Patent Application
20240128463
The present disclosure relates to a laminated resin film, a current collector, and a secondary battery.
Lithium secondary batteries are widely utilized as power sources for laptop computers, mobile phones, electric vehicles, and the like.
As a current collector for lithium secondary batteries, there is a laminated resin film in which a metal layer is formed on the surface of a resin layer.
Patent Document 1 discloses a current collector including: an insulating layer; and a conductive layer, in which the conductive layer is mounted on the insulating layer, an electrode active material layer is mounted on the conductive layer, the conductive layer is positioned on at least one surface of the insulating layer, and a metal protective layer is provided on at least one surface of the conductive layer. Patent Document 1 discloses at least one selected from metal conductive materials and carbon-based conductive materials as a material for the conductive layer.
However, when the laminated resin film in which a metal layer is formed on the surface of a resin layer is used as the current collector for lithium secondary batteries, there is a concern of a degradation of the current collector.
The present disclosure has been made in view of the above-mentioned problems, and an object thereof is to provide a laminated resin film that is less likely to be degraded.
Another object of the present disclosure is to provide a current collector made from the above-mentioned laminated resin film, and a secondary battery which has this current collector and is lightweight and excellent in safety.
In order to achieve the above-mentioned objects, a Cu film as a metal layer was formed on the surface of a resin layer, and intensive studies were conducted with a focus on its orientation.
As a result, it was found that it is sufficient for a Cu film to be formed on the surface of the resin layer, provided that in the Cu film, peak intensities of a (200) plane and a (220) plane are within a specific range when a peak intensity of a (111) plane in X-ray diffraction measurement is set to 100.
In other words, the present disclosure relates to the following.
[1] A laminated resin film including: a resin layer; and a Cu film provided on one surface or both surfaces of the resin layer,
y≥2.5×−7.5 Expression (1)
[2] The laminated resin film according to [1], in which the peak intensity x of the (220) plane is 5 or less.
[3] The laminated resin film according to [1] or [2], in which an underlayer is provided between the resin layer and the Cu film so as to be in contact with the resin layer and the Cu film.
[4] A current collector including the laminated resin film according to any one of [1] to [3].
[5] A secondary battery including: a negative electrode; a positive electrode facing the negative electrode; and a separator positioned between the negative electrode and the positive electrode,
A laminated resin film of the present disclosure includes: a resin layer; and a Cu film provided on one surface or both surfaces of the resin layer, in which in the Cu film, a peak intensity y of a (200) plane is 2 to 30 when a peak intensity of a (111) plane in X-ray diffraction measurement is set to 100, and Expression (1) is satisfied. Therefore, the laminated resin film of the present disclosure is less likely to be degraded.
A current collector of the present disclosure is made from the laminated resin film of the present disclosure. Therefore, the current collector of the present disclosure is less likely to be degraded.
In addition, in a secondary battery of the present disclosure, any one or both of a negative electrode and a positive electrode have the current collector of the present disclosure. Accordingly, the secondary battery of the present disclosure is lightweight and excellent in safety.
Hereinafter, the present embodiment will be described in detail with appropriate reference to the drawings. In the drawings used in the following description, characteristic portions may be shown by enlarging them for convenience to facilitate understanding characteristics of the present disclosure, and the dimensional ratios and the like of each of constituent elements may be different from those of actual constituent elements. Materials, dimensions, and the like exemplified in the following description are merely examples, and the present disclosure is not limited thereto and can be implemented with appropriate changes within a range not departing from the scope thereof.
[Lithium Secondary Battery]
(Power Generating Part)
In the power generating part 40, a positive electrode 20 and a negative electrode 30 are disposed to face each other with a separator 10 interposed therebetween.
<Positive Electrode>
The positive electrode 20 has a positive electrode current collector 22 and a positive electrode active material layer 24.
(Positive Electrode Active Material Layer)
The positive electrode active material layer 24 contains a positive electrode active material, a positive electrode binder, and a positive electrode conductive assistant.
