JP7259677B2 - All-solid battery - Google Patents

Description

The present disclosure relates to all-solid-state batteries.

2. Description of the Related Art In recent years, with the rapid spread of information-related equipment and communication equipment such as personal computers, video cameras, and mobile phones, the development of batteries used as power sources for these devices has been emphasized. In addition, in the automobile industry and the like, development of high-output and high-capacity batteries for electric vehicles or hybrid vehicles is underway.
Among batteries, lithium metal secondary batteries are attracting attention because they use lithium, which has the highest ionization tendency among metals, as the negative electrode, resulting in a large potential difference with the positive electrode and high output voltage.
In addition, all-solid-state batteries are attracting attention in that they use a solid electrolyte instead of an electrolyte solution containing an organic solvent as an electrolyte interposed between a positive electrode and a negative electrode.

In the field of lithium metal secondary batteries, the occurrence of short circuits caused by dendrites is known. A short circuit occurs when lithium deposited on the negative electrode layer during charging grows toward the positive electrode layer, and the negative electrode layer and the positive electrode layer physically contact each other. Developments are underway aimed at preventing short circuits caused by dendrite growth.

Patent Literature 1 discloses a lithium solid state battery having a Li-deposited negative electrode provided with a Li-absorbing layer made of a carbon material and a resin between a negative electrode current collector and a solid electrolyte layer.

Further, in Patent Document 2, a negative electrode active material layer containing a negative electrode active material containing Li and a conductive powder layer containing a conductive powder provided on the side opposite to the solid electrolyte layer side of the negative electrode active material layer and a non-aqueous electrolyte battery comprising a negative electrode having

JP 2019-033053 A JP 2013-089417 A

The lithium solid-state battery described in Patent Document 1 is provided with a Li-absorbing layer made of a carbon material and a resin between the negative electrode current collector and the solid electrolyte layer to suppress short circuits and improve the reversible capacity of the lithium solid-state battery. , there is room for further improvement in charge-discharge efficiency.
An object of the present disclosure is to provide an all-solid-state battery with high charge-discharge efficiency in view of the above circumstances.

The present disclosure is an all-solid-state battery that uses a deposition-dissolution reaction of metallic lithium as a negative electrode reaction,
Having a negative electrode current collector, a solid electrolyte layer, and a positive electrode layer in this order,
Provided is an all-solid battery characterized by having a Li-occlusion layer containing a fibrous carbon material and a resin between the negative electrode current collector and the solid electrolyte layer.

The present disclosure can provide an all-solid-state battery with high charge-discharge efficiency.

It is a cross-sectional schematic diagram showing an example of an all-solid-state battery of the present disclosure. FIG. 3 is a diagram showing the relationship between the thickness of each Li absorption layer and the charge/discharge efficiency of each all-solid lithium metal secondary battery in Examples and Comparative Examples.

The present disclosure is an all-solid-state battery that uses a deposition-dissolution reaction of metallic lithium as a negative electrode reaction,
Having a negative electrode current collector, a solid electrolyte layer, and a positive electrode layer in this order,
Provided is an all-solid battery characterized by having a Li-occlusion layer containing a fibrous carbon material and a resin between the negative electrode current collector and the solid electrolyte layer.

In the present disclosure, a lithium metal secondary battery means a battery that uses at least one of metallic lithium and a lithium alloy as a negative electrode active material, and that utilizes a deposition-dissolution reaction of metallic lithium as a negative electrode reaction. Further, in the present disclosure, a negative electrode means one including a negative electrode layer.
In the present disclosure, when the all-solid-state battery is fully charged means when the state-of-charge (SOC) value of the all-solid-state battery is 100%. The SOC indicates the ratio of the charge capacity to the full charge capacity of the battery, and the full charge capacity is SOC 100%.
The SOC may be estimated, for example, from the open circuit voltage (OCV) of the all-solid-state battery.

