The present invention relates to a method for manufacturing an electrochemical cell.
A proposed electrochemical cell uses a semisolid electrode. The electrochemical cell has a structure in which a separator is sandwiched between a first structure and a second structure. The first structure has a structure with a first current collector and a first electrode stacked, and the second structure has a structure with a second current collector and a second electrode stacked. The first electrode is one of a positive electrode and a negative electrode, and the second electrode is the other of the positive electrode and the negative electrode.
For such an electrochemical cell, a proposed technique covers the first structure, the second structure, and the separator with a package having a hole for releasing a gas that can be generated in electrodes such as the first electrode and the second electrode (e.g., Patent Document 1).
Patent Document 1: WO 2019/087956 pamphlet
A method for manufacturing an electrochemical cell according to one aspect of the disclosure includes: a process A of manufacturing a first structure by stacking a first film, a first current collector, and a first electrode; a process B of manufacturing a second structure by stacking a second film, a second current collector, and a second electrode; a process C of disposing a separator between the first structure and the second structure; a process D of manufacturing a unit cell by sealing an outer periphery of the first film and an outer periphery of the second film; and a process E of charging the unit cell while pressurizing the unit cell in a stacking direction of the first structure, the separator, and the second structure.
Embodiments will be described below with reference to the accompanying drawings. Note that in the following description of the drawings, the same or similar components will be denoted by the same or similar reference signs. However, the drawings are schematic.
Hereinafter, a unit cell according to an embodiment will be described with reference to
As illustrated in
The positive electrode structure 110 includes a positive electrode film 111, a positive electrode current collector 112, and a positive electrode 113. The positive electrode structure 110 is a stack body of the positive electrode film 111, the positive electrode current collector 112, and the positive electrode 113. In the embodiment, the positive electrode structure 110 is an example of a first structure.
The positive electrode film 111 is made of a material having insulating properties and air impermeability. In the embodiment, the positive electrode film 111 is an example of a first film. The positive electrode film 111 has a sheet shape. The positive electrode film 111 may have a multilayer structure made of two or more layers (e.g., three layers). For example, the positive electrode film 111 may include an outer layer exposed to the outside of the unit cell 100, an inner layer exposed to the inside of the unit cell 100, and an intermediate layer disposed between the outer layer and the inner layer.
The outer layer may be made of an insulating material. For example, the insulating material constituting the outer layer can use a polymer film made of at least one or more materials selected from the group consisting of polyethylene terephthalate (PET), polybutylene terephthalate (PBT), nylon, high purity polyethylene (HDPE), oriented polypropylene (o-PP), polyvinyl chloride (PVC), polyimide (PI), and polysulfone (PSU). The outer layer may be coated with flame-retardant PET.
The intermediate layer may be made of a metal material. The metal material constituting the intermediate layer can use a layer (a foil, a substrate, a film, or the like) made of one or more materials selected from the group consisting of aluminum (Al), copper (Cu), and stainless steel (SUS).
The inner layer may be made of an insulating material. The insulating material constituting the inner layer can use a polymer film made of one or more materials selected from the group consisting of cast polypropylene (c-PP), polyethylene (PE), ethylene vinyl acetate (EVA), polyethylene terephthalate (PET), polyvinyl acetate (PVA), polyamide (PA), tacky acrylic, an ultraviolet (UV) curable resin, an electron beam (EB) curable resin, and an infrared (IR) curable resin.
The inner layer may be made of a flame-retardant material. The flame-retardant material constituting the inner layer can use one or more materials selected from the group consisting of polyether ether ketone (PEEK), polyethylene naphthalene (PEN), polyether sulfone (PES), polyimide (PI), polyethylene sulfide (PPS), and polyethylene oxide (PPO).
The case where the positive electrode film 111 has a three-layer structure has been described here, but the embodiment is not limited to this. The positive electrode film 111 may have a two-layer structure or a single-layer structure. The positive electrode film 111 may contain a combustion inhibiting substance.
The positive electrode current collector 112 has a function of transferring electrons to and from the positive electrode 113. In the embodiment, the positive electrode current collector 112 is an example of a first current collector. The positive electrode current collector 112 is disposed between the positive electrode film 111 and the positive electrode 113. The positive electrode current collector 112 may have a sheet shape or may have a mesh shape. The thickness of the positive electrode current collector 112 may be 1 to 40 μm.
