Patent Application
20240014392
The present application claims priority to Korean Patent Application No. 10-2021-0002853 filed on Jan. 8, 2021 in the Republic of Korea, the disclosure of which is incorporated herein by reference.
The present disclosure relates to a positive electrode and a lithium secondary battery including the same. Particularly, the present disclosure relates to a positive electrode showing high initial efficiency and excellent quick charging performance, and a lithium secondary battery including the same.
As technical development and needs for mobile instruments have been increased, rechargeable secondary batteries that can be downsized and provided with high capacity have been increasingly in demand. In addition, among such secondary batteries, lithium secondary batteries having high energy density and operating voltage have been commercialized and used widely.
A lithium secondary battery has a structure including an electrode assembly having a positive electrode and a negative electrode, each of which includes an active material coated on an electrode current collector, and a porous separator interposed between both electrodes; and a lithium salt-containing electrolyte injected to the electrode assembly. The electrode is obtained by applying a slurry including an active material, a binder and a conductive material dispersed in a solvent to a current collector, followed by drying and pressing.
A lithium secondary battery is a secondary battery in which lithium ions participate in electric conduction between electrodes during charge/discharge, and shows higher energy density and a lower memory effect, as compared to the other secondary batteries, such as a nickel metal hydride battery or a nickel cadmium battery. Therefore, the use of such a lithium secondary battery has been extended from a compact power source for portable electronic devices, household electric instruments, or the like, to medium- or large-scale power sources for devices, such as electric power storage devices, UPS devices, electric power leveling devices, etc., or power sources for driving ships, railroad cars, hybrid vehicles, electric vehicles, etc., and there is a need for improvement of the performance of such a battery. For example, in the use for cars, such as hybrid vehicles or electric vehicles, there is a need for providing a secondary battery with high energy density in order to realize a long range of driving or with high output in order to improve acceleration response.
To realize a secondary battery for electric vehicles with high output and high energy density, a positive electrode having a high nickel (Ni) content has been used to obtain an electrode.
However, when using such a Ni-enriched positive electrode, the electrode affects a change in resistance depending on the state-of-charge (SOC) of a battery, as compared to a positive electrode having a low Ni content, and most secondary batteries show an increase in resistance. To solve the above-mentioned problem, there is still a need for studies of controlling the resistance of an electrode or cell through the structure of a positive electrode or the design of the composition of a positive electrode.
The present disclosure is designed to solve the problems of the related art, and therefore the present disclosure is directed to providing a positive electrode which prevents an increase in resistance at a low SOC during discharge, and a secondary battery including the same.
In one aspect of the present disclosure, there is provided a positive electrode according to any one of the following embodiments.
According to the first embodiment, there is provided a positive electrode including:
Li1+a[NixMnyCoz]M1tO2 [Chemical Formula 1]
Li1+b[NiuMnvCow]M2sO2 [Chemical Formula 2]
According to the second embodiment, there is provided the positive electrode as defined in the first embodiment, wherein the Ni content of the first positive electrode active material is 40-75 mol % based on the total transition metals of the first positive electrode active material, and the Ni content of the second positive electrode active material is 80-90 mol % based on the total transition metals of the second positive electrode active material.
According to the third embodiment, there is provided the positive electrode as defined in the first or the second embodiment, wherein the Ni content of the first positive electrode active material is 50-75 mol % based on the total transition metals of the first positive electrode active material, and the Ni content of the second positive electrode active material is 81-90 mol % based on the total transition metals of the second positive electrode active material.
According to the fourth embodiment, there is provided the positive electrode as defined in any one of the first to the third embodiments, wherein the Ni content of the first positive electrode active material is 65-70 mol % based on the total transition metals of the first positive electrode active material, and the Ni content of the second positive electrode active material is 86-90 mol % based on the total transition metals of the second positive electrode active material.
According to the fifth embodiment, there is provided the positive electrode as defined in any one of the first to the fourth embodiments, wherein the weight ratio of the lower layer region of the positive electrode active material layer to the upper layer region thereof is 20:80-80:20.