FIG. 1 is a cross-sectional schematic diagram showing an example of an all-solid-state battery of the present disclosure.
As shown in FIG. 1, the all-solid-state battery 100 includes a negative electrode current collector 11, a solid electrolyte layer 12, a positive electrode layer 13, and a positive electrode current collector 14 in this order. A Li occlusion layer 15 is provided between them. Although the negative electrode layer is not shown in FIG. 1, a negative electrode layer may exist between the negative electrode current collector 11 and the solid electrolyte layer 12 in the present disclosure. Further, if the negative electrode layer is between the negative electrode current collector 11 and the solid electrolyte layer 12, the may be present in at least one of the positions of Furthermore, when the negative electrode layer is made of metallic lithium, the negative electrode layer may be present in the all-solid-state battery 100 when fully charged, and the negative electrode layer is dissolved in the all-solid-state battery 100 before the initial charge or after the complete discharge. may have disappeared.

[Negative electrode current collector]
The material of the negative electrode current collector may be a material that does not alloy with Li, such as SUS, copper, and nickel. Examples of the shape of the negative electrode current collector include a foil shape and a plate shape. The shape of the negative electrode current collector in a plan view is not particularly limited, but examples thereof include a circular shape, an elliptical shape, a rectangular shape, and an arbitrary polygonal shape. The thickness of the negative electrode current collector varies depending on the shape, but is, for example, within the range of 1 μm to 50 μm, and may be within the range of 5 μm to 20 μm.

[Li storage layer]
The Li occlusion layer is a layer of a mixture containing a fibrous carbon material and a resin, and is a layer arranged between the negative electrode current collector and the solid electrolyte layer.
Examples of fibrous carbon materials include VGCF (vapor-grown carbon fiber), carbon nanotubes, and carbon nanofibers.
Examples of resins include acrylonitrile-butadiene rubber (ABR), butadiene rubber (BR), polyvinylidene fluoride (PVdF), and styrene-butadiene rubber (SBR).
The mass ratio of the fibrous carbon material and the resin in the Li storage layer is not particularly limited, but the mass ratio when the total mass of these two types of materials is 100% by mass is fibrous carbon material:resin=10: It may be 90 to 90:10, or fibrous carbon material:resin=25:75 to 75:25.
Examples of methods for producing a mixture composed of a fibrous carbon material and a resin include manual mixing using a mortar and pestle, homogenizer, mechanical milling, and the like. The mechanical milling may be dry mechanical milling or wet mechanical milling.
Mechanical milling is not particularly limited as long as it is a method of mixing a fibrous carbon material and a resin while applying mechanical energy. It may be, inter alia, a ball mill, in particular a planetary ball mill.
Examples of liquids used in preparing a mixture using a homogenizer include aprotic liquids such as polar aprotic liquids and non-polar aprotic liquids.
The thickness of the Li absorption layer is not particularly limited, but may be 14 to 33 μm.

[Negative electrode layer]
In the present disclosure, for example, an all-solid-state battery in which a negative electrode layer is provided between the Li absorption layer and the negative electrode current collector during assembly, or a negative electrode layer is not provided between the Li absorption layer and the negative electrode current collector during assembly, and then It may be an all-solid battery provided with a negative electrode layer formed by depositing metallic lithium as a negative electrode active material by charging. After the initial charge, metallic lithium deposited between the negative electrode current collector and the solid electrolyte layer is used as a negative electrode active material.
The negative electrode layer contains a negative electrode active material.
Examples of the negative electrode active material include metallic lithium (Li) and lithium alloys. Examples of lithium alloys include Li—Au, Li—Mg, Li—Sn, Li—Si, Li—Al, Li—B, Li— C, Li—Ca, Li—Ga, Li—Ge, Li—As, Li—Se, Li—Ru, Li—Rh, Li—Pd, Li—Ag, Li—Cd, Li—In, Li—Sb, Li--Ir, Li--Pt, Li--Hg, Li--Pb, Li--Bi, Li--Zn, Li--Tl, Li--Te and Li--At. As long as the negative electrode layer contains metallic lithium or a lithium alloy as a negative electrode active material as a main component, it may also contain other conventionally known negative electrode active materials. In the present disclosure, the main component means a component contained in the negative electrode layer in an amount of 50% by mass or more when the total mass of the negative electrode layer is 100% by mass.
The thickness of the negative electrode layer is not particularly limited, but may be 30 nm or more and 5000 nm or less.

