This application claims priority to Japanese Patent Application No. 2021-190443 filed Nov. 24, 2021, which is incorporated herein by reference in its entirety.
The present disclosure relates to an all-solid-state battery and to a method for producing it.
All-solid-state batteries have a construction in which the separator layer and electrolyte solution used in a conventional electrolyte solution lithium ion battery are replaced with a solid electrolyte, and due to the high flame retardance of the solid electrolyte and lack of requirement for a cooling unit, they are expected to have high pack energy density and to allow high rate charging, thus being highly suitable for use in automobiles.
In terms of all-solid-state battery structure, PTL 1 discloses a structure wherein unit cells each having a positive electrode layer formed on one side of a solid electrolyte and a negative electrode layer formed on the other side, are stacked across positive electrode collectors and negative electrode collectors, the positive electrode collectors being commonly connected to a positive electrode terminal and the negative electrode collectors being commonly connected to a negative electrode terminal, and the terminals leading out of the battery. One problem with this construction, however, is that the internal resistance of the cell increases due to electrical resistance at the connected sections between the collectors and terminals.
To counter this, PTL 2 discloses a stacked all-solid-state battery structure wherein the positive electrode collector has each of the positive electrode layers of the electrode stack disposed in a folded manner so as to be electrically connected together, and the negative electrode collector has each of the negative electrode layers of the electrode stack disposed in a folded manner so as to be electrically connected together. This can reduce electrical resistance at the connected sections between the positive electrodes and negative electrode collectors and the terminals, in a conventional construction. However, this structure has been problematic because it requires complex production steps.
Another issue is that the electrical resistance may increase due to copper sulfide formation if sulfur is included in the solid electrolyte and copper is used as the collector. PTL 3 discloses an all-solid-state battery with reduced copper sulfide formation and excellent conductivity, wherein the solid electrolyte has a negative electrode collector for an all-solid-state battery with a nickel film formed on both sides of an electrolytic copper foil, rolled copper foil or copper alloy foil, and a sulfur-containing solid electrolyte. However, since the layered stack is entirely joined in this structure, it has not been possible to replace specific defective layer portions, and the yield during production has also been low.
It is an object of the present disclosure to provide an all-solid-state battery with a novel construction.
The construction for solving the problem described above is as follows:
An all-solid-state battery having at least one structural unit cell comprising a positive electrode collector layer, a positive electrode active material layer, a solid electrolyte layer, a negative electrode active material layer and a negative electrode collector layer stacked in that order,
wherein a connecting conductor layer is layered on the surface of the positive electrode collector layer side and/or the negative electrode collector layer side of the structural unit cell.
The all-solid-state battery according to aspect 1, wherein the electric resistivity of the connecting conductor layer is lower than the electric resistivity of the positive electrode collector layer or negative electrode collector layer on which the connecting conductor is layered.
The all-solid-state battery according to aspect 1 or 2, wherein the electric resistivity of the connecting conductor layer is 1×10−6 Ωm or lower.
The all-solid-state battery according to any one of aspects 1 to 3, wherein the connecting conductor layer is made of copper and/or aluminum.
The all-solid-state battery according to any one of aspects 1 to 4, wherein the negative electrode active material layer comprises a sulfide-based solid electrolyte, and the negative electrode collector layer is made of stainless steel or nickel.
A method for producing an all-solid-state battery according to any one of aspects 1 to 5, wherein the method comprises the following steps in order:
a step of alternately layering the structural unit cell and the connecting conductor layer or layering subunits of the layered structural unit cell and connecting conductor, to form a stack,
a step of connecting a positive electrode terminal and a negative electrode terminal to the connecting conductor layer of the obtained stack, and
a step of sealing the stack with an exterior body.
According to the present disclosure it is possible to provide an all-solid-state battery having a novel construction.
The all-solid-state battery of the disclosure is an all-solid-state battery having a structural unit cell comprising a positive electrode collector layer, a positive electrode active material layer, a solid electrolyte layer, a negative electrode active material layer and a negative electrode collector layer stacked in that order, wherein a connecting conductor layer is layered on the surface of the positive electrode collector layer side and/or the negative electrode collector layer side of the structural unit cell.
