KR20230019035A - Positive electrode comprising insulating layer having excellent wet adhesion and lithium secondary battery comprising the same - Google Patents

Abstract

The present invention relates to a positive electrode for a lithium secondary battery including an insulating layer having excellent wet adhesion, and a lithium secondary battery including the same, wherein the insulating layer has excellent wet adhesion in an electrolyte to prevent the movement of lithium ions in the overlay region of an electrode, thereby suppressing the occurrence of capacity.

Description

Positive electrode for lithium secondary battery including an insulating layer having excellent wet adhesion and lithium secondary battery including the same

The present invention relates to a positive electrode for a lithium secondary battery including an insulating layer having excellent wet adhesion, a manufacturing method thereof, and a lithium secondary battery including the same.

As technology development and demand for mobile devices increase, the demand for secondary batteries as an energy source is rapidly increasing, and accordingly, a lot of research is being conducted on batteries that can meet various needs.

Typically, in terms of battery shape, there is a high demand for prismatic batteries and pouch-type batteries that can be applied to products such as mobile phones with thin thickness, and in terms of materials, lithium such as lithium cobalt polymer batteries with excellent energy density, discharge voltage, and safety. Demand for secondary batteries is high.

One of the main research tasks in these secondary batteries is to improve safety. The main cause of accidents related to battery safety is due to the arrival of an abnormal high temperature state due to a short circuit between an anode and a cathode. That is, under normal circumstances, a separator between the positive electrode and the negative electrode is positioned to maintain electrical insulation, but the battery causes overcharging or overdischarging, dendritic growth of the electrode material or internal short-circuit caused by foreign substances, or Existing separators have limitations in abnormal situations, such as when a sharp object such as a screw or a screw penetrates a battery or when excessive deformation is applied to the battery due to an external force.

In general, a microporous membrane made of polyolefin resin is mainly used as a separation membrane, but its heat resistance temperature is about 120 to 160° C., which is insufficient in heat resistance. Therefore, when an internal short circuit occurs, there is a problem in that the separator shrinks due to short reaction heat, and the short circuit part expands, leading to a thermal runaway state in which a larger and larger reaction heat is generated. Since this phenomenon mainly occurs at the electrode active material coated end of the electrode current collector coated with the electrode active material when electrodes are stacked, various methods have been tried to reduce the possibility of short circuit of the electrode under external shock or high temperature.

Specifically, in order to solve the internal short circuit of the battery, a method of forming an insulating layer by attaching an insulating tape to the uncoated portion of the electrode and a part of the active material layer or coating an insulating liquid has been proposed. For example, there is a method of applying an insulating binder to the uncoated portion of the positive electrode and a part of the active material layer, or coating an insulating liquid obtained by dispersing a mixture of the binder and inorganic particles in a solvent (hereinafter referred to as an insulating layer).

On the other hand, the electrodes in the actual secondary battery exist in a state of being impregnated with an electrolyte solution, but the conventional insulating layer has reduced adhesive strength (hereinafter referred to as wet adhesive force) in a state of being impregnated with an electrolyte solution, so that the overlay area of the electrode There was a problem in that the movement of lithium ions could not be prevented, and thus the capacity was expressed (see FIG. 1). In particular, lithium ions may be precipitated when capacity is developed in the overlay region of the electrode, which may cause a decrease in stability of the battery cell.

Therefore, it is necessary to develop an insulating layer having excellent wet adhesion.

Republic of Korea Patent Publication No. 10-2019-0093524

Accordingly, an object of the present invention is to provide a positive electrode for a lithium secondary battery including an insulating layer having excellent wet adhesion, a manufacturing method thereof, and a lithium secondary battery including the same.

In order to solve the above problems, the present invention in one embodiment, the current collector; An active material layer formed on one side or both sides of the current collector and including a positive electrode active material, a conductive material, and a non-aqueous binder; and an insulating layer positioned on a side surface of the active material layer. In addition, the insulating layer is formed of an aqueous binder substituted with a non-aqueous solvent.

In one embodiment, the insulating layer is positioned on the current collector and has a structure formed to cover a partial area of the active material layer applied to the current collector from a partial area of the current collector uncoated portion.

In one specific embodiment, the insulating layer is located on the current collector, has a structure formed to cover a portion of the sliding area of the active material layer applied to the current collector from a partial region of the current collector uncoated portion, and the height of the insulating layer is the active material layer. It ranges from 10 to 50% of the height.

In another embodiment, the insulating layer is located on the current collector, and has a structure formed to cover a portion of the sliding area of the active material layer applied to the current collector from a partial region of the current collector uncoated portion, and the height of the insulating layer is formed of the active material. It ranges from 50 to 100% of the layer height.

For example, the thickness of the insulating layer ranges from 1 μm to 50 μm on average.

In one embodiment, the insulating layer further includes inorganic particles dispersed in an aqueous binder substituted with a non-aqueous solvent. In addition, the weight ratio of the inorganic particles and the aqueous binder ranges from 1:99 to 95:5.

The inorganic particles include AlOOH, Al ₂ O ₃ , γ-AlOOH, Al(OH) ₃ , Mg(OH) ₂ , Ti(OH) ₄ , MgO, CaO, Cr ₂ O ₃ , MnO ₂ , selected from the group consisting of Fe ₂ O ₃ , Co ₃ O ₄ , NiO, ZrO ₂ , BaTiO ₃ , SnO ₂ , CeO ₂ , Y ₂ O ₃ , SiO ₂ , silicon carbide (SIC) and boron nitride (BN); It may be one or more.

In addition, the aqueous binder, styrene-butadiene rubber, acrylate styrene-butadiene rubber, acrylonitrile-butadiene rubber, acrylonitrile-butadiene-styrene rubber, acrylic rubber, butyl rubber, fluororubber, polytetrafluoroethylene, Polyethylene, polypropylene, ethylene propylene copolymer, polyethylene oxide, polyvinylpyrrolidone, polyepicrohydrin, polyphosphazene, polyacrylonitrile, polystyrene, ethylenepropylenediene copolymer, polyvinylpyridine, chloro It may be at least one selected from the group consisting of sulfonated polyethylene, latex, polyester resin, acrylic resin, phenol resin, epoxy resin, polyvinyl alcohol, hydroxypropylmethylcellulose, hydroxypropylcellulose, and diacetylcellulose.