(Positive Electrode Active Material)
As the positive electrode active material, an electrode active material is used, the electrode active material being capable of absorbing and desorbing lithium ions, deintercalating and intercalating (intercalation) lithium ions, or reversibly advancing doping and dedoping of lithium ions and lithium ion counter anions (for example, PF6−).
Examples of the positive electrode active material include lithium cobaltate (LiCoO2), lithium nickelate (LiNiO2), lithium manganese spinel (LiMn2O4), a composite metal oxide represented by General Formula: LiNixCoyMnzMaO2 (where x+y+z+a=1, 0≤x≤1, 0≤y≤1, 0≤z≤1, 0≤a ≤1, and M is one or more elements selected from Al, Mg, Nb, Ti, Cu, Zn, and Cr), a lithium vanadium compound (LiV2O5), olivine-type LiMPO4 (where M indicates one or more elements selected from Co, Ni, Mn, Fe, Mg, Nb, Ti, Al, and Zr, or VO), lithium titanate (Li4Ti5O12), and a composite metal oxide represented by LiNixCoyAlzO2 (0.9<x+y+z<1.1).
(Positive Electrode Binder)
The positive electrode binder binds the positive electrode active materials to each other and also binds the positive electrode active material to the positive electrode current collector 22.
As the positive electrode binder, it is possible to use polyvinylidene fluoride (PVDF), polyethersulfone (PESU), polytetrafluoroethylene (PTFE), a tetrafluoroethylene-hexafluoropropylene copolymer (FEP), a tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer (PFA), an ethylene-tetrafluoroethylene copolymer (ETFE), polychlorotrifluoroethylene (PCTFE), an ethylene-chlorotrifluoroethylene copolymer (ECTFE), polyvinyl fluoride (PVF), and the like, for example.
As the positive electrode binder, the following may also be used: vinylidene fluoride fluororubbers such as vinylidene fluoride-hexafluoropropylene fluororubber (VDF-HFP fluororubber), vinylidene fluoride-hexafluoropropylene-tetrafluoroethylene fluororubber (VDF-HFPTFE fluororubber), vinylidene fluoride-pentafluoropropylene fluororubber (VDF-PFP fluororubber), vinylidene fluoride-pentafluoropropylene-tetrafluoroethylene fluororubber (VDF-PFP-TFE fluororubber), vinylidene fluoride-perfluoromethyl vinyl ether-tetrafluoroethylene fluororubber (VDF-PFMVE-TFE fluororubber), and vinylidene fluoride-chlorotrifluoroethylene fluororubber (VDF-CTFE fluororubber).
As the positive electrode binder, a conductive polymer having electron conductivity and/or a conductive polymer having ion conductivity may be used. Examples of the conductive polymer having electron conductivity include polyacetylene. In this case, the positive electrode binder also exhibits a function as a positive electrode conductive assistant. Therefore, the positive electrode active material layer 24 may not contain the positive electrode conductive assistant. Examples of the conductive polymer having ion conductivity include those obtained by combining polymer compounds such as polyethylene oxide and polypropylene oxide with lithium salts or alkali metal salts mainly composed of lithium.
(Positive Electrode Conductive Assistant)
The positive electrode conductive assistant improves the conductivity of the positive electrode active material layer 24. A well-known conductive assistant can be used as the positive electrode conductive assistant. Examples of the positive electrode conductive assistant include carbon materials such as graphite and carbon black; fine powders of metals such as copper, nickel, stainless steel, and iron; and conductive oxides such as indium tin oxide (ITO).
(Positive Electrode Current Collector)
As the positive electrode current collector 22, it is possible to use a metal foil or metal thin plate made of metals such as aluminum, copper, and nickel, for example. The positive electrode current collector 22 may be a laminated resin film having a resin layer (not shown) and having a metal layer made of metals such as aluminum, copper, and nickel on one surface or both surfaces of the resin layer.
<Negative Electrode>
The negative electrode 30 has a negative electrode current collector 32 and a negative electrode active material layer 34.
(Negative Electrode Active Material Layer)
The negative electrode active material layer 34 contains a negative electrode active material and, if necessary, further contains a negative electrode binder and/or a negative electrode conductive assistant.
