Patent Application
20240396087
This application claims priority to and the benefit of Korean Patent Application No. 10-2023-0065731 filed in the Korean Intellectual Property Office on May 22, 2023, the entire contents of which are incorporated herein by reference.
Examples of this disclosure relate to an electrolyte for a rechargeable lithium battery, and a rechargeable lithium battery including the same.
A rechargeable lithium battery may be recharged and has three or more times as high energy density per unit weight as a conventional lead storage battery, nickel-cadmium battery, nickel hydrogen battery, nickel zinc battery and the like. A rechargeable lithium battery may be also charged at a high rate and thus, may be commercially manufactured for a laptop, a cell phone, an electric tool, an electric bike, and the like, and research on improvement of additional energy density is being actively pursued.
Such a rechargeable lithium battery is used by injecting an electrolyte into a battery cell including a positive electrode that has a positive electrode active material that can intercalate and de-intercalate lithium, and a negative electrode that has a negative electrode active material that can intercalate and de-intercalate lithium.
One of the recent development directions of a rechargeable lithium battery relates to high-rate charging. However, the high-rate charging of the rechargeable lithium battery may present challenges of deteriorating lifecycle characteristics and/or an increase in resistance due to lithium dendrite precipitated on the negative electrode surface (for example, on the interface of the negative electrode with the electrolyte).
Accordingly, an electrolyte that may improve the high-rate charging performance as well as reduce or minimize the deterioration of lifecycle characteristics and/or the increase in resistance of the rechargeable lithium battery may be advantageous.
Some example embodiments provide an electrolyte for a rechargeable lithium battery that improves high-rate charging performance while reducing or minimizing deterioration of lifecycle characteristics and/or increase in resistance.
Some example embodiments provide a rechargeable lithium battery with improved high-rate charging performance while reducing or minimizing deterioration of lifecycle characteristics and/or increase in resistance by using the electrolyte for a rechargeable lithium battery.
Some example embodiments provide an electrolyte for a rechargeable lithium battery including a non-aqueous organic solvent, a lithium salt, and a potassium imide salt.
In various examples, the potassium imide salt content may be or include about 0.15 to about 1.0 wt % based on 100 wt % of the electrolyte for a rechargeable lithium battery.
In other examples, the potassium imide salt content may be about 0.2 to about 0.3 wt % based on 100 wt % of the electrolyte for a rechargeable lithium battery.
For example, the potassium imide salt may be or include KFSI (potassium bis(fluorosulfonyl)imide), KTFSI (potassium bis(trifluoromethanesulfonyl)imide), KFTFSI (potassium (fluorosulfonyl) (trifluoromethanesulfonyl)imide), or a combination thereof.
The non-aqueous organic solvent may include a carbonate-based, ester-based, ether-based, ketone-based, alcohol-based, or aprotic solvent.
The non-aqueous organic solvent may include a carbonate-based solvent in which cyclic carbonate and chain carbonate are mixed in a volume ratio of about 5:95 to about 50:50.
The cyclic carbonate may include ethylene carbonate (EC), and the chain carbonate may include ethylmethyl carbonate (EMC) and dimethyl carbonate (DMC).
The lithium salt may include at least one selected from LiPF6, LiBF4, LiDFOP, LiDFOB, LiPO2F2, LiSbF6, LiAsF6, LiN(SO2C2F5)2, Li(CF3SO2)2N, LiN(SO3C2F5)2, Li(FSO2)2N ((lithium bis(fluorosulfonyl)imide: LiFSI), LiC4F9SO3, LiClO4, LiAlO2, LiAlCl4, LiN(CmF2m+1SO2)(CnF2n+1SO2), wherein, m and n are each independently integers from 1 to 20, LiCl, LiI, and LiB(C2O4)2(lithium bis(oxalato) borate: LiBOB).
A concentration of lithium salt in the electrolyte for a rechargeable lithium battery may be about 1.0 M to about 2.0 M.
Some example embodiments provide a rechargeable lithium battery including a positive electrode having a positive electrode active material, a negative electrode having a negative electrode active material, and the electrolyte.
The positive electrode active material may include a lithium nickel-based composite oxide represented by Chemical Formula 1:
Lia1Nix1M1y1M2z1O2−b1Xb1 [Chemical Formula 1]
In Chemical Formula 1,
For example, the negative electrode active material may include at least one of graphite and a Si—C composite
The Si—C composite may include a core having Si particles and amorphous carbon.
The core including the Si particles may have one or more of Si—C composite, SiOk (0<k≤2), and a Si alloy.
The Si—C composite may include a core having Si particles and amorphous carbon.
The central portion of the core may include pores.
A radius of the central portion may be about 30% to about 50% of a radius of the Si—C composite, and an average particle diameter of the Si particles may be about 10 nm to about 200 nm.
In various examples, the central portion may not include amorphous carbon, and the amorphous carbon may exist only in the surface portion of the negative electrode active material.
The negative electrode active material may further include crystalline carbon.