In addition, the non-aqueous binder of the active material layer is polyvinylidene fluoride (PVDF), polyvinylidene fluoride-co-hexafluoropropene (PVDF-co-HFP, Poly (vinylidene fluoride-co-hexafluoropropene)) , poly(ethylene oxide) ((PEO, Poly(ethylene oxide)), polyacrylic acid (PAA), polyimide (PI), polyamideimide (PAI) and polyimide-polyamideimide copolymer (PI-PAI). It may be one or more selected from the group consisting of.

In a specific example, the non-aqueous binder may be polyvinylidene fluoride (PVDF). In addition, the aqueous binder may be an aqueous binder substituted with a non-aqueous organic solvent, for example, styrene-butadiene rubber substituted with an N-methyl-2-pyrrolidone solvent.

Meanwhile, in one embodiment of the present invention, the insulating layer may also include a non-aqueous binder and an aqueous binder substituted with a non-aqueous solvent. For example, the insulating layer may have a composition in which an aqueous binder and a non-aqueous binder are mixed in a weight ratio of 20:80 to 80:20 or 40:60 to 60:40 in weight ratio.

Furthermore, the present invention provides a lithium secondary battery including the positive electrode for a secondary battery described above.

A positive electrode for a lithium secondary battery including an insulating layer having excellent wet adhesiveness according to the present invention and a lithium secondary battery including the same, wherein the insulating layer has excellent wet adhesiveness in an electrolyte solution to prevent the movement of lithium ions in the overlay region of the electrode, thereby reducing the capacity It has the advantage of being able to inhibit expression and the like.

1 is a diagram schematically showing the movement of lithium ions in an overlay region of an electrode.
2 is a flow chart showing a manufacturing method of a cathode for a lithium secondary battery according to the present invention.
Figure 3 is a view showing the results of measuring the wet adhesion of the insulating layer of Examples and Comparative Examples.
4 is a graph in which discharge capacities are measured to evaluate the capacity development of the battery cells of Examples 4 to 6 (room temperature discharge characteristics).
5 is a graph in which discharge capacities are measured to evaluate the capacity development of the battery cells of Examples 4 to 6 (high temperature discharge characteristics).

Since the present invention can have various changes and various embodiments, specific embodiments will be described in detail in the detailed description.

However, this is not intended to limit the present invention to specific embodiments, and should be understood to include all modifications, equivalents, and substitutes included in the spirit and scope of the present invention.

In the present invention, the term "comprises" or "has" is intended to designate that there is a feature, number, step, operation, component, part, or combination thereof described in the specification, but one or more other features It should be understood that the presence or addition of numbers, steps, operations, components, parts, or combinations thereof is not precluded.

Further, in the present invention, when a part such as a layer, film, region, plate, etc. is described as being “on” another part, this includes not only the case where it is “directly on” the other part, but also the case where another part is present in the middle thereof. . Conversely, when a part such as a layer, film, region, plate, or the like is described as being “under” another part, this includes not only being “directly under” the other part, but also the case where there is another part in the middle. In addition, in the present application, being disposed "on" may include the case of being disposed not only on the upper part but also on the lower part.

In the present invention, "insulating layer" means an insulating member formed by coating and drying from at least a portion of the uncoated portion of the current collector to at least a portion of the electrode active material layer.

In the present invention, "wet adhesive strength" means the adhesive strength of the insulating layer measured in the state impregnated in the electrolyte solution. More specifically, the wet adhesion may be measured by immersing a metal specimen on which an insulating layer is formed in an electrolyte solution, applying ultrasonic waves, and checking whether swelling or detachment of the insulating layer occurs.

In the present invention, the term "metal specimen" is a space in which an insulating layer is formed, and may mean a metal current collector used in manufacturing an electrode, and may be a metal current collector punched out to have a predetermined width and a predetermined length. For example, the metal specimen may be aluminum, copper or an aluminum alloy.

In the present invention, the term "overlay area" may refer to an area in which an insulating layer is formed in an electrode. More specifically, the insulating layer covers from at least a portion of the non-coated portion of the electrode on which the active material layer is formed to at least a portion of the active material layer, and a region where the insulating layer is formed in the active material layer may be referred to as an overlay region.

Hereinafter, the present invention will be described in more detail.

Cathode for lithium secondary battery

In one embodiment, the present invention includes a current collector; An active material layer formed on one side or both sides of the current collector and including a positive electrode active material, a conductive material, and a non-aqueous binder; and an insulating layer positioned on a side surface of the active material layer.

In addition, the insulating layer is formed of an aqueous binder substituted with a non-aqueous solvent. In the present invention, the insulating layer can be stably applied even to an anode vulnerable to moisture through replacement of a non-aqueous solvent while increasing wet adhesion by applying an aqueous binder when forming the insulating layer.

The electrode for a secondary battery according to the present invention includes an insulating layer having excellent wet adhesion, and thus has an advantage of preventing the movement of lithium ions in the overlay region of the electrode and suppressing the occurrence of capacity.

In general, the positive electrode in a secondary battery exists in a state of being impregnated with an electrolyte solution, and the conventional insulating layer has reduced wet adhesion in the state of being impregnated with an electrolyte solution, so that it cannot prevent the movement of lithium ions in the overlay region of the positive electrode, thereby reducing the capacity. There was a problem manifesting this. In particular, lithium ions may be precipitated when capacity is developed in the overlay region of the positive electrode, which may cause a decrease in stability of the battery cell. In the present invention, when manufacturing a positive electrode of a secondary battery, an insulating layer is formed using an aqueous binder substituted with a non-aqueous solvent that is the same as the solvent of the positive electrode slurry, thereby suppressing gelation due to a difference in the type of binder between the active material layer and the coating layer. In particular, the insulating layer is dried simultaneously with the solvent of the positive electrode slurry in the drying step, thereby preventing cracks between the active material layer and the insulating layer due to a drying speed or temperature difference.

In addition, the insulating layer has an effect of increasing electrical insulation and thermal safety and suppressing thermal expansion by further including inorganic particles.

On the other hand, the wet adhesion of the insulating layer can be measured by immersing the metal specimen on which the insulating layer is formed in an electrolyte solution, applying ultrasonic waves, and then checking whether the insulating layer formed on the metal specimen has swelling or detachment.

