Patent Application
20230253547
This patent document claims benefit of priority to Korean Patent Application No. 10-2022-0014955 filed on Feb. 4, 2022 in the Korean Intellectual Property Office, the disclosure of which is incorporated herein by reference in its entirety.
The technology in this patent document relates to a cathode for a lithium secondary battery and a lithium secondary battery including the same. More specifically, this patent document relates to a cathode for a lithium secondary battery which includes a lithium transition metal oxide-based cathode active material and a lithium secondary battery including the cathode.
A secondary battery is a battery which may be repeatedly charged and discharged. With rapid progress of information and communication, and display industries, the secondary battery has been widely applied to various portable telecommunication electronic devices such as a camcorder, a mobile phone, a laptop computer as a power source thereof. Recently, a battery pack including the secondary battery has also been developed and applied to an eco-friendly automobile such as a hybrid vehicle as a power source thereof.
Examples of the secondary battery may include a lithium secondary battery, a nickel-cadmium battery, and a nickel-hydrogen battery. Among them, the lithium secondary battery has a high operating voltage and a high energy density per unit weight, and is advantageous in terms of a charging speed and light weight. In this regard, the lithium secondary battery has been actively developed and applied as a power source.
For example, the lithium secondary battery may include: an electrode assembly including a cathode, an anode, and a separation membrane (separator); and an electrolyte in which the electrode assembly is impregnated. The lithium secondary battery may further include, for example, a pouch-shaped outer case in which the electrode assembly and the electrolyte are housed.
As a cathode active material for a lithium secondary battery, a lithium transition metal oxide having a secondary particle structure, in which primary particles are agglomerated, is used. In the case of secondary particles, there is a problem in that micro-cracks occur inside the secondary particles during long term charging and discharging. In addition, when increasing an electrode density to implement a high energy density, there is a problem in that the secondary particles are collapsed. Accordingly, in order to solve these problems, development of a structurally stable cathode active material by developing a cathode active material such as a single crystal or a single particle has recently been proceeded.
For example, Korean Patent Publication Laid-Open No. 10-2021-0120525 discloses a cathode active material including a lithium-based composite oxide having a single crystal structure, but has a limitation in providing minimization of an increase in resistance together with sufficient high-density characteristics of the electrode.
Various implementations of the disclosed technology can be used to provide a cathode for a lithium secondary battery having improved structural stability and operational reliability.
Implementations of the disclosed technology can also be sued to provide a lithium secondary battery including the cathode having improved structural stability and operational reliability.
According to an aspect of the disclosed technology, there is provided a cathode for a lithium secondary battery including: a cathode current collector; and a cathode active material layer comprising a first cathode active material layer and a second cathode active material layer, which are sequentially laminated on the cathode current collector, wherein the first cathode active material layer and the second cathode active material layer include first cathode active material particles and second cathode active material particles, which have different particle structures from each other in crystallography or morphology, and a mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the first cathode active material layer is different from a mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the second cathode active material layer.
In some embodiments, the first cathode active material particle may have a polycrystalline structure, and the second cathode active material particle may have a single crystal structure.
In some embodiments, the first cathode active material particle may have a secondary particle structure in which a plurality of primary particles are integrally aggregated, and the second cathode active material particle may have a single particle structure.
In some embodiments, the mixing weight ratios of the second cathode active material particles to the first cathode active material particles in the first cathode active material layer and the second cathode active material layer may be 1/9 to 1, respectively.
In some embodiments, the mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the first cathode active material layer may be 1/9 to 1/2, and the mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the second cathode active material layer may be 1/2 to 1.
In some embodiments, the mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the first cathode active material layer may be smaller than the mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the second cathode active material layer.
In some embodiments, the cathode active material layer may further include at least one additional cathode active material layer laminated between the first cathode active material layer and the second cathode active material layer or on the second cathode active material layer, and the additional cathode active material layer may include the first cathode active material particles and the second cathode active material particles.
In some embodiments, a mixing weight ratio of the second cathode active material particles to the first cathode active material particles of at least one layer included in the additional cathode active material layer may be different from each of the mixing weight ratios thereof in the first cathode active material layer and the second cathode active material layer.