[Solid electrolyte layer]
The solid electrolyte layer contains at least a solid electrolyte.
As the solid electrolyte to be contained in the solid electrolyte layer, known solid electrolytes that can be used in all-solid-state batteries can be appropriately used, and examples thereof include oxide-based solid electrolytes and sulfide-based solid electrolytes.
Examples of sulfide solid electrolytes include Li ₂ SP ₂ S ₅ , Li ₂ S—SiS ₂ , LiX—Li ₂ S—SiS ₂ , LiX—Li ₂ SP ₂ S ₅ , LiX—Li ₂ O—Li ₂ SP ₂ S ₅ , LiX—Li ₂ SP ₂ O ₅ , LiX—Li ₃ PO ₄ —P ₂ S ₅ , Li ₃ PS ₄ and the like. The above description of "Li ₂ SP ₂ S ₅ " means a material obtained by using a raw material composition containing Li ₂ S and P ₂ S ₅ , and the same applies to other descriptions. "X" in LiX above represents a halogen element. One or more kinds of LiX may be contained in the raw material composition containing LiX. When two or more types of LiX are included, the mixing ratio of the two or more types is not particularly limited.
The molar ratio of each element in the sulfide-based solid electrolyte can be controlled by adjusting the content of each element in the raw material. Also, the molar ratio and composition of each element in the sulfide-based solid electrolyte can be measured, for example, by ICP emission spectrometry.

The sulfide-based solid electrolyte may be sulfide glass, crystallized sulfide glass (glass ceramics), or a crystalline material obtained by solid-phase reaction treatment of a raw material composition. .
The crystalline state of the sulfide-based solid electrolyte can be confirmed, for example, by subjecting the sulfide-based solid electrolyte to powder X-ray diffraction measurement using CuKα rays.

Sulfide glass can be obtained by subjecting a raw material composition (for example, a mixture of Li ₂ S and P ₂ S ₅ ) to amorphous processing. Examples of amorphous processing include mechanical milling.

Glass-ceramics can be obtained, for example, by heat-treating sulfide glass.
The heat treatment temperature may be any temperature higher than the crystallization temperature (Tc) observed by thermal analysis measurement of sulfide glass, and is usually 195° C. or higher. On the other hand, the upper limit of the heat treatment temperature is not particularly limited.
The crystallization temperature (Tc) of sulfide glass can be measured by differential thermal analysis (DTA).
The heat treatment time is not particularly limited as long as the desired crystallinity of the glass-ceramics is obtained. is mentioned.
The method of heat treatment is not particularly limited, but for example, a method using a kiln can be mentioned.

Examples of oxide-based solid electrolytes include Li _6.25 La ₃ Zr ₂ Al _0.25 O ₁₂ , Li ₃ PO ₄ and Li _3+x PO _4-x N _x (1≦x≦3).

The shape of the solid electrolyte may be particulate from the viewpoint of ease of handling.
Moreover, the average particle diameter (D50) of the particles of the solid electrolyte is not particularly limited, but the lower limit may be 0.5 μm or more and the upper limit may be 2 μm or less.

In the present disclosure, unless otherwise specified, the average particle diameter of particles is the volume-based median diameter (D50) measured by laser diffraction/scattering particle size distribution measurement. In the present disclosure, the median diameter (D50) is the diameter (volume average diameter) at which the cumulative volume of particles is half (50%) of the total volume when the particles are arranged in order from the smallest particle size.

Solid electrolytes can be used singly or in combination of two or more. Moreover, when using two or more kinds of solid electrolytes, two or more kinds of solid electrolytes may be mixed, or two or more layers of each solid electrolyte may be formed to form a multilayer structure.
The proportion of the solid electrolyte in the solid electrolyte layer is not particularly limited. It may be within the range of mass % or less, and may be 100 mass %.

The solid electrolyte layer may contain a binder from the viewpoint of exhibiting plasticity. As such a binder, the materials exemplified as the resin used for the Li occluding layer can be exemplified. However, in order to facilitate high output, it is contained in the solid electrolyte layer from the viewpoint of preventing excessive aggregation of the solid electrolyte and making it possible to form a solid electrolyte layer having a uniformly dispersed solid electrolyte. The binder may be 5% by mass or less.

The thickness of the solid electrolyte layer is not particularly limited, and is usually 0.1 μm or more and 1 mm or less.
Examples of the method for forming the solid electrolyte layer include a method of pressure-molding powder of a solid electrolyte material containing a solid electrolyte and, if necessary, other components. When the solid electrolyte material powder is pressure-molded, a press pressure of about 1 MPa to 600 MPa is normally applied.
The pressurization method is not particularly limited, but includes the pressurization method exemplified in the later-described formation of the positive electrode layer.