An electrolyte solution used in measuring the wet adhesion may include an organic solvent and an electrolyte salt, and the electrolyte salt may be a lithium salt. As the lithium salt, those commonly used in non-aqueous electrolytes for lithium secondary batteries may be used without limitation. For example, the anion of the lithium salt is F ^- , Cl ^- , Br ^- , I ^- , NO ₃ ^- , N(CN) ₂ ^- , BF ₄ ^- , ClO ₄ ^- , PF ₆ ^- , (CF ₃ ) ₂ PF ₄ ^- , (CF ₃ ) ₃ PF ₃ ^- , (CF ₃ ) ₄ PF ₂ ^- , (CF ₃ ) ₅ PF ^- , (CF ₃ ) ₆ P ^- , CF ₃ SO ₃ ^- , CF ₃ CF ₂ SO ₃ ^- , (CF ₃ SO ₂ ) ₂ N ^- , (FSO ₂ ) ₂ N ^- , CF ₃ CF ₂ (CF ₃ ) ₂ CO ^- , (CF ₃ SO ₂ ) ₂ CH ^- , (SF ₅ ) ₃ C ^- , CF ₃ (CF ₂ ) ₇ SO ₃ ^- , CF ₃ CO ₂ ^- , CH ₃ CO ₂ ^- , SCN ^- and (CF ₃ CF ₂ SO ₂ ) ₂ N ^- any one or two or more selected from the group consisting of can include

As the organic solvent included in the above-described electrolyte solution, those commonly used in electrolyte solutions for lithium secondary batteries may be used without limitation. and can be used. Among them, cyclic carbonates, linear carbonates, or mixtures of these carbonate compounds may be typically included.

In the positive electrode for a lithium secondary battery according to the present invention, the insulating layer may include an aqueous binder.

In specific examples, the water-based binder is styrene-butadiene rubber, acrylate styrene-butadiene rubber, acrylonitrile-butadiene rubber, acrylonitrile-butadiene-styrene rubber, acrylic rubber, butyl rubber, fluororubber, polytetrafluoroethylene, Polyethylene, polypropylene, ethylene propylene copolymer, polyethylene oxide, polyvinylpyrrolidone, polyepicrohydrin, polyphosphazene, polyacrylonitrile, polystyrene, ethylenepropylenediene copolymer, polyvinylpyridine, chloro It may be at least one selected from the group consisting of sulfonated polyethylene, latex, polyester resin, acrylic resin, phenol resin, epoxy resin, polyvinyl alcohol, hydroxypropylmethylcellulose, hydroxypropylcellulose, and diacetylcellulose. In a specific example, the aqueous binder may be at least one selected from the group consisting of styrene-butadiene rubber, acrylate styrene-butadiene rubber, acrylonitrile-butadiene rubber, and acrylonitrile-butadiene-styrene rubber. For example, the water-based binder may be styrene-butadiene rubber.

Conventionally, polyvinylidene fluoride (hereinafter referred to as PVDF) has been used as a binder for the insulating layer of the anode, but it has a problem of deterioration in wet adhesion when impregnated with an electrolyte. Accordingly, in the present invention, styrene-butadiene rubber may be used as a binder polymer. Meanwhile, when styrene-butadiene rubber is used as the polymer binder, water may be used as a solvent. However, in this case, when the insulating composition and the positive electrode slurry are simultaneously coated, the difference in binder type between the insulating composition and the positive electrode slurry causes Gelation may occur.

In a specific example, the aqueous binder may be an aqueous binder substituted with a non-aqueous organic solvent. Here, the non-aqueous organic solvent is N-methyl-pyrrolidone (NMP), dimethylformamide (DMF) and dimethylacetamide (DMAc), dimethyl sulfoxide (DMSO), ethylene carbonate (EC), diethyl carbonate (DEC), Ethylmethylcarbonate (EMC), Dimethylcarbonate (DMC), Propylene Carbonate (PC), Dipropylcarbonate (DPC), Butyrene Carbonate (BC), Methylpropyl Carbonate (MPC), Ethylpropyl Carbonate (EPC) , Acetonitrile, Dimethoxyethane, Tetrahydrofuran (THF), γ-butyrolactone, methyl alcohol, ethyl alcohol, isopropyl alcohol alcohol) may be one or more selected from the group consisting of.

For example, the aqueous binder may be styrene-butadiene rubber substituted with NMP solvent. More specifically, an insulating layer may be formed by applying an insulating composition to cover at least a portion of the active material layer from at least a portion of the uncoated portion, and then drying the composition at a temperature of about 50 to 300° C. In this case, the insulating layer may be a styrene-butadiene rubber in which the solvent is removed during the drying process and the styrene-butadiene rubber dispersed in the solvent is substituted with the NMP.

In addition, since the insulating layer includes inorganic particles, the safety of the battery can be improved and the strength of the insulating layer can also be improved. The amount of the inorganic particles may be appropriately adjusted in consideration of viscosity, heat resistance, insulation, filling effect, dispersibility or stability of the insulating composition. In general, as the size of the inorganic particles increases, the viscosity of a composition including the inorganic particles increases, and the possibility of sedimentation in the insulating composition increases. Also, as the size becomes smaller, the thermal resistance tends to increase. Accordingly, inorganic particles of an appropriate type and size may be selected in consideration of the above points, and two or more types of inorganic particles may be used together if necessary.

In a specific example, the inorganic particles of the insulating layer are AlOOH, Al ₂ O ₃ , γ-AlOOH, Al(OH) ₃ , Mg(OH) ₂ , Ti(OH) ₄ , MgO, CaO, Cr ₂ O ₃ , group consisting of MnO ₂ , Fe ₂ O ₃ , Co ₃ O ₄ , NiO, ZrO ₂ , BaTiO ₃ , SnO ₂ , CeO ₂ , Y ₂ O ₃ , SiO ₂ , silicon carbide (SIC) and boron nitride (BN) It may be one or more selected from AlOOH, Al ₂ O ₃ , γ-AlOOH and Al (OH) ₃ It may be one or more selected from the group consisting of. For example, the inorganic particles may be AlOOH.

The weight ratio of the inorganic particles and the aqueous binder may range from 1:99 to 95:5, or from 10:90 to 70:30; It may be 20:80 to 60:40, or 40:60 to 60:40. For example, the weight ratio of the inorganic particles and the aqueous binder in the insulating composition may be 50:50. On the other hand, if the content of the aqueous binder is too small, it may be difficult to exhibit the desired insulating effect in the present invention, and the adhesive force with the electrode may be weakened. In addition, when the content of the water-based binder is too large, the insulating composition may flow down in the overlay region during coating of the electrode, which may cause a decrease in safety of the battery cell.

The average particle diameter of the inorganic particles may be 0.1 μm to 100 μm, 0.5 μm to 80 μm, 1 μm to 50 μm; 2 μm to 30 μm; It may be 3 μm to 20 μm or 5 μm to 10 μm. When the size of the inorganic particles is within the above range, the electrode may be uniformly coated, and the performance of the lithium secondary battery may be secured by minimizing lithium ion resistance.

