JPWO2020067378A1 - Electrodes for lithium-ion secondary batteries and lithium-ion secondary batteries - Google Patents

Abstract

The present invention includes an electrode active material layer (30) and an insulating resin layer (40) provided on the surface of the current collector (20) and the current collector (20), and the insulating resin layer (40) is an electrode. An electrode (10) for a lithium ion secondary battery that is arranged adjacent to an end (31) of the active material layer (30) and so as to cover the end (31), and is for a lithium ion secondary battery. The electrode (10) is arranged on the surface where the electrode active material layer (30) and the insulating resin layer (70) are provided on the end side of the electrode flat portion (11) and the electrode flat portion (11), and the electrode is flat. It is provided with an electrode raised portion (12) that is thicker than the portion (11), and the ratio (T2 / T1) of the thickness (T2) of the electrode raised portion (12) to the thickness (T1) of the electrode flat portion (11). ) Is less than 1.25, and the thickness difference represented by T2-T1 is less than 15 μm. Further, the lithium ion secondary battery of the present invention includes the electrode for the lithium ion secondary battery of the present invention. According to the present invention, it is possible to provide an electrode for a lithium ion secondary battery capable of extending the life of the battery and a lithium ion secondary battery provided with the electrode.

Description

The present invention relates to an electrode for a lithium ion secondary battery having an insulating resin layer arranged adjacent to an end portion of the electrode active material layer and arranged so as to cover the end portion, and a lithium ion secondary battery.

Lithium-ion secondary batteries are used as large-scale stationary power sources for power storage, power sources for electric vehicles, etc., and in recent years, research on miniaturization and thinning of batteries has been progressing. A lithium ion secondary battery is generally provided with both electrodes having an electrode active material layer formed on the surface of a metal foil and a separator arranged between the electrodes. The separator plays a role of preventing a short circuit between both electrodes and holding an electrolytic solution.
In a lithium ion secondary battery, the occurrence rate of short circuits is particularly high near the end of the active material layer on the current collector. On the other hand, in order to more reliably prevent a short circuit between both electrodes, a non-aqueous secondary battery in which a portion having a high occurrence rate of the short circuit is coated with an insulating tape is known as a prior art (for example, Patent Document). 1). In the non-aqueous secondary battery described in Patent Document 1, an insulating tape is attached to the boundary portion between the exposed portion of the current collector and the coating portion of the positive electrode mixture layer to more reliably prevent an internal short circuit. ..

JP-A-2009-134915

However, in the case of a laminated battery, as the number of layers of the electrodes increases, the thickness of the overlapping portion of the electrode ends to which the insulating tape is attached increases. For this reason, it may be difficult to store the laminated electrodes in the battery housing, or the pressure applied to the laminated electrodes after the laminated electrodes are stored in the housing may become non-uniform. In this case, the laminated electrodes may be locally deteriorated, resulting in a shortened battery life.
Therefore, an object of the present invention is to provide an electrode for a lithium ion secondary battery capable of extending the life of the battery and a lithium ion secondary battery provided with the electrode.

As a result of diligent studies, the present inventor has arranged an insulating resin layer adjacent to the end portion of the electrode active material layer and so as to cover the end portion, and further, the electrode with respect to the thickness (T1) of the electrode flat portion. It has been found that the life of the battery can be extended by setting the ratio (T2 / T1) of the thickness (T2) of the raised portion to less than a predetermined value and setting the thickness difference represented by T2-T1 to less than a predetermined value. .. Then, the present inventor has completed the following invention. The gist of the present invention is the following [1] to [7].
[1] The current collector is provided with an electrode active material layer and an insulating resin layer provided on the surface of the current collector, and the insulating resin layer is adjacent to an end portion of the electrode active material layer and An electrode for a lithium-ion secondary battery that is arranged so as to cover the end portion.
The electrode for a lithium ion secondary battery is arranged on the surface where the electrode active material layer and the insulating resin layer are provided, the electrode flat portion and the end side of the electrode flat portion, and the electrode flat portion. With a thicker electrode bulge,
The ratio (T2 / T1) of the thickness (T2) of the raised electrode portion to the thickness (T1) of the flat electrode portion is less than 1.25, and the thickness difference represented by T2-T1 is 15 μm. Electrodes for lithium-ion secondary batteries that are less than.
[2] The end portion of the electrode active material layer adjacent to the insulating resin layer is composed of an inclined portion whose thickness decreases as the distance from the central portion of the electrode active material layer increases.
The above [1], wherein the edge factor represented by the ratio (W / T1) of the width (W) of the inclined portion to the thickness (T1) of the flat electrode portion is 1.0 to 15.0. Electrode for lithium ion secondary battery.
[3] The electrode for a lithium ion secondary battery according to the above [1] or [2], wherein the electrode active material layer is a positive electrode active material layer.
[4] The electrode for a lithium ion secondary battery according to any one of the above [1] to [3], wherein the electrode active material layer contains an electrode active material and a binder.
[5] A lithium ion secondary battery comprising the electrode for the lithium ion secondary battery according to any one of the above [1] to [4].
[6] A negative electrode and a positive electrode are provided.
The lithium ion secondary battery according to the above [5], wherein the positive electrode is an electrode for the lithium ion secondary battery.
[7] The positive electrode and the negative electrode are alternately arranged so that a plurality of layers are provided, and the ends of the current collectors of the positive electrodes constituting each layer are collectively connected to the positive electrode terminal and constitute each layer. A lithium-ion secondary battery in which the ends of the current collectors of each of the negative electrodes are grouped together and connected to the negative electrode terminals.
At least one of the positive electrode and the negative electrode is composed of the electrode for a lithium ion secondary battery.
The lithium ion secondary battery according to the above [5] or [6], wherein the insulating resin layer is arranged so as to be adjacent to the end of the electrode active material layer on the bundled end side of the current collector. ..

According to the present invention, it is possible to provide an electrode for a lithium ion secondary battery capable of extending the life of the battery and a lithium ion secondary battery provided with the electrode.