In some embodiments, the number of the additional cathode active material layers may be 1 to 3.
In some embodiments, the first cathode active material particles and the second cathode active material particles may include a lithium-nickel composite metal oxide, respectively, and a molar ratio of nickel among metal elements except for lithium in the first cathode active material particles may be 0.8 or more.
In some embodiments, a molar ratio of nickel among metal elements except for lithium in the second cathode active material particles may be 0.8 or more.
In some embodiments, the molar ratio of nickel among metal elements except for lithium in the second cathode active material particles may be smaller than the molar ratio of nickel in the first cathode active material particles.
In some embodiments, an average particle diameter (D50) of the second cathode active material particles may be smaller than an average particle diameter (D50) of the first cathode active material particles.
In some embodiments, a density of the cathode active material layer may be 3.5 g/cc or more and 4.5 g/cc or less.
According to another aspect of the disclosed technology, there is provided a lithium secondary battery including: the cathode for a lithium secondary battery according to exemplary embodiments; and an anode disposed to face the cathode.
The lithium secondary battery cathode according to the above-described and other embodiments of the disclosed technology may include a cathode active material layer having a multilayer structure. In the multilayered cathode active material layer, the first cathode active material layer and the second cathode active material layer may include first cathode active material particles and second cathode active material particles, which have different particle structures from each other in crystallography or morphology, and a mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the first cathode active material layer may be different from a mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the second cathode active material layer.
Accordingly, it is possible to implement a lithium secondary battery with a minimized electrode resistance increase rate while maximizing the electrode density.
Various features and advantages of the disclosed technology will be more clearly understood from the following detailed description taken in conjunction with the accompanying drawings, in which:
According to embodiments of the disclosed technology, a cathode for a lithium secondary battery may include a cathode active material layer having a multilayer structure including first cathode active material particles and second cathode active material particles, which have different particle structures from each other in crystallography or morphology. Accordingly, it is possible to implement a lithium secondary battery with a minimized electrode resistance increase rate while maximizing the electrode density.
The drawings presented are provided for illustrating one of examples of embodiments of the disclosed technology.
As used herein, the terms “first” and “second” do not limit the number or order of subjects modified by the “first” and the “second,” but are used to distinguish the modified subjects which are different from each other.
Referring to
The cathode current collector 105 may include, for example, stainless steel, nickel, aluminum, titanium, copper, or an alloy thereof, and preferably includes aluminum or an aluminum alloy.
According to exemplary embodiments, the cathode active material layer 110 may include a first cathode active material layer 112 and a second cathode active material layer 114. Thereby, the cathode active material layer 110 may have a multilayer structure (e.g., a double-layer structure) in which a plurality of cathode active material layers are laminated.
In some embodiments, the cathode active material layer 110 may further include at least one additional cathode active material layer laminated between the first cathode active material layer 112 and the second cathode active material layer 114 or on the second cathode active material layer 114.
For example, one to three additional cathode active material layers may be laminated on the second cathode active material layer 114. Accordingly, the cathode active material layer 110 may have a multilayer structure in which the plurality of cathode active material layers are laminated.
As shown in
The first cathode active material layer 112 may directly contact with the surface of the cathode current collector 105. The second cathode active material layer 114 may directly contact with the upper surface of the first cathode active material layer 112.
The first cathode active material layer 112 and the second cathode active material layer 114 according to an exemplary embodiment may include first cathode active material particles and second cathode active material particles, which have different particle structures from each other in crystallography or morphology. The first cathode active material layer 112 and the second cathode active material layer 114 may include the first cathode active material particles and the second cathode active material particles, respectively.
In this case, a mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the first cathode active material layer 112 may be different from a mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the second cathode active material layer 114.
According to embodiments, the first cathode active material layer 112 and the second cathode active material layer 114 may include first cathode active material particles and second cathode active material particles, which have different particle structures from each other in crystallography. The first cathode active material particles and the second cathode active material particles, which have different particle structures from each other in crystallography, may mean first cathode active material particles having a polycrystalline structure and second cathode active material particles having a single crystal structure.
