Electrode manufacturing method

Abstract

To reduce mixing between unit layers in an active material layer having a multilayer structure.SOLUTION: A first layer is formed by attaching a first paint to the surface of a substrate. The first layer is compressed by applying first pressure to the first layer. A second layer is formed by attaching a second paint to the surface of the first layer after compression. The second layer is compressed by applying second pressure to the second layer. An active material layer that includes the first layer and the second layer is formed. The second paint is dry. The first paint and the second paint each independently contain an active material and a binder.SELECTED DRAWING: Figure 1

Description

[Technical Field]

[0001] The present disclosure relates to a method for manufacturing an electrode and the electrode. [Background technology]

[0002] JP-A-2009-525568 (Patent Document 1) discloses a multilayer material including at least two layers. [Prior art documents] [Patent documents]

[0003] [Patent Document 1] Special Publication No. 2009-525568 Summary of the Invention [Problem to be solved by the invention]

[0004] An electrode is manufactured by forming an active material layer on the surface of a substrate. Active material layers with a multilayer structure have also been proposed. The multilayer structure includes multiple unit layers. The multiple unit layers are stacked in the thickness direction of the active material layer. For example, the composition, thickness, density, etc. can be changed for each unit layer. Controlling the composition, thickness, density, etc. for each unit layer may improve battery performance.

[0005] Generally, an active material layer (unit layer) is formed by a wet process. That is, an active material, a binder, a dispersion medium (liquid), etc. are mixed to form a wet paint. The wet paint is also called a slurry or a paste. The unit layer is formed by applying the wet paint to the surface of a substrate and drying it.

[0006] However, in wet processes, it is difficult to precisely control the composition, thickness, density, etc. of each unit layer. In wet processes, after the lower layer dries, a wet paint is applied to the surface of the lower layer and then dried to form the upper layer. During the process of forming the upper layer, liquids (dispersion medium, binder solution, etc.) contained in the wet paint may penetrate into the lower layer. This may cause materials to mix between the upper and lower layers. This mixing of materials may result in the target composition, etc. not being achieved.

[0007] An object of the present disclosure is to reduce intermixing between unit layers in an active material layer having a multi-layer structure. [Means for solving the problem]

[0008] The technical configuration and effects of the present disclosure will be described below. However, the mechanism of action in this specification includes speculation. The mechanism of action does not limit the technical scope of the present disclosure.

[0009] 1. The method for producing an electrode includes the following steps (a) to (e): (a) A first coating material is applied to the surface of the substrate to form a first layer. (b) compressing the first layer by applying a first pressure to the first layer; (c) A second layer is formed by applying a second coating material to the surface of the first layer after compression. (d) compressing the second layer by applying a second pressure to the second layer; (e) Forming an active material layer including a first layer and a second layer. The second paint is in a dry state. The first paint and the second paint each independently contain an active material and a binder.

[0010] In the manufacturing method "1" above, the second layer is formed by applying a second paint (dry paint) to the surface of the first layer. The dry paint is substantially free of liquid. In other words, there is substantially no liquid that can penetrate the first layer. Therefore, mixing of materials at the interface between the first and second layers can be reduced.

[0011] 2. The first paint may be in a dry state.

[0012] The first layer (lower layer) may also be formed by a dry process. In a wet process, binder migration may occur during evaporation of the dispersion medium (liquid). "Migration" refers to the phenomenon in which the binder rises to the surface of the coating layer. When migration occurs, unevenness in the binder distribution may occur in the thickness direction of the active material layer. In a dry process, binder migration is not thought to occur. Therefore, a homogeneous first layer can be formed.

[0013] 3. The second pressure may be different from the first pressure.

[0014] The second applied pressure may be different from the first applied pressure, causing the second layer to have a different density than the first layer.

[0015] 4. The second pressure may be lower than the first pressure.

[0016] By applying a second pressure force lower than the first pressure force, the second layer (upper layer) can have a lower density than the first layer (lower layer). The lower density of the upper layer is expected to facilitate permeation of the electrolyte into the active material layer. Permeation of the electrolyte into the active material layer is expected to reduce battery resistance, for example. The higher density of the lower layer is expected to achieve a balance between electrolyte permeability and high energy density.