The positive electrode current collector 112 is made of a metal material. The metal material constituting the positive electrode current collector 112 can use one or more materials selected from the group consisting of stainless steel, nickel, a nickel-chromium alloy, aluminum, titanium, copper, lead, a lead alloy, a heat-resistant metal, and a noble metal. The positive electrode current collector 112 may be coated with a conductive material. The conductive material can use one or more materials selected from the group consisting of a metal, a metal oxide, and carbon. The metal can use one or more materials selected from the group consisting of platinum (Pt), gold (Au), and nickel (Ni). The metal oxide can use vanadium oxide.
In the embodiment, the positive electrode current collector 112 may include a positive electrode terminal 112A. The positive electrode terminal 112A may extend outward the positive electrode film 111 in a plan view. The positive electrode terminal 112A may extend outward the positive electrode film 111 at the lateral side 101A. The positive electrode terminal 112A may be formed integrally with the positive electrode current collector 112. The positive electrode 113 may be stacked on at least part of the positive electrode terminal 112A. In an aspect in which two or more of the unit cells 100 are stacked (the stack cell 200 described later), the positive electrode terminal 112A is electrically connected to the positive electrode terminal 112A of another unit cell 100 (parallel connection).
The positive electrode 113 is electrically connected to the positive electrode current collector 112. In the embodiment, the positive electrode is an example of a first electrode. The positive electrode 113 receives electrons from the positive electrode current collector 112 in the discharge operation and emits electrons to the positive electrode current collector 112 in the charge operation. The positive electrode 113 is an electrochemically active semisolid. In other words, the positive electrode 113 is a mixture of a positive electrode active material and an electrolytic solution. The positive electrode 113 may be a mixture of a liquid phase and a solid phase such as a clay-like slurry, a particulate suspension, a colloidal suspension, an emulsion, a gel, or a micelle. The positive electrode 113 is disposed between the positive electrode current collector 112 and the separator 130. The positive electrode 113 has a layer shape. The thickness of the positive electrode may be 250 to 2000 μm.
The positive electrode 113 may contain, as a positive electrode active material, a nickel-cobalt-aluminum-based lithium composite oxide (NCA), a spinel-based lithium manganese oxide (LMO), a lithium iron phosphate (LFP), a lithium cobalt oxide (LCO), a nickel-cobalt-manganese-based lithium composite oxide (NCM), or the like. The positive electrode 113 may contain, as a positive electrode active material, a solid-state compound known to those skilled in the art, for example, used in a nickel-hydrogen battery, a nickel-cadmium battery, or the like. The positive electrode 113 may contain, as a positive electrode active material, LiCoO2 or LiNiO2 doped with Mg, for example.
The negative electrode structure 120 includes a negative electrode film 121, a negative electrode current collector 122, and a negative electrode 123. The negative electrode structure 120 is a stack body of the negative electrode film 121, the negative electrode current collector 122, and the negative electrode 123. In the embodiment, the negative electrode structure 120 is an example of a second structure.
The negative electrode film 121 is made of a material having insulating properties and air impermeability. In the embodiment, the negative electrode film 121 is an example of a second film. The negative electrode film 121 has a sheet shape. The negative electrode film 121 may have a multilayer structure made of two or more layers (e.g., three layers). The configuration of the negative electrode film 121 may be same as, and/or similar to, that of the positive electrode film 111, and the details of the negative electrode film 121 are omitted.
The negative electrode current collector 122 has a function of transferring electrons to and from the negative electrode 123. In the embodiment, the negative electrode current collector 122 is an example of a second current collector. The negative electrode current collector 122 is disposed between the negative electrode film 121 and the negative electrode 123. The negative electrode current collector 122 may have a sheet shape or may have a mesh shape. The thickness of the negative electrode current collector 122 may be 1 to 20 μm.
The negative electrode current collector 122 is made of a metal material. The metal material constituting the negative electrode current collector 122 can use one or more materials selected from the group consisting of stainless steel, nickel, a nickel-chromium alloy, titanium, lead oxide, and a noble metal. The negative electrode current collector 122 may be coated with a conductive material.
In the embodiment, the negative electrode current collector 122 may include a negative electrode terminal 122A. The negative electrode terminal 122A may extend outward the negative electrode film 121 in a plan view. The negative electrode terminal 122A may extend outward the negative electrode film 121 at the lateral side 101A. The negative electrode terminal 122A may be formed integrally with the negative electrode current collector 122. The negative electrode 123 may be stacked on at least part of the negative electrode terminal 122A. In an aspect in which the two or more unit cells 100 are stacked (the stack cell 200 described later), the negative electrode terminal 122A is electrically connected to the negative electrode terminal 122A of another unit cell 100 (parallel connection).