As used herein, the term “single crystal” may refer to a structure which has only one crystal in a particle and does not include a grain or grain boundary inside the particle.
As used herein, the term “polycrystal” may refer to a structure which has a plurality of crystals in a particle and includes a crystal grain or crystal grain boundary inside the particle.
For example, electron-backscattered diffraction (EBSD) is a crystal orientation analysis method located in the middle of X-ray diffraction analysis (XRD) and transmission electron microscopy (TEM) analysis methods, and enables to confirm and obtain orientation information of crystal grains which form a microstructure of a material. For example, the polycrystal or single crystal may be distinguished through the crystal grain orientation distribution of the particles measured by EBSD.
According to embodiments, the first cathode active material layer 112 and the second cathode active material layer 114 may include a mixture or blend of the first cathode active material particles having a polycrystalline structure and the second cathode active material particles having a single crystal structure.
According to embodiments, the first cathode active material layer 112 and the second cathode active material layer 114 may include the first cathode active material particles and the second cathode active material particles, which have different particle structures from each other in morphology. The first cathode active material particles and the second cathode active material particles, which have different particle structures from each other in morphology, may mean first cathode active material particles having a secondary particle structure and second cathode active material particles having a single particle structure.
As used herein, the term “secondary particle” may mean a particle in which a plurality of primary particles are aggregated or assembled to be substantially considered or observed as one particle. For example, the secondary particle may have greater than 10, 30 or more, 50 or more, or 100 or more of primary particles aggregated therein.
As used herein, the term “single particle” may mean a monolith formed of one particle regardless of the type and number of particle crystals, and may exclude a secondary particle structure in which the primary particles are aggregated or assembled. However, the single particle does not exclude: a form in which fine particles (e.g., particles having a volume of 1/100 or less based on a volume of the single particle) are attached to the surface of the particle; and a form in which 10 or less of the fine particles are included inside the particle.
For example, in the cathode active material layer 110, the single particles may be present in contact with each other. The form in which the single particles are present in contact with each other and the form of the secondary particle may be distinguished from each other, which can be confirmed through an SEM image. For example, 2 to 10 single particles may be present in contact with each other. That is, the particles are not distinguished in crystallography, and the primary particle and the single particle may have a single crystal or polycrystal.
According to embodiments, the first cathode active material layer 112 and the second cathode active material layer 114 may include a mixture or blend of first cathode active material particles having a secondary particle structure in which a plurality of primary particles are integrally aggregated, and second cathode active material particles having a single particle structure.
Hereinafter, the contents of the first cathode active material particle and the second cathode active material particle, which will be described below, may be commonly applied to both the case of having different particle structures in crystallography and the case of having different particle structures in morphology.
According to embodiments, the first cathode active material particle may have a polycrystalline or secondary particle structure. Thereby, the movement of ions between the crystal grain boundaries or the primary particles may be facilitated, charging/discharging speeds may be enhanced, and capacity retention characteristics may be improved.
However, in the case of the polycrystalline or secondary particle structure, since the plurality of crystal grains or primary particles are included therein, cracks may easily propagate inside the particle due to an impact upon occurring a penetration of the cell caused by an external object. Accordingly, when an electrode short-circuit occurs due to penetration, a generation amount or propagation speed of thermal energy may be rapidly increased due to overcurrent. In addition, when involving a process of applying a cathode active material slurry to the cathode current collector 105, followed by rolling the same to form the cathode 100, structurally weak first cathode active material particles may be pulverized or cracked due to a pressure propagated through crystal grain boundaries or voids between the primary particles. In this case, desired capacity and output characteristics may not be secured.
To solve these problems, by adding the second cathode active material particles having a structurally stable single crystal or single particle structure to the cathode active material layer 110, heat and shock propagation through the cracks generated inside the particles may be reduced. Thereby, a cathode having a high density may be prepared without damage to the cathode active material, and an increase in the electrode resistance may be minimized.
According to embodiments, the mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the first cathode active material layer 112 may be different from the mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the second cathode active material layer 114.