[0017] 5. The second paint may have the same chemical composition as the first paint.

[0018] For example, the first and second layers having different densities may be formed using a single type of paint, which can reduce the number of parts.

[0019] 6. The first coating material may adhere to the surface of the substrate by electrostatic forces. The second coating material may adhere to the surface of the first layer by electrostatic forces.

[0020] As a method for applying dry paint (powder paint), for example, electrostatic coating is considered.

[0021] 7. The second paint may have a solid content of 95 to 100% by mass.

[0022] The dry state shows a solid content of 95% or more.

[0023] 8. The electrode includes a substrate and an active material layer. The active material layer is disposed on the surface of the substrate. The active material layer includes a first layer and a second layer. The first layer is disposed between the substrate and the second layer. The second layer is in contact with the first layer. The first layer and the second layer each independently include an active material and a binder. At the interface between the first layer and the second layer, the surface of the first layer is flat.

[0024] When the first layer is dried and pressed, the surface of the first layer becomes flat. However, if the second layer is formed by a wet process, the liquid penetrates the first layer, causing the materials to mix, resulting in a disturbance on the surface of the first layer. In other words, the surface of the first layer becomes uneven.

[0025] In the manufacturing method "1" above, the second layer is formed by a dry process. Therefore, a flat surface can be maintained at the interface between the first layer and the second layer. As a result, the first layer can be in flush contact with the second layer.

[0026] 9. At the interface between the first and second layers, the first layer may have a flatness of 1.15 or less. The flatness is determined by the following formula (I): F=L' / L …(I) It is calculated by In the above formula (I), F indicates flatness. L represents the width of the active material layer in a cross section parallel to the thickness direction of the active material layer. L' represents the length of the contour line of the surface of the first layer at the interface between the first and second layers in a cross section parallel to the thickness direction of the active material layer.

[0027] The surface of the first layer can be evaluated by the flatness of "9" above. The closer the flatness value is to 1, the flatter the target surface is. In the manufacturing method of "1" above, a flatness of 1.15 or less can be achieved. If the second layer is formed by a wet process, the flatness is considered to exceed 1.15.

[0028] 10. The second layer may have a different density than the first layer.

[0029] 11. The second layer may have a lower density than the first layer.

[0030] 12. The second layer may have the same chemical composition as the first layer.

[0031] Hereinafter, an embodiment of the present disclosure (hereinafter may be abbreviated as "the present embodiment") and an example of the present disclosure (hereinafter may be abbreviated as "the present example") will be described. However, the present embodiment and the example do not limit the technical scope of the present disclosure. [Brief explanation of the drawings]

[0032] [Figure 1] FIG. 1 is a schematic flowchart of a method for producing an electrode according to this embodiment. [Figure 2] FIG. 2 is a schematic diagram showing an example of an electrostatic coating device. [Figure 3] FIG. 3 is a schematic cross-sectional view showing an electrode in this embodiment. [Figure 4] FIG. 4 is a cross-sectional SEM image of the electrode in this example. [Figure 5] FIG. 5 shows an example of flatness measurement in this example. DETAILED DESCRIPTION OF THE INVENTION

[0033] <Definitions of terms, etc.> In this specification, the terms "comprise," "include," "have," and variations thereof (e.g., "consisting of") are open-ended. Open-ended terms may or may not include additional elements in addition to the required elements. The term "consisting of" is closed-ended. However, even in closed-ended terms, additional elements that are normally incidental impurities or unrelated to the disclosed technology are not excluded. The term "consisting essentially of..." is semi-closed. Semi-closed terms allow for the addition of elements that do not substantially affect the basic and novel characteristics of the disclosed technology.

[0034] In this specification, expressions such as "may" and "can" are used in the permissive sense of "possibly" rather than the obligatory sense of "must."

[0035] In this specification, the order of execution of multiple steps, actions, operations, etc. included in various methods is not limited to the order described unless otherwise specified. For example, multiple steps may proceed simultaneously. For example, multiple steps may occur one after the other.