According to the sixth embodiment, there is provided a method for manufacturing a positive electrode, including the steps of:
Li1+a[NixMnyCoz]M1tO2 [Chemical Formula 1]
Li1+b[NiuMnvCow]M2sO2 [Chemical Formula 2]
According to the seventh embodiment, there is provided the method for manufacturing a positive electrode as defined in the sixth embodiment, wherein the Ni content of the first positive electrode active material is 40-75 mol % based on the total transition metals of the first positive electrode active material, and the Ni content of the second positive electrode active material is 80-90 mol % based on the total transition metals of the second positive electrode active material.
According to the eighth embodiment, there is provided the method for manufacturing a positive electrode as defined in the sixth or the seventh embodiment, wherein the Ni content of the first positive electrode active material is 50-75 mol % based on the total transition metals of the first positive electrode active material, and the Ni content of the second positive electrode active material is 81-90 mol % based on the total transition metals of the second positive electrode active material.
According to the ninth embodiment, there is provided the method for manufacturing a positive electrode as defined in any one of the sixth to the eighth embodiments, wherein the Ni content of the first positive electrode active material is 65-70 mol % based on the total transition metals of the first positive electrode active material, and the Ni content of the second positive electrode active material is 86-90 mol % based on the total transition metals of the second positive electrode active material.
According to the tenth embodiment, there is provided a lithium secondary battery including the positive electrode as defined in any one of the first to the fifth embodiments.
The positive electrode according to an embodiment of the present disclosure includes a positive electrode active material layer, which has a lower layer region facing the positive electrode current collector and containing a first positive electrode active material and a first binder polymer, and an upper layer region disposed on the lower layer region, wherein the Ni content of the second positive electrode active material in the upper layer region is controlled to be larger than the Ni content of the first positive electrode active material in the lower layer region. In this manner, it is possible to prevent an increase in resistance which may cause rapid degradation of output at a low SOC, and to provide a positive electrode and a secondary battery including the same with improved high-temperature cycle characteristics.
In addition, according to an embodiment of the present disclosure, the above-effects may be realized more predominantly in a high-loading positive electrode having a high coating amount of positive electrode active material. As a result, it is possible to realize a battery for electric vehicles (EV) having high capacity and high energy density.
The accompanying drawings illustrate a preferred embodiment of the present disclosure and together with the foregoing disclosure, serve to provide further understanding of the technical features of the present disclosure, and thus, the present disclosure is not construed as being limited to the drawing.
FIGURE is a graph illustrating the high-temperature capacity retention of the secondary battery according to each of Examples 1 and 2 and Comparative Examples 1 and 2, depending on cycle number.
Hereinafter, preferred embodiments of the present disclosure will be described in detail with reference to the accompanying drawings. Prior to the description, it should be understood that the terms used in the specification and the appended claims should not be construed as limited to general and dictionary meanings, but interpreted based on the meanings and concepts corresponding to technical aspects of the present disclosure on the basis of the principle that the inventor is allowed to define terms appropriately for the best explanation.
In one aspect of the present disclosure, there is provided a positive electrode including:
Li1+a[NixMnyCoz]M1tO2 [Chemical Formula 1]
Li1+b[NiuMnvCow]M2sO2 [Chemical Formula 2]
The present disclosure suggests a method for manufacturing a positive electrode by disposing two different types of positive electrode active materials having a different Ni content in the upper layer and lower layer of the positive electrode through a double layer (DLD) coating technology for a positive electrode, wherein the Ni content of the positive electrode active material in the upper layer is controlled to be larger than the Ni content of the positive electrode active material in the lower layer. The present disclosure is directed to controlling the resistance in a lower SOC region that may affect the output of a secondary battery by using the positive electrode.
In addition, the present disclosure shows a higher effect in a high-loading electrode having a high coating amount of positive electrode active material, and may be applied to the manufacture of a battery for electric vehicles (EV) having high capacity and high energy density. In general, a high-Ni positive electrode active material, i.e. a positive electrode active material having a high Ni content, refers to a positive electrode active material containing Ni at 80 mol % or more based on the total transition metals.