As the potassium imide salt is added to the electrolyte for a rechargeable lithium battery in some example embodiments, a lithiophilic film can be formed on the surface of the negative electrode, and precipitates at the interface between the negative electrode and the electrolyte can be reduced or minimized. As a result, it is possible to implement a rechargeable lithium battery with improved high-rate charging performance while suppressing or reducing deterioration of lifecycle characteristics and/or increase in resistance.
When the terms “about” or “substantially” are used in this specification in connection with a numerical value, it is intended that the associated numerical value include a tolerance of ±10% around the stated numerical value. The expression “up to” includes amounts of zero to the expressed upper limit and all values therebetween. When ranges are specified, the range includes all values therebetween such as increments of 0.1%. Moreover, when the words “generally” and “substantially” are used in connection with geometric shapes, it is intended that precision of the geometric shape is not required but that latitude for the shape is within the scope of the disclosure.
Hereinafter, a rechargeable lithium battery according to some example embodiments is described with reference to the accompanying drawings. However, these embodiments are exemplary, the present invention is not limited thereto and example embodiments are defined by the scope of claims.
Herein, as an example of a rechargeable lithium battery, a cylindrical rechargeable lithium battery is described.
Some example embodiments of the present invention provide an electrolyte for a rechargeable lithium battery including a non-aqueous organic solvent, a lithium salt, and a potassium imide salt.
In various examples, when potassium imide salt is added as an additive to the electrolyte of a rechargeable lithium battery, the potassium imide salt may simultaneously or contemporaneously coexist with the lithium salt in the rechargeable lithium battery. Accordingly, cations (i.e., K+ and Li+) of the two salts may be simultaneously or contemporaneously electrodeposited on the negative electrode surface, forming a lithiophilic film that includes both K+ and Li+ on the negative electrode surface and having a uniform thickness; and a LiF inorganic film. In examples, when potassium imide salt is not added as an additive to the electrolyte of the rechargeable lithium battery, cations of the lithium salt (i.e., Li) may be electrodeposited on the negative electrode surface and may form lithium dendrites, e.g., sharp lithium dendrites, on the negative electrode surface. Formation of the lithium dendrites may damage the lifecycle and safety of the rechargeable lithium battery.
The lithiophilic film including both K+ and Li+ on the negative electrode surface and having a uniform thickness may suppress or reduce the formation of the sharp lithium dendrite and may also reduce or minimize the formation of precipitates on the interface between the negative electrode and the electrolyte. In addition, the LiF inorganic film may lower a resistance increase rate of the negative electrode.
Furthermore, the potassium imide salt, compared with a potassium phosphate salt, has the desired or advantageous effect of forming the lithiophilic film. Specifically, the potassium imide salt includes an electron donating group, compared with a sodium phosphate salt not including the corresponding group, exhibits a desired or advantageous effect of stabilizing phosphorus pentafluoride (PF) and the like.
Based on 100 wt % of the electrolyte for a rechargeable lithium battery, a content of the potassium imide salt may be about 0.15 wt % to about 1.0 wt %, and for example, about 0.2 wt % to about 0.5 wt %, or about 0.2 wt % to about 0.3 wt %.
When the content of the potassium imide salt satisfies the above-discussed example ranges, the lithiophilic film is formed at a desired level on the negative electrode surface and thus may reduce or minimize the formation of precipitates on the interface of the negative electrode with the electrolyte. Accordingly, a rechargeable lithium battery exhibiting improved high-rate charging performance as well as suppressed or reduced deterioration of lifecycle characteristics such as duration and performance, and/or suppressed or reduced increase in resistance may be realized.
The potassium imide salt may include, e.g., KFSI (potassium bis(fluorosulfonyl)imide), KTFSI (potassium bis(trifluoromethanesulfonyl) imide), KFTFSI (potassium (fluorosulfonyl) (trifluoromethanesulfonyl) imide), or a combination thereof. For example, the potassium imide salt may be or include any one of the above-discussed three (3) types of compounds.
In various examples, the non-aqueous organic solvent in the electrolyte may constitute a medium for transmitting ions taking part in the electrochemical reaction of a battery.
For example, the non-aqueous organic solvent may include a carbonate-based, ester-based, ether-based, ketone-based, alcohol-based, or aprotic solvent.
The carbonate-based solvent may include, e.g., ethylmethyl carbonate (EMC), dimethyl carbonate (DMC), diethyl carbonate (DEC), dipropyl carbonate (DPC), methylpropyl carbonate (MPC), ethylpropyl carbonate (EPC), methylethyl carbonate (MEC), ethylene carbonate (EC), propylene carbonate (PC), butylene carbonate (BC), and the like. The ester-based solvent may include methyl acetate, ethyl acetate, n-propyl acetate, t-butyl acetate, methylpropionate, ethylpropionate, propylpropionate, decanolide, mevalonolactone, caprolactone, and the like. The ether-based solvent may include dibutyl ether, tetraglyme, diglyme, dimethoxyethane, 2-methyltetrahydrofuran, tetrahydrofuran, and the like. The ketone-based solvent may include, e.g., cyclohexanone and the like. The alcohol-based solvent may include, e.g., ethyl alcohol, isopropyl alcohol, and the like, and the aprotic solvent may include, e.g., nitriles such as R—CN (wherein R is a C2 to C20 linear, branched, or cyclic hydrocarbon group, a double bond, an aromatic ring, or an ether bond), amides such as dimethylformamide, dioxolanes such as 1,3-dioxolane, sulfolanes, and the like.