The all-solid-state battery of the disclosure may have a monolayer structure with one structural unit cell, or a multilayer structure with a plurality of alternately layered structural unit cells and connecting conductor layers.
With a plurality of layered structural unit cells, it is possible to further increase the charge-discharge capacity per volume and to further reduce the internal resistance of the battery. If a connecting conductor layer is also provided between each of the structural unit cells in the all-solid-state battery of the disclosure, then the structural unit cells will not be joined together, resulting in a different construction from the construction disclosed in PTL 3 in which the stack is joined throughout, and therefore since it is possible to exchange only a specific structural unit cell when a problem has occurred in part of that structural unit cell, this structure can improve production yield.
A serial structure is a structure with stacking such that the positive electrode collector sides of the structural unit cells are disposed in contact with one of the sides of the connecting conductors and the negative electrode collector sides of the structural unit cells are disposed in contact with the other sides, and the polarities of the plurality of structural unit cells are in the same direction (bipolar structure), while a parallel structure is a structure with stacking such that the positive electrode collector sides of the structural unit cells are disposed in contact with both sides of the positive electrode connecting conductors, and the negative electrode collector sides of the structural unit cells are disposed in contact with both sides of the negative electrode connecting conductors, so that the polarities of the plurality of structural unit cells alternate in opposite directions (monopolar structure). A serial structure can increase the voltage of the battery. A parallel structure can further increase the charge-discharge capacity and further lower the internal resistance of the battery.
As shown in
With the insulator 16 described above, the structural unit cell 10A can inhibit short circuiting caused by contact between the positive electrode collector layer 11 and/or positive electrode active material layer 12 and the negative electrode active material layer 14 and/or negative electrode collector layer 15.
In
In the all-solid-state battery 1A shown in
The all-solid-state battery 1B of the second embodiment of the disclosure shown in
When a plurality of structural unit cells 10A are layered as shown in
The all-solid-state battery 1C of the third embodiment of the disclosure shown in
In some embodiments, in the all-solid-state battery 1C shown in
The all-solid-state battery 1D of the fourth embodiment of the disclosure shown in
The all-solid-state battery 1E of the fifth embodiment of the disclosure shown in
As shown in
The structural unit cell of the all-solid-state battery of the present disclosure has a construction in which a positive electrode collector layer, positive electrode active material layer, solid electrolyte layer, negative electrode active material layer and negative electrode collector layer are stacked in that order.
As seen from the stacking direction of the structural unit cell, the positive electrode collector layer and positive electrode active material layer are disposed on the inner side of the outer periphery of the solid electrolyte layer, negative electrode active material layer and negative electrode collector layer. As seen from the stacking direction of the structural unit cell, the positive electrode collector layer and positive electrode active material layer may also have their outer peripheries aligned with the solid electrolyte layer, in which case the positive electrode collector layer, positive electrode active material layer and solid electrolyte layer may be disposed on the inner sides of the outer peripheries of the negative electrode active material layer and negative electrode collector layer.
This is in order to cause the positive electrode active material layer, and especially the edges, to reliably face the solid electrolyte layer and negative electrode active material layer, thereby allowing lithium ions migrating from the positive electrode active material during charge to easily intercalate into the negative electrode active material. This can help prevent deposition of lithium metal onto the positive electrode active material layer surface and the interface between the positive electrode active material layer and solid electrolyte layer, thus inhibiting internal short circuiting of the structural unit cells.
In the construction in which the positive electrode collector layer and positive electrode active material layer are disposed on the inner sides of the outer peripheries of the solid electrolyte layer, negative electrode active material layer and negative electrode collector layer, the insulator may also be disposed in a manner surrounding the outer peripheries of the positive electrode collector layer and positive electrode active material layer. The insulator may have a frame-like shape that surrounds the outer peripheries of the positive electrode collector layer and positive electrode active material layer.