The negative electrode 123 is electrically connected to the negative electrode current collector 122. In the embodiment, the negative electrode 123 is an example of a second electrode. The negative electrode 123 emits electrons from the negative electrode current collector 122 in the discharge operation and receives electrons from the negative electrode current collector 122 in the charge operation. The negative electrode 123 is an electrochemically active semisolid. In other words, the negative electrode 123 is a mixture of a negative electrode active material and an electrolytic solution. The negative electrode 123 may be a mixture of a liquid phase and a solid phase such as a clay-like slurry, a particulate suspension, a colloidal suspension, an emulsion, a gel, or a micelle. The negative electrode 123 is disposed between the negative electrode current collector 122 and the separator 130.
The negative electrode 123 has a layer shape. The thickness of the negative electrode may be 250 to 2000 μm.
The negative electrode 123 may contain, as a negative electrode active material, a carbon-based material such as graphite, hard carbon, soft carbon, a carbon nanotube, graphene, or the like. The negative electrode 123 may contain, for example, a titanium-based oxide such as lithium titanate or titanium dioxide. The negative electrode 123 may contain, for example, a transition metal compound containing iron, cobalt, copper, manganese, nickel, or the like.
The positive electrode 113 and the negative electrode 123 may contain an electrolytic solution. The electrolytic solution may be a carbonate-based solvent. The carbonate-based solvent may be γ-butyrolactone, ethylene carbonate, or both γ-butyrolactone and ethylene carbonate. The carbonate-based solvent may contain another solvent as long as it contains at least one of γ-butyrolactone and ethylene carbonate. Examples of other solvents include propylene carbonate, dimethyl carbonate, dimethoxyethane, diethyl carbonate, tetrahydrofuran, and triethylene glycol dimethyl ether. When γ-butyrolactone and ethylene carbonate are used in combination with other solvents, the carbonate-based solvent may have a vapor pressure of less than 0.1 kPa at 25° C.
The positive electrode 113 and the negative electrode 123 may contain an additive. The additive may contain, for example, at least one of maleic anhydride, lithium bis (oxalate) borate, or biphenyl.
The separator 130 is disposed between the positive electrode structure 110 and the negative electrode structure 120. The unit cell 100 has a function of reducing a short circuit between the positive electrode structure 110 and the negative electrode structure 120. The separator 130 may be made of an insulator. The separator 130 may be made of a polymer having ductility and elasticity. For example, the separator 130 may be made of one or more materials selected from the group consisting of polyolefin, polyvinyl chloride, nylon, fluorocarbon, and polystyrene.
The positive electrode film 111 and the negative electrode film 121 are respectively sealed outside the positive electrode 113 and the negative electrode 123 in a plan view, and the positive electrode 113 and the negative electrode 123 are accommodated in respective packages made of the positive electrode film 111 and the negative electrode film 121.
Under such a premise, the package made of the positive electrode film 111 and the negative electrode film 121 has an opening 105A and an opening 105B. For example, the opening 105A may be an opening communicating with the inside and the outside of the package on the positive electrode 113 side from the separator 130. The opening 105B may be an opening communicating with the inside and the outside of the package on the negative electrode 123 side from the separator 130.
The opening 105A may be formed in the lateral side 101B provided on the opposite side of the lateral side 101A. The opening 105A may be formed at a corner formed by the lateral side 101A and the longitudinal side 102B. That is, the opening 105A may be formed at a diagonal position of the unit cell 100 with respect to the positive electrode terminal 112A. The size of the opening 105A may be 0.1 to 10 mm in the lateral direction of the unit cell 100 or may be 10 to 30 mm in the longitudinal direction of the unit cell 100.
The opening 105B may be formed in the lateral side 101B provided on the opposite side of the lateral side 101A. The opening 105B may be formed at a corner formed by the lateral side 101A and the longitudinal side 102A. That is, the opening 105B may be formed at a diagonal position of the unit cell 100 with respect to the negative electrode terminal 122A. The size of the opening 105B may be 0.1 to 10 mm in the lateral direction of the unit cell 100 or may be 10 to 30 mm in the longitudinal direction of the unit cell 100.