Preferably, the mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the first cathode active material layer 112 may be smaller than the mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the second cathode active material layer. When the structurally stable second cathode active material is included in the upper layer of the cathode active material layer 110 in high content, the active material particles may not be cracked or collapsed even when rolled at a high density during manufacturing the electrode, and it is possible to prevent the electrode resistance from being greatly increased.
According to embodiments, the mixing weight ratios of the second cathode active material particles to the first cathode active material particles in the first cathode active material layer 112 and the second cathode active material layer 114 may be 1/9 to 1, respectively.
Preferably, the mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the first cathode active material layer 112 may be 1/9 to 1/2, and the mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the second cathode active material layer 114 may be 1/2 to 1. Within the above range, it is possible to provide an optimal mixing ratio that maximizes the density of the electrode and minimizes an increase in the electrode resistance.
According to embodiments, the first cathode active material particles and the second cathode active material particles may include a lithium-nickel composite metal oxide, respectively. In this case, the first cathode active material particles and the second cathode active material particles may include nickel in the largest content (molar ratio) among metals except for lithium.
For example, the first cathode active material particles may have a nickel content of about 80 mol % or more among the metals except for lithium, and the second cathode active material particles may have a nickel content of about 80 mol % or more among the metals except for lithium.
According to some embodiments, the nickel content (or molar ratio) of the second cathode active material particles may be smaller than the nickel content of the first cathode active material particles.
In some embodiments, the first cathode active material particles may have a layered structure or chemical structure represented by Formula 1 below.
LixM1aM2bM3cOy [Formula 1]
In Formula 1, M1, M2 and M3 may be selected from the group consisting of Ni, Co, Mn, Na, Mg, Ca, Ti, V, Cr, Cu, Zn, Ge, Sr, Ag, Ba, Zr, Nb, Mo, Al, Ga and B, and x, y, a, b and c may be in a range of 0<x≤1.2, 2≤y≤2.02, 0.8≤a≤0.99, 0.01≤b+c≤0.2 and 0<a+b+c≤1, respectively.
In some embodiments, M1, M2 and M3 in Formula 1 may be nickel (Ni), manganese (Mn) and cobalt (Co), respectively.
For example, nickel may be provided as a metal associated with an output and/or a capacity of the lithium secondary battery. As described above, by employing a polycrystalline or lithium transition metal oxide of the secondary particles, of which a molar ratio of nickel is 0.8 or more, as the first cathode active material particles, and forming the first cathode active material layer 112 to be in contact with the cathode current collector 105, high power and capacitance characteristics of the cathode 100 may be effectively obtained.
For example, manganese (Mn) may be provided as a metal associated with the mechanical and electrical stabilities of the lithium secondary battery. For example, cobalt (Co) may be a metal associated with the conductivity or resistance of the lithium secondary battery.
In some embodiments, a concentration ratio (or molar ratio) of nickel:cobalt:manganese in the particles of the first cathode active material may be adjusted to about 8:1:1. In this case, conductivity and life-span characteristics may be reinforced by including cobalt and manganese in substantially equal amount while increasing the capacity and output through the nickel in a molar ratio of about 0.8.
In some embodiments, the second cathode active material particles may have a layered structure or chemical structure represented by Formula 2 below.
LixM1′aM2′bM3′cOy [Formula 2]
In Formula 2, M1′, M2′ and M3′ may be selected from the group consisting of Ni, Co, Mn, Na, Mg, Ca, Ti, V, Cr, Cu, Zn, Ge, Sr, Ag, Ba, Zr, Nb, Mo, Al, Ga, W and B, and x, y, a, b and c may be in a range of 0<x≤1.2, 2≤y≤2.02, 0.8≤a≤0.99, 0.01≤b+c≤0.2 and 0<a+b+c≤1, respectively.
In some embodiments, the second cathode active material particles may also improve electrode resistance characteristics and reinforce stability by controlling the contents of cobalt and manganese while improving the capacity and output through the nickel in a molar ratio of about 0.8 or more.