[Positive electrode layer]
The positive electrode layer contains a positive electrode active material, and may contain a solid electrolyte, a conductive material, a binder, and the like as optional components.

There are no particular restrictions on the type of positive electrode active material, and any material that can be used as an active material for an all-solid-state battery can be used. When the all-solid battery is an all-solid lithium metal secondary battery, the positive electrode active material is, for example, metallic lithium (Li), a lithium alloy, LiCoO ₂ , LiNi _x Co _1-x O ₂ (0<x<1), LiNi _1/3 Co _1/3 Mn _1/3 O ₂ , LiMnO ₂ , heteroelement-substituted Li—Mn spinels (e.g., LiMn _1.5 Ni _0.5 O ₄ , LiMn _1.5 Al _0.5 O ₄ , LiMn _{1.5Mg0.5O4 , LiMn1.5Co0.5O4} , _{LiMn1.5Fe0.5O4 ,} and _{LiMn1.5Zn0.5O4 , etc. ) , lithium} titanate ₍ Li ₄ Ti ₅ O ₁₂ ), lithium metal phosphates (e.g. LiFePO ₄ , LiMnPO ₄ , LiCoPO ₄ and LiNiPO ₄ ), lithium compounds such as LiCoN, Li ₂ SiO ₃ and Li ₄ SiO ₄ , transition metal oxides materials (such as _V2O5 and _MoO3 ), _TiS2 , Si, _SiO2 , and lithium-storing intermetallic compounds (such _{as Mg2Sn} , _Mg2Ge , _Mg2Sb , and _Cu3Sb ), etc. can be mentioned. Examples of lithium alloys include the lithium alloys exemplified as the lithium alloys used for the negative electrode active material.
Although the shape of the positive electrode active material is not particularly limited, it may be particulate.
A coat layer containing a Li ion conductive oxide may be formed on the surface of the positive electrode active material. This is because the reaction between the positive electrode active material and the solid electrolyte can be suppressed.
Li ion conductive oxides include, for example, LiNbO ₃ , Li ₄ Ti ₅ O ₁₂ , Li ₃ PO ₄ and the like. The thickness of the coat layer is, for example, 0.1 nm or more, and may be 1 nm or more. On the other hand, the thickness of the coat layer is, for example, 100 nm or less, and may be 20 nm or less. The coverage of the coat layer on the surface of the positive electrode active material is, for example, 70% or more, and may be 90% or more.

Examples of the solid electrolyte include solid electrolytes that can be contained in the solid electrolyte layer described above.
The content of the solid electrolyte in the positive electrode layer is not particularly limited, but may be in the range of, for example, 1% by mass to 80% by mass when the total mass of the positive electrode layer is 100% by mass.

As the conductive material, a known material can be used, and examples thereof include carbon materials, metal particles, and the like. Examples of the carbon material include at least one selected from the group consisting of carbon black such as acetylene black and furnace black, VGCF, carbon nanotubes, and carbon nanofibers. At least one selected from the group consisting of VGCF, carbon nanotubes, and carbon nanofibers may be used. Metal particles include particles of Ni, Cu, Fe, SUS, and the like.
The content of the conductive material in the positive electrode layer is not particularly limited.

As the binder, the materials exemplified as the resin used for the Li occluding layer can be exemplified. The content of the binder in the positive electrode layer is not particularly limited.

The thickness of the positive electrode layer is not particularly limited.

The positive electrode layer can be formed by a conventionally known method.
For example, the positive electrode active material and, if necessary, other components are put into a solvent and stirred to prepare a positive electrode layer slurry. The positive electrode layer is obtained by coating on top and drying.
Solvents include, for example, butyl acetate, butyl butyrate, heptane, N-methyl-2-pyrrolidone, and the like.
The method for applying the positive electrode layer slurry onto one surface of a support such as a positive electrode current collector is not particularly limited, and may be a doctor blade method, a metal mask printing method, an electrostatic coating method, a dip coating method, a spray coating method, a roll coating method, or the like. Examples include a coating method, a gravure coating method, and a screen printing method.
As the support, one having self-supporting properties can be appropriately selected and used, and there is no particular limitation. For example, metal foils such as Cu and Al can be used.