In some embodiments, material composing the positive electrode collector layer is one that does not react when in contact with the solid electrolyte or upon charge-discharge within the action potential of the positive electrode, and that has low electric resistivity. Examples include aluminum, stainless steel (SUS, austenite, martensite, ferrite, and austenite-ferrite (biphase)) and nickel. Two or more different types may also be used. In some embodiments, aluminum is used among those mentioned above.
The positive electrode collector layer in the all-solid-state battery of the disclosure may be made of aluminum, stainless steel or nickel. These metals have low reactivity with sulfide-based solid electrolytes.
In some embodiments, the positive electrode active material layer is composed mainly of a positive electrode active material and a solid electrolyte.
Examples of positive electrode active materials include LiCoO2, LiMnO2, LiNiO2, oxides of lithium ternary oxides of Ni, Co and Mn, lithium ternary oxides of Ni, Co and Al, and LiFePO4. Two or more different types may also be used.
Examples of solid electrolytes include sulfide-based solid electrolytes such as Li2S—P2S5 (Li7P3S11), Li10GeP2S12, Li6PS5Cl and Li6PS5I, and oxide-based solid electrolytes such as Li1.4Al0.4Ti1.6(PO4)3, Li7La3Zr2O12 and Li1.5Al0.5Ge1.5(PO4)3. Two or more different types may also be used. In some embodiments, sulfide-based solid electrolytes are used among those mentioned above. In some embodiments, when a sulfide-based solid electrolyte is to be used, the positive electrode active material surface may be coated with LiNbO3 in order to inhibit reaction with the positive electrode active material.
The solid electrolyte layer is composed mainly of a solid electrolyte. The solid electrolyte may be any of the solid electrolytes mentioned above for composing the positive electrode active material layer.
In some embodiments, the negative electrode active material layer is composed mainly of a negative electrode active material and a solid electrolyte.
Negative electrode active materials include graphite, hard carbon, lithium titanate, titanium oxide, silicon and silicon oxide. Two or more different types may also be used.
The solid electrolyte may be any of the solid electrolytes mentioned above for composing the positive electrode active material layer.
In some embodiments, the material composing the negative electrode collector layer is one that does not react when in contact with the solid electrolyte or upon charge-discharge within the action potential of the negative electrode, and that has low electric resistivity. Examples include stainless steel (SUS), carbon, nickel and copper. Two or more different types may also be used.
Examples of materials to compose the insulator include resins such as polyethylene terephthalate (PET), polyimide (PI) and polyphenylenesulfide (PPS), and ceramics such as alumina. Two or more different types may also be used.
In some embodiments, when the negative electrode active material layer in the all-solid-state battery of the disclosure comprises a sulfide-based solid electrolyte, the negative electrode collector layer is made of stainless steel or nickel. These metals have low reactivity with sulfide-based solid electrolytes.
In the all-solid-state battery of the disclosure, the connecting conductor layer is layered on the surface of the positive electrode collector layer side and/or the surface of the negative electrode collector layer side of the structural unit cell.
By joining the positive electrode terminal and negative electrode terminal to the connecting conductor layer in the all-solid-state battery of the disclosure, it is possible to obtain a structure in which the positive electrode terminal and negative electrode terminal are not directly joined to the positive electrode collector layers and negative electrode collector layers of the structural unit cells. It is also possible to obtain a structure in which the positive electrode collector layers and negative electrode collector layers of the structural unit cells are simply layered without contact with the connecting conductor layer.
Unlike in a conventional all-solid-state battery having a construction with the positive electrode collector layers and negative electrode collector layers joined to the positive electrode terminal and negative electrode terminal, the all-solid-state battery of the disclosure thus makes it possible to easily separate the structural unit cells from the all-solid-state battery even when they have been assembled in the all-solid-state battery. Therefore, when a problem arises with any of the structural unit cells during the all-solid-state battery production process, for example, the problematic structural unit cell alone can be easily exchanged to a non-problematic structural unit cell.
It is therefore possible to eliminate waste of the other structural unit cells or other parts of the all-solid-state battery, thereby improving yields during production of the all-solid-state battery.
An all-solid-state battery can also be formed by alternately layering structural unit cells and connecting conductor layers (positive electrode connecting conductor layers and negative electrode connecting conductor layers). This can further facilitate production of the all-solid-state battery.