In another example, the insulating composition may include first and second inorganic particles having different particle sizes, but may have a bimodal particle size distribution. This means that the inorganic particles are mixed with the elementary particles and the opposite, the empty space between the first inorganic particles of the opposite can be filled with the second inorganic particles of the elementary particles, and an appropriate amount of inorganic particles can be dispersed. . However, it is not limited thereto.

On the other hand, the thickness of the insulating layer may be determined in the range of 0.2 ㎛ to 100 ㎛, specifically, may be 1 ㎛ to 50 ㎛, more specifically, 1 ㎛ to 30 ㎛; 2 μm to 30 μm; 3 μm to 20 μm; Or it may be 5 μm to 15 μm. When the thickness of the coating portion is too thin, it may be difficult to expect an effect for improving safety due to the application of the insulating layer.

Furthermore, the active material layer may include a cathode active material. In a specific example, as the cathode active material, all commonly used cathode active materials may be used, and lithium manganese oxide, lithium cobalt oxide, lithium nickel oxide, lithium iron oxide, or a lithium composite oxide obtained by combining these may be used, but is not limited thereto. don't

In addition, the content of the cathode active material may be 85 to 95 parts by weight, specifically 88 to 95 parts by weight, 90 to 95 parts by weight, 86 to 90 parts by weight, or 92 to 95 parts by weight based on 100 parts by weight of the active material layer. can

At this time, the conductive material may be used to improve performance such as electrical conductivity of the anode, and at least one selected from the group consisting of natural graphite, artificial graphite, carbon black, acetylene black, ketjen black, and carbon fiber may be used. . For example, the conductive material may include acetylene black.

In addition, the conductive material may be included in 1 to 10 parts by weight based on 100 parts by weight of the active material layer, specifically 2 to 8 parts by weight; or 2 to 6 parts by weight.

In addition, the binder is polyvinylidene fluoride-hexafluoropropylene copolymer (PVDF-co-HFP), polyvinylidene fluoride, polyacrylonitrile, polymethylmethacrylate and at least one resin selected from the group consisting of copolymers thereof. As one example, the binder may include polyvinylidenefluoride.

In addition, the binder may be included in an amount of 1 to 10 parts by weight, specifically 2 to 8 parts by weight, based on 100 parts by weight of the active material layer; or 2 to 6 parts by weight.

In addition, the average thickness of the active material layer is not particularly limited, but may be specifically 0.1 μm to 20 μm, more specifically 0.1 μm to 15 μm; 0.1 μm to 10 μm; 2 μm to 10 μm; 4 μm to 10 μm; Or it may be 5 μm to 9 μm.

On the other hand, the positive electrode for a lithium secondary battery according to the present invention can be used as a current collector that has high conductivity without causing chemical change in the battery. For example, stainless steel, aluminum, nickel, titanium, calcined carbon, etc. may be used, and aluminum or stainless steel may be surface-treated with carbon, nickel, titanium, silver, or the like. In addition, the current collector may form fine irregularities on the surface to increase the adhesion of the positive electrode active material, and various forms such as films, sheets, foils, nets, porous materials, foams, and nonwoven fabrics are possible. In addition, the average thickness of the current collector may be appropriately applied in the range of 3 to 500 μm in consideration of the conductivity and total thickness of the anode to be manufactured.

Manufacturing method of positive electrode for lithium secondary battery

In one embodiment, the present invention includes applying a positive electrode slurry including a positive electrode active material, a conductive material, and a non-aqueous binder to one or both surfaces of a current collector; applying an insulating composition including an aqueous binder substituted with a non-aqueous solvent to cover a portion of the positive electrode slurry applied to the current collector from at least a portion of the uncoated portion of the current collector; and drying the positive electrode slurry and the insulating composition applied to the current collector. In addition, the positive electrode slurry and the insulating composition contain the same non-aqueous solvent.

2 is a flowchart of a method for manufacturing a positive electrode for a lithium secondary battery according to the present invention. Referring to FIG. 2, in the method of manufacturing a positive electrode for a lithium secondary battery according to the present invention, a positive electrode slurry is applied to one or both surfaces of a current collector, and a portion of the positive electrode slurry applied to the current collector from at least a part of the uncoated portion of the current collector An insulating composition may be applied to cover. Meanwhile, the insulating composition may be applied while the positive electrode slurry is not dried. Here, "undried" may mean a slurry in a state that has not undergone a separate drying process in a drying device or equipment. And, in the present invention, a step of drying the positive electrode slurry and the insulating composition applied to the current collector may be included. In particular, according to the method for manufacturing a positive electrode for a lithium secondary battery according to the present invention, the positive electrode slurry and the insulating composition applied to the current collector are simultaneously dried to increase the adhesive strength between the positive electrode active material and the insulating layer, thereby reducing the interface resistance, It is possible to form a dense insulating layer in which problems in mechanical properties such as brittleness are improved. In addition, the efficiency of the manufacturing process of the positive electrode can be increased.

Meanwhile, in the method for manufacturing a positive electrode for a lithium secondary battery according to the present invention, the positive electrode slurry and the insulating composition are characterized in that they contain the same non-aqueous organic solvent. When the same solvent is used for the positive electrode slurry and the insulating composition, problems such as gelation of heterogeneous binders and generation of cracks during drying due to a difference in boiling point may be solved.

The non-aqueous organic solvent is N-methyl-pyrrolidone (NMP), dimethylformamide (DMF) and dimethylacetamide (DMAc), dimethyl sulfoxide (DMSO), ethylene carbonate (EC), diethyl carbonate (DEC ), ethyl methyl carbonate (EMC), dimethyl carbonate (DMC), propylene carbonate (PC), dipropyl carbonate (DPC), butyrene carbonate (BC), methylpropyl carbonate (MPC), ethylpropyl carbonate (EPC), aceto Acetonitrile, Dimethoxyethane, Tetrahydrofuran (THF), γ-butyrolactone, methyl alcohol, ethyl alcohol, isopropyl alcohol It may be one or more selected from the group consisting of.

In a specific example, the non-aqueous organic solvent is at least one selected from the group consisting of N-methyl-pyrrolidone (NMP), dimethylformamide (DMF), dimethylacetamide (DMAc), and dimethyl sulfoxide (DMSO). It may be at least one selected from the group consisting of N-methyl-pyrrolidone (NMP), dimethylformamide (DMF), and dimethylacetamide (DMAc).