The opening 105A and the opening 105B allow a gas generated by a side reaction of charge and discharge to be released from the inside to the outside of the unit cell 100 (the positive electrode structure 110 or the negative electrode structure 120). Therefore, a gas can be less likely to be accumulated between the positive electrode current collector 112 and the positive electrode 113, between the negative electrode current collector 122 and the negative electrode 123, between the positive electrode 113 and the separator 130, or between the negative electrode 123 and the separator 130. As a result, the efficiency of the main reaction of charge and discharge can be less likely to decrease, and the battery capacity can be less likely to decrease.
Hereinafter, a stack cell according to an embodiment will be described.
As illustrated in
The package 150 may be made of two members (a first package member 150A and a second package member 150B) having a sheet shape. The first package member 150A has a tray shape having a first recessed portion 151A and a first flange portion 152A. The unit cells 100 are disposed in the first recessed portion 151A with a gap formed between the inner wall of the first recessed portion 151A formed in the first package member 150A and the unit cells 100. Similarly, the second package member 150B has a tray shape having a second recessed portion 151B and a second flange portion 152B. The unit cells 100 are disposed in the second recessed portion 151B with a gap formed between the inner wall of the second recessed portion 151B formed in the second package member 150B and the unit cells 100. The first flange portion 152A is formed over the entire outer periphery of the first recessed portion 151A, and the second flange portion 152B is formed over the entire outer periphery of the second recessed portion 151B. Therefore, sealing the first flange portion 152A and the second flange portion 152B allows the package 150 made of the first package member 150A and the second package member 150B to accommodate the stack body of the unit cells 100.
The package 150 may be made of an air impermeable member. The package 150 may be made of a hydrophobic member. For example, the package 150 may be made of a metal material. The metal material can use one or more materials selected from the group consisting of stainless steel, aluminum, and copper.
The positive electrode terminal 112A of the unit cell 100 is electrically connected to the positive electrode terminal 112A of another unit cell 100 (parallel connection). Similarly, the negative electrode terminal 122A of unit cell 100 is electrically connected to the negative electrode terminal 122A of another unit cell 100 (parallel connection). Finally, as the stack cell 200, a pair of extraction terminals 210 is exposed to the outside of the package 150. The pair of extraction terminals 210 may be made of the positive electrode terminal 112A and the negative electrode terminal 122A of at least one unit cell 100 included in the stack cell 200 or may be made of a member different from the positive electrode terminal 112A and the negative electrode terminal 122A of the unit cells 100.
From distinction from the package 150, the package made of the positive electrode film 111 and the negative electrode film 121 may be referred to as a first package. For the same purpose, the package 150 may be referred to as a second package.
Hereinafter, the method for manufacturing the unit cell 100 will be described. Hereinafter, the manufacturing method will be described using the B-B cross section illustrated in
First, a method for manufacturing the positive electrode structure 110 will be described with reference to
As illustrated in
Subsequently, the positive electrode 113 is stacked on the positive electrode current collector 112. The positive electrode 113 may be stacked by applying a material constituting the positive electrode 113 to the positive electrode current collector 112. The positive electrode 113 may be stacked extending outward the positive electrode current collector 112 in a plan view.
Second, a method for manufacturing the negative electrode structure 120 will be described with reference to
As illustrated in
Subsequently, the negative electrode 123 is stacked on the negative electrode current collector 122. The negative electrode 123 may be stacked by applying a material constituting the negative electrode 123 to the negative electrode current collector 122. The negative electrode 123 may be stacked extending outward the negative electrode current collector 122 in a plan view.
Third, an assembly process of the unit cell 100 will be described with reference to
As illustrated in
Subsequently, the outer periphery of the positive electrode film 111 and the outer periphery of the negative electrode film 121 are sealed. The method for sealing may be ultrasonic sealing or thermocompression bonding sealing. In a plan view, the separator 130 is sealed together with the positive electrode film 111 and the negative electrode film 121 on the inside of the outer periphery of the separator 130.
In the sealing, the outer periphery of the positive electrode film 111 and the outer periphery of the negative electrode film 121 are respectively sealed outside the positive electrode 113 and the negative electrode 123 while leaving a positive electrode non-sealing region in at least part of the positive electrode film 111.
Specifically, as illustrated in
Similarly, in the sealing, the outer periphery of the positive electrode film 111 and the outer periphery of the negative electrode film 121 are respectively sealed outside the positive electrode 113 and the negative electrode 123 while leaving a negative electrode non-sealing region in at least part of the negative electrode film 121.