FIG. 1 is a schematic cross-sectional view of an electrode for a lithium ion secondary battery according to an embodiment of the present invention. FIG. 2 is a diagram showing an example of a die head used for coating the composition for the electrode active material layer. FIG. 3 is a diagram for explaining the application of the composition for the electrode active material layer. FIG. 4 is a diagram showing an example of a die head used for applying the composition for an insulating resin layer. FIG. 5 is a diagram for explaining the application of the composition for the insulating resin layer. FIG. 6 is a diagram for explaining the division of the current collector forming the electrode active material layer and the insulating resin layer. FIG. 7 is a schematic cross-sectional view of a modified example of the electrode for a lithium ion secondary battery according to the embodiment of the present invention. FIG. 8 is a schematic cross-sectional view of the lithium ion secondary battery according to the embodiment of the present invention. FIG. 9 is a schematic cross-sectional view of a modified example of the lithium ion secondary battery according to the embodiment of the present invention.

[Electrodes for lithium-ion secondary batteries]
Hereinafter, the electrode for a lithium ion secondary battery according to the embodiment of the present invention will be described with reference to FIG. FIG. 1 is a schematic cross-sectional view of an electrode for a lithium ion secondary battery according to an embodiment of the present invention.
As shown in FIG. 1, the electrode 10 for a lithium ion secondary battery in one embodiment of the present invention includes a current collector 20, an electrode active material layer 30 provided on the surfaces of both sides of the current collector 20, and an insulating resin. It includes a layer 40. Then, each insulating resin layer 40 is arranged so as to be adjacent to the end portion 31 of the electrode active material layer 30 and to cover the end portion 31. Further, the electrode 10 for a lithium ion secondary battery is arranged on the surface where the electrode active material layer 30 and the insulating resin layer 40 are provided, the electrode flat portion 11 and the end side of the electrode flat portion 11, and the electrode is flat. The electrode bulging portion 12 which is thicker than the portion 11 is provided. Further, the electrode active material layer 30 preferably constitutes the electrode flat portion 11, and is arranged on the electrode active material layer flat portion 33 having a flat surface and the end side of the electrode active material layer flat portion 33. A raised portion 34 of the electrode active material layer, which is thicker than the flat portion 33 of the electrode active material layer, is provided. Reference numeral T1 indicates the thickness of the flat electrode portion 11, and reference numeral T2 indicates the thickness of the raised electrode portion 12. When the thickness of the electrode raised portion 12 is not constant, the reference numeral T2 indicates the maximum value of the thickness of the electrode raised portion 12.

The ratio (T2 / T1) of the thickness (T2) of the electrode raised portion 12 to the thickness (T1) of the electrode flat portion 11 is less than 1.25. When the above ratio (T2 / T1) is 1.25 or more, when the electrodes are laminated, the thickness of the overlapping portion of the electrode raised portion 12 becomes too large as compared with the overlapping portion of the electrode flat portion 11, and the layers are laminated. The pressure applied to the laminated electrodes after the electrodes are housed in the housing may become non-uniform. In this case, the laminated electrodes may be locally deteriorated, resulting in a shortened battery life. From the viewpoint of battery life, the ratio (T2 / T1) of the thickness (T2) of the electrode raised portion 12 to the thickness (T1) of the electrode flat portion 11 is preferably 1.20 or less, more preferably. It is 1.10 or less, more preferably 1.05 or less. The lower limit of the range of the above ratio (T2 / T1) is 1.

The thickness difference between the thickness (T2) of the electrode raised portion 12 and the thickness (T1) of the electrode flat portion 11, that is, the thickness difference represented by T2-T1, is less than 15 μm. When the thickness difference represented by T2-T1 is 15 μm or more, when the electrodes are laminated, the thickness of the overlapping portion of the electrode raised portion 12 becomes too large as compared with the overlapping portion of the electrode flat portion 11. After the laminated electrodes are housed in the housing, the pressure applied to the laminated electrodes may become non-uniform. In this case, the laminated electrodes may be locally deteriorated, resulting in a shortened battery life. From the viewpoint of battery life, the thickness difference represented by T2-T1 is preferably 10 μm or less, more preferably 5 μm or less. The lower limit of the thickness difference range represented by T2-T1 is 0.
As will be described later, by adjusting the viscosity of the composition for the electrode active material layer and the composition for the insulating resin layer, and the pressure of the press during pressure pressing, the swelling at the end of the electrode is suppressed and the ratio is reduced. The values of (T2 / T1) and T2-T1 can be within the above range.

The end portion 31 of the electrode active material layer 30 adjacent to the insulating resin layer 40 is preferably composed of an inclined portion 31 whose thickness decreases as the distance from the central portion 32 of the electrode active material layer 30 increases. As a result, when the current collector on which the electrode active material layer and the insulating resin layer are formed is pressure-pressed, the current collector may be wrinkled or the electrode active material layer and the insulating resin layer may be powdered. Can be further suppressed.
The pressure press of the current collector on which the electrode active material layer and the insulating resin layer are formed will be described later. Further, the inclined portion 31 can be formed by adjusting the viscosity of the composition for the electrode active material layer.

The edge factor represented by the ratio (W / T1) of the width (W) of the inclined portion 31 to the thickness (T1) of the flat electrode portion 11 is preferably 1.0 to 15.0, and more preferably 1.0 to 15.0. It is 4.0 to 13.0. When the edge factor is 1.0 to 15.0, when the current collector forming the electrode active material layer and the insulating resin layer is pressure-pressed, the current collector may be wrinkled or the electrode active material layer and insulation may be wrinkled. It is possible to further suppress the occurrence of powder falling off of the resin layer. The pressure press of the current collector on which the electrode active material layer and the insulating resin layer are formed will be described later.
Further, the value of the edge factor can be set within the above range by adjusting the viscosity of the composition for the electrode active material layer described later and the pressure of the press during pressure pressing.

(Current collector)
Examples of the material constituting the current collector 20 include conductive metals such as copper, aluminum, titanium, nickel, and stainless steel. Among these, when the current collector 20 is a positive electrode current collector, aluminum, titanium, nickel and stainless steel are preferable, and aluminum is more preferable. When the current collector 20 is a negative electrode current collector, copper, titanium, nickel and stainless steel are preferable, and copper is more preferable. The current collector 20 is generally made of a metal foil, and the thickness thereof is not particularly limited, but is preferably 1 to 50 μm, more preferably 5 to 20 μm. When the thickness of the current collector 20 is 1 to 50 μm, the current collector 20 can be easily handled and a decrease in energy density can be suppressed.