[0036] In this specification, unless otherwise specified, a numerical range such as "m to n%" includes both the upper and lower limits. That is, "m to n%" indicates a numerical range of "m% or more and n% or less." Furthermore, "m% or more and n% or less" includes "more than m% and less than n%." Furthermore, a numerical value arbitrarily selected from within the numerical range may be set as a new upper or lower limit. For example, a new numerical range may be set by arbitrarily combining a numerical value within the numerical range with a numerical value described elsewhere in this specification, in a table, a figure, or the like.

[0037] In this specification, all numerical values ​​are modified by the term "about." The term "about" may mean, for example, ±5%, ±3%, ±1%, etc. All numerical values ​​may be approximate values ​​that may vary depending on the application of the disclosed technology. All numerical values ​​may be expressed with significant figures. Measured values ​​may be the average value of multiple measurements. The number of measurements may be three or more, five or more, or ten or more. In general, the more measurements are made, the more reliable the average value is expected to be. Measured values ​​may be rounded off based on the number of significant figures. Measured values ​​may include errors, such as those associated with the detection limits of the measuring device.

[0038] Geometric terms used in this specification (e.g., "parallel," "perpendicular," "orthogonal," etc.) should not be interpreted in a strict sense. For example, "parallel" may deviate slightly from the strict meaning of "parallel." Geometric terms used in this specification may include, for example, tolerances, errors, etc. in design, work, manufacturing, etc. The dimensional relationships in each drawing may not match the actual dimensional relationships. To facilitate understanding of the disclosed technology, the dimensional relationships (length, width, thickness, etc.) in each drawing may be changed. Furthermore, some configurations may be omitted.

[0039] In this specification, when a compound is expressed by a stoichiometric formula (e.g., "LiCoO2"), the stoichiometric formula is merely a representative example of the compound. The compound may have a non-stoichiometric composition. For example, when lithium cobalt oxide is expressed as "LiCoO2," unless otherwise specified, the lithium cobalt oxide is not limited to a composition ratio of "Li / Co / O = 1 / 1 / 2" and may contain Li, Co, and O in any composition ratio. Furthermore, doping or substitution with trace elements may be permitted.

[0040] In this specification, the term "solid content" refers to the total mass fraction of components other than the liquid. For example, when a paint contains a dispersion medium (liquid), a binder (solute), a conductive material (dispersoid), and an active material (dispersoid), the solid content of the paint refers to the total mass fraction of the binder, conductive material, and active material relative to the total mass of the paint. The solid content may be abbreviated as "NV (Nonvolatile Content)." In this specification, the term "dry state" refers to a solid content of 95 to 100%. The solid content in the dry state may be 98% or more, or may be 99% or more.

[0041] In this specification, "D50" is defined as the particle size at which the cumulative frequency of smaller particle sizes reaches 50% in the volume-based particle size distribution.

[0042] As used herein, the term "melting point" refers to the peak-top temperature of the melting peak (endothermic peak) in a DSC (Differential Scanning Calorimetry) curve. The DSC curve can be measured in accordance with JIS K 7121. "Near the melting point" can refer to, for example, a range of ±20°C from the melting point.

[0043] In this specification, "electrode" is a general term for a positive electrode and a negative electrode. That is, an electrode may be a positive electrode or a negative electrode. The electrode may be used for any purpose. In this embodiment, an electrode for a lithium ion battery is described as an example. The lithium ion battery may be a liquid battery or an all-solid-state battery.

[0044] <Electrode manufacturing method> 1 is a schematic flowchart of a method for manufacturing an electrode according to this embodiment. Hereinafter, the "method for manufacturing an electrode according to this embodiment" may be abbreviated as "the present manufacturing method." The present manufacturing method includes "(a) formation of a first layer," "(b) first pressing," "(c) formation of a second layer," "(d) second pressing," and "(e) formation of an active material layer."

[0045] (a) Formation of the first layer The method includes applying a first coating material to a surface of a substrate to form a first layer.