(Negative Electrode Active Material)
The negative electrode active material is a compound capable of absorbing and desorbing lithium ions, and known negative electrode active materials for lithium secondary batteries can be used. As the negative electrode active material, it is possible to use metallic lithium, carbon materials such as graphite (natural graphite, artificial graphite), carbon nanotubes, low graphitizability carbons, high graphitizability carbons, and low-temperature fired carbons; metals that can combine with lithium such as aluminum, silicon, and tin; amorphous compounds mainly including oxides such as SiOx (0<x<2) and tin dioxide; particles including lithium titanate (Li4TisO12) and the like; and the like, for example.
(Negative Electrode Binder)
As the negative electrode binder, the same binders as those usable as the positive electrode binder can be used. As the negative electrode binder, in addition to those that can be used as the positive electrode binder, for example, one or two or more selected from cellulose, carboxymethyl cellulose, styrene-butadiene rubber, ethylene-propylene rubber, a polyimide resin, a polyamide-imide resin, and an acrylic resin may also be used.
(Negative Electrode Conductive Assistant)
As the negative electrode conductive assistant, it is possible to use carbon materials such as carbon powders such as carbon black, and carbon nanotubes; fine powders of metals such as copper, nickel, stainless steel, and iron; mixtures of carbon materials and fine powders of metals; conductive oxides such as ITO; and the like, for example.
(Negative Electrode Current Collector)
In the lithium secondary battery 100 of the present embodiment, the negative electrode current collector 32 is made from a laminated resin film 3 shown in
By using the laminated resin film 3 shown in
In the laminated resin film 3 shown in
As shown in
When a plurality of the power generating parts 40 are laminated and accommodated in the exterior body 50, as the negative electrode current collector 32, it is preferable to use the laminated resin film 3 in which the Cu films 3b are provided on both surfaces of the resin layer 3a. In this case, by providing the negative electrode active material layers 34 on both surfaces of the laminated resin film 3, one laminated resin film 3 can serve as the negative electrode current collector 32 of two negative electrodes 30.
Examples of the resin layer 3a forming the laminated resin films 3 and 33 include film-like ones made of polyethylene terephthalate (PET), polyethylene (PE), polypropylene (PP), polyamide, polyimide, polystyrene, polyvinyl chloride, an acrylonitrile-butadiene-styrene copolymer, polybutylene terephthalate, poly-p-phenylene terephthalamide, polypropylene ethylene, polyformaldehyde, an epoxy resin, a phenolic resin, polytetrafluoroethylene, polyvinylidene fluoride, silicone rubber, polycarbonate, and the like. Among these, it is preferable to use a film made of PET because it has excellent chemical resistance, stretchability, and tensile strength.
The thickness of the resin layer 3a forming the laminated resin films 3 and 33 can be appropriately determined according to the usage of the lithium secondary battery 100. The thickness of the resin layer 3a is preferably 3 μm to 12 μm, and is more preferably 3 μm to 6 μm, for example. When the thickness of the resin layer 3a is 3 μm or more, deformation of the laminated resin films 3 and 33 can be inhibited, and fracture of the Cu film 3b and peeling of the Cu film 3b from the resin layer 3a can further be prevented. In addition, when the thickness of the resin layer 3a is 12 μm or less, this is preferable because then the laminated resin films 3 and 33 do not hinder the miniaturization of the lithium secondary battery 100.
In the Cu film 3b forming the laminated resin films 3 and 33, a peak intensity y of the (200) plane is 2 to 30 when a peak intensity of the (111) plane in X-ray diffraction measurement is set to 100, and Expression (1) is satisfied. Therefore, the laminated resin films 3 and 33 are less likely to be degraded for the following reason.
y≥2.5×−7.5 Expression (1)
As a result of intensive studies by the inventors of the present invention, it was found that the main cause of the degradation of the laminated resin films 3 and 33 is that the Cu film 3b is eroded and degraded due to the decomposition products generated by the decomposition of an electrolyte by charging and discharging. In particular, the degradation of the Cu film is accelerated due to HF generated by the decomposition of an electrolyte such as LiPF6 as the lithium secondary battery 100 is repeatedly charged and discharged in a high-temperature environment. Specific examples of the degradation of the Cu film by the decomposition products include cracks and fractures of the Cu film, peeling of the Cu film from the resin layer 3a, and dissolution and loss of the Cu film.