(Electrode active material layer)
The electrode active material layer 30 typically contains an electrode active material and an electrode binder. When the electrode is a positive electrode, the electrode active material layer becomes a positive electrode active material layer, and the electrode active material becomes a positive electrode active material. On the other hand, when the electrode is a negative electrode, the electrode active material layer becomes a negative electrode active material layer, and the electrode active material becomes a negative electrode active material. Lithium-ion secondary batteries are usually loaded with a larger amount of negative electrode active material that accepts lithium than a positive electrode active material that contains lithium. That is, a negative electrode is used in which the amount of the negative electrode active material is larger than the amount of the positive electrode active material of the positive electrode. This is a measure for preventing the negative electrode from accepting lithium ions during charging and depositing lithium metal on the negative electrode. Therefore, it is preferable that the positive electrode and the negative electrode facing each other are configured so that the amount of the negative electrode active material is larger than the amount of the positive electrode active material. For the same reason, it is preferable to design the negative electrode to have a larger area of the opposite positive electrode / negative electrode than the positive electrode. This is to maintain a state in which the amount of the negative electrode active material is always large even when the position is displaced. Then, by forming an insulating resin layer at the boundary between the region of the positive electrode active material layer having a smaller area than the negative electrode active material layer and the region where the positive electrode active material layer is not formed, an internal short circuit is more reliably prevented. it can. Therefore, the electrode active material layer 30 provided with the insulating resin layer 40 is preferably a positive electrode active material layer, and the electrode active material is preferably a positive electrode active material.

The thickness of the electrode active material layer 30 is not particularly limited, but is preferably 10 to 100 μm, more preferably 20 to 80 μm per one side of the current collector. The thickness of the electrode active material layer 30 is specifically the thickness of the flat portion 33 of the electrode active material layer.

<Positive electrode active material>
Examples of the positive electrode active material used for the positive electrode active material layer include a lithium metallic acid compound. Examples of the lithium metal acid compound include lithium cobalt oxide (LiCoO ₂ ), lithium nickel oxide (LiNiO ₂ ), lithium manganate (LiMn ₂ O ₄ ), and the like. Further, as the positive electrode active material, olivine-type lithium iron phosphate (LiFePO ₄ ) or the like may be used. Further, as the positive electrode active material, a material using a plurality of metals other than lithium may be used, and NCM (nickel cobalt manganese) oxide, NCA (nickel cobalt aluminum) oxide, etc., which are called ternary oxides, may be used. You may use it. As the positive electrode active material, these substances may be used alone or in combination of two or more.

<Negative electrode active material>
Examples of the negative electrode active material used for the negative electrode active material layer include carbon materials such as graphite and hard carbon, composites of tin compounds, silicon and carbon, lithium and the like. Among these, carbon materials are preferable, and graphite is preferable. More preferred. As the negative electrode active material, one of the above substances may be used alone, or two or more of them may be used in combination.

<Average particle size of electrode active material>
The average particle size of the electrode active material is not particularly limited, but is preferably 0.5 to 50 μm, more preferably 1 to 30 μm, and even more preferably 5 to 25 μm. The average particle size means the particle size (D50) when the volume integration is 50% in the particle size distribution of the electrode active material obtained by the laser diffraction / scattering method.

<Contents of electrode active material>
The content of the electrode active material in the electrode active material layer 30 is preferably 60 to 99% by mass, more preferably 80 to 99% by mass, still more preferably 90 to 98% by mass, based on the total amount of the electrode active material layer.

<Binder for electrodes>
Specific examples of the binder for the electrode include polyvinylidene fluoride (PVdF), polyvinylidene fluoride-hexafluoropropylene copolymer (PVdF-HFP), fluorine-containing resin such as polytetrafluoroethylene (PTFE), and polymethyl acrylate (PMA). ), Acrylic resin such as polyvinylidene methacrylate (PMMA), polyvinylidene acetate, polyimide (PI), polyamide (PA), polyvinylidene chloride (PVC), polyether nitrile (PEN), polyethylene (PE), polypropylene (PP) , Polyacrylonitrile (PAN), acrylonitrile-butadiene rubber, styrene butadiene rubber (SBR), poly (meth) acrylic acid, carboxymethyl cellulose (CMC), hydroxyethyl cellulose, polyvinyl alcohol and the like. These binders may be used alone or in combination of two or more. Further, carboxymethyl cellulose and the like may be used in the form of a salt such as a sodium salt.

The content of the binder for the electrode in the electrode active material layer 30 is preferably 0.5 to 20% by mass, more preferably 1.0 to 10% by mass, based on the total amount of the electrode active material layer.

<Conductive aid>
The electrode active material layer 30 may contain a conductive auxiliary agent. As the conductive auxiliary agent, a material having higher conductivity than the above-mentioned electrode active material is used, and specific examples thereof include carbon materials such as Ketjen black, acetylene black, carbon nanotubes, and rod-shaped carbon. The conductive auxiliary agent may be used alone or in combination of two or more. When the conductive auxiliary material is contained in the electrode active material layer 30, the content of the conductive auxiliary agent is preferably 0.5 to 15% by mass based on the total amount of the electrode active material layer, and is preferably 1 to 10% by mass. Is more preferable. When the content of the conductive auxiliary agent is 0.5 to 15% by mass, it is possible to suppress an increase in battery resistance and a decrease in output performance, and the conductive auxiliary agent absorbs the binder to cause powder falling. Can be suppressed.

The electrode active material layer 30 may contain an optional component other than the electrode active material, the conductive auxiliary agent, and the binder for the electrode as long as the effect of the present invention is not impaired. However, the total content of the electrode active material, the conductive auxiliary agent, and the binder for the electrode is preferably 90% by mass or more, and more preferably 95% by mass or more, based on the total mass of the electrode active material layer. ..