[0046] <Base material> The substrate may be, for example, in the form of a sheet. The substrate may be, for example, conductive. The substrate may include, for example, a metal foil. The substrate may include, for example, an aluminum (Al) foil, a copper (Cu) foil, or the like. The substrate may have a thickness of, for example, 5 to 50 μm.

[0047] <1st paint> The first coating material may be a wet coating material or a dry coating material. The first coating material may be a slurry, a wet powder, or a dry powder. The slurry may have a solid content of, for example, 50 to 70%. The wet powder may have a solid content of, for example, 70 to 95%. The dry powder may have a solid content of, for example, 95 to 100%. In other words, the first coating material may be in a dry state.

[0048] The wet paint may be made by mixing, for example, an active material, a binder, and a liquid. The dry paint may be made by mixing, for example, an active material and a binder. That is, the first paint contains an active material and a binder. The first paint may further contain, for example, a conductive material, a solid electrolyte, etc.

[0049] <Active material> The active material may be, for example, in powder form. The active material may have a D50 of, for example, 1 to 30 μm. The active material may include, for example, a positive electrode active material. The active material may include, for example, at least one selected from the group consisting of LiCoO2, LiNiO2, LiMnO2, LiMn2O4, Li(NiCoMn)O2, Li(NiCoAl)O2, and LiFePO4. For example, "(NiCoMn)" in "Li(NiCoMn)O2" indicates that the sum of the composition ratios in parentheses is 1. As long as the sum is 1, the amounts of the individual components are arbitrary. Li(NiCoMn)O2 may be, for example, Li(Ni 1 / 3 Co 1 / 3 Mn 1 / 3)O2, Li(Ni 0.5 Co 0.2 Mn 0.3 )O2, Li(Ni 0.8 Co 0.1 Mn 0.1 ) O2, etc.

[0050] The active material may include, for example, a negative electrode active material, such as graphite, soft carbon, hard carbon, silicon, silicon oxide, silicon-based alloy, tin, tin oxide, tin-based alloy, and Li4Ti5O 12 It may contain at least one selected from the group consisting of:

[0051] <Binder> The binder may be, for example, in powder form. The binder binds the solid materials together in the active material layer. The amount of binder may be, for example, 0.1 to 10 parts by mass per 100 parts by mass of the active material. The binder may contain any component. The binder may contain, for example, at least one selected from the group consisting of polyvinylidene fluoride (PVdF), polytetrafluoroethylene (PTFE), vinylidene fluoride-hexafluoropropylene copolymer (PVdF-HFP), styrene butadiene rubber (SBR), carboxymethyl cellulose (CMC), polyimide (PI), polyamideimide (PAI), and polyacrylic acid (PAA).

[0052] <liquid> The liquid may function, for example, as a dispersion medium in a slurry or as a granulation promoter in a wet powder. The liquid may, for example, dissolve a binder. The liquid may, for example, contain at least one selected from the group consisting of water, N-methyl-2-pyrrolidone (NMP), and butyl butyrate. Note that the dry paint (dry powder) is substantially free of liquid.

[0053] <Optional ingredients> The first coating material may further contain, for example, a conductive material. The conductive material may be, for example, in powder form. The conductive material can form an electron conduction path in the active material layer. The amount of the conductive material may be, for example, 0.1 to 10 parts by mass per 100 parts by mass of the active material. The conductive material may contain any component. The conductive material may include, for example, conductive carbon particles, conductive carbon fibers, etc. The conductive material may include, for example, at least one selected from the group consisting of carbon black, vapor-grown carbon fiber, carbon nanotubes, and graphene flakes. The carbon black may include, for example, at least one selected from the group consisting of acetylene black, furnace black, channel black, and thermal black.

[0054] The first coating material may further contain, for example, a solid electrolyte. The solid electrolyte may be in powder form. The solid electrolyte may form an ion conduction path in the active material layer. The solid electrolyte may contain any component. For example, the solid electrolyte may contain at least one selected from the group consisting of Li2S-P2S5, LiI-Li2S-P2S5, LiBr-Li2S-P2S5, and LiI-LiBr-Li2S-P2S5.