The Cu film 3b in which the above-mentioned peak intensity y of the (200) plane satisfies Expression (1) has favorable adhesiveness to the resin layer 3a. Therefore, the decomposition products generated by the decomposition of an electrolyte are less likely to enter between the Cu film 3b and the resin layer 3a, and the Cu film 3b is less likely to be peeled off from the resin layer 3a. In addition, the Cu film 3b in which the above-mentioned peak intensity y of the (200) plane is 2 or more has excellent ductility. Cracks are less likely to be generated in the Cu film 3b having excellent ductility. Furthermore, the Cu film 3b in which the peak intensity y of the (200) plane is 30 or less is less likely to be eroded even when it comes into contact with the decomposition products generated by decomposition of an electrolyte. These synergistic effects inhibit the degradation of the Cu film 3b from advancing in the laminated resin films 3 and 33. Therefore, the laminated resin films 3 and 33 are less likely to be degraded.
The peak intensity y of the (200) plane is preferably 2.5 or more when the peak intensity of the (111) plane in X-ray diffraction measurement is set to 100 because then cracks are less likely to be generated in the Cu film 3b.
The peak intensity y of the (200) plane is preferably 15 or less when the peak intensity of the (111) plane in X-ray diffraction measurement is set to 100 because then the Cu film 3b is further less likely to be eroded.
In the Cu film 3b, the peak intensity x of the (220) plane is preferably 5 or less, and is more preferably 2 or less when the peak intensity of the (111) plane in X-ray diffraction measurement is set to 100. The Cu film 3b in which the above-mentioned peak intensity x of the (220) plane is 5 or less has much better adhesiveness to the resin layer 3a. Therefore, the Cu film 3b is further less likely to be peeled off from the resin layer 3a.
The thickness of the Cu film 3b in the laminated resin films 3 and 33 of the present embodiment is preferably 0.3 μm to 2.0 μm, and is more preferably 0.5 μm to 1.0 μm. When the thickness of the Cu film 3b is 0.3 μm or more, the laminated resin films 3 and 33 having even lower electric resistance are obtained. In addition, when the thickness of the Cu film 3b is 0.5 μm or more, fracture of the Cu film 3b and peeling of the Cu film 3b from the resin layer 3a can further be prevented. Furthermore, when the thickness of the Cu film 3b is 2.0 μm or less, by using the laminated resin films 3 and 33 as the negative electrode current collector 32, the weight of the lithium secondary battery 100 can be further reduced.
“Method for Manufacturing Laminated Resin Film”
Next, a method for manufacturing the laminated resin films 3 and 33 will be described with reference to an example.
First, the resin layer 3a having a predetermined thickness is formed by a known method using a predetermined resin. A commercially available resin film may be used as the resin layer 3a.
Next, the Cu film 3b is formed on one surface or both surfaces of the resin layer 3a so as to be in contact with the resin layer 3a. The peak intensities of the (200) plane and the (220) plane when the peak intensity of the (111) plane in X-ray diffraction measurement of the Cu film 3b is set to 100 can be controlled by a method for forming the Cu film 3b.
In the present embodiment, the Cu film 3b is preferably formed by performing, in the following order, the following steps: a step of forming a Cu seed layer on one surface or both surfaces of the resin layer 3a; and a step of forming a Cu plated layer on the Cu seed layer by an electrolytic plating method.