As another method of forming the positive electrode layer, the positive electrode layer may be formed by pressure-molding a powder of a positive electrode mixture containing the positive electrode active material and, if necessary, other components. When the powder of the positive electrode mixture is pressure-molded, a press pressure of about 1 MPa to 600 MPa is normally applied.
The pressurizing method is not particularly limited, but examples thereof include a method of applying pressure using a flat plate press, a roll press, and the like.

[Positive collector]
An all-solid-state battery usually has a positive electrode current collector that collects the current of the positive electrode layer.
A known metal that can be used as a current collector for an all-solid battery can be used as the positive electrode current collector. Such metals include one or more elements selected from the group consisting of Cu, Ni, Al, V, Au, Pt, Mg, Fe, Ti, Co, Cr, Zn, Ge, and In. A metal material can be exemplified. Examples of positive electrode current collectors include SUS, aluminum, nickel, iron, titanium and carbon.
The shape of the positive electrode current collector is not particularly limited, and various shapes such as a foil shape and a mesh shape can be used.

An all-solid-state battery is provided with an exterior body that accommodates a positive electrode layer, a negative electrode layer, a solid electrolyte layer, and the like, if necessary.
The material of the exterior body is not particularly limited as long as it is stable in the electrolyte, and examples thereof include polypropylene, polyethylene, and resins such as acrylic resins.

The all-solid-state battery may be a primary battery, a secondary battery, or a secondary battery. This is because they can be repeatedly charged and discharged, and are useful, for example, as batteries for vehicles. Also, the all-solid battery may be an all-solid lithium metal secondary battery.
Examples of the shape of the all-solid-state battery include coin type, laminate type, cylindrical type, rectangular type, and the like.

In the manufacturing method of the all-solid-state battery of the present disclosure, for example, first, the solid electrolyte layer is formed by pressure-molding the powder of the solid electrolyte material. Then, on one surface of the solid electrolyte layer, a positive electrode layer is obtained by pressure-molding a positive electrode mixture powder containing at least one positive electrode active material selected from the group consisting of metallic lithium, lithium alloys and lithium compounds. Thereafter, a slurry containing a material for the Li occlusion layer is applied to one surface of the negative electrode current collector and dried to form a Li occlusion layer to obtain a negative electrode current collector-Li occlusion layer laminate, and the positive electrode layer of the solid electrolyte layer is formed. The negative electrode current collector-Li occlusion layer laminate is mounted on the surface opposite to the formed surface so that the Li occlusion layer is in contact with the solid electrolyte layer. Then, if necessary, a positive electrode current collector may be attached on the surface of the positive electrode layer opposite to the solid electrolyte layer to form the all-solid-state battery of the present disclosure.
In this case, the press pressure when the powder of the solid electrolyte material and the powder of the positive electrode material mixture is pressure-molded is usually about 1 MPa or more and 600 MPa or less.
The pressurization method is not particularly limited, but includes the pressurization method exemplified in the formation of the positive electrode layer.

(Example 1)
[Preparation of Li storage layer]
VGCF as a fibrous carbon material and PVDF as a resin were weighed at a mass ratio of 75:25, mixed by hand, heptane was added, and mixed for 3 minutes using a homogenizer (manufactured by SMTE Co., Ltd., UH-50). , to obtain a Li occlusion layer material, which is the material for the Li occlusion layer.
A Cu foil is prepared as a negative electrode current collector, and a Li occluding layer material is applied on one side of the Cu foil and dried to form a Li occluding layer on one side of the Cu foil. A laminate was obtained. The thickness of the Li absorption layer was set to 14 μm.

[Preparation of positive electrode mixture]
Particles of LiNi _1/3 Co _1/3 Mn _1/3 O ₂ (manufactured by Nichia Corporation) were used as the positive electrode active material. The particles of the positive electrode active material are previously surface-treated with LiNbO ₃ . This positive electrode active material, VGCF (manufactured by Showa Denko) as a conductive material, and a sulfide-based solid electrolyte (Li ₂ SP ₂ S _5- based material containing LiBr and LiI) were mixed in a mass ratio of 85.3:1.3: The positive electrode mixture was obtained by weighing and mixing so as to obtain 13.4.