In other examples, the non-aqueous organic solvent may be used alone or in combination with one or more of any of the above carbonate-based, ester-based, ether-based, ketone-based, alcohol-based, or aprotic solvents, and when used in combination with one or more of these solvents, a mixing ratio may be appropriately adjusted according to the desired battery performance.
The carbonate-based solvent may be prepared by mixing a cyclic carbonate and a chain carbonate. The cyclic carbonate and chain carbonate may be mixed together in a volume ratio of about 5:95 to about 50:50. When the mixture is used as an electrolyte, the mixture may have enhanced performance.
For example, ethylene carbonate (EC) may be used as the cyclic carbonate, and ethylmethyl carbonate (EMC) and dimethyl carbonate (DMC) may be used as the chain carbonate.
In other examples, the non-aqueous organic solvent may include a carbonate-based solvent in which ethylene carbonate (EC), ethylmethyl carbonate (EMC), and dimethyl carbonate (DMC) are mixed. For example, the carbonate-based solvent in which ethylene carbonate (EC), ethylmethyl carbonate (EMC), and dimethyl carbonate (DMC) may be mixed is mixed in a volume ratio of EC:EMC:DMC=about 1:0.5:5 to about 5:3:10, which may improve performance of the electrolyte.
The non-aqueous organic solvent may further include an aromatic hydrocarbon-based solvent as well as the carbonate-based solvent. The carbonate-based solvent and aromatic hydrocarbon-based solvent may be mixed together in a volume ratio of about 1:1 to about 30:1.
The aromatic hydrocarbon-based solvent may be or include an aromatic hydrocarbon-based compound of Chemical Formula 3.
In Chemical Formula 3, R201 to R206 may be the same or different from each other and are selected from hydrogen, a halogen, a C1 to C10 alkyl group, a haloalkyl group, or a combination thereof.
Examples of the aromatic hydrocarbon-based solvent may be selected from benzene, fluorobenzene, 1,2-difluorobenzene, 1,3-difluorobenzene, 1,4-difluorobenzene, 1,2,3-trifluorobenzene, 1,2,4-trifluorobenzene, chlorobenzene, 1,2-dichlorobenzene, 1,3-dichlorobenzene, 1,4-dichlorobenzene, 1,2,3-trichlorobenzene, 1,2,4-trichlorobenzene, iodobenzene, 1,2-diiodobenzene, 1,3-diiodobenzene, 1,4-diiodobenzene, 1,2,3-triiodobenzene, 1,2,4-triiodobenzene, toluene, fluorotoluene, 2,3-difluorotoluene, 2,4-difluorotoluene, 2,5-difluorotoluene, 2,3,4-trifluorotoluene, 2,3,5-trifluorotoluene, chlorotoluene, 2,3-dichlorotoluene, 2,4-dichlorotoluene, 2,5-dichlorotoluene, 2,3,4-trichlorotoluene, 2,3,5-trichlorotoluene, iodotoluene, 2,3-diiodotoluene, 2,4-diiodotoluene, 2,5-diiodotoluene, 2,3,4-triiodotoluene, 2,3,5-triiodotoluene, xylene, or a combination thereof.
In order to improve battery lifecycle, the electrolyte may further include vinylene carbonate, vinyl ethylene carbonate, or an ethylene carbonate-based compound of Chemical Formula 4 as a lifecycle improving additive.
In Chemical Formula 4, R207 and R208 may be the same or different and are selected from hydrogen, a halogen, a cyano group (CN), a nitro group (NO2), or a C1 to C5 fluoroalkyl group, and at least one of R207 and R208 is a halogen, a cyano group (CN), a nitro group (NO2), or a C1 to C5 fluoroalkyl group, and R207 and R208 are not both hydrogen.
Examples of the ethylene carbonate-based compound include difluoro ethylenecarbonate, chloroethylene carbonate, dichloroethylene carbonate, bromoethylene carbonate, dibromoethylene carbonate, nitroethylene carbonate, cyanoethylene carbonate or fluoroethylene carbonate. The amount of the additive for improving lifecycle may be used within an appropriate range.