[0055] <Composite powder> When the first coating material is a dry powder, the first coating material may be a composite powder. The composite powder may be formed by combining an active material with other solid materials. For example, the composite powder may be formed by adhering a binder, a conductive material, etc. to the surface of the active material (particles). The composite powder may be formed, for example, by mixing the active material with other solid materials under conditions in which a strong shear force is applied. After the composite powder is formed, the composite powder may be subjected to heat treatment, for example, at a temperature near the melting point of the binder. The heat treatment softens, melts, and re-solidifies the binder. As a result, the binder, the conductive material, etc. are expected to be firmly fixed to the surface of the active material.

[0056] <Attachment method> In this manufacturing method, the first coating material can be attached to the surface of the substrate by any method. When the first coating material is a slurry, the slurry may be applied to the surface of the substrate by, for example, a die coater. When the first coating material is a wet powder, the wet powder may be applied to the surface of the substrate by, for example, a roll coater.

[0057] When the first coating material is a dry powder, the dry powder may be applied to the surface of the substrate by, for example, electrostatic coating. In electrostatic coating, the dry powder adheres to the surface of the substrate by electrostatic force. That is, in the present manufacturing method, the first coating material may adhere to the surface of the substrate by electrostatic force. In this embodiment, electrostatic coating is described as an example of a dry process.

[0058] FIG. 2 is a schematic diagram showing an example of an electrostatic coating device. The electrostatic coating device 200 includes a container 205, a first roll 201, a second roll 202, and a power source 204. For example, a composite powder 101 (first paint or second paint) is supplied to the container 205. The composite powder 101 may be stirred in the container 205. For example, the composite powder 101 may be mixed with a magnetic powder (hereinafter also referred to as a "magnetic carrier") in the container 205. The magnetic carrier 102 includes a ferromagnetic material. The composite powder 101 may adhere to the surface of the magnetic carrier 102.

[0059] The first roll 201 is equipped with a magnet. The first roll 201 may also be referred to as a "magnet roll." The magnetic carriers 102 are attracted to the surface of the first roll 201 by a magnetic force F1 from the first roll 201. This causes the composite powder 101 to be placed on the surface of the first roll 201. The power source 204 applies a DC voltage between the first roll 201 and the second roll 202. This forms an electric field between the first roll 201 and the second roll 202. The power source 204 supplies an electric charge to the first roll 201. The electric charge is injected into the composite powder 101 on the surface of the first roll 201.

[0060] The first roll 201 rotates in the direction of the arrow. As the first roll 201 rotates, the composite powder 101 is transported into the gap between the first roll 201 and the second roll 202. An electric field is formed between the first roll 201 and the second roll 202. When the composite powder 101 is introduced into the electric field, an electrostatic force F2 acts on the composite powder 101. When the electric field is formed so that the electrostatic force F2 is greater than the magnetic force F1, the composite powder 101 can be detached from the surface of the first roll 201.

[0061] The second roll 202 rotates in the direction of the arrow. Due to the rotation of the second roll 202, the substrate 110 is transported into the gap between the first roll 201 and the second roll 202. The composite powder 101 released from the first roll 201 flies toward the substrate 110. The composite powder 101 adheres to the surface of the substrate 110, thereby forming a first layer 121.

[0062] (b) First Pressing The present manufacturing method includes compressing the first layer by applying a first pressure to the first layer. For example, the first layer may be compressed by a roll press. The first pressure may be, for example, 1 to 10 kN. The first roll linear pressure is determined by dividing the first pressure by the width of the first layer. The first roll linear pressure may be, for example, 0.2 to 2 kN / cm. The first layer may be heated during pressing. Applying pressure and heat to the first layer is expected to improve, for example, the fixing strength of the first layer. For example, the first layer may be pressed by a heat roll or the like. The heating temperature may be, for example, a temperature near the melting point of the binder. The heating temperature may be, for example, 100 to 200°C.

[0063] (c) Formation of the second layer The manufacturing method includes forming a second layer by applying a second coating material to the surface of the compressed first layer. For example, electrostatic coating may be performed. That is, in the manufacturing method, the second coating material may be applied to the surface of the first layer by electrostatic force. Details of electrostatic coating are as described above.