(Insulating resin layer)
The insulating resin layer 40 may include a resin component as long as it can secure insulation at the end of the electrode. Examples of the resin component include fluorine-containing resins such as polyvinylidene fluoride (PVdF), polyvinylidene fluoride-hexafluoropropylene copolymer (PVdF-HFP), and polytetrafluoroethylene (PTFE), and polymethyl acrylate (PMA). Acrylic resin such as polymethylmethacrylate (PMMA), polyvinylidene acetate, polyimide (PI), polyamide (PA), polyvinylidene chloride (PVC), polyethernitrile (PEN), polyethylene (PE), polypropylene (PP), poly Examples thereof include acrylonitrile (PAN), acrylonitrile-butadiene rubber, styrene butadiene rubber (SBR), poly (meth) acrylic acid, carboxymethyl cellulose (CMC), hydroxyethyl cellulose, polyvinyl alcohol and the like. These binders may be used alone or in combination of two or more. Further, carboxymethyl cellulose and the like may be used in the form of a salt such as a sodium salt. These polymers may be used alone or may be used as a multilayer body by superimposing these polymers. Further, various additives may be used for these polymers, and the type and content thereof are not particularly limited. In addition, insulating fine particles may be added to the resin component, if necessary. Examples of the insulating fine particles include inorganic particles and organic particles.
When inorganic particles are used as an additive, the rigidity of the insulating layer can usually be increased and the drying shrinkage can be reduced. Examples of the material of such inorganic particles include aluminum oxide (alumina), hydrate of aluminum oxide (bemite (AlOOH)), gibsite (Al (OH) ₃ ), silicon oxide, magnesium oxide (magnesia), and water. Oxide particles such as magnesium oxide, calcium oxide, titanium oxide (titania), BaTIO ₃ , ZrO ₂ , alumina-silica composite oxide, nitride particles such as aluminum nitride and boron nitride, covalent crystals such as silicon and diamond. Examples thereof include particles, sparingly soluble ion crystal particles such as barium sulfate, calcium fluoride and barium fluoride, and clay fine particles such as talc and montmorillonite. Among these, oxide particles are preferable from the viewpoint of stability in an electrolytic solution and potential stability, and among them, titanium oxide and aluminum oxide are preferable from the viewpoint of low water absorption and excellent heat resistance (for example, resistance to high temperatures of 180 ° C. or higher). , Aluminum oxide hydrate, magnesium oxide and magnesium hydroxide are more preferable, aluminum oxide, aluminum oxide hydrate, magnesium oxide and magnesium hydroxide are more preferable, and aluminum oxide is particularly preferable.
As the organic particles, polymer particles are usually used. By adjusting the type and amount of functional groups on the surface of the organic particles, the affinity for water can be controlled, and the amount of water contained in the insulating layer can be controlled. In addition, organic particles are usually excellent in that metal ions are less eluted. Examples of the material of such organic particles include various polymer compounds such as polystyrene, polyethylene, polyimide, melamine resin, and phenol resin. The polymer compound forming the particles may be, for example, a mixture, a modified product, a derivative, a random copolymer, an alternating copolymer, a graft copolymer, a block copolymer, a crosslinked product, or the like. Further, the organic particles may be formed of a mixture of two or more kinds of polymer compounds.
One of these inorganic particles and organic particles may be used alone, or two or more of them may be mixed and used.
The content of the insulating fine particles when the insulating resin layer contains the insulating fine particles is not particularly limited. When the content of the insulating fine particles is small, voids are unlikely to be generated in the insulating layer, and when the electrodes are compacted, they may swell without following the deformation of the electrode active material layer. Further, when the content of the insulating fine particles is large, the follow-up to the deformation of the electrode active material layer is excellent, but the press roll may be damaged depending on the material of the fine particles. From this point of view, it is preferable that the content of the insulating fine particles is appropriately selected depending on the type of the electrode active material and the press setting.

The thickness of the insulating resin layer 40 is preferably 1 to 100 μm from the viewpoint of the short circuit suppressing effect. The thickness of the insulating resin layer 40 is the thickness of the current collector 20 in the thickness direction.

[Manufacturing method of electrodes for lithium-ion secondary batteries]
The electrode for a lithium ion secondary battery in one embodiment of the present invention can be manufactured by, for example, the following manufacturing method. In an example of the method for manufacturing an electrode for a lithium ion secondary battery according to an embodiment of the present invention, first, a composition for an electrode active material layer is applied onto a current collector to form an electrode active material layer on the current collector. To do. Then, the composition for the insulating resin layer is applied so as to be adjacent to the end portion of the electrode active material layer and to cover the end portion thereof to form the insulating resin layer.

(Electrode active material layer forming process)
In the electrode active material layer forming step, first, a composition for an electrode active material layer containing an electrode active material, an electrode binder, and a solvent is prepared. Examples of the solvent used in the composition for the electrode active material layer include cyclohexanone, methyl ethyl ketone, methyl isobutyl ketone, tetrahydrofuran, toluene, isopropyl alcohol, N-methylpyrrolidone (NMP), ethanol, water and the like. The composition for the electrode active material layer may contain other components such as a conductive additive to be blended if necessary. Details of the electrode active material, the binder for the electrode, and the like are as described above. The composition for the electrode active material layer is in the state of a slurry.

The viscosity of the composition for the electrode active material layer is preferably 2500 to 12000 mPa · s, more preferably 3000 to 10000 mPa · s. The viscosity is a viscosity measured 2 minutes after the start of rotation of the spindle under the conditions of 60 rpm and 25 ° C. with a B-type viscometer. By keeping the viscosity within the above range, the thickness of the raised portion 34 of the electrode active material layer can be reduced. Then, by reducing the thickness of the raised portion 34 of the electrode active material layer, it becomes easy to reduce the values of the ratio (T2 / T1) and T2-T1 as described above.

The electrode active material layer can be formed, for example, by applying the composition for an electrode active material layer on a current collector and drying it by a known coating method. Examples of the method of applying the composition for the electrode active material layer on the current collector sheet include a die coating method, a slit coating method, a comma coating method, a lip coating method, a dip coating method, a spray coating method, and a roll coating method. Examples include the method, the doctor blade method, the bar coating method, the gravure coating method, and the screen printing method. Among these coating methods, the die coating method is preferable from the viewpoint that an inclined portion can be easily formed at the end portion of the electrode active material layer. Hereinafter, application of the composition for the electrode active material layer onto the current collector will be described with reference to FIGS. 2 and 3 by taking the die coating method as an example.