The lithium salt dissolved in the non-aqueous organic solvent supplies lithium ions in the battery, enables the basic operation of a rechargeable lithium battery, and improves transportation of the lithium ions between positive and negative electrodes. Examples of the lithium salt may include at least one selected from LiPF6, LiBF4, LiDFOP, LiDFOB, LiPO2F2, LiSbF6, LiAsF6, LiN(SO2C2F5)2, Li(CF3SO2)2N, LiN(SO3C2F5)2, Li(FSO2)2N (lithium bis(fluorosulfonyl)imide: LiFSI), LiC4F9SO3, LiClO4, LiAlO2, LiAlCl4, LiN(CmF2m+1SO2)(CnF2n+1SO2), wherein, m and n are natural numbers, for example an integer of 1 to 20, LiCl, LiI, and LiB(C2O4)2(lithium bis(oxalato) borate: LiBOB). The lithium salt may be used in a concentration ranging from about 0.1 M to about 2.0 M. When the lithium salt is included at the above concentration range, an electrolyte may have desired or advantageous performance and lithium ion mobility due to improved electrolyte conductivity and viscosity.
Some example embodiments provide a rechargeable lithium battery including a positive electrode having a positive electrode active material; a negative electrode having a negative electrode active material; and the aforementioned electrolyte.
The positive electrode may include a positive electrode current collector and a positive electrode active material layer on the positive electrode current collector, and the positive electrode active material layer may include a positive electrode active material.
The positive electrode active material may include, e.g., lithiated intercalation compounds that reversibly intercalate and de-intercalate lithium ions.
For example, at least one composite oxide of lithium and a metal of cobalt, manganese, nickel, or a combination thereof may be used.
The composite oxide having a coating layer on the surface thereof may be used, or a mixture of the composite oxide and the composite oxide having a coating layer may be used. The coating layer may include a coating element compound selected from an oxide of the coating element, a hydroxide of the coating element, an oxyhydroxide of the coating element, an oxycarbonate of the coating element, or a hydroxycarbonate of the coating element. The compound for the coating layer may be either amorphous or crystalline. The coating element included in the coating layer may be or include Mg, Al, Co, K, Na, Ca, Si, Ti, V, Sn, Ge, Ga, B, As, Zr, or a mixture thereof. The coating process may include any conventional processes as long as the process does not cause any side effects on the properties of the positive electrode active material (e.g., spray coating, dipping), and thus a detailed description thereof is omitted.
Specifically, the positive electrode active material may include a lithium nickel-based composite oxide represented by Chemical Formula 1 below:
Lia1Nix1M1y1M2z1O2−b1Xb1 [Chemical Formula 1]
In Chemical Formula 1, 0.9≤a1≤1.2, 0.7≤x1≤1, 0≤y1≤0.2, 0≤z1≤0.2, 0.9≤x1+y1+z1≤1.1, and 0≤b1≤0.1; M1 and M2 are each independently one or more element selected from Al, B, Ba, Ca, Ce, Co, Cr, Cu, Fe, Mg, Mn, Mo, Nb, Si, Sr, Ti, V, W, and Zr; and X is one or more element selected from F, P, and S.
In Chemical Formula 1, 0.75≤x1≤1, 0≤y1≤0.18, and 0≤z1≤0.18; 0.85≤x1≤1, 0≤y1≤0.15, and 0≤z1≤0.15; or 0.9≤x1≤1, 0≤y1≤0.1, and 0≤z1≤0.1.
For example, the positive electrode active material may include a lithium nickel-based composite oxide represented by Chemical Formula 2 below. The compound represented by Chemical Formula 2 may be referred to as a lithium nickel cobalt-based complex oxide:
Lia2Nix2COy2M3z2O2−b2Xb2 [Chemical Formula 2]
In Chemical Formula 2, 0.9≤a2≤1.8, 0.7≤x2<1, 0<y2≤0.2, 0≤z2≤0.2, 0.9≤x2+y2+z2≤1.1, and 0≤b2≤0.1, M3 is one or more element selected from Al, B, Ba, Ca, Ce, Cr, Fe, Mg, Mn, Mo, Nb, Si, Sr, Ti, V, W, and Zr, and X is one or more element selected from F, P, and S.
In Chemical Formula 2, 0.75≤x2≤0.99, 0≤y2≤0.15, and 0≤z2≤0.15; 0.85≤x2≤0.99, 0.01≤y2≤0.15, and 0.01≤z2≤0.15; or 0.9≤x2≤0.99, 0.01≤y2≤0.1, and 0.01≤z2≤0.1.
As an example, the positive electrode active material may include a lithium nickel-based composite oxide represented by Chemical Formula 3 below. The compound of Chemical Formula 3 may be referred to as lithium nickel-cobalt-aluminum oxide or lithium nickel-cobalt-manganese oxide.
Lia3Nix3COy3M4z3M5w3O2−b3Xb3 [Chemical Formula 3]
In Chemical Formula 3, 0.9≤a3≤1.8, 0.7≤x3≤0.98, 0.01≤y3≤0.19, 0.01≤z3≤0.19, 0≤w3≤0.19, 0.9≤x3+y3+z3+w3≤1.1, and 0≤b3≤0.1, M4 is one or more element selected from Al, and Mn, M5 is one or more element selected from B, Ba, Ca, Ce, Cr, Fe, Mg, Mo, Nb, Si, Sr, Ti, V, W, and Zr, and X is one or more element selected from F, P, and S.