A slurry for forming a first cathode active material layer may be prepared by mixing the above-described blend of the first cathode active material particles and second cathode active material particles with a binder, a conductive material and/or a dispersant in a solvent, followed by stirring the mixture. The slurry for forming the first cathode active material layer may be coated on the cathode current collector 105, followed by compressing and drying the same to form the first cathode active material layer 112.
In addition, a slurry for forming a second cathode active material layer may be prepared in the same manner as the slurry for forming a first cathode active material layer, and coated on the first cathode active material layer 112, followed by compressing and drying the same to form the second cathode active material layer 114. For example, a binder and a conductive material substantially the same as or similar to those used in forming the first cathode active material layer 112 may also be used in forming the second cathode active material layer 114. However, in this case, the mixing weight ratios of the second cathode active material particles to the first cathode active material particles included in the slurry for forming a first cathode active material layer and the slurry for forming a second cathode active material layer may be different from each other.
That is, the cathode active material layer having a multilayer structure may effectively implement desired properties (improvement of electrode density and minimization of increase in the electrode resistance) by differently adjusting the mixing weight ratios of the second cathode active material particles to the first cathode active material particles included in each cathode active material layer.
The binder may include, for example, an organic binder such as vinylidene fluoride-hexafluoropropylene copolymer (PVDF-co-HFP), polyvinylidene fluoride (PVDF), polyacrylonitrile, polymethyl methacrylate, etc., or an aqueous binder such as styrene-butadiene rubber (SBR), and may be used together with a thickener such as carboxymethyl cellulose (CMC).
For example, a PVDF-based binder may be used as a binder for forming the cathode. In this case, an amount of the binder for forming the first cathode active material layer 112 may be reduced and an amount of first cathode active material particles may be relatively increased, thereby improving the output and capacity of the secondary battery.
The conductive material may be included to facilitate the movement of electrons between the active material particles. For example, the conductive material may include a carbon-based conductive material such as graphite, carbon black, graphene, or carbon nanotubes and/or a metal-based conductive material including tin, tin oxide, titanium oxide, or a perovskite material such as LaSrCoO3, and LaSrMnO3.
In one embodiment, the cathode active material layer 110 may further include at least one additional cathode active material layer laminated between the first cathode active material layer 112 and the second cathode active material layer 114 or on the second cathode active material layer 114. The additional cathode active material layer may include the first cathode active material particles and the second cathode active material particles.
For example, the number of additional cathode active material layers may be 1 to 3. When forming the cathode active material layer 110 in a multilayer structure by further laminating the additional cathode active material layers, each layer of the cathode active material may include first cathode active material particles and second cathode active material particles, which have different particle structures from each other in crystallography or morphology.
The additional cathode active material layer further laminated may be prepared in the same manner as the above-described slurry for forming a first cathode active material layer, and coated between the first cathode active material layer 112 and the second cathode active material layer 114, or on the second cathode active material layer 114, followed by compressing and drying the same to form the additional cathode active material layer. In this case, the mixing weight ratio of the second cathode active material particles to the first cathode active material particles of at least one layer included in the additional cathode active material layer may be different from each of the mixing weight ratios thereof in the first cathode active material layer 112 and the second cathode active material layer 114. The mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the additional cathode active material layer further laminated may be 1/9 to 1, and preferably 1/2 to 1. Accordingly, a high-density cathode and a battery with minimized increase in the electrode resistance may be implemented.
In one embodiment, an average particle diameter (e.g., D50) of the second cathode active material particles may be smaller than an average particle diameter of the first cathode active material particles. Accordingly, propagation of heat and cracks due to penetration or rolling may be more effectively suppressed or reduced.
For example, the average particle diameter (D50) of the second cathode active material particles may be about 1 to 20 preferably about 1 to 17 and more preferably about 2 to 15 μm.
The average particle diameter (D50) of the first cathode active material particles may be about to 30 μm, preferably about 7 to 25 μm, and more preferably about 10 to 20 μm.