FIG. 2 is a diagram showing an example of a die head used for coating the composition for the electrode active material layer. The die head 50 is provided with a discharge port 51. The composition for the electrode active material layer supplied to the die head 50 is discharged from the discharge port 51.

As shown in FIG. 3, the composition for the electrode active material layer is discharged from the die head 50 onto the current collector 120 moving in the direction of reference numeral 121. As a result, the electrode active material layer 130 can be formed on the current collector 120. By adjusting the viscosity of the composition for the electrode active material layer, the side surface 131 of the electrode active material layer 130 can be tilted. Further, by adjusting the viscosity of the composition for the electrode active material layer, the thickness of the raised portion 34 of the electrode active material layer is reduced (see FIG. 1), and the values of T2 / T1 and T2-T1 are set as described above. It can also be adjusted within the specified range. The current collector 120 on which the electrode active material layer 130 is formed passes through a dryer (not shown). As a result, the electrode active material layer 130 formed on the current collector 120 is dried. The drying temperature is not particularly limited as long as the solvent can be removed, but is, for example, 40 to 120 ° C, preferably 50 to 90 ° C. The drying time is not particularly limited, but is, for example, 30 seconds to 10 minutes.
After the electrode active material layer 130 is dried, the electrode active material layer 130 is also formed on the surface opposite to the current collector 120 in the same manner.

(Insulating resin layer forming process)
Next, the composition for the insulating resin layer is applied so that the applied composition for the edge resin layer is adjacent to the end 131 of the electrode active material layer 130 and covers the end 131. First, a composition for an insulating resin layer containing insulating fine particles, a binder for electrodes, and a solvent is prepared. Specific examples of the solvent in the composition for the insulating resin layer include one or more selected from N-methylpyrrolidone, N-ethylpyrrolidone, dimethylacetamide, and dimethylformamide. In addition, the composition for the insulating resin layer may contain other optional components to be blended as needed. Details of the insulating fine particles, the binder for the insulating resin layer, and the like are as described above. The composition for the insulating resin layer is in the state of a slurry.

The solid content concentration of the composition for the insulating resin layer is preferably 5 to 75% by mass, more preferably 15 to 50% by mass. When the solid content concentration of the composition for the insulating resin layer is 5 to 75% by mass, the applied composition for the insulating resin layer can be sufficiently dried, and the film thickness of the applied composition for the insulating resin layer becomes too small. The thickness accuracy of the insulating resin layer is stable. The viscosity of the composition for the insulating resin layer is preferably 1000 to 10000 mPa · s, more preferably 2000 to 6000 mPa · s. When the viscosity of the composition for the insulating resin layer is 1000 to 10000 mPa · s, it is possible to suppress the occurrence of bleeding in the electrode active material layer, and the insulating resin layer is prevented from having a large swelling or streaks. Can be suppressed. The viscosity is a viscosity measured 2 minutes after the start of rotation of the spindle under the conditions of 60 rpm and 25 ° C. with a B-type viscometer.

The insulating resin layer may be formed by a known method using the composition for the insulating resin layer. For example, the composition for the insulating resin layer may be formed near the end of the electrode active material layer 130 of the current collector 120. It can be formed by applying and drying. Examples of the method for applying the insulating resin layer composition onto the current collector 120 include a die coating method, a slit coating method, a comma coating method, a lip coating method, a dip coating method, a spray coating method, and a roll coating method. Doctor blade method, bar coat method, gravure coat method, screen printing method and the like can be mentioned. Among these coating methods, the die coating method is preferable from the viewpoint that the composition for the insulating resin layer can be accurately coated near the end portion of the electrode active material layer 130. Hereinafter, application of the composition for the insulating resin layer will be described with reference to FIGS. 4 and 5 by taking the die coating method as an example.

FIG. 4 is a diagram showing an example of a die head used for applying the composition for an insulating resin layer. The die head 60 is provided with two discharge ports 61 and 62. The positions of the two discharge ports 61 and 62 correspond to the positions near the ends of the electrode active material layer 130, respectively. The composition for the electrode active material layer supplied to the die head 60 is discharged from the two discharge ports 61 and 62. Thereby, the composition for the insulating resin layer can be applied so that the applied composition for the insulating resin layer is adjacent to the end 131 of the electrode active material layer 130 and covers the end 131.

As shown in FIG. 5, the composition for the insulating resin layer is discharged from the die head 60 onto the current collector 120 on which the electrode active material layer 130 is formed, which is moving in the direction of reference numeral 121. As a result, the insulating resin layer 140 can be formed on the current collector 120 so that the insulating resin layer 140 is adjacent to the end 131 of the electrode active material layer 130 and covers the end 131. The current collector 120 having the insulating resin layer 140 formed on the current collector 120 passes through a dryer (not shown). As a result, the insulating resin layer 140 formed on the current collector 120 is dried. The drying temperature is not particularly limited as long as the solvent can be removed, but is, for example, 40 to 120 ° C, preferably 50 to 90 ° C. The drying time is not particularly limited, but is, for example, 30 seconds to 10 minutes.
After the insulating resin layer 140 is dried, the insulating resin layer 140 is also formed on the surface opposite to the current collector 120 in the same manner.

(Pressure press process)
The current collector 120 having the electrode active material layer 130 and the insulating resin layer 140 formed on the current collector 120 is preferably pressure-pressed. By pressure pressing, the swelling near the end of the electrode active material layer 130 can be further reduced, and the ratio (T2 / T1) and the value of T2-T1 can be easily adjusted within the above ranges. The pressure press may be performed by a roll press or the like.
The pressure of the pressure press is not particularly limited as long as the desired electrode density can be achieved and wrinkles or the like do not occur in the current collector 120. For example, from the viewpoint that the thickness of the raised electrode portion can be reduced, the pressure of the pressure press is a linear pressure in the case of a roll press, preferably 100 to 2000 kN / m, and more preferably 200 to 1000 kN / m. Is.