Examples of the step of forming the Cu seed layer include a method in which a Cu seed layer made from a Cu film is formed on one surface or both surfaces of the resin layer 3a by film formation methods such as an electroless plating method, a sputtering method, a vapor deposition method, and a chemical vapor deposition method (CVD method). Among the above-mentioned film formation methods, it is preferable to form the Cu seed layer by using any method selected from the electroless plating method, the sputtering method, and the vapor deposition method, and it is particularly preferable to use the sputtering method. This is because, by forming the Cu plated layer on the Cu seed layer, this makes it possible to obtain a Cu seed layer that facilitates the formation of the Cu film 3b in which the peak intensities of the (200) plane and the (220) plane satisfy a specific condition when the peak intensity of the (111) plane in X-ray diffraction measurement is set to 100.
When the sputtering method is used in the step of forming the Cu seed layer, it is preferable to form the Cu seed layer in an atmosphere containing argon. The atmosphere containing argon may be an atmosphere consisting only of argon gas, or may be an atmosphere of a mixed gas of argon gas and hydrogen gas, but is preferably the atmosphere consisting only of argon gas. This is because it is possible to obtain a Cu seed layer that facilitates the formation of the Cu film 3b in which the peak intensities of the (200) plane and the (220) plane satisfy a specific condition when the peak intensity of the (111) plane in X-ray diffraction measurement is set to 100.
In the step of forming the Cu seed layer, it is preferable to form a Cu seed layer made from a Cu film having a thickness of 10 to 300 nm. When the thickness of the Cu seed layer is 300 nm or less, this is preferable because, by performing the step of forming the Cu plated layer, this further facilitates obtaining of the Cu film 3b in which the peak intensities of the (200) plane and the (220) plane satisfy a specific condition when the peak intensity of the (111) plane in X-ray diffraction measurement is set to 100. When the thickness of the Cu seed layer is 10 nm or more, this is preferable because, in the step of forming the Cu plated layer, holes (pinholes) reaching the resin layer 3a can be inhibited from being generated when the Cu seed layer is dissolved in a plating liquid. By performing the step of forming the Cu plated layer, the Cu seed layer is integrated with the Cu plated layer to become a part of the Cu film.
Examples of the step of forming the Cu plated layer include a method in which the Cu film 3b having a thickness of 0.3 μm to 2.0 μm, for example, is formed on the Cu seed layer formed on one surface or both surfaces of the resin layer 3a by the electrolytic plating method. In the electrolytic plating method, a plating liquid having a known composition can be used. Plating conditions such as a plating temperature and a plating time in the electrolytic plating method can be appropriately determined according to the thickness of the Cu film 3b of the laminated resin films 3 and 33, and the like.
The current density in the electrolytic plating method can be 2.5 to 4.8 A/dm2, for example. By changing the current density in the electrolytic plating method, it is possible to control the peak intensity of the (200) plane when the peak intensity of the (111) plane in X-ray diffraction measurement of the Cu film 3b is set to 100. Specifically, when the current density is low, the Cu film 3b in which the above-mentioned peak intensity of the (200) plane is strong is obtained, and when the current density is high, the Cu film 3b in which the above-mentioned peak intensity of the (200) plane is weak is obtained.
A method for forming the Cu film 3b on one surface or both surfaces of the resin layer 3a is not limited to the method of performing the step of forming the Cu seed layer and the step of forming the Cu plated layer by the electrolytic plating method. For example, the Cu film 3b may be formed on one surface or both surfaces of the resin layer 3a by using only one film formation method selected from the electroless plating method, the sputtering method, the vapor deposition method, and the chemical vapor deposition method (CVD method). In this case, the resin layer 3a can be efficiently formed with fewer manufacturing steps as compared to the case in which the step of forming the Cu seed layer and the step of forming the Cu plated layer are performed.
When the Cu films 3b are formed on both surfaces of the resin layer 3a, the Cu films 3b may be formed on both surfaces of the resin layer 3a at the same time, or, alternatively, the Cu film 3b may be formed on one surface, and thereafter the Cu film 3b may be formed on the opposite surface. When the Cu films 3b are formed on both surfaces of the resin layer 3a, it is preferable to form the Cu films 3b on both surfaces of the resin layer 3a at the same time because then the laminated resin film 3 can be manufactured efficiently.
