Patent Application
20230361345
It relates to a non-aqueous electrolyte for a lithium secondary battery and a lithium secondary battery including the same.
Lithium secondary batteries are attracting attention as power sources for various electronic devices because of a high discharge voltage and a high energy density.
As for positive active materials of lithium secondary batteries, a lithium-transition metal oxide having a structure capable of intercalating lithium ions such as LiCoO2, LiMn2O4, LiNi1-xCoxO2 (0<x<1), and the like has been used.
As for negative active materials, various carbon-based materials such as artificial graphite, natural graphite, and hard carbon capable of intercalating and deintercalating lithium ions have been used. As electrolytes for a lithium secondary battery, organic solvents in which lithium salts are dissolved have been used.
One embodiment provides a non-aqueous electrolyte for a lithium secondary battery exhibiting improved high temperature-safety by suppressing gas generation at high temperatures.
Another embodiment provides a lithium secondary battery including the non-aqueous electrolyte.
According to one embodiment, an electrolyte for a lithium secondary battery including a non-aqueous organic solvent a lithium salt and a first additive represented by Chemical Formula 1 and a second additive represented Chemical Formula 2, and a mixing ratio of the first additive and the second additive is 0.5:1 to 10:1 by weight.
(In Chemical Formula 1,
R1 to R8 are each independently a hydrogen atom, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C2 to C30 alkenyl group, a substituted or unsubstituted C2 to C30 alkynyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C3 to C30 cycloalkenyl group, a substituted or unsubstituted C3 to C30 cycloalkynyl group, or a substituted or unsubstituted C6 to C30 aryl group.)
(In Chemical Formula 2, A is a substituted or unsubstituted aliphatic chain or (—C2H4—O—C2H4—)n, and n is an integer of 1 to 10.)
In Chemical Formula 1, R1 to R8 may each independently be hydrogen atom, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C2 to C10 alkenyl group, a substituted or unsubstituted C2 to C10 alkynyl group, a substituted or unsubstituted C3 to C10 cycloalkyl group, a substituted or unsubstituted C3 to C10 cycloalkenyl group, a substituted or unsubstituted C3 to C10 cycloalkynyl group, or a substituted or unsubstituted C6 to C10 aryl group.
The mixing ratio of the first additive and the second additive may be 0.5:1 to 5:1 by weight.
In one embodiment, an amount of the first additive may be 0.25 wt % or more and less than 10 wt % when amounts of the non-aqueous organic solvent and the lithium salt are to be 100 wt %, and an amount of the first additive may be 0.5 wt % to 5 wt %, when amounts of the non-aqueous organic solvent and the lithium salt are to be 100 wt %.
An amount of the second additive may be 0.1 wt % or more, and less than 10 wt %, when amounts of the non-aqueous organic solvent and the lithium salt are to be 100 wt %, and an amount of the second additive may be 0.1 wt % to 5 wt % when amounts of the non-aqueous organic solvent and the lithium salt are to be 100 wt %.
The non-aqueous organic solvent may include a propionate-based solvent.
The propionate-based solvent may be methyl propionate, ethyl propionate, propyl propionate, or combinations thereof. In addition, an amount of the propionate-based solvent may be 30 volume % to 80 volume % based on the total volume of the non-aqueous organic solvent.
Another embodiment provides a lithium secondary battery including the non-aqueous electrolyte, a positive electrode, and a negative electrode. Other embodiments are included in the following detailed description.
An electrolyte for a lithium secondary battery according to one embodiment of the present invention may suppress gas generation at high temperatures and thus it may provide a lithium secondary battery exhibiting good high-temperature safety.
Hereinafter, embodiments of the present invention are described in detail. However, these embodiments are examples, the present invention is not limited thereto, and the present invention is defined by the scope of claims.