[Fabrication of all-solid-state battery]
101.7 mg of powder of a sulfide-based solid electrolyte (Li ₂ SP ₂ S _5- based material containing LiBr and LiI) was prepared in a ceramic mold (cross-sectional area: 1 cm ² , using a cylindrical container), Press molding was performed at a pressure of 1 ton/cm ² to obtain a solid electrolyte layer.
A positive electrode layer was formed by adding 31.3 mg of the above positive electrode mixture to one side of the solid electrolyte layer and pressing at 6 ton/cm ² .
The negative electrode current collector-Li occlusion layer laminate is placed on the surface of the solid electrolyte layer opposite to the positive electrode layer so that the Li occlusion layer is in contact with the solid electrolyte layer, and pressed at 1 ton/cm ² to compact. turned into a battery.
An all-solid lithium metal secondary battery of Example 1 was obtained by placing a positive electrode current collector (aluminum foil) on the surface of the positive electrode layer of the dust battery opposite to the solid electrolyte layer and restraining it. . All operations using the sulfide-based solid electrolyte were performed in a glove box in a dry Ar atmosphere.

(Example 2)
An all-solid lithium metal secondary battery was obtained in the same manner as in Example 1, except that the thickness of the Li absorption layer was 18 μm.

(Example 3)
An all-solid lithium metal secondary battery was obtained in the same manner as in Example 1, except that the thickness of the Li occluding layer was 25 μm.

(Example 4)
An all-solid lithium metal secondary battery was obtained in the same manner as in Example 1, except that the thickness of the Li absorption layer was 28 μm.

(Example 5)
An all-solid lithium metal secondary battery was obtained in the same manner as in Example 1, except that the thickness of the Li absorption layer was 33 μm.

(Comparative example 1)
An all solid lithium metal secondary battery was obtained in the same manner as in Example 1, except that no Li absorption layer was formed.

(Comparative example 2)
An all-solid lithium metal secondary battery was fabricated in the same manner as in Example 1, except that spherical Ketjenblack (KB) was used instead of VGCF as the carbon material for the Li occlusion layer, and the thickness of the Li occlusion layer was set to 11 μm. got

(Comparative Example 3)
An all-solid lithium metal secondary battery was obtained in the same manner as in Example 1, except that spherical Ketjenblack was used instead of VGCF as the carbon material for the Li occlusion layer, and the thickness of the Li occlusion layer was set to 18 μm. .

(Comparative Example 4)
An all-solid lithium metal secondary battery was obtained in the same manner as in Example 1, except that spherical Ketjenblack was used instead of VGCF as the carbon material for the Li occlusion layer, and the thickness of the Li occlusion layer was set to 25 μm. .

(Comparative Example 5)
An all-solid lithium metal secondary battery was obtained in the same manner as in Example 1, except that spherical ketjen black was used instead of VGCF as the carbon material for the Li occlusion layer, and the thickness of the Li occlusion layer was set to 40 μm. .

[evaluation]
(Charge/discharge measurement)
Using the all-solid lithium metal secondary battery obtained in Example 1, charging and discharging measurements were performed after being left in a constant temperature bath at 60° C. for 3 hours. As the measurement conditions, constant current (CC) charging was performed at 60° C. and a current density of 8.7 mA/cm ² (rate: 2C) ^. paused. After that, CC discharge was performed at 60° C. and a current density of 0.435 mA/cm ² (rate: 0.1 C), and when the lower limit voltage reached 3.0 V, the discharge was terminated.
From the discharge capacity and charge capacity of the all-solid lithium metal secondary battery of Example 1 obtained by charge-discharge measurement, the charge-discharge efficiency was obtained from the following formula.
Charge/discharge efficiency (%) = (discharge capacity/charge capacity) x 100
The all-solid lithium metal secondary batteries obtained in Examples 2 to 5 and Comparative Examples 1 to 5 were also charged and discharged in the same manner as the all-solid lithium metal secondary battery of Example 1. , each charge-discharge efficiency was obtained.
The results are shown in Table 1 and FIG.