In Chemical Formula 3, 0.75≤x3≤0.98, 0≤y3≤0.16, and 0≤z3≤0.16; 0.85≤x3≤0.98, 0.01≤y3≤0.14, 0.01≤z3≤0.14, and 0≤w3≤0.14; or 0.9≤x3≤0.98, 0.01≤y3≤0.09, 0.01≤z3≤0.09, and 0≤w3≤0.09.
As an example, the positive electrode active material may include a lithium nickel-based composite oxide represented by Chemical Formula 4 below. The compound of Chemical Formula 4 may be referred to be a cobalt-free lithium nickel-manganese oxide.
Lia4Nix4Mny4M6z4O2−b4Xb4 [Chemical Formula 4]
In Chemical Formula 4, 0.9≤a2≤1.8, 0.7≤x4<1, 0<y4≤0.2, 0≤z4≤0.2, 0.9≤x4+y4+z4≤1.1, and 0≤b4≤0.1, M6 is one or more element selected from Al, B, Ba, Ca, Ce, Cr, Fe, Mg, Mo, Nb, Si, Sr, Ti, V, W, and Zr, and X is one or more element selected from F, P, and S.
In the positive electrode active material according to some example embodiments, the first positive electrode active material may be included in an amount of about 50 wt % to about 90 wt %, and the second positive electrode active material may be included in an amount of about 10 wt % to about 50 wt %, based on a total amount of the first positive electrode active material and the second positive electrode active material. For example, the first positive electrode active material may be included in an amount of about 60 wt % to about 90 wt %, or about 70 wt % to about 90 wt %, and the second positive electrode active material may be included in an amount of about 10 wt % to about 40 wt %, or about 10 wt % to about 30 wt %. When the content ratio of the first and second positive electrode active materials is within the above-discussed ranges, the positive electrode active material including the same can achieve improved or high capacity, improved mixture density, and exhibit improved or high energy density.
In the positive electrode of some example embodiments, a content of the positive electrode active material may be about 90 wt % to about 98 wt %, about 50 wt % to about 99 wt %, about 60 wt % to about 99 wt %, about 70 wt % to 99 wt %, about 80 wt % to about 99 wt %, or about 90 wt % to about 99 wt % based on a total weight of the positive electrode active material layer.
In some example embodiments of the present invention, the positive electrode active material layer may also include a conductive material and a binder. In this case, the content of the conductive material and of the binder may be about 1.0 wt % to about 5.0 wt %, based on a total weight of the positive electrode active material layer.
The conductive material is used to impart conductivity to the negative electrode, and any electrically conductive material may be used as a conductive material unless the conductive material causes a chemical change in the battery. Examples of the conductive material may include a carbon-based material such as natural graphite, artificial graphite, carbon black, acetylene black, Ketjen black, carbon fiber, and the like; a metal-based material of a metal powder or a metal fiber including copper, nickel, aluminum, silver, and the like; a conductive polymer such as a polyphenylene derivative; or a mixture thereof.
The binder improves binding properties of positive electrode active material particles with one another and with a current collector. Examples of the binder may be or include polyvinyl alcohol, carboxylmethyl cellulose, hydroxypropyl cellulose, diacetyl cellulose, polyvinylchloride, carboxylated polyvinylchloride, polyvinylfluoride, an ethylene oxide-containing polymer, polyvinylpyrrolidone, polyurethane, polytetrafluoroethylene, polyvinylidene fluoride, polyethylene, polypropylene, a styrene-butadiene rubber, an acrylated styrene-butadiene rubber, an epoxy resin, nylon, and the like, but are not limited thereto.
The positive electrode current collector may include aluminum (Al), but is not limited thereto.
The negative electrode includes a negative electrode current collector and a negative electrode active material layer including a negative electrode active material formed on the negative electrode current collector.
The negative electrode active material may be or include a material that reversibly intercalates/de-intercalates lithium ions, a lithium metal, a lithium metal alloy, a material capable of doping and de-doping lithium, or a transition metal oxide.
The material that reversibly intercalates/de-intercalates lithium ions includes carbon materials. The carbon material may be or include any generally-used carbon-based negative electrode active material in a rechargeable lithium battery. Examples of the carbon material include crystalline carbon, amorphous carbon, or a combination thereof. The crystalline carbon may be non-shaped, or sheet, flake, spherical, or fiber shaped natural graphite or artificial graphite. The amorphous carbon may be or include a soft carbon, a hard carbon, a mesophase pitch carbonized product, fired coke, and the like.
The lithium metal alloy may include lithium and a metal selected from Na, K, Rb, Cs, Fr, Be, Mg, Ca, Sr, Si, Sb, Pb, In, Zn, Ba, Ra, Ge, Al, and Sn.