In the lithium secondary battery 100 of the present embodiment, instead of the laminated resin film 3, as shown in
As shown in
The underlayer 3c is preferably a metal layer containing at least one element selected from the group consisting of Cr, Ti, and Ni. When the laminated resin film 35 is used as the negative electrode current collector 32, the underlayer 3c may be a metal layer containing at least one element selected from the group consisting of Cr, Ti, Ni, Ta, Zn, Nb, and Cu, but is preferably a metal layer containing Ni, and is more preferably a metal layer consisting of an alloy of Ni and Cr because then the erosion resistance against HF is improved.
The laminated resin film 35 shown in
<Separator>
As the separator 10, a known separator such as one having electrical insulation and consisting of a porous structure can be used. Specific examples thereof include a single layer body or a laminated body of films made of polyolefin resins such as polyethylene and polypropylene; a stretched film of a mixture made of a plurality of types of polyolefin resins; and a fibrous nonwoven fabric made of at least one constituent material selected from the group consisting of cellulose, polyester, and polypropylene.
(Electrolyte Solution)
The power generating part 40 is impregnated with the electrolyte solution. As the electrolyte solution, an electrolytic solution or a non-aqueous electrolytic solution can be used. When the non-aqueous electrolytic solution is used as the electrolyte solution, this is preferable because then a tolerable voltage during charging can be increased as compared to the case of using the aqueous electrolytic solution.
The non-aqueous electrolytic solution is obtained by dissolving an electrolyte in a non-aqueous solvent. As the non-aqueous solvent, cyclic carbonates and chain carbonates can be used, for example.
As the cyclic carbonate, one that can solvate the electrolyte is used. Examples of the cyclic carbonates include ethylene carbonate, propylene carbonate, and butylene carbonate.
As the chain carbonate, one that lowers the viscosity of the cyclic carbonate is used. Examples of the chain carbonates include diethyl carbonate, dimethyl carbonate, and ethyl methyl carbonate.
As the non-aqueous solvent, methyl acetate, ethyl acetate, methyl propionate, ethyl propionate, γ-butyrolactone, 1,2-dimethoxyethane, 1,2-diethoxyethane, and the like may also be used in addition to the cyclic carbonates and the chain carbonates.
Examples of electrolytes contained in the non-aqueous electrolytic solution include lithium salts such as LiPF6, LiClO4, LiBF4, LiCF3SO3, LiCF3CF2SO3, LiC(CF3SO2)3, LiN(CF3SO2)2, LiN(CF3CF2SO2)2, LiN(CF3SO2)(C4F9SO2), LiN(CF3CF2CO)2, and LiBOB. For these lithium salts, one type may be used alone, or two or more types may be used in combination. From the viewpoint of a degree of ionization, the electrolyte preferably includes LiPF6.
As the non-aqueous electrolytic solution, an ionic liquid may be used, for example. The ionic liquid is a salt (room temperature molten salt) in the liquid state even at a low temperature of, for example, lower than 100° C., and is a combination of cations and anions. The ionic liquid has a strong electrostatic interaction and is nonvolatile and nonflammable. Therefore, the lithium secondary battery 100 using the ionic liquid as the non-aqueous electrolytic solution is excellent in safety.
As a cation component and an anion component of the ionic liquid, known ones can be used.
(Lead)
The leads 60 and 62 are formed of a conductive material such as aluminum. As shown in
(Exterior Body)
The exterior body 50 seals the power generating part 40 and the electrolyte solution inside. The exterior body 50 is not particularly limited as long as it can restrain the leakage of the electrolyte solution to an external device and the invasion of water or the like from an external device into the inside.
As the exterior body 50, it is possible to use one made from a metal laminate film in which both surfaces of a metal foil 52 are coated with a polymer film 54, for example, as shown in
As the metal foil 52, an aluminum foil can be used, for example. As the polymer film 54 on the outer side, it is preferable to use one made of a polymer having a high melting point. For example, a film made of polyethylene terephthalate (PET), polyamide, or the like can be used. As the polymer film 54 on the inner side, it is possible to use a film made of polyethylene (PE), polypropylene (PP), or the like, for example.