(Split)
The current collector 120 forming the electrode active material layer 130 and the insulating resin layer 140 is, for example, cut along the dotted line of reference numeral 150 in FIG. 6 and divided into a plurality of electrodes for a lithium ion secondary battery. As a result, the electrode 10 for a lithium ion secondary battery according to the embodiment of the present invention shown in FIG. 1 can be manufactured.

The electrode 10 for a lithium ion secondary battery in one embodiment of the present invention can be deformed as follows.
(Modification example 1)
The electrode 10 for a lithium ion secondary battery in the above embodiment of the present invention has an electrode active material layer 30 and an insulating resin layer 40 formed on both surfaces of the current collector 20. However, as in the lithium ion secondary battery electrode 10A shown in FIG. 7, the electrode active material layer 30 and the insulating resin layer 40 may be formed only on one surface of the current collector 20.

(Modification 2)
In the above example of the method for manufacturing an electrode for a lithium ion secondary battery according to an embodiment of the present invention, when the electrode for a lithium ion secondary battery according to the embodiment of the present invention is manufactured, the composition for an electrode active material layer and insulation are used. The composition for the resin layer was applied separately. However, the composition for the electrode active material layer and the composition for the insulating resin layer may be applied at the same time.

The electrode for a lithium ion secondary battery and a modification thereof in one embodiment of the present invention are only one embodiment of the electrode for a lithium ion secondary battery of the present invention. Therefore, the electrode for a lithium ion secondary battery and a modification thereof in one embodiment of the present invention do not limit the electrode for a lithium ion secondary battery of the present invention.

[Lithium secondary ion battery]
A lithium ion secondary battery according to an embodiment of the present invention will be described with reference to FIG. FIG. 8 is a schematic cross-sectional view of the lithium ion secondary battery according to the embodiment of the present invention. As shown in FIG. 8, the lithium ion secondary battery 1 according to the embodiment of the present invention includes the lithium ion secondary battery electrode 10 according to the embodiment of the present invention as a positive electrode and a negative electrode.

In the lithium ion secondary battery 1 according to the embodiment of the present invention, the lithium ion secondary battery electrode 10 as the positive electrode and the lithium ion secondary battery electrode 10 as the negative electrode are alternately provided in a plurality of layers. It is located in. Then, the ends of the current collectors 20 of the electrodes 10 for the lithium ion secondary battery as the positive electrodes constituting each layer are collectively connected to the positive electrode terminal 2, and the lithium ion secondary battery as the negative electrode constituting each layer is connected. The ends of the current collectors 20 of each of the electrodes 10 are grouped together and connected to the negative electrode terminal 3. Further, the insulating resin layer 40 is arranged so as to be adjacent to the end portion of the electrode active material layer 30 on the bundled end portion side of the current collector 120. As a result, it is possible to prevent the thickness of the overlapping portions 4 and 5 of the ends of the lithium ion secondary battery electrodes 10 from increasing. Then, it becomes easy to store the laminated electrodes 10 in the housings 6 and 7 of the battery 1, and the pressure applied to the laminated electrodes 10 after the laminated electrodes 10 are stored in the housings 6 and 7 becomes non-uniform. It can be suppressed from becoming. As a result, local deterioration of the laminated electrodes 10 can be prevented and the life of the battery can be extended. Further, the utilization rate of the electrode 10 is increased, and the energy density of the lithium ion secondary battery 1 can be increased. The housings 6 and 7 may be of a square type, a cylindrical type, a laminated type, or the like.

The lithium ion secondary battery 1 in one embodiment of the present invention preferably further includes a separator 8 arranged between the positive electrode 10 and the negative electrode 10. By providing the separator 8, a short circuit between the positive electrode 10 and the negative electrode 10 is more effectively prevented. Further, the separator 8 may hold the electrolyte 9 described later. The insulating resin layer 40 provided on the positive electrode 10 or the negative electrode 10 may or may not be in contact with the separator, but is preferably in contact with the separator.

Examples of the separator 8 include a porous polymer film, a non-woven fabric, and glass fiber, and among these, a porous polymer film is preferable. Examples of the porous polymer film include an olefin-based porous film. The separator 8 may be heated by heat generated when the lithium ion secondary battery is driven to cause heat shrinkage, and even during such heat shrinkage, the provision of the insulating resin layer makes it easier to suppress a short circuit.

The lithium ion secondary battery of the present invention comprises an electrolyte 9. The electrolyte is not particularly limited, and a known electrolyte 9 used in the lithium ion secondary battery 1 may be used. As the electrolyte 9, for example, an electrolytic solution is used. The electrolyte 9 is filled in the housings 6 and 7, for example, after the laminated electrodes 10 are housed in the housings 6 and 7.

Examples of the electrolytic solution include an organic solvent and an electrolytic solution containing an electrolyte salt. Examples of the organic solvent include ethylene carbonate (EC), propylene carbonate (PC), dimethyl carbonate (DMC), diethyl carbonate (DEC), ethyl methyl carbonate (EMC), γ-butyrolactone, sulfolane, dimethyl sulfoxide, acetonitrile, and dimethyl. Polar solvents such as formamide, dimethylacetamide, 1,2-dimethoxyethane, 1,2-diethoxyethane, tetrahydrofuran, 2-methyltetrahydrofuran, 1,3-dioxolane, methyl acetate, or a mixture of two or more of these solvents Can be mentioned. Electrolyte salts include LiClO ₄ , LiPF ₆ , LiBF ₄ , LiAsF ₆ , LiSbF ₆ , LiCF ₃ CO ₂ , LiPF ₆ SO ₃ , LiN (SO ₂ CF ₃ ) ₂ , LiN (SO ₂ CF ₂ CF ₃ ) ₂ , Examples thereof include salts containing lithium such as LiN (COCF ₃ ) _2, LiN (COCF ₂ CF ₃ ) ₂ , and lithium bisoxalate boronate (LiB (C ₂ O ₄ ) ₂ ). In addition, a complex such as an organic acid lithium salt-boron trifluoride complex and a complex hydride such as LiBH ₄ can be mentioned. These salts or complexes may be used alone or as a mixture of two or more. Further, the electrolyte 9 may be a gel-like electrolyte in which the above-mentioned electrolyte solution further contains a polymer compound. Examples of the polymer compound include a fluoropolymer such as polyvinylidene fluoride and a polyacrylic polymer such as methyl poly (meth) acrylate. The gel electrolyte may be used as a separator.