The material capable of doping and de-doping lithium may include Si, SiOx (0<x<2), a Si—Q alloy (wherein Q is selected from an alkali metal, an alkaline-earth metal, a Group 13 element, a Group 14 element, a Group 15 element, a Group 16 element, a transition metal, a rare earth element, or a combination thereof, and not Si), Sn, SnO2, a Sn—R alloy (wherein R is an alkali metal, an alkaline-earth metal, a Group 13 element, a Group 14 element, a Group 15 element, a Group 16 element, a transition element, a rare earth element, or a combination thereof, and not Sn), and the like. At least one of them may be mixed with SiO2.
The elements Q and R may be selected from Mg, Ca, Sr, Ba, Ra, Sc, Y, Ti, Zr, Hf, Rf, V, Nb, Ta, Db, Cr, Mo, W, Sg, Tc, Re, Bh, Fe, Pb, Ru, Os, Hs, Rh, Ir, Pd, Pt, Cu, Ag, Au, Zn, Cd, B, Al, Ga, Sn, In, TI, Ge, P, As, Sb, Bi, S, Se, Te, Po, and combination thereof.
The transition metal oxide may be or include a vanadium oxide, a lithium vanadium oxide, and the like.
In some example embodiments, the negative electrode active material may include at least one of graphite and a Si—C composite.
The Si—C composite may include a core including Si particles and amorphous carbon, and for example, the Si particles may include at least one of Si, SiOk (0<k≤2), and an Si alloy.
For example, the Si—C composite may include a core including Si particles and amorphous carbon.
The central portion of the core may include pores, and a radius of the central portion may be about 30% to about 50% of a radius of the Si—C composite.
The Si particles may have an average particle diameter of about 10 nm to about 200 nm.
As used herein, the average particle diameter of the Si particle may be a particle size (D50) at a volume ratio of 50% in a cumulative size-distribution curve.
When the average particle diameter of the Si particle is within the above range, volume expansion occurring during charging and discharging of the battery may be suppressed or reduced, and disconnection of a conductive path due to particle crushing during charging and discharging may be reduced or prevented.
The Si particles may be included in an amount of about 1 wt % to about 60 wt %, for example, about 3 wt % to about 60 wt %, based on a total weight of the Si—C composite.
The central portion may not include amorphous carbon, and the amorphous carbon may be present only in the surface portion of the negative electrode active material.
Herein, the surface portion indicates a region from the central portion of the negative electrode active material to the outermost surface of the negative electrode active material.
In addition, the Si particles are substantially uniformly included over the negative electrode active material, that is, present at a substantially uniform concentration in the central portion and the surface portion thereof.
The amorphous carbon may be or include soft carbon, hard carbon, mesophase pitch carbonized product, calcined coke, or a combination thereof.
The negative electrode active material may further include crystalline carbon.
When the negative electrode active material includes a Si—C composite and crystalline carbon together, the Si—C composite and crystalline carbon may be included in the form of a mixture, and in this case, the Si—C composite and crystalline carbon may be included in a weight ratio of about 1:99 to about 50:50. More specifically, the Si—C composite and crystalline carbon may be included in a weight ratio of about 3:97 to about 20:80 or about 5:95 to about 20:80.
The crystalline carbon may be or include, for example, graphite, and more specifically natural graphite, artificial graphite, or a mixture thereof.
The crystalline carbon may have an average particle diameter of about 5 μm to about 30 μm.
The amorphous carbon precursor may include a coal-based pitch, mesophase pitch, petroleum-based pitch, coal-based oil, petroleum-based heavy oil, or a polymer resin such as a phenol resin, a furan resin, or a polyimide resin.
In the negative electrode active material layer, the negative electrode active material may be included in an amount of about 95 wt % to about 99 wt % based on the total weight of the negative electrode active material layer.
In some example embodiments, the negative electrode active material layer may include a binder, and optionally a conductive material. In the negative electrode active material layer, the amount of the binder may be about 1 wt % to about 5 wt % based on a total weight of the negative electrode active material layer. When it further includes the conductive material, it may include about 90 wt % to about 98 wt % of the negative electrode active material, about 1 wt % to about 5 wt % of the binder, and about 1 wt % to about 5 wt % of the conductive material.
The binder improves binding properties of negative electrode active material particles with one another and with a current collector. The binder may be or include a non-water-soluble binder, a water-soluble binder, or a combination thereof.
The non-water-soluble binder may be or include polyvinylchloride, carboxylated polyvinylchloride, polyvinylfluoride, polyurethane, polytetrafluoroethylene, polyvinylidene fluoride, polyethylene, polypropylene, polyamideimide, polyimide, or a combination thereof.
The water-soluble binder may be or include a rubber-based binder or a polymer resin binder. The rubber-based binder may be selected from a styrene-butadiene rubber, an acrylated styrene-butadiene rubber (SBR), an acrylonitrile-butadiene rubber, an acrylic rubber, a butyl rubber, a fluorine rubber, or a combination thereof. The polymer resin binder may be selected from polytetrafluoroethylene, ethylenepropylene copolymer, polyethyleneoxide, polyvinylpyrrolidone, polyepichlorohydrin, polyphosphazene, polyacrylonitrile, polystyrene, an ethylene propylenediene copolymer, polyvinylpyridine, chlorosulfonated polyethylene, latex, a polyester resin, an acrylic resin, a phenolic resin, an epoxy resin, polyvinylalcohol, or a combination thereof.