[Method for Manufacturing Lithium Secondary Battery]
Next, a method for manufacturing the lithium secondary battery 100 shown in
To manufacture the lithium secondary battery 100 of the present embodiment, first, the positive electrode 20 and the negative electrode 30 are produced.
As a method for manufacturing the positive electrode 20, for example, it is possible to use a method in which a paint containing the positive electrode active material is applied onto the positive electrode current collector 22 and dried.
As the paint containing the positive electrode active material, it is possible to use one containing the positive electrode active material, the positive electrode binder, the positive electrode conductive assistant, and a solvent. As the solvent, water, N-methyl-2-pyrrolidone, or the like can be used. The paint containing the positive electrode active material can be produced by mixing each component used for the paint containing the positive electrode active material by a known method. A method of mixing each component used for the paint containing the positive electrode active material is not particularly limited, and the order of mixing is also not particularly limited.
A method of applying the paint containing the positive electrode active material to the positive electrode current collector 22 is not particularly limited, and a method that is usually employed when manufacturing the positive electrode 20 can be used. Examples of the method of applying the paint containing the positive electrode active material include a slit die coating method and a doctor blade method.
A method in which a coating film is formed by applying the paint containing the positive electrode active material and thereafter drying is performed by removing the solvent in the coating film is not particularly limited. For example, it is possible to use a method in which the positive electrode current collector 22 to which the paint containing the positive electrode active material is applied is dried in an atmosphere of 80° C. to 150° C. Thereby, the positive electrode 20 in which the positive electrode active material layer 24 is formed on the positive electrode current collector 22 is obtained.
To manufacture the negative electrode 30, first, the laminated resin film 3 shown in
As the paint containing the negative electrode active material, it is possible to use one containing the negative electrode active material, the negative electrode binder, the negative electrode conductive assistant, and a solvent. As the solvent, water, N-methyl-2-pyrrolidone, or the like can be used. The paint containing the negative electrode active material can be produced by mixing each component used for the paint containing the negative electrode active material by a known method. A method of mixing each component used for the paint containing the negative electrode active material is not particularly limited, and the order of mixing is also not particularly limited.
Next, as shown in
In the lithium secondary battery 100 of the present embodiment, the negative electrode current collector 32 is made from the laminated resin film 3 shown in
Although the embodiments of the present disclosure have been described in detail with reference to the drawings, each of the configurations, combinations thereof, and the like in each of the embodiments is an example, and additions, omissions, replacements, and other changes can be made within a range not deviating from the gist of the present disclosure.
For example, in the lithium secondary battery 100 of the above-mentioned embodiment, the case in which the laminated resin film 3 shown in
A resin layer 3a (trade name: DIAFOIL, manufactured by Mitsubishi Chemical Corporation) made of polyethylene terephthalate (PET) and having a thickness of 4.5 μm was prepared. Next, a Cu seed layer having a thickness of 50 nm was formed using a sputtering method in the atmosphere shown in Table 1. Thereafter, a Cu plated layer was formed on the Cu seed layer at the current density shown in Table 1 by an electrolytic plating method. By carrying out the steps described above, Cu films 3b having a thickness of 0.5 km were formed on both surfaces of the resin layer 3a at the same time, thereby obtaining the laminated resin film 3 shown in
The term “Ar+O2” written in Sputtering film formation atmosphere shown in Table 1 is a mixed gas containing argon gas and oxygen gas at a volume fraction of 9999:1. The term “Ar+H2” is a mixed gas containing argon gas and hydrogen gas at a volume fraction of 999:1.
For the laminated resin film 3 thus obtained, X-ray diffraction measurement of the Cu films 3b was performed using an X-ray diffraction (XRD) machine (trade name: X'Pert PRO MRD, manufactured by PANalytical) to obtain the peak intensities of a (111) plane, a (200) plane, and a (200) plane. From the results, the peak intensities of the (200) plane and the (220) plane were calculated when the peak intensity of the (111) plane in the X-ray diffraction measurement was set to 100. Table 1 shows the results.