Such a high-Ni positive electrode active material undergoes a larger change in structure during charge/discharge and shows low structural stability, and thus is problematic in that it causes a rapid increase in resistance in a lower SOC region, resulting in degradation of output.
According to the present disclosure, a positive electrode active material having a low Ni content is disposed in the lower layer region of the bilayer-type positive electrode active material layer to increase the structural stability, thereby improving the problem of an increase in resistance.
According to an embodiment of the present disclosure, the first positive electrode active material may have a Ni content of 40-75 mol %, 50-75 mol %, 55-75 mol %, 60-75 mol %, 65-75 mol %, or 65-70 mol %, based on the total transition metals of the first positive electrode active material.
In addition, the second positive electrode active material may have a Ni content of 80-90 mol %, 81-90 mol %, 82-90 mol %, 84-90 mol %, or 86-90 mol %, based on the total transition metals of the second positive electrode active material.
Each of the first positive electrode active material and the second positive electrode active material may be primary particles, or secondary particles formed by agglomeration of primary particles through a granulation process.
In the particle size distribution, the first positive electrode active material may have an average particle diameter (D50) of 3-15 μm, particularly 5-12 μm, and more particularly 6-10 μm.
In addition, the second positive electrode active material may have a D50 of 5-20 μm, particularly 7-18 μm, and more particularly 10-15 μm.
As used herein, ‘particle diameter, Dn’ means a particle diameter corresponding to n % of the accumulated particle number distribution depending on particle diameter. Therefore, ‘D50’ means a particle diameter corresponding to 50% of the accumulated particle number distribution depending on particle diameter, ‘D90’ means a particle diameter corresponding to 90% of the accumulated particle number distribution depending on particle diameter, and ‘D10’ means a particle diameter corresponding to 10% of the accumulated particle number distribution depending on particle diameter.
In addition, Dn may be determined by using a laser diffraction method. Particularly, a powder to be analyzed is dispersed in a dispersion medium and introduced to a commercially available laser diffraction particle size analyzer (e.g. Microtrac S3500), and then a difference in diffraction pattern depending on particle size is determined, when particles pass through laser beams, and then a particle size distribution is calculated. Then, the particle diameter at each point of 10%, 50% and 90% of the accumulated particle number distribution depending on a particle diameter is calculated to determine each of D10, D50 and D90.
According to an embodiment of the present disclosure, the first positive electrode active material contained in the lower layer region of the positive electrode and the second positive electrode active material contained in the upper layer region thereof are different types of lithium oxide of nickel cobalt manganese active materials having a different Ni content, and thus an intermixing region in which such different types of active materials are mixed may be present at the portion where the lower layer region is in contact with the upper layer region. This is because when the slurry for a lower layer containing the first positive electrode active material and the slurry for an upper layer containing the second positive electrode active material are coated at the same time or continuously with a very short time interval and then dried at the same time to form an active material layer, a certain intermixing zone is generated at the interface where the slurry for a lower layer is in contact with the slurry for an upper layer before drying, and then the intermixing zone is formed in the shape of a layer of intermixing region, while the slurry for a lower layer and the slurry for an upper layer are dried subsequently.
According to an embodiment of the present disclosure, the weight ratio (ratio of loading amount per unit area) of the lower layer region to the upper layer region of the positive electrode active material layer may be 20:80-80:20, particularly 30:70-70:30. When the above-defined weight ratio is satisfied, the adhesion between the current collector and the positive electrode active material layer is enhanced, and excellent quick charging performance may be realized.
According to an embodiment of the present disclosure, the thickness ratio of the lower layer region to the upper layer region may be 20:80-80:20, particularly 30:70-70:30. When the above-defined thickness ratio is satisfied, the adhesion between the current collector and the positive electrode active material layer is enhanced, and excellent quick charging performance may be realized.
According to an embodiment of the present disclosure, the total thickness of the positive electrode active material layer is not particularly limited. For example, the positive electrode active material layer may have a total thickness of 40-200 μm. In addition, the lower layer region in the positive electrode active material layer may have a thickness of 20-150 μm, or 30-100 μm, and the upper layer region may have a thickness of 20-150 μm, or 30-100 μm.