Specifically, as illustrated in
Hereinafter, the method for manufacturing the stack cell 200 will be described. Hereinafter, the manufacturing method will be described using the A-A cross section illustrated in
First, as illustrated in
Second, the stack body of the unit cells 100 is disposed in the package 150. For example, the unit cells 100 are disposed in the first recessed portion 151A with a gap formed between the inner wall of the first recessed portion 151A formed in the first package member 150A and the unit cells 100. The unit cells 100 are disposed in the second recessed portion 151B with a gap formed between the inner wall of the second recessed portion 151B formed in the second package member 150B and the unit cells 100. The first package member 150A in which the unit cells 100 are disposed and the second package member 150B in which the unit cells 100 are disposed are stacked. At this stage, first portions of the first package member 150A (the first flange portion 152A) and the second package member 150B (the second flange portion 152B) need not be sealed, and second portions of the first package member 150A (the first flange portion 152A) and the second package member 150B (the second flange portion 152B) may be sealed. The first portion may be a portion through which the extraction terminal 210 is extracted to the outside of the package 150. The second portion may be a portion other than the first portion.
Third, as illustrated in
Fourth, the first package member 150A and the second package member 150B are entirely sealed. In other words, the first portion described above is sealed. The first portion may be a portion through which the extraction terminal 210 is extracted to the outside of the package 150.
Hereinafter, a summary of the manufacturing method according to an embodiment will be described.
As illustrated in
In step S12, the negative electrode structure 120 is manufactured by stacking the negative electrode film 121, the negative electrode current collector 122, and the negative electrode 123 (see
In step S13, the separator 130 is disposed between the positive electrode structure 110 and the negative electrode structure 120 (see
In step S14, the unit cell 100 is manufactured by sealing the outer periphery of the positive electrode film 111 and the outer periphery of the negative electrode film 121 (see
Steps S11 to S14 are the processes of manufacturing the unit cell 100. In
In step S21, the two or more unit cells 100 are stacked, and the stack body of the unit cells 100 is disposed in the package 150 (see
In step S22, the second portions of the first package member 150A and the second package member 150B are sealed (see
In step S23, the two or more unit cells 100 are charged while the two or more unit cells 100 are pressurized in the stacking direction of the two or more unit cells 100 (see FIG. 11). Step S23 (precharge) may be performed under a reduced-pressure atmosphere. The reduced-pressure atmosphere may include a vacuum atmosphere.
In step S24, the stack cell 200 is manufactured by sealing the first portions of the first package member 150A and the second package member 150B (see
That is, the precharge (step S23) is performed after the unit cells 100 are disposed in the package 150 and before the package 150 is completely sealed.
Steps S21 to S24 are the processes of manufacturing the stack cell 200. In
In the embodiment, the unit cell 100 may be manufactured by sealing the outer periphery of the positive electrode film 111 and the outer periphery of the negative electrode film 123 outside the positive electrode 113 and the negative electrode 111, respectively, while leaving the positive electrode non-sealing region (e.g., the positive electrode cutout region 111B) in at least part of the outer periphery of the positive electrode film 121. Such a configuration allows the positive electrode non-sealing region (the opening 105A) to be formed as a part of the process of sealing the positive electrode film 111 and the negative electrode film 121. In particular, the positive electrode cutout region 111B is formed at a position overlapping with the sealing position, allowing the opening 105A to be easily formed. Therefore, the unit cell 100 that can release the gas that can be generated in the positive electrode 113 can be appropriately manufactured.
In the embodiment, the unit cell 100 may be manufactured by sealing the outer periphery of the positive electrode film 111 and the outer periphery of the negative electrode film 123 outside the positive electrode 113 and the negative electrode 121, respectively, while leaving the negative electrode non-sealing region (e.g., the negative electrode cutout region 121B) in at least part of the outer periphery of the negative electrode film 121. Such a configuration allows the negative electrode non-sealing region (the opening 105B) to be formed as a part of the process of sealing the positive electrode film 111 and the negative electrode film 121. In particular, the positive electrode cutout region 111B is formed at a position overlapping with the sealing position, allowing the opening 105A to be easily formed. Therefore, the unit cell 100 that can release the gas that can be generated in the negative electrode 123 can be appropriately manufactured.
In the embodiment, in the process of manufacturing the stack cell 200, a gap may be formed between the inner wall of the package 150 and the unit cells 100. Therefore, the gas that can be generated in the positive electrode 113 or the negative electrode 123 can be accommodated in the gap, allowing the accumulation of the gas at least in the unit cells 100 to be reduced.
