion conductivity of 0.5 × 10 ^-3 S · cm ^-1 or more by the AC impedance method under measurement conditions of 27.0 ° C., an applied voltage of 10 mV, and a measurement frequency range of 0.1 Hz to 7 MHz. In the solid electrolyte membrane according to any one of claims 1 to 4 .
A solid electrolyte membrane used for the solid electrolyte layer constituting an all-solid-state lithium-ion battery. An all-solid-state lithium-ion battery in which a positive electrode layer, a solid electrolyte layer, and a negative electrode layer are laminated in this order.
An all-solid-state lithium-ion battery in which the solid electrolyte layer is formed of the solid electrolyte membrane according to any one of claims 1 to 5 .

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