In some embodiments, the positive electrode connecting conductor layer and negative electrode connecting conductor layer have shapes that partially or fully cover the positive electrode collector layers and negative electrode collector layers, respectively. In some embodiments, while planar shapes are used from the viewpoint of further reducing electrical resistance per unit volume, they may also be lattice-like or mesh-like. The positive electrode connecting conductor layer and negative electrode connecting conductor layer may have the positive electrode terminal and negative electrode terminal connected at locations that do not overlap with the positive electrode collector layers and negative electrode collector layers, respectively. In some embodiments, the method of connection is ultrasonic welding or spot welding/resistance spot welding from the viewpoint of further reducing electrical resistance at the connected sections.
The electric resistivity of the positive electrode connecting conductor layer and negative electrode connecting conductor layer will be inversely proportional to the thickness. In some embodiments, a smaller thickness of the connecting conductor layer, on the other hand, increases the energy density per battery volume, and therefore smaller thicknesses are used for the positive electrode connecting conductor layer and negative electrode connecting conductor layer. Specifically, in some embodiments, a thickness of 100 μm or smaller is used, 50 μm or smaller is used, and 20 μm or smaller is used.
In some embodiments, the materials composing the positive electrode connecting conductor layer and negative electrode connecting conductor layer have low electrical resistance. Examples include aluminum, copper, nickel and stainless steel (SUS). Two or more different types may also be used. In some embodiments, the electric resistivity of the connecting conductor layer is lower than that of the positive electrode collector layer or negative electrode collector layer with which it contacts.
Specifically, in some embodiments, the electric resistivity of the positive electrode connecting conductor layer is lower than the electric resistivity of the positive electrode collector layer, and the electric resistivity of the negative electrode connecting conductor layer is lower than the electric resistivity of the negative electrode collector layer.
More specifically, in some embodiments, the electric resistivity of the connecting conductor layer is 1×10−6 Ωm or lower. The electric resistivity is measured according to JIS C2525:1999.
The electric resistivity of the connecting conductor layer may be 1×10−6 Ωm or lower, 5×10−7 Ωm or lower, 1×10−7 Ωm or lower or 5×10−8 Ωm or lower.
The method for lowering the electrical resistance of the connecting conductor layer may be, for example, a method of using a metal material having lower electric resistivity than the material forming the positive electrode collector layer or negative electrode collector layer, as the material to form the positive electrode connecting conductor layer or negative electrode connecting conductor layer, or a method of increasing the thickness of the connecting conductor to enlarge the cross-sectional area.
Specifically, the connecting conductor layer may be made of copper and/or aluminum.
When the all-solid-state battery of the disclosure uses a sulfide-based solid electrolyte as the solid electrolyte, the negative electrode collector layer and sulfide-based solid electrolyte can potentially react depending on the material employed for the negative electrode collector layer, thus increasing the internal resistance of the all-solid-state battery. In such cases a material with low reactivity with the sulfide-based solid electrolyte, such as stainless steel or nickel, may be used as the material of the negative electrode collector layer.
A metal such as stainless steel or nickel generally has high electric resistivity. For example, the electric resistivity of stainless steel is 10 or more times that of copper. If such a metal is used as the collector, therefore, the internal resistance of the all-solid-state battery as a whole will increase.
In this regard, in some embodiments, when a sulfide-based solid electrolyte is used as the solid electrolyte, a material having low reactivity with the sulfide-based solid electrolyte, such as stainless steel or nickel, is used as the current collector layer, and a material having low electric resistivity, such as aluminum or copper, is used as the connecting conductor layer disposed on the current collector layer. With such a construction it is possible to use a material having low reactivity with sulfide-based solid electrolytes in the current collector layer and to inhibit reaction of the current collector layer with the sulfide-based solid electrolyte, thereby inhibiting increase in internal resistance, while also offsetting the high electric resistivity of the current collector layer by the connecting conductor layer that has low electric resistivity, and reducing the internal resistance of the all-solid-state battery as a whole.