[0064] <Second paint> The second coating material is in a dry state. The second coating material has a solid content of 95 to 100%. The second coating material may be a dry powder. The second coating material contains an active material and a binder. The second coating material may be a composite powder. Details of the active material, etc. are as described above. By forming the second layer by a dry process, mixing at the interface between the first layer and the second layer can be reduced.

[0065] The second paint may have a different chemical composition from the first paint. This allows the formation of a second layer having a different chemical composition from the first layer. For example, the type of active material may be different between the second paint and the first paint. For example, the compounding ratio of the active material to the binder may be different between the second paint and the first paint. The second paint may have the same chemical composition as the first paint. This allows the formation of a second layer having the same chemical composition as the first layer.

[0066] (d) Second Press The present manufacturing method includes compressing the second layer by applying a second pressure to the second layer. For example, the second layer may be compressed by a roll press. The second pressure may be the same as the first pressure. The second pressure may be different from the first pressure. This allows the second layer to have a different density than the first layer. The second pressure may be lower than the first pressure. This allows the second layer to have a lower density than the first layer. The second pressure may be, for example, 0.1 to 1 kN. The second roll linear pressure is calculated by dividing the second pressure by the width of the second layer. The second roll linear pressure may be, for example, 0.02 to 0.2 kN / cm. The second layer may be heated during pressing. Applying pressure and heat to the second layer is expected to improve, for example, the fixing strength of the second layer. For example, the second layer may be pressed by a heat roll or the like. The heating temperature may be, for example, a temperature near the melting point of the binder. The heating temperature may be, for example, 100 to 200°C.

[0067] (e) Formation of Active Material Layer The present manufacturing method includes forming an active material layer including a first layer and a second layer. For example, the active material layer may be completed by forming the first layer and the second layer. That is, the active material layer may consist of the first layer and the second layer. For example, after forming the first layer and the second layer, a third layer, a fourth layer, etc. may be further formed on the second layer by repeating the above-described steps (c) to (d).

[0068] <Electrode> FIG. 3 is a schematic cross-sectional view showing an electrode in this embodiment. Hereinafter, the "electrode in this embodiment" may be abbreviated as "the electrode." The electrode 100 may be manufactured by the manufacturing method. The electrode 100 includes a substrate 110 and an active material layer 120. Details of the substrate 110 are as described above. The active material layer 120 is disposed on the surface of the substrate 110. The active material layer 120 may be disposed on only one surface of the substrate 110, or on both the front and back surfaces.

[0069] The active material layer 120 includes a first layer 121 and a second layer 122. As long as the active material layer 120 includes the first layer 121 and the second layer 122, it may further include a third layer, a fourth layer (not shown), etc. For example, the third layer may be stacked on the second layer 122. For example, the fourth layer may be stacked on the third layer.

[0070] The first layer 121 is, so to speak, a lower layer. The first layer 121 is disposed between the substrate 110 and the second layer 122. That is, the first layer 121 is closer to the substrate 110 than the second layer 122. The first layer 121 may be formed directly on the surface of the substrate 110.

[0071] The second layer 122 is, so to speak, an upper layer. The second layer 122 is laminated on the first layer 121. The second layer 122 is closer to the surface of the active material layer 120 than the first layer 121. The second layer 122 may include the surface of the active material layer 120.

[0072] The second layer 122 is in contact with the first layer 121. At the interface between the first layer 121 and the second layer 122, the surface of the first layer 121 is flat. Therefore, the first layer 121 can be in contact with the second layer 122 at the same level.

[0073] The first layer 121 may have a flatness of, for example, 1.15 or less. The smaller the flatness value, the flatter the surface. The first layer 121 may have a flatness of, for example, 1 to 1.15, or 1 to 1.10.