The lithium ion secondary battery according to the above embodiment of the present invention can be modified as follows.
(Modification example 1)
The lithium ion secondary battery according to the embodiment of the present invention includes the electrode 10 for the lithium ion secondary battery of the embodiment of the present invention as the positive electrode and the negative electrode, but the positive electrode and the negative electrode of the embodiment of the present invention. A modified example 10A of the electrode for a lithium ion secondary battery may be provided.

(Modification 2)
The lithium ion secondary battery according to the embodiment of the present invention includes the electrode 10 for the lithium ion secondary battery according to the embodiment of the present invention as the positive electrode and the negative electrode, but the present invention is used as one of the positive electrode and the negative electrode. The electrode 10 for a lithium ion secondary battery according to the embodiment of the present invention may be provided. Further, as one of the positive electrode and the negative electrode, a modified example 10A of the electrode for a lithium ion secondary battery according to the embodiment of the present invention may be provided. As described above, since the electrode area of the positive electrode is usually smaller than that of the negative electrode, the insulating resin layer 40 can more reliably prevent an internal short circuit in the positive electrode than in the negative electrode. Therefore, it is preferable that the lithium ion secondary battery according to the embodiment of the present invention includes at least the electrode 10 for the lithium ion secondary battery according to the embodiment of the present invention or a modification 10A thereof as a positive electrode.
For example, as in the lithium ion secondary battery 1A shown in FIG. 9, the electrode 10 for the lithium ion secondary battery according to the embodiment of the present invention is used only for the positive electrode, and the negative electrode is not formed with an insulating resin layer. 10B may be used.

The lithium ion secondary battery and its modifications according to the embodiment of the present invention are only one embodiment of the lithium ion secondary battery of the present invention. Therefore, the lithium ion secondary battery and its modifications in one embodiment of the present invention do not limit the lithium ion secondary battery of the present invention.

Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not limited to these Examples.

The obtained electrode for a lithium ion secondary battery was evaluated by the following evaluation method.

(Life characteristics)
The cells prepared in Examples and Comparative Examples were repeatedly charged and discharged under the following conditions.
Charging: 0.2A, 4.2V constant current, then constant voltage charge until 0.01A current value Discharge: 0.2A constant current, discharge under 3.0V termination condition Number of repetitions: 1000 times 1000 The ratio obtained by dividing the discharge capacity after each charge / discharge by the value of the first discharge capacity was defined as the capacity retention rate, and was evaluated as follows.
◯: 80% ≤ capacity retention rate ×: capacity retention rate <80%
(Thickness of flat electrode portion (T1), thickness of raised electrode portion (T2))
The thickness of the flat electrode portion (T1) and the thickness of the raised electrode portion (T2) were measured using a thickness gauge (trade name “Digimicro MF-501”, manufactured by Nikon Corporation).
(Width of inclined part (W))
The electrode was cut using a cutting machine to prepare a sample for observing the cross section of the electrode. Then, the electrode cross section of the sample was observed at a magnification of 100 to 200 times using a laser microscope (trade name "LEXT OLS450", manufactured by Olympus Corporation), and the length of the inclined portion (W) was measured.

[Example 1]
(Formation of positive electrode active material layer)
NCA-based oxide (average particle size 10 μm) as a positive electrode active material, acetylene black as a conductive auxiliary agent, polyvinylidene fluoride (PVdF) as a binder for electrodes, and N-methylpyrrolidone (NMP) as a solvent are mixed. A slurry for the positive electrode active material layer was obtained. The content of the NCA-based oxide in the slurry for the positive electrode active material layer was 62% by mass, and the content of acetylene black was 1.4% by mass. The PVdF content was 1.6% by mass, and the NMP content was 35% by mass. The viscosity of the slurry for the positive electrode active material layer was 7460 mPa · s. The viscosity was measured with a B-type viscometer under the conditions of 60 rpm and 25 ° C., 2 minutes after the start of rotation of the spindle. This slurry for the positive electrode active material layer was applied to both sides of an aluminum foil having a thickness of 15 μm as a positive electrode current collector using a die coater as shown in FIG. 2, pre-dried, and then vacuum dried at 120 ° C. The positive electrode active material layer was formed on the aluminum foil. Next, the opposite side was similarly coated to form positive electrode active material layers on both sides of the aluminum foil.

Using a die coater as shown in FIG. 4, an aluminum foil having a positive electrode active material layer formed so that the applied slurry for an insulating resin layer is adjacent to and covers the end portion of the positive electrode active material layer. A slurry for the insulating resin layer was applied. As the slurry for the insulating resin layer, a slurry having a viscosity of 5430 mPa · s and a resin component of polyimide resin was used. The viscosity was measured with a B-type viscometer under the conditions of 60 rpm and 25 ° C., 2 minutes after the start of rotation of the spindle. Then, the coating film was dried at 60 ° C. for 10 minutes to form an insulating resin layer on the aluminum foil on which the positive electrode active material layer was formed. Next, the opposite side was similarly coated to obtain an aluminum foil having insulating resin layers on both sides. Then, the aluminum foil on which the insulating resin layer was formed was pressure-pressed by a roller at a linear pressure of 400 kN / m and further punched into an electrode size of 100 mm × 200 mm square to obtain a positive electrode having an insulating resin layer on both sides. Of the dimensions, the area coated with the positive electrode polar active material was 100 mm × 180 mm. The thickness of the positive electrode active material layer formed on both sides was 50 μm per side.

(Preparation of negative electrode)
100 parts by mass of graphite (average particle diameter 10 μm) as the negative electrode active material, 1.5 parts by mass of sodium salt of carboxymethyl cellulose (CMC) and 1.5 parts by mass of styrene butadiene rubber (SBR) as the binder for the negative electrode, and as a solvent. It was mixed with water to obtain a slurry for a negative electrode active material layer adjusted to have a solid content of 50% by mass. This slurry for the negative electrode active material layer was applied to both sides of a copper foil having a thickness of 12 μm as a negative electrode current collector and vacuum dried at 100 ° C. After that, the negative electrode current collector coated with the slurry for the negative electrode active material layer on both sides is pressure-pressed by a roller at a linear pressure of 300 kN / m, and further punched into an electrode size of 110 mm × 210 mm square, and the negative electrode active material is punched on both sides. It was a negative electrode having a layer. Of the dimensions, the area to which the negative electrode active material was applied was 110 mm × 190 mm. The thickness of the negative electrode active material layer formed on both sides was 50 μm per side. Moreover, the insulating resin layer was not formed on the negative electrode.