When the thickness of the lower layer region and the upper layer region satisfies the above-defined range, the adhesion between the current collector and the positive electrode active material layer is enhanced, and excellent quick charging performance may be realized.
The weight percentage (wt %) of the first binder polymer in the lower layer region may be larger than the weight percentage (wt %) of the second binder polymer in the upper layer region.
Particularly, the ratio (a/b) of the weight percentage (wt %) (a) of the first binder polymer in the solid content of the slurry for a lower layer to the weight percentage (wt %) (b) of the second binder polymer in the solid content of the slurry for an upper layer may be 1-5, 1.1-5, 1-4, 1.2-4, 1-3, 1.5-3, or 2.1-3.
Herein, when the ratio of the weight percentage (wt %) of the first binder polymer in the lower layer region to the weight percentage (wt %) of the second binder polymer in the upper layer region satisfies the above-defined range, it is possible to realize excellent adhesion between the current collector and the positive electrode active material layer and excellent quick charging performance.
According to an embodiment of the present disclosure, the weight percentage (wt %) of the first binder polymer in the lower layer region of the positive electrode active material layer may be 1-3 wt %, 1.5-2.5 wt %, or 1.5-2.4 wt %, and the weight percentage (wt %) of the second binder polymer in the upper layer region of the positive electrode active material layer may be 0.5-3 wt %, 1-2.5 wt %, or 1-2.4 wt %.
According to an embodiment of the present disclosure, the ratio (wt %) of the combined weight of the first binder polymer and the second binder polymer to the total weight of the positive electrode active material layer may be 1-3 wt %, 1-2 wt %, 2-3 wt %, 1-2.4 wt %, or 2.4-3 wt %.
In another aspect of the present disclosure, there is provided a method for manufacturing a positive electrode, including the steps of:
Li1+a[NixMnyCoz]M1tO2 [Chemical Formula 1]
Li1+b[NiuMnvCow]M2sO2 [Chemical Formula 2]
The positive electrode current collector is not particularly limited, as long as it has conductivity, while not causing any chemical change in the corresponding battery. For example, stainless steel, aluminum, nickel, titanium, baked carbon, copper or stainless steel surface-treated with carbon, nickel, titanium, silver, etc., aluminum-cadmium alloy, or the like, may be used. Although the positive electrode current collector is not particularly limited in its thickness, it may have a currently used thickness of 3-500 μm.
The first positive electrode active material and the second positive electrode active material may be present in an amount of 80-99 wt % based on the total weight of the slurry for a lower layer and the slurry for an upper layer, respectively.
The positive electrode active material layer may further include a conductive material, and thus each of the slurry for a lower layer and the slurry for an upper layer may further include a conductive material.
The conductive material is not particularly limited, as long as it causes no chemical change in the corresponding battery and has conductivity. Particular examples of the conductive material include: a carbon black-based carbonaceous material, such as carbon black, acetylene black, Ketjen black, channel black, furnace black, lamp black or thermal black; conductive fibers, such as carbon fibers or metallic fibers; metal powder, such as fluorocarbon, aluminum or nickel powder; conductive whisker, such as zinc oxide or potassium titanate; conductive metal oxide, such as titanium oxide; conductive materials, such as polyphenylene derivatives, or the like. The conductive material may be added in an amount of 0.1-20 wt % based on the total weight of the positive electrode slurry composition.
Each of the first binder polymer and the second binder polymer is an ingredient that assist the binding of the conductive material, the active material or the positive electrode current collector and may be present in an amount of 0.1-20 wt % based on the total weight of the positive electrode slurry composition. Particular examples of each of the first binder polymer and the second binder polymer independently include polyvinylidene fluoride-co-hexafluoropropylene (PVDF-co-HFP), polyvinylidene fluoride, polyacrylonitrile, polymethyl methacrylate, polyvinyl alcohol, carboxymethyl cellulose (CMC), starch, hydroxypropyl cellulose, regenerated cellulose, polyvinyl pyrrolidone, polytetrafluoroethylene, polyethylene, polypropylene, polyacrylic acid, styrene butadiene rubber (SBR), lithium polyacrylate (Li-PAA), or the like.