In the specification, when a definition is not otherwise provided, the term ‘substituted’ refers to one in which hydrogen of a compound is substituted with a substituent selected from a halogen atom (F, Br, Cl, or I), a hydroxy group, an alkoxy group, a nitro group, a cyano group, an amino group, an azido group, an amidino group, a hydrazine group, a hydrazono group, a carbonyl group, a carbamyl group, a thiol group, an ester group, a carboxyl group or a salt thereof, a sulfonic acid group or a salt thereof, phosphoric acid or a salt thereof, a C1 to C20 alkyl group, a C2 to C20 alkenyl group, a C2 to C20 alkynyl group, a C6 to C30 aryl group, a C7 to C30 arylalkyl group, a C1 to C4 alkoxy group, a C1 to C20 heteroalkyl group, a C3 to C20 heteroarylalkyl group, a C3 to C30 cycloalkyl group, a C3 to C15 cycloalkenyl group, a C6 to C15 cycloalkynyl group, a C2 to C20 heterocycloalkyl group, or a combination thereof.
A non-aqueous electrolyte for a lithium secondary battery according to one embodiment includes a non-aqueous organic solvent, a lithium salt, a first additive represented by Chemical Formula 1, and a second additive represented by Chemical Formula 2.
In Chemical Formula 1,
R1 to R8 are each independently a hydrogen atom, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C2 to C30 alkenyl group, a substituted or unsubstituted C2 to C30 alkynyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C3 to C30 cycloalkenyl group, a substituted or unsubstituted C3 to C30 cycloalkynyl group, or a substituted or unsubstituted C6 to C30 aryl group.
In one embodiment, the R1 to R8 may each independently be a hydrogen atom, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C2 to C10 alkenyl group, a substituted or unsubstituted C2 to C10 alkynyl group, a substituted or unsubstituted C3 to C10 cycloalkyl group, a substituted or unsubstituted C3 to C10 cycloalkenyl group, a substituted or unsubstituted C3 to C10 cycloalkynyl group, or a substituted or unsubstituted C6 to C10 aryl group.
In Chemical Formula 2, A is a substituted or unsubstituted aliphatic chain or (—C2H4—O—C2H4—)n, and n is an integer of 1 to 10.
According to one embodiment, the A may be a C2 to C20 hydrocarbon chain or (—C2H4—O—C2H4—)n, and n may be an integer of 1 to 5.
Herein, a mixing ratio of the first additive and the second additive may be 0.5:1 to 10:1 by weight, 0.5:1 to 5:1 by weight, or 1:1 to 5:1 by weight.
The electrolyte for the lithium secondary battery according to one embodiment includes both a first additive and a second additive, and particularly, in a weight ratio of 0.5:1 to 10:1 by weight, and the first additive may form a rigid thin layer on a surface of a positive electrode, thereby preventing the deterioration of the positive electrode at high temperature, and the second additive may be reduction-decomposed to form a thin layer on a surface of a negative electrode, thereby suppressing breakdown of an SEI layer due to a side reaction of the electrolyte at high temperatures. Furthermore, the second additive may render to stabilize the lithium salt so that elution of the metal from the positive active material by generation of HF and decomposition of a solvent due to the decomposition of the lithium salt decomposition may be suppressed.
Using of the both the first additive and the second additive allows formation of a suitable thin layer on the positive electrode and the negative electrode, thereby not largely increasing the initial thickness and inhibiting the deterioration of the positive electrode and the decomposition of the thin layer of the negative electrode at high temperatures, and thus, a generated amount of gas may be effectively reduced during storage at high temperatures. Even though both the first additive and the second additive are included, if the mixing ratio is out of the range, that is, the first additive is used in an amount of less than ½ times that of the second additive, high-temperature characteristics may be deteriorated, and when the first additive is used in an amount of more than 10 times that of the second additive, the viscosity of the electrolyte is increased to deteriorate the charge characteristics of the battery.
The effects of using both the first additive and the second additive may be realized by only using the compound represented by Chemical Formula 1 as the first additive.