For example, the non-aqueous organic solvent may be an amide-based organic solvent, and the same solvent as the solvent used in preparing the cathode slurry may be used, and the non-aqueous organic solvent may be N-methyl-pyrrolidone (NMP). can

When NMP is used as the solvent of the positive electrode slurry, the solvent of the insulating composition may be NMP. In particular, NMP is used as the solvent of the insulating composition to prevent the occurrence of the Cracks can be prevented. The insulation composition for an electrode of a secondary battery according to the present invention may be coated and dried simultaneously with the cathode slurry. In particular, in the drying process, NMP may be used as a substitution solvent.

A method for manufacturing a cathode for a lithium secondary battery according to the present invention is described in detail as follows.

Applying a cathode slurry to one side or both sides of the current collector (S10)

A method of manufacturing a positive electrode for a lithium secondary battery according to the present invention includes applying a positive electrode slurry to one side or both sides of a current collector.

At this time, as the current collector, a positive electrode for a lithium secondary battery according to the present invention may be used as a current collector that has high conductivity without causing chemical change in the battery. For example, stainless steel, aluminum, nickel, titanium, calcined carbon, etc. may be used, and aluminum or stainless steel may be surface-treated with carbon, nickel, titanium, silver, or the like. For example, the current collector may be aluminum.

In addition, in the slurry for the positive electrode active material, all positive electrode active materials commonly used in positive electrodes can be used as the positive electrode active material, and lithium manganese oxide, lithium cobalt oxide, lithium nickel oxide, lithium iron oxide, or a combination of these lithium composite oxides may be used, but is not limited thereto.

The non-aqueous binder included in the slurry for the cathode active material is polyvinylidene fluoride-hexafluoropropylene copolymer (PVDF-co-HFP), polyvinylidenefluoride, polyacrylonitrile, poly It may include one or more resins selected from the group consisting of methyl methacrylate (polymethylmethacrylate) and copolymers thereof. As one example, the binder may include polyvinylidenefluoride.

At this time, the conductive material may be used to improve performance such as electrical conductivity of the anode, and at least one selected from the group consisting of natural graphite, artificial graphite, carbon black, acetylene black, ketjen black, and carbon fiber may be used. . For example, the conductive material may include acetylene black.

Furthermore, the solvent used in the positive electrode slurry is a non-aqueous organic solvent, N-methyl-pyrrolidone (NMP), dimethylformamide (DMF) and dimethylacetamide (DMAc), dimethyl sulfoxide (DMSO), ethylene carbonate ( EC), diethyl carbonate (DEC), ethyl methyl carbonate (EMC), dimethyl carbonate (DMC), propylene carbonate (PC), dipropyl carbonate (DPC), butyrene carbonate (BC), methylpropyl carbonate (MPC), Ethylpropyl Carbonate (EPC), Acetonitrile, Dimethoxyethane, Tetrahydrofuran (THF), γ-butyrolactone, Methyl Alcohol, Ethyl Alcohol , isopropyl alcohol (isopropyl alcohol) may be at least one selected from the group consisting of, for example, it may be N-methyl-2-pyrrolidone (NMP).

Applying an insulating composition to cover a portion of the positive electrode slurry applied to the current collector from at least a portion of the uncoated portion of the current collector (S20)

In the method of manufacturing a positive electrode for a lithium secondary battery according to the present invention, an insulating composition containing inorganic particles and a water-based binder may be applied to cover a portion of the positive electrode slurry applied to the current collector from at least a portion of the uncoated portion of the current collector.

At this time, the cathode slurry may be in an undried state. Here, "undried" may mean a slurry in a state that has not undergone a separate drying process in a drying device or equipment.

In this case, the insulating composition may provide excellent wet adhesion by including inorganic particles and a water-based binder. Accordingly, it is possible to suppress the movement of lithium ions in the overlay region of the positive electrode and prevent the precipitation of lithium ions.

lithium secondary battery

In addition, the present invention, in one embodiment,

Provided is a lithium secondary battery including the positive electrode for a lithium secondary battery according to the present invention described above.

The lithium secondary battery according to the present invention may include the positive electrode, the negative electrode, and the separator positioned between the positive electrode and the negative electrode.

In particular, the lithium secondary battery according to the present invention has an advantage in that the insulating layer has excellent wet adhesion in the electrolyte solution, so that the movement of lithium ions in the overlay region of the electrode can be prevented, thereby suppressing capacity development. Accordingly, the lithium secondary battery according to the present invention can improve stability.

Here, the negative electrode may include a negative electrode current collector and a negative electrode active material layer disposed on the negative electrode current collector and containing an negative electrode active material. Specifically, the anode is manufactured by applying, drying, and pressing an anode active material on an anode current collector, and, if necessary, the above-described conductive material, organic binder polymer, filler, and the like may be optionally further included.

In addition, the negative electrode active material has a complete layered crystal structure, such as natural graphite.

graphite, soft carbon having a low-crystalline graphene structure (a structure in which hexagonal honeycomb planes of carbon are arranged in layers) and such a structure

carbon and graphite materials such as hard carbon, artificial graphite, expanded graphite, carbon fiber, non-graphitizable carbon, carbon black, carbon nanotube, fullerene, activated carbon, etc., in which they are mixed with amorphous portions; Li _x Fe ₂ O ₃ (0≤x≤1), Li _x WO ₂ (0≤x≤1), Sn _x Me _1-x Me' _y O _z (Me: Mn, Fe, Pb, Ge; Me' , Al, B, P, Si, elements of groups 1, 2 and 3 of the periodic table, halogens; 0<x≤1;1≤y≤3;1≤z≤8); lithium metal; lithium alloy; silicon-based alloys; tin-based alloys; SnO, SnO ₂ , PbO, PbO ₂ , Pb ₂ O ₃ , Pb ₃ O ₄ , Sb ₂ O ₃ , Sb ₂ O ₄ , Sb ₂ O ₅ , GeO, GeO ₂ , Bi ₂ O ₃ , Bi ₂ O ₄ and metal oxides such as Bi ₂ O ₅ ; conductive polymers such as polyacetylene; Li-Co-Ni-based materials; titanium oxide; Lithium titanium oxide and the like can be used.

As an example, the negative electrode active material may include both graphite and silicon (Si)-containing particles, and the graphite may include at least one of natural graphite having a layered crystal structure and artificial graphite having an isotropic structure. The silicon (Si)-containing particles are particles containing silicon (Si) as a main component as a metal component, silicon (Si) particles, silicon oxide (SiO ₂ ) particles, or the silicon (Si) particles and oxides. It may include a mixture of silicon (SiO2) particles.