Each of the first dispersion medium and the second dispersion medium may independently include water or an organic solvent, such as N-methyl-2-pyrrolidone (NMP), and may be used in such an amount that the slurry for an upper layer and the slurry for a lower layer containing the first positive electrode active material/the second positive electrode active material, the first binder polymer/the second binder polymer, the conductive material, or the like may have a desired level of viscosity.
In addition, the method for coating the slurry for a lower layer and the slurry for an upper layer is not particularly limited, as long as it is used conventionally in the art. For example, a coating process using a slot die may be used, and a Mayer bar coating process, a gravure coating process, a dip coating process, a spray coating process, or the like, may also be used.
According to an embodiment of the present disclosure, when the step of coating the slurry for a lower layer on one surface of the positive electrode current collector and the step of coating the slurry for an upper layer on the slurry for a lower layer are carried out at the same time or with a very short time interval, a device, such as a double slot die, may be used.
The step of drying the coated slurry for a lower layer and the coated slurry for an upper layer at the same time to form an active material layer may include drying the coated slurry for a lower layer and slurry for an upper layer at the same time to remove the dispersion medium in each slurry, carrying out pressing, and carrying out vacuum drying to form an active material layer.
Herein, the pressing may be carried out by using a method, such as roll pressing, used conventionally in the art, for example, under a pressure of 1-20 MPa at a temperature of 15-30° C. In addition, the pressing may be carried out under such a condition that the electrode (active material layer) may have a porosity of 20-40%, 25-35%, 20-30%, or 30-40%, after pressing.
The step of drying the coated slurry may be carried out at 70-110° C., 75-100° C., or 80-90° C., for 10-30 minutes, 15-25 minutes, or 20-30 minutes. The drying temperature and time may be controlled suitably depending on the type and content of the dispersion medium.
In addition, after pressing the dried slurry layer, vacuum drying may be carried out at a temperature of 100-170° C., 120-150° C., or 130-150° C., for about 3-10 hours, or 5-8 hours, but the drying temperature and time may be controlled suitably depending on the type and content of the dispersion medium.
The ratio (a/b) of the weight percentage (wt %) (a) of the first binder polymer in the solid content of the slurry for a lower layer to the weight percentage (wt %) (b) of the second binder polymer in the solid content of the slurry for an upper layer may be 1-5, 1.1-5, 1-4, 1.2-4, 1-3, 1.5-3, or 2.1-3.
Herein, when the ratio of the weight percentage (wt %) of the first binder polymer in the coated slurry for a lower layer to the weight percentage (wt %) of the second binder polymer in the coated slurry for an upper layer satisfies the above-defined range, it is possible to realize excellent adhesion and quick charging performance.
The weight percentage (wt %) of the first binder polymer in the solid content of the slurry for a lower layer may be 1-3 wt %, 1.5-2.5 wt %, or 1.5-2.4 wt %, and the weight percentage (wt %) of the second binder polymer in the solid content of the slurry for an upper layer may be 0.5-3 wt %, 1-2.5 wt %, or 1-2.4 wt %.
The ratio (wt %) of the combined weight of the first binder polymer and the second binder polymer to the total solid content of the slurry for a lower layer and the slurry for an upper layer may be 1-3 wt %, 1-2 wt %, 2-3 wt %, 1-2.4 wt %, or 2.4-3 wt %.
As described above, the positive electrode active material layer has a bilayer structure, and includes a lower layer region facing the positive electrode current collector and containing a first positive electrode active material and a first binder polymer, and an upper layer region facing the lower layer region and containing a second positive electrode active material and a second binder polymer.
In still another aspect of the present disclosure, there is provided a lithium secondary battery including the above-described positive electrode. Particularly, the lithium secondary battery may be obtained by injecting a lithium salt-containing electrolyte to an electrode assembly including the positive electrode, a negative electrode and a separator interposed between both electrodes.