[0074] The flatness is determined by the above formula (I). L and L' in the above formula (I) are measured on a cross section of the present electrode 100. A sample is cut out from the present electrode 100. The sample includes a cross section (surface to be observed) parallel to the thickness direction of the active material layer 120. The surface to be observed is flattened. The surface to be observed may be subjected to, for example, a CP (Cross-section Polisher) process. After flattening, the surface to be observed is observed with a SEM (Scanning Electron Microscope). A cross-sectional SEM image is thereby obtained. L and L' are measured on the cross-sectional SEM image. The observation magnification can be adjusted depending on the thickness of each layer, the thickness and width of the active material layer, etc. The observation magnification may be, for example, 100 to 1000 times.

[0075] The first layer 121 and the second layer 122 may have any thickness. The first layer 121 and the second layer 122 may each independently have a thickness of, for example, 5 to 200 μm, or 10 to 100 μm. The second layer 122 may be thicker than the first layer 121, for example. The second layer 122 may be thinner than the first layer 121, for example.

[0076] The first layer 121 and the second layer 122 may have any density. The second layer 122 may have the same density as the first layer 121. The second layer 122 may have a density different from that of the first layer 121. The second layer 122 may have a density lower than that of the first layer 121. A low density of the second layer 122 is expected to facilitate permeation of the electrolyte into the active material layer 120. A high density of the first layer 121 is expected to achieve a balance between permeability of the electrolyte and high energy density. The second layer 122 has a density of, for example, 1 to 2.5 g / cm. 3 and may have a density of 1.5 to 2.0 g / cm 3 The first layer 121 may have a density of, for example, 2.5 to 4.0 g / cm 3 and may have a density of 2.5 to 3.0 g / cm 3 The density may be

[0077] The first layer 121 and the second layer 122 each independently contain an active material and a binder. The second layer 122 may have, for example, a different chemical composition from the first layer 121. The second layer 122 may have, for example, the same chemical composition as the first layer 121. The first layer 121 and the second layer 122 may each independently further contain a conductive material, a solid electrolyte, etc. Details of the active material, etc. are as described above. [Example]

[0078] <Electrode manufacturing> (a) Formation of the first layer The following materials were prepared: Active material: Li(NiCoMn)O2 Conductive material: acetylene black Binder: PVdF Base material: Al foil

[0079] A particle compositing device (product name "Multi-Purpose Mixer", manufactured by Nippon Coke & Engineering Co., Ltd.) was prepared. In the particle compositing device, an active material, a conductive material, and a binder were mixed to produce a composite powder. The mixing ratio was "active material / conductive material / binder = 93.5 / 1.5 / 5 (mass ratio)". The mixing time in the particle compositing device was 10 minutes, and the rotation speed was 10,000 rpm. In this example, the composite powder was used as the first paint and the second paint.

[0080] 14.2 parts by mass of the first paint and 85.8 parts by mass of the magnetic carrier were placed in a plastic container. The plastic container was placed on a tabletop turntable and rotated at 277 rpm for 30 minutes.

[0081] An electrostatic coating device 200 was prepared (see FIG. 2). A mixture of a first coating material (composite powder 101) and magnetic carriers 102 was supplied to a container 205. The first coating material (composite powder 101) was attached to the surface of the substrate 110 by electrostatic force F2. This formed a first layer 121. The rotation speed of the first roll 201 (magnetic roll) was 100 rpm.

[0082] (b) First Pressing A roll press was prepared. The roll press was equipped with a heat roll. The temperature of the heat roll was set to 160°C. A first pressure was applied to the first layer by the roll press. This compressed the first layer. The first pressure was 7 kN. The linear pressure of the first roll was 1.17 kN / cm.

[0083] (c) Formation of the second layer A second paint was prepared. The second paint was the same composite powder as the first paint. Using an electrostatic coating device 200 (FIG. 2), the second paint (composite powder 101) was attached to the surface of the first layer 121. This resulted in the formation of a second layer 122 (see FIG. 3). The second layer 122 had the same chemical composition as the first layer 121.

[0084] (d) Second Press A roll press was prepared. The roll press was equipped with a heat roll. The temperature of the heat roll was set to 160°C. A second pressure was applied to the second layer by the roll press. This compressed the second layer. The second pressure was 0.7 kN. The second roll linear pressure was 0.117 kN / cm.

[0085] (e) Formation of Active Material Layer As a result of the above, an active material layer consisting of the first and second layers was formed. The specifications of the active material layer are shown in Table 1 below.