Examples of materials for the positive electrode terminal and negative electrode terminal include aluminum, copper and nickel. Two or more different types may also be used. A sealant film employing a thermoplastic resin such as polypropylene may also be disposed at a location in contact with the exterior body, creating a firm seal by thermocompression bonding.
The exterior body is formed of a laminate film, for example. In some embodiments, the exterior body has a gas barrier property in order to inhibit reaction of the solid electrolyte in the structural unit cell with moisture in the air atmosphere, which results in deterioration. In some embodiments, the exterior body is vacuum sealed to reduce interfacial resistance between the layers.
<Method for Producing all-Solid-State Battery>
The method for producing an all-solid-state battery according to the disclosure comprises, for example, a step of alternately layering a plurality of structural unit cells and connecting conductor layers or alternately layering a structural unit cell and connecting conductor layer, to form a stack, a step of connecting a positive electrode terminal and a negative electrode terminal to the connecting conductor layer of the obtained stack, and a step of sealing the stack with an exterior body, in that order.
The method for producing the all-solid-state battery 1A illustrated in
Another method may comprise, in order, a step of anchoring a positive electrode terminal 30-connected positive electrode connecting conductor layer 20a and a negative electrode terminal 40-connected negative electrode connecting conductor layer 20b to an exterior body 50 in advance, and a step of inserting structural unit cells 10A between the positive electrode connecting conductor layer 20a and negative electrode connecting conductor layer 20b before sealing the exterior body 50.
In some embodiments, the former method is used to further facilitate production with stacking in order in the same direction.
The method for producing the all-solid-state battery 1B illustrated in
The method for producing the all-solid-state battery 1C illustrated in
In the all-solid-state battery 1C shown in
The method for producing the all-solid-state battery 1D shown in
The method for producing the all-solid-state battery 1E illustrated in
When the structural unit cells are layered, an adhesive may be coated onto some of the structural unit cells or insulators, positive electrode connecting conductor layers, negative electrode connecting conductor layers or connecting conductor layers to anchor them, in order to inhibit dislocation of the layered stack.
In the production method described above for all-solid-state batteries 1B to 1E illustrated in
In order to firmly join together each of the layers of a stacked structure of a plurality of structural unit cells and reduce interfacial resistance in a conventional stacked all-solid-state battery it has been necessary to press the stack as a whole, but because of the differences in sizes, materials, thicknesses and elastic moduli of the different layers, concentration of pressure at parts of the structure has tended to result in damage or short circuiting. The method for producing an all-solid-state battery as illustrated in
In the method for producing all-solid-state batteries 1B to 1E according to the present embodiment illustrated in
Examples of the present disclosure will now be described. However, the present disclosure is in no way limited by the examples. The evaluation methods used in the Examples and Comparative Examples will be explained first.
The electric resistivities of the current collector layers and connecting conductor layers used in the Examples and Comparative Examples were measured according to JIS C2525:1999.
All-solid-state batteries fabricated for the Examples and Comparative Examples were each subjected to a charge-discharge test at 25° C. and a 0.1 C rate while applying pressure through flat plates on either side, and the charge capacity and discharge capacity of each was measured to evaluate the internal resistance of the battery. For the C rate, 1 C is the current at which the battery is charged to full capacity in 1 hour, and 0.1 C is the current at which it is charged to full capacity in 10 hours.
This was followed by charging at 60° C., 2 C and measurement of the charge capacity, and subsequently discharge at a 0.1 C followed by measurement of the charge capacity at a 6 C, to evaluate the internal resistance of the battery.
Aluminum foil (electric resistivity: 2.7×10−8 Ωm, thickness: 20 μm) as the positive electrode collector layer was coated with a positive electrode active material slurry comprising a mixture of a LiNbO3-coated lithium ternary oxide of Ni, Co and Mn (positive electrode active material), an argyrodite-based sulfide-based solid electrolyte, VGCF™-H carbon nanofibers (conductive aid) and an organic system binder, to form a positive electrode active material layer on the positive electrode collector layer.