The negative electrode may be obtained by allowing a negative electrode active material to be bound to a negative electrode current collector through a method generally known in the art. Non-limiting examples of the negative electrode active material include conventional negative electrode active materials that may be used for the negative electrodes for conventional electrochemical devices. Particularly, lithium intercalation materials, such as lithium metal or lithium alloys, carbon, petroleum coke, activated carbon, graphite or other carbonaceous materials, are used preferably. Non-limiting examples of the negative electrode current collector include foil made of copper, gold, nickel, copper alloys or a combination thereof.
The negative electrode active material, a conductive material, a binder and a solvent are mixed to prepare a slurry, and then the slurry may be coated directly on the negative electrode current collector. In a variant, the slurry may be cast onto another support, and the negative electrode active material film obtained by peeling it from the support may be laminated on the negative electrode current collector to obtain a negative electrode.
The separator may be a conventional porous polymer film used conventionally as a separator. For example, the porous polymer film may be a porous polymer film made of a polyolefinic polymer, such as ethylene homopolymer, propylene homopolymer, ethylene-butene copolymer, ethylene/hexene copolymer or ethylene/methacrylate copolymer. Such a porous polymer film may be used alone or in the form of a laminate. In addition, an insulating thin film having high ion permeability and mechanical strength may be used. The separator may include a safety reinforced separator (SRS) including a ceramic material coated on the surface of the separator to a small thickness. In addition, a conventional porous non-woven web, such as a non-woven web made of high-melting point glass fibers or polyethylene terephthalate fibers, may be used, but the scope of the present disclosure is not limited thereto.
The electrolyte includes a lithium salt as an electrolyte salt and an organic solvent for dissolving the lithium salt.
Any lithium salt used conventionally for an electrolyte for a secondary battery may be used without particular limitation. For example, the anion of the lithium salt may be any one selected from the group consisting of F−, Cl−, Br−, I−, NO3−, N(CN)2−, BF4−, ClO4−, PF6−, (CF3)2PF4−, (CF3)3PF−, (CF3)4PF−, (CF3)5PF−, (CF3)6P−, CF3SO3−, CF3CF2SO3−, (CF3SO2)2N−, (FSO2)2N−, CF3CF2(CF3)2CO−, (CF3SO2)2CH−, (SF5)3C−, (CF3SO2)3C−, CF3(CF2)7SO3−, CF3CO2−, CH3CO2−, SCN−, and (CF3CF2SO2)2N−, or two or more of them.
The organic solvent contained in the electrolyte may be any organic solvent used conventionally without particular limitation. Typical examples of the organic solvent include at least one selected from the group consisting of propylene carbonate, ethylene carbonate, diethyl carbonate, dimethyl carbonate, ethyl methyl carbonate, methyl propyl carbonate, dipropyl carbonate, dimethyl sulfoxide, acetonitrile, dimethoxyethane, diethoxyethane, vinylene carbonate, sulfolane, gamma-butyrolactone, propylene sulfite, and tetrahydrofuran.
Particularly, among the carbonate-based organic solvents, ethylene carbonate and propylene carbonate, which are cyclic carbonates, are organic solvents having high viscosity and a high dielectric constant, and thus may be used preferably, since they can dissociate the lithium salt in the electrolyte with ease. When such a cyclic carbonate is used after mixing it with a linear carbonate having low viscosity and a low dielectric constant, such as dimethyl carbonate or diethyl carbonate, it is possible to prepare an electrolyte having higher electrical conductivity, more preferably.
Optionally, the electrolyte used according to the present disclosure may further include additives contained in the conventional electrolyte, such as an overcharge-preventing agent, or the like.
The lithium secondary battery according to an embodiment of the present disclosure may be obtained by interposing the separator between the positive electrode and the negative electrode to form an electrode assembly, introducing the electrode assembly to a pouch, a cylindrical battery casing or a prismatic battery casing, and then injecting the electrolyte thereto to finish a secondary battery. In a variant, the lithium secondary battery may be obtained by stacking the electrode assemblies, impregnating the stack with the electrolyte, and introducing the resultant product to a battery casing, followed by sealing.
According to an embodiment of the present disclosure, the lithium secondary battery may be a stacked, wound, stacked and folded or cable type battery.