[0086] [Table 1]

[0087] <Evaluation> FIG. 4 is a cross-sectional SEM image of the electrode in this example. It can be seen that the surface of the first layer 121 is flat. This is thought to be because the first layer 121 and the second layer 122 are less likely to mix with each other.

[0088] FIG. 5 shows an example of flatness measurement in this example. In the cross-sectional SEM image, the width (L) of the active material layer 120 was 241.83 μm. The width (L) indicates the length in the direction perpendicular to the thickness direction of the active material layer 120. The width (L) is the overall width of the active material layer 120 in the cross-sectional SEM image. The length (L') of the contour line of the surface of the first layer 121 was 278.99 μm. According to the above formula (I), the flatness (F) was 1.15.

[0089] The present embodiment and examples are illustrative in all respects. The present embodiment and examples are not limiting. The technical scope of the present disclosure encompasses all modifications within the meaning and scope equivalent to the claims. For example, it is also intended from the beginning that any configuration may be extracted from the present embodiment and examples and that they may be combined in any desired manner. [Explanation of symbols]

[0090] 100 electrode, 101 composite powder, 102 magnetic carrier, 110 substrate, 120 active material layer, 121 first layer, 122 second layer, 200 electrostatic coating device, 201 first roll, 202 second roll, 204 power source, 205 container, F1 magnetic force, F2 electrostatic force.

Claims

1. A method for manufacturing an electrode comprising: a substrate; and an active material layer, the active material layer being disposed on a surface of the substrate; the active material layer comprising a first layer and a second layer, the first layer being disposed between the substrate and the second layer, (a) forming the first layer by applying a first coating material to a surface of the substrate; (b) compressing the first layer by applying a first compressive force to the first layer; (c) applying a second coating material to the surface of the first layer after compression to form the second layer; (d) compressing the second layer by applying a second compressive force to the second layer; and (e) forming the active material layer including the first layer and the second layer; Including, the second paint is in a dry state; the first paint and the second paint are each independently a composite powder in which an active material and a binder are composited, In the above (c), a roll having the second coating material applied thereto is disposed vertically below the first layer; causing the second coating material to fly by electrostatic force, thereby adhering the second coating material from the roll to the surface of the first layer; Electrode manufacturing method.

2. The first paint is in a dry state. A method for manufacturing the electrode according to claim 1.

3. The second pressure force is different from the first pressure force. The method for manufacturing the electrode according to claim 1 or 2.

4. the second pressure is lower than the first pressure, the roll linear pressure generated by the first pressure is 0.2 to 2 kN / cm; The roll linear pressure generated by the second pressure is 0.02 to 0.2 kN / cm. The method for manufacturing the electrode according to any one of claims 1 to 3.

5. The second paint has the same chemical composition as the first paint. The method for manufacturing the electrode according to any one of claims 1 to 4.

6. The first coating material adheres to the surface of the substrate by electrostatic force. The method for manufacturing the electrode according to any one of claims 1 to 5.

7. The second coating material has a solid content of 95 to 100% by mass. The method for manufacturing the electrode according to any one of claims 1 to 6.

8. the second layer is in contact with the first layer; the first layer and the second layer each independently contain the active material and the binder, the surface of the first layer is flat at the interface between the first layer and the second layer; At the interface between the first layer and the second layer, the first layer has a flatness of 1.15 or less. Has, The flatness is determined by the formula (I): F=L' / L It is found by In the formula (I), F indicates the flatness, L represents the width of the active material layer in a cross section parallel to the thickness direction of the active material layer, L′ represents the length of the contour line of the surface of the first layer at the interface between the first layer and the second layer in the cross section parallel to the thickness direction of the active material layer, A method for manufacturing the electrode according to claim 1.

9. the second layer has a different density than the first layer; The method for producing the electrode according to claim 8.

10. The second layer has a lower density than the first layer. The method for producing the electrode according to claim 8 or 9.

11. the second layer has the same chemical composition as the first layer; The method for manufacturing the electrode according to any one of claims 8 to 10.

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