In some exemplary embodiments, the first cathode active material particles and/or the second cathode active material particles may further include a coating layer formed on the surface thereof. For example, the coating layer may include Al, Ti, Ba, Zr, Si, B, Mg, P, W, or an alloy thereof, or an oxide thereof. These may be used alone or in combination of two or more thereof. The first cathode active material particles are passivated by the coating layer, thereby stability and life-span against penetration of an external object may be more improved.
In one embodiment, the above-described elements, alloys or oxides of coating layer may be inserted into the cathode active material particles as a dopant.
In some embodiments, for example, the first cathode active material layer 112 and the second cathode active material layer 114 may have a thickness of about 50 μm to about 200 respectively. The thickness may be adjusted as necessary.
In one embodiment, a charge capacity and a discharge capacity of the second cathode active material may be 200 mAh/g or more. Preferably, the charge capacity may be 210 to 240 mAh/g, and the discharge capacity may be 180 to 220 mAh/g. Accordingly, a high-capacity electrode may be prepared while securing structural stability.
In one embodiment, a density of the cathode active material layer may be 3.5 g/cc or more and 4.5 g/cc or less, and preferably, 3.5 g/cc or more and 4.0 g/cc or less. As used herein, the term “density of the cathode active material layer” is a value obtained by dividing a total weight of the cathode active material layer by a total volume, and may be calculated, for example, by punching an electrode in a predetermined size and measuring the mass and volume of a portion except for the current collector.
As described above, by including the first cathode active material particles and the second cathode active material particles, which have different particle structures from each other in crystallography or morphology, in each layer of the cathode active material having a multilayer structure, it is possible to suppress cracks from occurring in the cathode active material particles even when rolling at a high pressure, such that a high-density cathode may be implemented.
Referring to
The cathode 100 may include a cathode active material layer 110 coated on the cathode current collector 105. Although not illustrated in detail in
The anode 130 may include an anode current collector 125 and an anode active material layer 120 formed by coating the anode current collector 125 with the anode active material.
The anode active material useable for implementing the disclosed technology may include any material known in the related art, so long as it can intercalate and deintercalate lithium ions, without particular limitation thereof. For example, carbon-based materials such as crystalline carbon, amorphous carbon, carbon composite, carbon fiber, etc.; a lithium alloy; silicon or tin may be used. Examples of the amorphous carbon may include hard carbon, cokes, mesocarbon microbead (MCMB) calcined at a temperature of 1500° C. or lower, mesophase pitch-based carbon fiber (MPCF) or the like. Examples of the crystalline carbon may include graphite-based carbon such as natural graphite, graphite cokes, graphite MCMB, graphite MPCF or the like. Other elements included in the lithium alloy may include, for example, aluminum, zinc, bismuth, cadmium, antimony, silicone, lead, tin, gallium, indium or the like.
The anode current collector 125 may include, for example, gold, stainless steel, nickel, aluminum, titanium, copper, or an alloy thereof, and preferably includes copper or a copper alloy.
In some embodiments, a slurry may be prepared by mixing the anode active material with a binder, a conductive material and/or a dispersing material in a solvent, followed by stirring the mixture. At least one surface of the anode current collector 125 may be coated with the slurry, followed by compressing and drying to prepare the anode 130.
As the binder and the conductive material, materials which are substantially the same as or similar to the above-described materials used in the cathode active material layer 110 may be used. In some embodiments, the binder for forming the anode may include, for example, an aqueous binder such as styrene-butadiene rubber (SBR) for consistency with the carbon-based active material, and may be used together with a thickener such as carboxymethyl cellulose (CMC).
The separation membrane 140 may be interposed between the cathode 100 and the anode 130. The separation membrane 140 may include a porous polymer film made of a polyolefin polymer such as ethylene homopolymer, propylene homopolymer, ethylene/butene copolymer, ethylene/hexene copolymer, ethylene/methacrylate copolymer. The separation membrane 140 may include a nonwoven fabric made of glass fiber having a high melting point, polyethylene terephthalate fiber or the like.
In some embodiments, the anode 130 may have an area (e.g., a contact area with the separation membrane 140) and/or volume larger than those/that of the cathode 100. Thereby, lithium ions generated from the cathode 100 may be smoothly diffused to the anode 130 without being precipitated in the middle, for example. Therefore, effects of simultaneously improving output and stability through a combination of the above-described first cathode active material layer 112 and the second cathode active material layer 114 may be more easily implemented.