A stainless steel foil (electric resistivity: 5.4×10−7 Ωm, thickness: 10 μm) as the negative electrode collector layer was coated with a negative electrode active material slurry comprising a mixture of graphite (negative electrode active material), an argyrodite-based sulfide-based solid electrolyte and an organic system binder, to form a negative electrode active material layer on the negative electrode collector layer.
A mixture of an argyrodite-based sulfide-based solid electrolyte and an organic system binder was coated onto a stainless steel foil to form a solid electrolyte layer.
The aforementioned positive electrode active material layer, solid electrolyte layer and negative electrode active material layer were integrated to obtain a structural unit cell. The stainless steel foil of the solid electrolyte layer was detached during integration.
An all-solid-state battery composed of one structural unit cell was fabricated in the following manner. A stainless steel foil (electric resistivity: 5.4×10−7 Ω·m, thickness: 10 μm) as the positive electrode connecting conductor layer was connected with an aluminum positive electrode terminal by ultrasonic welding. A stainless steel foil as the negative electrode connecting conductor layer was similarly connected with a nickel-coated copper negative electrode terminal, by ultrasonic welding. The negative electrode collector layer side of the structural unit cell was layered onto the negative electrode connecting conductor layer, and an insulation film cut out to the same inside size as the positive electrode active material layer was disposed at the edge of the positive electrode active material layer of the structural unit cell. The connecting conductor layer of an aluminum foil (electric resistivity: 2.7×10−8 Ω·m, thickness: 20 μm) already connected to a lead was placed on the positive electrode collector layer side of the structural unit cell. The layered structure was vacuum sealed with an exterior body laminate film.
An all-solid-state battery was fabricated in the same manner as Example 1, except that an aluminum foil was used as the positive electrode connecting conductor layer and a copper foil (electric resistivity: 1.7×10−8 Ω·m, thickness: 17 μm) was used as the negative electrode connecting conductor layer.
An all-solid-state battery was fabricated in the same manner as Example 1, except that the structural unit cell was fabricated without using a positive electrode connecting conductor layer and negative electrode connecting conductor layer, but using a positive electrode collector layer with an aluminum foil having one side larger than the positive electrode active material layer, and a negative electrode collector layer with a copper foil having one side larger than the negative electrode active material layer, and a positive electrode terminal and negative electrode terminal were connected by ultrasonic welding outside of the layered region of the positive electrode collector layer and negative electrode collector layer.
The evaluation results for Examples 1 and 2 and Comparative Example 1 are shown in Table 1 below.
Examples 1 and 2 which employed stainless steel foils for the negative electrode collector layers, and also employed connecting conductor layers, had higher discharge capacity and charge capacity compared to Comparative Example 1. Example 2, which employed an aluminum foil as the positive electrode connecting conductor and a copper foil as the negative electrode connecting conductor, had an even higher charge capacity at 6 C.
An all-solid-state battery for Example 3 was fabricated in the same manner as Example 1. However, the all-solid-state battery of Example 1 and the all-solid-state battery of Example 3 had slightly different basis weights of the positive electrode active material layer and negative electrode active material layer combinations.
A stacked all-solid-state battery for Example 4 was fabricated by layering ten of the structural unit cells fabricated in Example 3, in mutual parallel connection, and vacuum sealing with an exterior body laminate film.
A stacked all-solid-state battery for Comparative Example 2 was fabricated by layering in parallel ten structural unit cells fabricated in the same manner as Comparative Example 1 except for using an aluminum foil as the positive electrode collector layer and a stainless steel foil as the negative electrode collector layer, and vacuum sealing with an exterior body laminate film.
The all-solid-state battery of Example 3 and the stacked all-solid-state batteries of Example 4 and Comparative Example 2 were subjected to charge-discharge, and the charge capacities and discharge capacities were measured. The measurement results are shown in Table 2.
As shown in Table 2, the stacked all-solid-state battery of Example 4 had approximately 10 times the charge capacity and discharge capacity of the all-solid-state battery of Example 3.
The stacked all-solid-state battery of Comparative Example 2, however, exhibited damage and short circuiting during layering.
Number | Date | Country | Kind |
---|---|---|---|
2021-190443 | Nov 2021 | JP | national |