In this case, the anode active material may include 80 to 95 parts by weight of graphite based on 100 parts by weight of the total; and 1 to 20 parts by weight of silicon (Si)-containing particles. The present invention can improve the charging capacity per unit mass while reducing lithium consumption and irreversible capacity loss during initial charging and discharging of the battery by adjusting the content of graphite and silicon (Si)-containing particles included in the negative electrode active material within the above ranges. there is.

In addition, the negative electrode active material layer may have an average thickness of 100 μm to 200 μm, specifically 100 μm to 180 μm; 100 μm to 150 μm; 120 μm to 200 μm; It may have an average thickness of 140 μm to 200 μm or 140 μm to 160 μm.

In addition, the anode current collector is not particularly limited as long as it does not cause chemical change in the battery and has high conductivity. For example, copper, stainless steel, nickel, titanium, fired carbon, etc. may be used, and copper However, in the case of stainless steel, surface treatment with carbon, nickel, titanium, silver, etc. may be used.

In addition, like the positive electrode current collector, the negative electrode current collector may form fine irregularities on the surface to strengthen the bonding force with the negative electrode active material, and various forms such as films, sheets, foils, nets, porous bodies, foams, and nonwoven fabrics are available. possible. In addition, the average thickness of the negative electrode current collector may be appropriately applied in the range of 3 to 500 μm in consideration of the conductivity and total thickness of the negative electrode to be manufactured.

In addition, the separator is interposed between the anode and the cathode, and an insulating thin film having high ion permeability and mechanical strength is used. The separator is not particularly limited as long as it is commonly used in the art, but specifically, chemical resistant and hydrophobic polypropylene; glass fiber; Alternatively, a sheet or non-woven fabric made of polyethylene may be used. In some cases, a composite separator in which inorganic particles/organic particles are coated with an organic binder polymer may be used on a porous polymer substrate such as the sheet or non-woven fabric. When a solid electrolyte such as a polymer is used as the electrolyte, the solid electrolyte may serve as a separator. In addition, the separator may have an average pore diameter of 0.01 to 10 μm and an average thickness of 5 to 300 μm.

Meanwhile, the positive and negative electrodes may be rolled in a jelly roll form and stored in a cylindrical battery, prismatic battery, or pouch type battery, or may be stored in a pouch type battery in a folding or stack-and-folding form, but are not limited thereto.

In addition, the lithium salt-containing electrolyte solution according to the present invention may be composed of an electrolyte solution and a lithium salt, and a non-aqueous organic solvent, an organic solid electrolyte, an inorganic solid electrolyte, or the like may be used as the electrolyte solution.

As the non-aqueous organic solvent, for example, N-methyl-2-pyrrolidinone, ethylene carbonate, propylene carbonate, butylene carbonate, dimethyl carbonate, diethyl carbonate, gamma-butyrolactone, 1,2-dimethine Toxy ethane, tetrahydroxy franc, 2-methyl tetrahydrofuran, dimethyl sulfoxide, 1,3-dioxorane, formamide, dimethylformamide, dioxorane, acetonitrile, nitromethane, methyl formate, Methyl acetate, phosphoric acid triesters, trimethoxy methane, dioxolane derivatives, sulfolane, methyl sulfolane, 1,3-dimethyl-2-imidazolidinone, propylene carbonate derivatives, tetrahydrofuran derivatives, ether, propion An aprotic organic solvent such as methyl acid or ethyl propionate may be used.

Examples of the organic solid electrolyte include polyethylene derivatives, polyethylene oxide derivatives, polypropylene oxide derivatives, phosphoric acid ester polymers, poly agitation lysine, polyester sulfide, polyvinyl alcohol, polyvinylidene fluoride, ions A polymerizer containing a sexual dissociation group or the like can be used.

Examples of the inorganic solid electrolyte include Li ₃ N, LiI, Li ₅ Ni ₂ , Li ₃ N-LiI-LiOH, LiSiO ₄ , LiSiO ₄ -LiI-LiOH, Li ₂ SiS ₃ , Li ₄ SiO ₄ , Nitride, halide, sulfate, and the like of Li such as Li ₄ SiO ₄ -LiI-LiOH, Li ₃ PO ₄ -Li ₂ S-SiS ₂ , etc. may be used.

The lithium salt is a material that is easily soluble in non-aqueous electrolytes, for example, LiCl, LiBr, LiI, LiClO ₄ , LiBF ₄ , LiB10Cl ₁₀ , LiPF ₆ , LiCF ₃ SO ₃ , LiCF ₃ CO ₂ , LiAsF ₆ , LiSbF ₆ , LiAlCl ₄ , CH ₃ SO ₃ Li, (CF ₃ SO ₂ ) ₂ NLi, lithium chloroborane, lithium lower aliphatic carboxylic acid, lithium 4-phenylborate, imide and the like can be used.

In addition, for the purpose of improving charge and discharge characteristics, flame retardancy, etc. in the electrolyte solution, for example, pyridine, triethylphosphite, triethanolamine, cyclic ether, ethylene diamine, n-glyme, hexaphosphoric acid triamide, nitro Benzene derivatives, sulfur, quinone imine dyes, N-substituted oxazolidinones, N,N-substituted imidazolidines, ethylene glycol dialkyl ethers, ammonium salts, pyrrole, 2-methoxy ethanol, aluminum trichloride, etc. may be added. there is. In some cases, halogen-containing solvents such as carbon tetrachloride and ethylene trifluoride may be further included to impart incombustibility, and carbon dioxide gas may be further included to improve storage properties at high temperatures. Fluoro-Ethylene Carbonate (FEC) ), PRS (Propene sultone), etc. may be further included.

Meanwhile, in one embodiment, the present invention provides a battery module including the above-described secondary battery as a unit cell, and provides a battery pack including the battery module.

The battery pack can be used as a power source for medium or large sized devices requiring high temperature stability, long cycle characteristics, high rate characteristics, etc. Specific examples of such medium or large sized devices include a power tool powered by an omniscient motor and moving; electric vehicles, including electric vehicles (EVs), hybrid electric vehicles (HEVs), plug-in hybrid electric vehicles (PHEVs), and the like; electric two-wheeled vehicles including electric bicycles (E-bikes) and electric scooters (E-scooters); electric golf carts; A power storage system may be mentioned, and more specifically, a hybrid electric vehicle (HEV) may be cited, but is not limited thereto.