The lithium secondary battery according to the present disclosure may be used for a battery cell used as a power source for a compact device, and may be used preferably as a unit battery for a medium- or large-size battery module including a plurality of battery cells. Particular examples of such medium- or large-size devices include electric vehicles, hybrid electric vehicles, plug-in hybrid electric vehicles, power storage systems, or the like. Particularly, the lithium secondary battery may be useful for batteries for hybrid electric vehicles and new & renewable energy storage batteries, requiring high output.
Examples will be described more fully hereinafter so that the present disclosure can be understood with ease. The following examples may, however, be embodied in many different forms and should not be construed as limited to the exemplary embodiments set forth therein. Rather, these exemplary embodiments are provided so that the present disclosure will be thorough and complete, and will fully convey the scope of the present disclosure to those skilled in the art.
First, Denka black as a conductive material was introduced to N-methyl pyrrolidone (NMP), and the resultant mixture was introduced to a high-speed dispersion system (Spike mill, available from Inoue) and dispersed to prepare a pre-dispersion of conductive material. Next, a positive electrode active material and a binder polymer were mixed with the pre-dispersion of conductive material to prepare a slurry for a lower layer having a viscosity of 10,000 cps.
Herein, the slurry for a lower layer includes 96.3 wt % of a positive electrode active material represented by the chemical formula of Li[Ni0.65Mn0.15Co0.20]O2 and having a Ni content of 65% based on the total transition metals, 1.3 wt % of Denka black as a conductive material and 2.4 wt % of polyvinylidene fluoride (PVDF) as a binder polymer.
In addition, a slurry for an upper layer having a viscosity of 10,000 cps was prepared in the same manner as described above. Herein, the slurry for an upper layer includes 96.3 wt % of a positive electrode active material represented by the chemical formula of Li[Ni0.86Mn0.05Co0.07]Al0.02O2 and having a Ni content of 86% based on the total transition metals, 1.3 wt % of Denka black as a conductive material and 2.4 wt % of polyvinylidene fluoride (PVDF) as a binder polymer.
The slurry for a lower layer was introduced to the lower layer slurry tank of a dual layer coating instrument, and the slurry for an upper layer was introduced to the upper layer slurry tank thereof to apply the slurry for a lower layer and the slurry for an upper layer onto an aluminum positive electrode current collector having a thickness of 12 μm at the same time.
Then, each slurry was dried at 110° C., and pressing was carried out to obtain a positive electrode having a bilayer-type coating layer. Herein, the positive electrode active material layer of the positive electrode had a total thickness of 175 μm, the lower layer region of the positive electrode active material layer had a thickness of 87 μm, and the upper layer region of the positive electrode active material layer had a thickness of 87 μm. The positive electrode had a porosity of 29%. The weight ratio of the lower layer to the upper layer of the positive electrode active material layer was 50:50.
First, 95.6 wt % of a negative electrode active material (artificial graphite), 1.0 wt % of a conductive material (Super-C) and 3.4 wt % of a binder polymer (styrene butadiene rubber) were dispersed in water to prepare a negative electrode active material slurry. The slurry was applied onto a copper negative electrode current collector having a thickness of 8 μm and dried at 150° C., and then pressing was carried out to obtain a negative electrode. Herein, the negative electrode active material layer had a total thickness of 212 μm and a porosity of 29.0%.
A polyethylene porous film as a separator was interposed between the negative electrode and the positive electrode, the resultant structure was introduced to a battery casing, and then an electrolyte was injected thereto to obtain a secondary battery. Herein, the electrolyte was a mixed solution including ethylene carbonate and ethyl methyl carbonate (volume ratio 3/7) and containing 1.1 M LiPF6 dissolved therein.
A positive electrode, a negative electrode and a secondary battery were obtained in the same manner as Example 1, except that the Ni content in the positive electrode active material was changed as shown in the following Table 1.