When the water-soluble binder is used as the negative electrode binder, a cellulose-based compound may be further used to provide viscosity as a thickener. The cellulose-based compound includes one or more of carboxylmethyl cellulose, hydroxypropylmethyl cellulose, methyl cellulose, or alkali metal salts thereof. The alkali metal may be or include Na, K, or Li. Such a thickener may be included in an amount of 0.1 parts by weight to 3 parts by weight based on 100 parts by weight of the negative electrode active material.
In various examples, the conductive material may be included to provide electrode conductivity and any electrically conductive material may be used as a conductive material unless it causes a chemical change. Examples thereof may be a carbon-based material such as natural graphite, artificial graphite, carbon black, acetylene black, Ketjen black, carbon fiber and the like; a metal-based material such as a metal powder or a metal fiber of copper, nickel, aluminum, silver, and the like; a conductive polymer such as a polyphenylene derivative and the like, or a mixture thereof.
The negative electrode current collector may be selected from a copper foil, a nickel foil, a stainless steel foil, a titanium foil, a nickel foam, a copper foam, a polymer substrate coated with a conductive metal, or a combination thereof.
The rechargeable lithium battery may further include a separator between the negative electrode and the positive electrode, depending on a type of the rechargeable lithium battery. This separator may be or include a porous substrate; or may be or include a composite porous substrate.
The porous substrate may be or include a substrate including pores, and lithium ions may move through the pores. The porous substrate may be or include for example polyethylene, polypropylene, polyvinylidene fluoride, and multi-layers thereof such as a polyethylene/polypropylene double-layered separator, a polyethylene/polypropylene/polyethylene triple-layered separator, and a polypropylene/polyethylene/polypropylene triple-layered separator.
The composite porous substrate may have a form including a porous substrate and a functional layer on the porous substrate. The functional layer may be or include, for example, at least one of a heat-resistant layer and an adhesive layer from the viewpoint of enabling additional function. For example, the heat-resistant layer may include a heat-resistant resin and optionally a filler.
In other examples, the adhesive layer may include an adhesive resin and optionally a filler.
The filler may be or include an organic filler or an inorganic filler.
Referring to
Hereinafter, examples and comparative examples of the present invention will be described. The following example is only an example of the present invention, and the present inventive concepts are not limited to the following examples.
As a non-aqueous organic solvent, a carbonate-based solvent is prepared by mixing ethylene carbonate (EC):ethylmethyl carbonate (EMC):dimethyl carbonate (DMC)=20:20:40 in a volume ratio.
To the non-aqueous organic solvent, a 1.0 M lithium salt (LiPF6) is added, and about 0.15 wt % of a potassium imide salt (KFSI) as an additive is subsequently added thereto to obtain an electrolyte for a rechargeable lithium battery.
In this disclosure, the content (wt %) of the potassium imide salt is indicative of the content (wt %) of the potassium imide salt based on 100 wt % of the electrolyte for a rechargeable lithium battery.
An electrolyte for a rechargeable lithium battery is manufactured in the same manner as in Preparation Example 1, with the difference that about 0.2 wt % of the potassium imide salt (KFSI) is used as an additive instead of the 0.15 wt % in Preparation Example 1.
An electrolyte for a rechargeable lithium battery is manufactured in the same manner as in Preparation Example 1, with the difference that about 0.3 wt % of the potassium imide salt (KFSI) is used as an additive instead of the 0.15 wt % in Preparation Example 1.
An electrolyte for a rechargeable lithium battery is manufactured in the same manner as in Preparation Example 1, with the difference that about 0.5 wt % of the potassium imide salt (KFSI) is used as an additive instead of the 0.15 wt % in Preparation Example 1.
An electrolyte for a rechargeable lithium battery is manufactured in the same manner as in Preparation Example 1, with the difference that about 1.0 wt % of the potassium imide salt (KFSI) is used as an additive instead of the 0.15 wt % in Preparation Example 1.
An electrolyte for a rechargeable lithium battery is manufactured in the same manner as in Preparation Example 1, with the difference that about 0.3 wt % of the potassium imide salt (KTFSI) is used as an additive instead of the 0.15 wt % KFSI in Preparation Example 1.
An electrolyte for a rechargeable lithium battery is manufactured in the same manner as in Preparation Example 1, with the difference that about 0.3 wt % of the potassium imide salt (KFTFSI) is used as an additive instead of the 0.15 wt % KFSI in Preparation Example 1.
An electrolyte for a rechargeable lithium battery is manufactured in the same manner as in Preparation Example 1, with the difference that no additive is used at all unlike in in Preparation Example 1.
An electrolyte for a rechargeable lithium battery is manufactured in the same manner as in Preparation Example 1, with the difference that 0.15 wt % of a potassium phosphate salt (KPF6) instead of KFSI is used as an additive.