In the embodiment, the separator 130 may extend outward the outer periphery of the positive electrode structure 110 and the outer periphery of the negative electrode structure 120 in a plan view, and the separator 130 may be sealed together with the positive electrode film 111 and the negative electrode film 121. Such a configuration allows a short circuit between the positive electrode structure 110 and the negative electrode structure 120 to be appropriately reduced.
In the embodiment, the unit cells 100 may be charged while being pressurized in the stacking direction of the positive electrode structure 110, the separator 130, and the negative electrode structure 120 (precharge). Such a configuration allows the precharge to generate a gas at the positive electrode 113 and the negative electrode 123 in the production stage of the unit cells 100 and the gas generated at the positive electrode 113 and the negative electrode 123 to be released in advance. Therefore, the gas generated in the positive electrode 113 and the negative electrode 123 can be effectively released in advance.
In an embodiment, the precharge may be performed under a reduced-pressure atmosphere. Such a configuration allows the gas generated in the positive electrode 113 and the negative electrode 123 to be efficiently released.
In the embodiment, regarding the unit cell 100, the positive electrode non-sealing region (e.g., the positive electrode cutout region 111B) may be formed. Such a configuration allows the gas generated in the positive electrode 113 to be effectively released in advance. Similarly, regarding the unit cell 100, the negative electrode non-sealing region (e.g., the negative electrode cutout region 121B) may be formed. Such a configuration allows the gas generated in the negative electrode 123 to be effectively released in advance.
In the embodiment, regarding the stack cell 200, precharge may be performed with the two or more unit cells 100 stacked. Such a configuration allows precharge of the two or more unit cells 100 to be simultaneously performed and the precharge to be efficiently performed.
In the embodiment, precharge may be performed before the package 150 is completely sealed. Such a configuration, the gas generated in the positive electrode 113 and the negative electrode 123 to be efficiently released.
Although the present invention is described by the above-described disclosure, it should not be understood that the description and the drawings, which form a part of this disclosure, limit this invention. Various alternative embodiments, examples, and operational techniques will be apparent from this disclosure to those skilled in the art.
In the disclosure described above, the case where the positive electrode structure 110 is the first structure has been exemplified. However, the disclosure described above is not limited to this example. The positive electrode structure 110 may be the second structure. In such a case, the “positive electrode” may be read as “second”. Similarly, the case where the negative electrode structure 120 is the second structure has been exemplified. However, the disclosure described above is not limited to this example. The negative electrode structure 120 may be the first structure. In such a case, the “negative electrode” may be read as “first”.
In the disclosure described above, the package 150 covers the stack body of the two or more unit cells 100. However, the disclosure described above is not limited to this example. The package 150 may cover one unit cell 100.
In the disclosure described above, the case where the precharge (step S23 illustrated in
In the above disclosure, the charge of the unit cells 100 is exemplified as the process for releasing the gas in the process of manufacturing the unit cells 100. However, the disclosure described above is not limited to this example. The above-described process may include discharge of the unit cells 100 in addition to charge of the unit cells 100.
In the disclosure described above, the case where the package 150 is made of the first package member 150A and the second package member 150B has been exemplified. However, the disclosure described above is not limited to this example. For example, the package 150 may have a bag shape without the second portion. In such a case, the process of sealing the second portion (S22 illustrated in
The disclosure described above exemplifies the case where the opening 105A and the opening 105B are configured with the unit cell 100 being formed by sealing the positive electrode film 111 having the positive electrode non-sealing region and the negative electrode film 121 having the negative electrode non-sealing region. However, the disclosure described above is not limited to this example. For example, the opening 105A and the opening 105B may be formed after the unit cell 100 is sealed without a non-sealing region. In other words, the opening 105A and the opening 105B may be formed by cutting out part of the unit cell 100 after sealing the positive electrode film 111 not having the positive electrode non-sealing region and the negative electrode film 121 not having the negative electrode non-sealing region. The opening 105A and the opening 105B may be formed by making a hole in the unit cell 100 after sealing the positive electrode film 111 not having the positive electrode non-sealing region and the negative electrode film 121 not having the negative electrode non-sealing region.
This application is national stage application of International Application No. PCT/JP2021/016216, filed on Apr. 21, 2021.
Filing Document | Filing Date | Country | Kind |
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PCT/JP2021/016216 | 4/21/2021 | WO |