According to exemplary embodiments, an electrode cell is defined by the cathode 100, the anode 130, and the separation membrane 140, and a plurality of electrode cells are laminated to form, for example, a jelly roll type electrode assembly 150. For example, the electrode assembly 150 may be formed by winding, lamination, folding, or the like of the separation membrane 140.
The electrode assembly 150 may be housed in an outer case 160 together with an electrolyte to define the lithium secondary battery. According to exemplary embodiments, a non-aqueous electrolyte may be used as the electrolyte.
The non-aqueous electrolyte includes a lithium salt of an electrolyte and an organic solvent. The lithium salt is represented by, for example, Li+X−, and as an anion (X−) of the lithium salt, F−, Cl−, Br−, I−, NO3−, N(CN)2−, BF4−, C1O4−, PF6−, (CF3)2PF4−, (CF3)3PF3−, (CF3)4PF2−, (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−, etc. may be exemplified.
As the organic solvent, for example, propylene carbonate (PC), ethylene carbonate (EC), diethyl carbonate (DEC), dimethyl carbonate (DMC), ethylmethyl carbonate (EMC), methylpropyl carbonate, dipropyl carbonate, dimethylsulfuroxide, acetonitrile, dimethoxyethane, diethoxyethane, vinylene carbonate, sulfolane, gamma-butyrolactone, propylene sulfite and tetrahydrofuran, etc. may be used. These may be used alone or in combination of two or more thereof.
As shown in
The lithium secondary battery may be manufactured, for example, in a cylindrical shape using a can, a square shape, a pouch type or a coin shape.
Hereinafter, specific experimental examples are for illustrating various features and implementations of the disclosed technology; various alterations, improvements and modifications of the disclosed examples and other implementations can be made based on what is described and/or illustrated.
After preparing a first cathode active material slurry by mixing first cathode active material particles (LiNi1.08Co0.1Mn0.1O2, secondary particles in morphology that can be confirmed by EBSD, 11.5 μm) and second cathode active material particles (LiNi0.82Co0.135Mn0.045O2, single particles in morphology that can be confirmed by EBSD, 5.5 μm) in a weight ratio of 90:10 (a mixing weight ratio of the second cathode active material particles to the first cathode active material particles is about 1/5.6) to prepare a mixture, and then mixing the prepared mixture with CNT as a conductive material and PVDF as a binder in a weight ratio of 98.25:0.75:1.0, respectively, an aluminum current collector was coated with the prepared slurry, followed by drying and pressing the same to form a first cathode active material layer.
After a second cathode active material slurry by mixing the first cathode active material particles and the second cathode active material particles in a weight ratio of 60:40 (a mixing weight ratio of the second cathode active material particles to the first cathode active material particles was about 1/1.2) to prepare a mixture, and then mixing the prepared mixture with CNT as a conductive material and PVDF as a binder in a weight ratio of 98.25:0.75:1.0, the surface of the first cathode active material layer was coated with the prepared slurry, followed by drying and pressing the same to form a second cathode active material layer. Accordingly, a cathode, in which the first cathode active material layer and the second cathode active material layer are sequentially laminated on the cathode current collector, was prepared.
Electrode densities of the finally formed first cathode active material layer and second cathode active material layer were 3.7 g/cc, respectively.
An anode slurry, which includes 91.95% by weight (“wt. %”) of natural graphite and 5 wt. % of silicon as an anode active material, 0.25 wt. % of single-walled carbon nanotubes (SWCNTs) as a conductive material, 1.5 wt. % of styrene-butadiene rubber (SBR) as a binder, and 1.3 wt. % of carboxymethyl cellulose (CMC) as a thickener, was prepared. A copper substrate was coated with the prepared anode slurry, followed by drying and pressing the same to prepare an anode.