[Examples 2 and 3 and Comparative Examples 1 to 3]
In Examples 2 and 3 and Comparative Examples 1 to 3, the viscosity of the slurry for the positive electrode active material layer and the press pressure of the positive electrode current collector coated with the slurry for the positive electrode active material layer were changed as shown in Table 1. As a result, Examples 2 and 3 having the thickness of the flat electrode portion (T1), the thickness of the raised electrode portion (T2), and the width of the inclined portion of the electrode active material layer (W) shown in Table 2 below. The positive electrodes of Comparative Examples 1 to 3 were prepared.
[Comparative Example 4]
Example 1 except that the insulating resin layer was formed by using an insulating tape (manufactured by Teraoka Seisakusho Co., Ltd., model number: 652S, thickness: 25 μm) after the pressure pressing step instead of the slurry for the insulating resin layer. The positive electrode of Comparative Example 4 was prepared in the same manner as the positive electrode.

(Preparation of electrolyte)
LiPF ₆ as an electrolyte salt was dissolved in a solvent in which ethylene carbonate (EC) and diethyl carbonate (DEC) were mixed at a volume ratio of 3: 7 (EC: DEC) so as to be 1 mol / liter to prepare an electrolytic solution. Prepared.

(Battery manufacturing)
A laminate was obtained by laminating 10 negative electrodes having the insulating resin layer obtained above, 9 positive electrodes, and 18 separators. Here, the negative electrode and the positive electrode were arranged alternately, and a separator was arranged between each negative electrode and the positive electrode. Further, as the separator, a polyethylene porous film was used. The exposed ends of the positive electrode current collectors of each positive electrode were joined together by ultrasonic fusion, and the terminal tabs protruding to the outside were joined. Similarly, the exposed ends of the negative electrode current collectors of each negative electrode were joined together by ultrasonic fusion, and the terminal tabs protruding to the outside were joined. Next, the laminate was sandwiched between aluminum laminate films, the terminal tabs were projected to the outside, and the three sides were sealed by laminating. A laminated cell was manufactured by injecting the electrolytic solution obtained above from one side left unsealed and vacuum-sealing.

The measurement results and evaluation results are shown in Table 2 below.

As shown in Examples 1 to 3 above, the value of T2 / T1 of the electrode for the lithium ion secondary battery should be less than 1.25, and the value of T2-T1 should be less than 15 μm. It was found that the life characteristics of the lithium ion secondary battery can be improved. On the other hand, in the lithium ion secondary batteries of Comparative Examples 1, 2 and 4, the T2 / T1 value of the lithium ion secondary battery electrode is 1.25 or more, and the T2-T1 value is 15 μm or more. Because it was there, the life characteristics were bad. In the lithium ion secondary battery of Comparative Example 3, the value of T2 / T1 of the electrode for the lithium ion secondary battery was less than 1.25, but the value of T2-T1 was 15 μm or more, so that the life characteristic was long. It was bad.

1,1A Lithium-ion secondary battery 2 Positive electrode terminal 3 Negative electrode terminal 6,7 Housing 8 Separator 9 Electrolyte 10,10A, 10B Electrode for lithium-ion secondary battery (positive electrode, negative electrode)
11 Electrode flat part 12 Electrode raised part 20,120 Current collector 30,130 Electrode active material layer 31,131 End (inclined part)
32 Central part 33 Electrode active material layer Flat part 34 Electrode active material layer raised part 40,140 Insulating resin layer 50,60 Die head 51,61,62 Discharge port

Claims (7)

A current collector and an electrode active material layer and an insulating resin layer provided on the surface of the current collector are provided, and the insulating resin layer is adjacent to an end portion of the electrode active material layer and the end portion is formed. An electrode for a lithium-ion secondary battery that is placed so as to cover it.
The electrode for a lithium ion secondary battery is arranged on the surface where the electrode active material layer and the insulating resin layer are provided, the electrode flat portion and the end side of the electrode flat portion, and the electrode flat portion. With a thicker electrode bulge,
The ratio (T2 / T1) of the thickness (T2) of the raised electrode portion to the thickness (T1) of the flat electrode portion is less than 1.25, and the thickness difference represented by T2-T1 is 15 μm. Electrodes for lithium-ion secondary batteries that are less than. The end portion of the electrode active material layer adjacent to the insulating resin layer is composed of an inclined portion whose thickness decreases as the distance from the central portion of the electrode active material layer increases.
The lithium according to claim 1, wherein the edge factor represented by the ratio (W / T1) of the width (W) of the inclined portion to the thickness (T1) of the flat electrode portion is 1.0 to 15.0. Electrode for ion secondary battery. The electrode for a lithium ion secondary battery according to claim 1 or 2, wherein the electrode active material layer is a positive electrode active material layer. The electrode for a lithium ion secondary battery according to any one of claims 1 to 3, wherein the electrode active material layer contains an electrode active material and a binder. A lithium ion secondary battery comprising the electrode for a lithium ion secondary battery according to any one of claims 1 to 4. It has a negative electrode and a positive electrode,
The lithium ion secondary battery according to claim 5, wherein the positive electrode is an electrode for the lithium ion secondary battery. The positive electrode and the negative electrode are alternately arranged so that a plurality of layers are provided, and the ends of the current collectors of the positive electrodes constituting each layer are collectively connected to the positive electrode terminal, and each of the negative electrodes constituting each layer is connected. A lithium-ion secondary battery in which the ends of the current collector are grouped together and connected to the negative electrode terminal.
At least one of the positive electrode and the negative electrode is composed of the electrode for a lithium ion secondary battery.
The lithium ion secondary battery according to claim 5 or 6, wherein the insulating resin layer is arranged so as to be adjacent to the end portion of the electrode active material layer on the bundled end side of the current collector.

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