Further, the positive electrode and the negative electrode may be rolled in a jelly roll shape and stored in a cylindrical battery, prismatic battery, or pouch type battery, or stored in a pouch type in a folding or stack-and-folding shape. For example, the lithium secondary battery according to the present invention may be a pouch type battery.

As described above, the lithium secondary battery including the cathode active material according to the present invention may be used in a battery module or battery pack including a plurality of unit cells. Specifically, it is useful for portable devices such as mobile phones, notebook computers, digital cameras, and electric vehicles such as hybrid electric vehicles (HEVs).

Hereinafter, the present invention will be described in more detail by examples and experimental examples.

However, the following Examples and Experimental Examples are merely illustrative of the present invention, and the contents of the present invention are not limited to the following Examples and Experimental Examples.

Example 1.

N-methyl-2-pyrrolidone (NMP) solvent for 100 g of a state in which a styrene-butadiene rubber (hereinafter referred to as SBR, a product of ZEON's BM451B) binder is dispersed in water as a solvent at a ratio of 60: 40 (parts by weight) 500 g was added and stirred. Then, while heating the stirred mixture at 100 to 120 ° C. for 2 hours, the contained water was completely evaporated to prepare an NMP-substituted SBR binder. Then, an insulating composition was prepared by mixing and stirring the NMP-substituted SBR binder and the inorganic particles in a weight ratio of 50:50. The viscosity of the prepared insulating composition is 5,000 cP.

Examples 2-4, Comparative Examples 1-2.

An insulating coating solution was obtained in the same manner as in Example 1, except that the contents of the inorganic particles and the binder were changed when preparing the insulating composition.

Specific compositions of Examples 1 to 4 and Comparative Examples 1 to 2 are shown in Table 1 below.

division insulation composition menstruum inorganic particles bookbinder Inorganic particles:binder (weight ratio) Example 1 NMP AlOOH SBR 50:50 Example 2 NMP AlOOH SBR 60:40 Example 3 NMP AlOOH SBR 75:25 Example 4 NMP AlOOH SBR 80:20 Comparative Example 1 NMP AlOOH PVDF 80:20 Comparative Example 2 NMP AlOOH PVDF 88:12

Experimental Example 1. Measurement of Wet Adhesion of Insulation Layer

In order to evaluate the adhesive strength of the insulating layer according to the present invention, the following experiment was performed.

Metal specimen with insulating layer

The insulating compositions prepared in Examples 1-4 and Comparative Examples 1 and 2 were coated on aluminum metal foil and dried to prepare a metal specimen having an insulating layer having a thickness of about 10 μm. The metal specimen on which the insulating layer was formed was punched into a size of 2 cm × 2 cm using a punching machine for measuring adhesion.

ultrasonic application

200 g of electrolyte EC/EMC = 3/7 (vol.%) was put into a 250 ml beaker, and a metal specimen having an insulating layer was impregnated into the electrolyte. In order to control the movement of the metal specimen, the metal specimen was fixed with a jig.

In addition, ultrasonic waves were applied to the electrolyte solution impregnated with the metal specimen using an ultrasonic disperser (BANDELIN, 4200). At this time, the ultrasonic application conditions are as follows.

- Frequency: 20kHz

- Tip diameter: 13 mm (TS-113)

-Amplitude: 100%

(Peak-to-peak 132 ㎛ when using 13 mm tip)

And, the results are shown in Table 2 and FIG. 2 below.

division Example 1 Example 2 Example 3 Example 4 Comparative Example 1 Comparative Example 2 Furtherance AlOOH:SBR
=50:50 AlOOH:SBR
=60:40 AlOOH:SBR
=75:25 AlOOH:SBR
=80:20 AlOOH:PVDF
=80:20 AlOOH:PVDF
=88:12 time (minutes) 19 19 19 15 5 10 End temperature (℃) 109 109 109 100 71 87 Wet Adhesion Comparison No swelling and tally No swelling and tally No swelling and tally No swelling and tally swelling occurs Swelling and tally occur

2 is a view showing the results of measuring the wet adhesive strength of the insulating layers of Examples 1 and 4 and Comparative Examples 1-2.

Looking at Table 2 and FIG. 2, the electrode specimen of Example 1 did not have swelling or detachment in the insulating layer. However, in the case of Example 1, the boiling point of EMC was 107.5 ° C due to the temperature increase of the electrolyte solution by the application of ultrasonic waves, and the measurement environment was changed due to the evaporation of the solvent, and the measurement was stopped when the temperature reached 109 ° C.

In addition, in the case of Examples 2 and 3, although not shown in the photograph, swelling or detachment did not occur in the insulating layer in the electrode specimen as in Example 1. However, the boiling point of EMC was 107.5 ℃, the solvent evaporated and the measurement environment changed, so the measurement was stopped when it reached 109 ℃.

In the case of Example 4, no swelling or detachment occurred in the electrode specimen for 15 minutes after ultrasonic wave was applied to the electrolyte. However, although not disclosed in the drawings, swelling and detachment of the electrode specimen occurred when the temperature of the electrolyte solution reached 108° C. due to the continuous application of ultrasonic waves.

In addition, in the case of Comparative Examples 1 and 2, swelling and detachment occurred in the electrode specimen 5 minutes after ultrasonic wave was applied to the electrolyte.

Through this, it was confirmed that the insulating layer of Example had excellent wet adhesive strength compared to the insulating layer of Comparative Example 1-2.

Experimental Example 2. Capacity Expression Evaluation of Battery Cells

In order to evaluate the performance of the positive electrode including the insulating layer according to the present invention, capacity development was evaluated after manufacturing a half cell.

Manufacture of Half Cells

96 parts by weight of LiNi _0.8 Co _0.1 Mn _0.1 O ₂ as a cathode active material, 2 parts by weight of PVdF as a binder, and 2 parts by weight of carbon black as a conductive material were weighed and mixed in N-methylpyrrolidone (NMP) solvent to prepare a cathode slurry. . The slurry for the active material layer was applied to aluminum foil, dried, and then rolled to prepare a positive electrode having a positive electrode active material layer (average thickness: 130 μm).

And, after dip-coating the insulating coating solution obtained in Examples 1 to 3 on the positive electrode, it was dried in a convection oven (130 ° C.) to form an insulating layer having a thickness of 10 μm on the positive electrode. Coin-type half cells were fabricated using lithium foil as an anode and an electrolyte containing 1M LiPF ₆ in a solvent of EC:DMC:DEC=1:2:1.

insulation layer battery Example 1 Example 5 Example 2 Example 6 Example 3 Example 7

Discharge capacity measurement

The discharge characteristics of the batteries of Examples 5 to 7 were evaluated under the following conditions. In addition, the discharge characteristics were measured at room temperature (25° C.) and high temperature (45° C.), respectively.