In addition, whether or not the Cu film 3b satisfied Expression (1) above was examined by substituting the peak intensities of the (200) plane and the (220) plane shown in Table 1 into Expression (1). Table 1 shows the results. In Table 1, the case of satisfying Expression (1) is indicated as “0”, and the case of not satisfying Expression (1) is indicated as “X”.
Using the laminated resin film 3 thus obtained as a negative electrode current collector, a lithium secondary battery was obtained by the method described below.
First, a negative electrode was manufactured by a method of applying a paint containing a negative electrode active material onto the negative electrode current collector made from the laminated resin film 3 of Experimental Examples 1 to 31 such that the film thickness after drying was 70 μm, and thereafter performing drying.
As the paint containing the negative electrode active material, one composed of 95 parts by mass of graphite (negative electrode active material), 1 part by mass of carbon black (conductive assistant material), 1.5 parts by mass of styrene-butadiene rubber (binder), 2.5 parts by mass of carboxymethyl cellulose (binder), and a solvent was used.
Next, a positive electrode was manufactured by a method of applying a paint containing a positive electrode active material onto a positive electrode current collector made from an aluminum foil having a thickness of 8 μm such that the film thickness after drying was 70 μm, and then performing drying.
As the paint containing the positive electrode active material, one composed of 94 parts by mass of lithium cobaltate (LiCoO2) (positive electrode active material), 2 parts by mass of carbon black (conductive assistant material), 4 parts by mass of polyvinylidene fluoride (binder), and a solvent was used.
Thereafter, the positive electrode and the negative electrode were laminated with a separator 10 made of polyethylene interposed therebetween to form a power generating part. Then, the power generating part was put into a pouch-shaped exterior body made from an aluminum laminate film together with an electrolyte solution, and the entrance of the exterior body was sealed. As the electrolyte solution, one in which 1 mol/L of LiPF6 had been added to dimethyl carbonate was used.
Through the steps described above, lithium secondary batteries of Experimental Examples 1 to 31 were obtained.
The lithium secondary battery thus obtained was put in a constant-temperature tank at 60° C. and charged and discharged for 100 cycles. Thereafter, the power generating part of the lithium secondary battery was cut, and using a scanning electron microscope (SEM) (Hitachi High-Tech Corporation S-4800), the negative electrode current collector (laminated resin film) was observed at a magnification of 5,000 to evaluate the “fracture resistance” and the “peeling resistance” according to the criteria shown below.
“Fracture Resistance”
(OK) 30 visual fields were observed, and no cracked sites were recognized.
(NG) 30 visual fields were observed, and one or more cracked sites were recognized.
“Peeling Resistance”
(EXCELLENT) 30 visual fields were observed, and no peeled sites were recognized.
(GOOD) 30 visual fields were observed, and three or less peeled sites were recognized.
(NG) 30 visual fields were observed, and four or more peeled sites were recognized.
As shown in Table 1, the fracture resistance was evaluated as (OK), and the peeling resistance was evaluated as (EXCELLENT) or (GOOD) in Experimental Examples 2 to 6, 9 to 12, 14, 15, 17, 18, 21, 30, and 31 using the laminated resin film having the Cu film in which the peak intensity y of the (200) plane was 2 to 30 when the peak intensity of the (111) plane in the X-ray diffraction measurement was set to 100, and Expression (1) was satisfied.
In particular, in Experimental Examples 2 to 6, 9, 10, 12, 30, and 31 using the laminated resin film having the Cu film in which the peak intensity x of the (220) plane was 5 or less when the peak intensity of the (111) plane in the X-ray diffraction measurement was set to 100, the peeling resistance was evaluated as (EXCELLENT), showing favorable peeling resistance.
On the other hand, as shown in Table 1, the fracture resistance and the peeling resistance were evaluated as (NG) in Experimental Examples 1, 7, 8, 13, 16, 19, 20, and 22 to 29 using the laminated resin film having the Cu film in which the peak intensity y of the (200) plane was not 2 to 30 when the peak intensity of the (111) plane in the X-ray diffraction measurement was set to 100, and/or Expression (1) was no satisfied.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2021/006097 | 2/18/2021 | WO |