A positive electrode, a negative electrode and a secondary battery were obtained in the same manner as Example 1, except that 96.3 wt % of a positive electrode active material represented by the chemical formula of Li[Ni0.86Mn0.05Co0.07]Al0.02O2 and having a Ni content of 86% based on the total transition metals, 1.3 wt % of Denka black as a conductive material and 2.4 wt % of polyvinylidene fluoride (PVDF) as a binder polymer were mixed to prepare a slurry for a lower layer having a viscosity of 10,000 cps; and
96.3 wt % of a positive electrode active material represented by the chemical formula of Li[Ni0.65Mn0.15Co0.20]O2 and having a Ni content of 65% based on the total transition metals, 1.3 wt % of Denka black as a conductive material and 2.4 wt % of polyvinylidene fluoride (PVDF) as a binder polymer were mixed to prepare a slurry for an upper layer having a viscosity of 10,000 cps.
First, Denka black as a conductive material was introduced to N-methyl pyrrolidone (NMP), and the resultant mixture was introduced to a high-speed dispersion system (Spike mill, available from Inoue) and dispersed to prepare a pre-dispersion of conductive material. Next, a positive electrode active material and a binder polymer were mixed with the pre-dispersion of conductive material to prepare a slurry having a viscosity of 10,000 cps.
Herein, the slurry includes 96.3 wt % of a positive electrode active material represented by the chemical formula of Li[Ni0.86Mn0.05Co0.07]Al0.02O2 and having a Ni content of 86% based on the total transition metals, 1.3 wt % of Denka black as a conductive material and 2.4 wt % of polyvinylidene fluoride (PVDF) as a binder polymer.
The slurry was applied onto an aluminum positive electrode current collector having a thickness of 12 μm by using a single layer coating system.
Then, the slurry was dried at 110° C., and pressing was carried out to obtain a positive electrode having a monolayer-type coating layer. Herein, the positive electrode active material layer of the positive electrode had a total thickness of 175 μm.
A lithium secondary battery was obtained in the same manner as Example 1, except that the positive electrode obtained as described above was used.
Each of the positive electrodes and the lithium secondary batteries according to Examples 1 and 2 and Comparative Examples 1 and 2 was evaluated in terms of its characteristics as follows.
Each of the lithium secondary batteries according to Examples 1 and 2 and Comparative Examples 1 and 2 was used to evaluate an increase in resistance in a lower SOC (5-20%) region as compared to the resistance at SOC 50% under the following conditions by using the following method. The results are shown in the following Table 1.
The resistance of each lithium secondary battery was determined when it was discharged to each level of SOC at 2.5 C, while the state-of-charge (SOC) was reduced from 100% to 0% at a rate of 5% in an operating voltage range of 2.5-4.25 V at room temperature, and the results are compared.
In addition, the increase in resistance in a lower SOC (5-20%) region as compared to the resistance at SOC 50% was calculated according to the following formula:
Increase in resistance (%)=[(Resistance in lower SOC (5-20%))/(Resistance at SOC 50%)]×100,
wherein the resistance in lower SOC (5-20%) is an average value of resistance values determined at SOC 5%, 10%, 15% and 20%.
Each of the lithium secondary batteries according to Examples 1 and 2 and Comparative Examples 1 and 2 was charged/discharged for 170 cycles at 45° C. under the following conditions to evaluate the high-temperature capacity retention.
The high-temperature capacity retention was calculated as a ratio of the discharge capacity after 170 cycles based on the discharge capacity after the first cycle. The results are shown in the following Table 1 and the FIGURE.
Referring to Table 1, each of the secondary batteries including a bilayer type active material layer controlled to have a Ni content of the second positive electrode active material in the upper layer region larger than the Ni content of the first positive electrode active material in the lower layer region according to Examples 1 and 2 shows a lower increase in resistance in a lower SOC (5-20%) based on the resistance at SOC 50% and a higher high-temperature retention, as compared to the secondary battery using a positive electrode including a bilayer-type active material layer, in which the Ni content of the second positive electrode active material and that of the first positive electrode active material are reversed according to Comparative Example 1, and the secondary battery using a positive electrode including a monolayer-type active material layer according to Comparative Example 2.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2021-0002853 | Jan 2021 | KR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2022/000312 | 1/7/2022 | WO |