LiNi0.88Co0.07Al0.05O2 as a positive e electrode active material, polyvinylidene fluoride as a binder, and Ketjen black as a conductive material are mixed respectively in a weight ratio of about 97:2:1, and subsequently dispersed in N-methyl pyrrolidone to prepare a positive electrode active material slurry.
The positive electrode active material slurry is coated on an Al foil about 14 μm-thick, dried at about 110° C., and pressed to manufacture the positive electrode.
A mixture of artificial graphite and a Si—C composite in a weight ratio of about 93:7 is prepared as a negative electrode active material, and the negative electrode active material, a styrene-butadiene rubber binder, and carboxylmethyl cellulose in a weight ratio of about 97:1:2 are dispersed in distilled water to prepare a negative electrode active material slurry.
The Si—C composite includes a core including artificial graphite and silicon particles, and a coal pitch coated on the surface of the core.
The negative electrode active material slurry is coated on a Cu foil about 10 μm-thick, dried at about 100° C., and pressed to manufacture a negative electrode.
As a counter electrode, which is a negative electrode, a Li metal about 10 μm-thick is used.
The manufactured positive and negative electrodes are assembled with a polyethylene separator about 25 μm-thick to manufacture an electrode assembly, and the electrolyte for a rechargeable lithium battery according to Preparation Example 1 is injected thereinto to manufacture the rechargeable lithium battery cell.
A rechargeable lithium battery cell is manufactured in the same manner as in Example 1, with the difference that the electrolyte for a rechargeable lithium battery according to Preparation Example 2 is injected thereinto.
A rechargeable lithium battery cell is manufactured in the same manner as in Example 1, with the difference that the electrolyte for a rechargeable lithium battery according to Preparation Example 3 is injected thereinto.
A rechargeable lithium battery cell is manufactured in the same manner as in Example 1, with the difference that the electrolyte for a rechargeable lithium battery according to Preparation Example 4 is injected thereinto.
A rechargeable lithium battery cell is manufactured in the same manner as in Example 1, with the difference that the electrolyte for a rechargeable lithium battery according to Preparation Example 5 is injected thereinto.
A rechargeable lithium battery cell is manufactured in the same manner as in Example 1, with the difference that the electrolyte for a rechargeable lithium battery according to Preparation Example 6 is injected thereinto.
A rechargeable lithium battery cell is manufactured in the same manner as in Example 1, with the difference that the electrolyte for a rechargeable lithium battery according to Preparation Example 7 is injected thereinto.
A rechargeable lithium battery cell is manufactured in the same manner as in Example 1, with the difference that the electrolyte for a rechargeable lithium battery according to Comparative Preparation Example 1 is injected thereinto.
A rechargeable lithium battery cell is manufactured in the same manner as in Example 1, with the difference that the electrolyte for a rechargeable lithium battery according to Comparative Preparation Example 2 is injected thereinto.
The rechargeable lithium battery half-cells of Examples 1 to 7 and Comparative Examples 1 to 2 are constant-current (CC)-charged at a 1.5 C charging rate to a state-of-charge (SOC) of 80%, and discharged at a 0.1 C discharging rate, and a lithium dendrite precipitation amount is subsequently measured according to Equation 1 below. The results are shown in Table 1:
Referring to Table 1, Examples 1 to 7, compared with Comparative Examples 1 and 2, exhibit a suppressed or reduced lithium dendrite precipitation on the interface of the negative electrode with the electrolyte. Such suppression or reduction contributes to high-rate charging.
The rechargeable lithium battery full-cells according to Examples 1 to 6 and Comparative Examples 1 to 4 are evaluated with respect to a resistance increase rate under the following conditions, and the results are shown in Table 2.
The cells are constant current-charged to 4.2 V at a current charging rate of 1.5 C at 25° C. Subsequently, the cells were 120 cycles (120th cycle) constant current-discharged to 2.8 V at a current discharging rate of 1 C. In some or all the charge and discharge cycles, a pause of 10 minutes is set after each charge/discharge cycle.
After performing the 120 cycles' charges and discharges, the capacity retention rate (%) is calculated according to Equation 2.
In addition, after the 120 cycles' charges and discharges, the direct resistance current internal resistance (DC-IR) is measured to obtain a DC-IR increase rate (%) according to Equation 3.
In Equation 3, DC-IR (at the 120th charge and discharge cycle) is DC-IR after the 120th charge and discharge cycle at 25° C., and DC-IR (0d.) is DC-IR right before the 120th charge and discharge cycle.
Referring to Table 2, Examples 1 to 7, compared with Comparative Examples 1 and 2, exhibit increased capacity retention and exhibit a suppressed or reduced increase in resistance during the high-rate charging, thereby improving high-rate charging lifecycle.
While this disclosure has been described in connection with what is presently considered to be practical example embodiments, it is to be understood that the invention is not limited to the disclosed embodiments, but, on the contrary, is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2023-0065731 | May 2023 | KR | national |