- Discharge: 0.1C, 0.33C, 0.5C, 1.0C, 2.5, cut-off

On the other hand, in order to compare the capacity development of each battery, a battery cell including an electrode on which an insulating layer was not formed was used as Comparative Example 3. And, the results are shown in Table 4 and Figure 3, Table 5 and Figure 4.

division insulation composition Room temperature discharge rate (%) menstruum inorganic particles bookbinder Inorganic Particles: Binder
(weight ratio) 0.1C 0.33C 0.5C 1.0C Comparative Example 3 - - - - 100.00 100.00 100.00 100.00 Example 5 NMP AlOOH SBR 50:50 0.33 0.06 0.05 0.00 Example 6 NMP AlOOH SBR 60:40 0.60 0.09 0.05 0.03 Example 7 NMP AlOOH SBR 75:25 0.27 0.06 0.03 0.00

division insulation composition High temperature discharge rate (%) menstruum inorganic particles bookbinder Inorganic Particles: Binder
(weight ratio) 0.1C 0.33C 0.5C 1.0C Comparative Example 3 - - - - 100.00 100.00 100.00 100.00 Example 5 NMP AlOOH SBR 50:50 2.23 0.21 0.15 0.05 Example 6 NMP AlOOH SBR 60:40 1.41 0.18 0.15 0.03 Example 7 NMP AlOOH SBR 75:25 15.35 0.18 0.15 0.03

Referring to Tables 4 and 5 and FIGS. 3 and 4, in the case of Example 7 at high temperature discharge (45 ° C.), it was confirmed that some capacity was expressed at 0.1 C discharge, but the batteries of Examples 5 and 6 were room temperature There was little capacity development at discharge (25°C).

As a result, it seems that the insulating layer has excellent wet adhesion in the electrolyte to prevent the movement of lithium ions in the overlay region of the electrode and suppress the development of capacity during discharge. Accordingly, it seems that the lithium secondary battery according to the present invention can improve safety while suppressing capacity degradation due to an increase in cycles.

Although the above has been described with reference to preferred embodiments of the present invention, those skilled in the art or those having ordinary knowledge in the art do not deviate from the spirit and technical scope of the present invention described in the claims to be described later. It will be understood that various modifications and changes can be made to the present invention within the scope.

Therefore, the technical scope of the present invention is not limited to the contents described in the detailed description of the specification, but should be defined by the claims.

Claims (11)

current collector;
An active material layer formed on one side or both sides of the current collector and including a positive electrode active material, a conductive material, and a non-aqueous binder; and
Including an insulating layer located on the side of the active material layer,
The insulating layer is a cathode for a lithium secondary battery, characterized in that formed of an aqueous binder substituted with a non-aqueous solvent.
According to claim 1,
The insulating layer is located on the current collector, and has a structure formed to cover a partial region of the active material layer applied to the current collector from a partial region of the current collector uncoated portion.
According to claim 1,
The insulating layer is located on the current collector, and has a structure formed to cover a part of the sliding area of the active material layer applied to the current collector from a partial area of the current collector uncoated portion,
A positive electrode for a lithium secondary battery in which the formation height of the insulating layer ranges from 10 to 50% of the height of the active material layer.
According to claim 1,
The insulating layer is located on the current collector, and has a structure formed to cover a part of the sliding area of the active material layer applied to the current collector from a partial area of the current collector uncoated portion,
A positive electrode for a lithium secondary battery in which the formation height of the insulating layer ranges from 50 to 100% of the height of the active material layer.
According to claim 1,
A cathode for a lithium secondary battery having an average thickness of the insulating layer in the range of 1 μm to 50 μm.
According to claim 1,
The insulating layer is
Further comprising inorganic particles dispersed in an aqueous binder substituted with a non-aqueous solvent,
A positive electrode for a lithium secondary battery, characterized in that the weight ratio of the inorganic particles and the aqueous binder is in the range of 1:99 to 95:5.
According to claim 6,
Inorganic particles are AlOOH, Al ₂ O ₃ , γ-AlOOH, Al(OH) ₃ , Mg(OH) ₂ , Ti(OH) ₄ , MgO, CaO, Cr ₂ O ₃ , MnO ₂ , Fe ₂ O ₃ , Co ₃ O ₄ , NiO, ZrO ₂ , BaTiO ₃ , SnO ₂ , CeO ₂ , Y ₂ O ₃ , SiO ₂ , at least one lithium secondary selected from the group consisting of silicon carbide (SIC) and boron nitride (BN) Anode for battery.
According to claim 1,
The water-based binder is styrene-butadiene rubber, acrylate styrene-butadiene rubber, acrylonitrile-butadiene rubber, acrylonitrile-butadiene-styrene rubber, acrylic rubber, butyl rubber, fluororubber, polytetrafluoroethylene, polyethylene, poly Propylene, ethylene propylene copolymer, polyethylene oxide, polyvinyl pyrrolidone, polyepicrohydrin, polyphosphazene, polyacrylonitrile, polystyrene, ethylene propylene diene copolymer, polyvinylpyridine, chlorosulfonated polyethylene , Latex, polyester resin, acrylic resin, phenol resin, epoxy resin, polyvinyl alcohol, hydroxypropyl methyl cellulose, hydroxypropyl cellulose, and at least one selected from the group consisting of diacetyl cellulose positive electrode for lithium secondary battery.
According to claim 1,
The non-aqueous binder is polyvinylidene fluoride (PVDF), polyvinylidene fluoride-co-hexafluoropropene (PVDF-co-HFP, Poly(vinylidene fluoride-co-hexafluoropropene)), poly(ethylene oxide) 1 selected from the group consisting of ((PEO, Poly(ethylene oxide)), polyacrylic acid (PAA), polyimide (PI), polyamideimide (PAI) and polyimide-polyamideimide copolymer (PI-PAI) Cathode for lithium secondary battery with more than one species.
According to claim 1,
The non-aqueous binder is polyvinylidene fluoride (PVDF),
A positive electrode for a lithium secondary battery, characterized in that the water-based binder is a styrene-butadiene rubber substituted with N-methyl-2-pyrrolidone.
A lithium secondary battery comprising the cathode for a lithium secondary battery according to any one of claims 1 to 10.

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