[Evaluation results]
The charge/discharge efficiency is the ratio of the discharge capacity to the charge capacity, and the charge/discharge efficiency decreases when a short circuit occurs or the movement of Li ions is inhibited.
First, regardless of the shape of the carbon material, the all-solid lithium metal secondary batteries of Comparative Examples 2 to 4 and Examples 1 to 5, which have a Li absorption layer containing a carbon material and a resin, are comparative examples having no Li absorption layer. 1 showed higher charge-discharge efficiency than the all-solid-state lithium metal secondary battery of No. 1. It is considered that this is because the presence of the Li occluding layer suppresses the occurrence of a short circuit due to the growth of lithium dendrites.
Next, focusing on the shape of the carbon material contained in the Li occlusion layer, the all-solid lithium metal secondary battery using the Li occlusion layer containing VGCF, which is a fibrous carbon material, as the carbon material of Examples 1 to 5, As compared with the all-solid lithium metal secondary battery using the Li absorption layer containing KB, which is a spherical carbon material, as the carbon material of Comparative Examples 2 to 5, good charge-discharge efficiency was exhibited. The reason for such a result is presumed to be as follows. When the carbon material comes into contact with the Li ions, it reacts with the Li ions and the surface exhibits ionic conductivity. When the carbon material is fibrous, the surface area exhibiting ionic conductivity is larger than when the carbon material is spherical. Therefore, when metallic lithium is dissolved, an ionic conduction path is easily secured, and Li ions easily move to the positive electrode. It is thought that
In addition, although the all-solid lithium metal secondary battery of Comparative Example 5 using the Li occlusion layer containing KB has the Li occlusion layer, the all-solid lithium metal secondary battery of Comparative Example 1 having no Li occlusion layer The charge/discharge efficiency was lower than that of the metal secondary battery. Comparing the all-solid-state lithium metal secondary batteries of Comparative Examples 2 to 5 using the Li occlusion layer containing KB, when the thickness of the Li occlusion layer exceeds 18 μm, the charging and discharging efficiency tends to decrease significantly as the thickness increases. Admitted. Even with the Li occlusion layer containing VGCF, the charge-discharge efficiency decreased slightly when the thickness exceeded 18 μm, but the decrease was smaller than in the case of the all-solid-state lithium metal secondary battery with the Li occlusion layer containing KB. Good charge/discharge efficiency was shown even at 33 μm. From this result, it can be seen that the use of the fibrous carbon material for the Li-absorbing layer can improve the charge-discharge efficiency of the all-solid-state lithium metal secondary battery even if the Li-absorbing layer is thickened. When a spherical carbon material such as KB is used, it is necessary to bond particles of the carbon material together with a binder in order to form a uniform Li-absorbing layer. If the thickness of the Li occlusion layer is increased beyond a certain value, the binding force between the particles of the carbon material due to the binder will become insufficient, and cracks will occur in the Li occlusion layer. As a result, the contact area between the Li storage layer and the solid electrolyte layer is reduced. When an all-solid-state lithium metal secondary battery having the Li occlusion layer is charged, the current concentrates at the point where the Li occlusion layer and the solid electrolyte layer are in contact, so that the battery is likely to short circuit. It is considered that the charge-discharge efficiency decreased significantly as the thickness increased. On the other hand, in fibrous carbon materials such as VGCF, the need for bonding between carbon materials is low, so cracks are less likely to occur in the Li occlusion layer even if the Li occlusion layer is thickened. As a result, the contact area between the Li occlusion layer and the solid electrolyte layer can be kept wider than when the Li occlusion layer contains a spherical carbon material, and the charge/discharge efficiency of the all-solid-state battery is improved regardless of the thickness of the Li occlusion layer. It is thought that it is possible to
Therefore, according to the present disclosure, it was demonstrated that an all-solid-state battery with high charge-discharge efficiency can be provided.

11 negative electrode current collector 12 solid electrolyte layer 13 positive electrode layer 14 positive electrode current collector 15 Li occlusion layer 100 all-solid battery

Claims (1)

An all-solid-state battery that utilizes a deposition-dissolution reaction of metallic lithium as a negative electrode reaction,
Having a negative electrode current collector, a solid electrolyte layer, and a positive electrode layer in this order,
a Li occlusion layer containing a fibrous carbon material and a resin between the negative electrode current collector and the solid electrolyte layer ;
The fibrous carbon material is a vapor-grown carbon fiber,
The resin is polyvinylidene fluoride,
The mass ratio of the fibrous carbon material and the resin in the Li storage layer is fibrous carbon material:resin=75:25,
The all-solid-state battery , wherein the thickness of the Li absorption layer is 14 to 33 μm .

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