After the cathode and anode prepared as described above were respectively notched in a predetermined size and laminated, then an electrode cell was fabricated by interposing a separator (polyethylene, thickness: 25 μm) between the cathode and the anode. Thereafter, tap parts of the cathode and the anode were welded, respectively. An assembly of the welded cathode/separator/anode was put into a pouch, followed by sealing three sides of the pouch except for one side into which an electrolyte is injected. At this time, a portion having the electrode tab was included in the sealing part. After injecting the electrolytic through the remaining one side except for the sealing part, the remaining one side was also sealed, followed by impregnation for 12 hours or more to prepare a lithium secondary battery.
The electrolyte used herein was prepared by dissolving 1M LiPF6 in a mixed solvent of EC/EMC/DEC (25/45/30; volume ratio), then adding 1 wt. % of vinylene carbonate (VC), 0.5 wt. % of 1,3-propene sultone (PRS), and 0.5 wt. % of lithium bis(oxalato)borate (LiBOB) thereto.
A lithium secondary battery was manufactured according to the same procedures as described in Example 1, except that mixtures were prepared by changing the mixing weight ratios of the first cathode active material particles and the second cathode active material particles included in the first cathode active material layer and the second cathode active material layer as described in Table 1 below, and the mixture, CNT as a conductive material and PVDF as a binder were mixed in a weight ratio of 98.25:0.75:1.0, respectively to form a cathode.
Lithium secondary batteries were manufactured according to the same procedures as described in Example 1, except that the mixing weight ratios of the first cathode active material particles and the second cathode active material particles included in the first to a third cathode active material layer were changed as described in Table 1 below.
After a cathode active material slurry was prepared by mixing the first cathode active material particles and the second cathode active material particles in a weight ratio of 85:15 (the mixing weight ratio of the second cathode active material particles to the first cathode active material particles was about 1/5.6) to prepare a mixture, and then mixing the prepared mixture with CNT as a conductive material and PVDF as a binder, an aluminum current collector was coated with the prepared slurry, followed by drying and pressing the same to form a cathode active material in a single layer.
Lithium secondary batteries were manufactured according to the same procedures as described in Example 1, except that the mixing weight ratios of the first cathode active material particles and the second cathode active material particles included in the first cathode active material layer and the second cathode active material layer were changed as described in Table 1 below.
1. Evaluation of Adhesion
For each of the cathodes prepared in the above examples and comparative examples, adhesion was measured using an adhesion measurement equipment (IMADA Z Link 3.1). Specifically, the adhesion was evaluated by measuring a force when peeling-off a surface of the cathode at an angle of 90 degrees after attaching the same to a tape. Result values are described in Table 1 below.
2. Measurement of Direct Current Internal Resistance (D_DCIR)
At 50% point of state-of-charge (SOC), when sequentially increasing the C-rate to 0.2C, 0.5C, 1.0C, 1.5C, 2.0C, 2.5C and 3.0C, and performing charging and discharging on the secondary batteries manufactured in the examples and comparative examples at the C-rate for 10 seconds, terminal points of the voltage were composed with an equation of a straight line and a slope thereof was adopted as the DCIR. Result values are described in Table 1 below.
Referring to Table 1, in the case of examples including a blend of secondary particles of the cathode active material particles and single particles of the cathode active material particles in each layer of the cathode active material layer having a multilayer structure, the electrode resistance increase rate was reduced. In addition, it was confirmed that the cathode active material maintained excellent adhesion without being broken even when increasing the density of the cathode
In addition, it was confirmed that, when the mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the first cathode active material layer was smaller than the mixing weight ratio of the second cathode active material particles to the first cathode active material particles in the second cathode active material layer, improvement of both adhesion and electrode resistance was excellent.
On the other hand, it was confirmed that, in the case of the comparative examples in which, even if single particles were included in the cathode active material layer and the cathode active material layer had a single layer structure or a multilayer structure, both polycrystalline cathode active material particles and single crystalline cathode active material particles were not included in each layer, the electrode resistance increase rate was higher than that of the examples. Further, it was confirmed that the adhesion was reduced when increasing the cathode density.
Referring to
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2022-0014955 | Feb 2022 | KR | national |