Such effects may be obtained as the compound of Chemical Formula 1 may from a firm film on a surface of the positive electrode, rather than a compound such as a sulfoxide, even though the compound of Chemical Formula 1 includes sulfur. Accordingly, when any compound including sulfur, but not having the structure of Chemical Formula 1 is used as the first additive, effects derived therefrom are insufficient which is undesired.
Herein, an amount of the first additive represented by Chemical Formula 1 may be 0.25 wt % or more and less than 10 wt % based on the weight of the non-aqueous organic solvent and the lithium salt, that is, the amounts of the non-aqueous organic solvent and the a lithium salt are to be 100 wt % (based on the total, 100 wt %, of the non-aqueous organic solvent and the lithium salt), and according to one embodiment, may be 0.5 wt % to 5 wt %. When the amount of the first additive represented by Chemical Formula 1 is satisfied in the range, the high-temperature reliability characteristics, for example, the improvement in high-temperature capacity retention and the decrease in high temperature resistance may be realized.
Furthermore, the amount of the second additive represented by Chemical Formula 2 may be 0.1 wt % or more and less than 10 wt % based on the weight of the non-aqueous organic solvent and the lithium salt, that is, the amounts of the non-aqueous organic solvent and the lithium salt are to be 100 wt % (based on the total, 100 wt %, of the non-aqueous organic solvent and the lithium salt), and according to one embodiment, 0.1 wt % to 5 wt %, or 0.1 wt % to 3 wt %. When the amount of the second additive represented by Chemical Formula 2 is satisfied in the range, the high-temperature reliability characteristics, for example, the improvement in high-temperature capacity retention and the decrease in high temperature resistance, may be realized.
In the electrolyte according to one embodiment, the non-aqueous organic solvent may include a carbonate-based solvent, and may further include a propionate-based solvent. The propionate-based solvent may be methyl propionate, ethyl propionate, propyl propionate, or combinations thereof. When the propionate-based solvent is used in a mixture, the mixing ratio may be suitably controlled.
In the non-aqueous organic solvent, an amount of the propionate-based solvent may be 30 volume % to 80 volume % based on the total volume of the non-aqueous organic solvent, and according to one embodiment, may be 40 volume % to 80 volume %. When the amount of the propionate-based solvent is within the range, the electrolyte solution impregnation may be improved.
The carbonate-based solvent may be 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), or combinations thereof. When the carbonate-based solvent is used in a mixture, the mixing ratio may be suitably controlled. Furthermore, the carbonate-based solvent may desirably include a mixture with a cyclic carbonate and a linear carbonate. Herein, the cyclic carbonate and the linear carbonate are mixed together in a volume ratio of about 1:1 to about 1:9, and when the mixture is used as an electrolyte, it may have enhanced performance.
In one embodiment, the non-aqueous organic solvent may further include an ester-based, ether-based, ketone-based, alcohol-based, or aprotic solvent.
The ester-based solvent may be methyl acetate, ethyl acetate, n-propyl acetate, t-butyl acetate, methyl propionate, ethyl propionate, propyl propionate, γ-butyrolactone, decanolide, valerolactone, mevalonolactone, caprolactone, and the like.
The ether-based solvent may be dibutyl ether, tetraglyme, diglyme, dimethoxyethane, 2-methyltetrahydrofuran, tetrahydrofuran, and the like, and the ketone-based solvent may be cyclohexanone, and the like.
The alcohol-based solvent may include ethyl alcohol, isopropyl alcohol, and the like, and the aprotic solvent may include nitriles such as T-CN (where T is a C2 to C20 linear, branched, or cyclic hydrocarbon, and may include a double bond, an aromatic ring, or an ether bond), amides such as dimethylformamide, dioxolanes such as 1,3-dioxolane, and the like.
In addition, the organic solvent may further include an aromatic hydrocarbon-based solvent. The aromatic hydrocarbon-based organic solvent may be an aromatic hydrocarbon-based compound represented by Chemical Formula 3.
(In Chemical Formula 3, R9 to R14 are the same or different, and are selected from hydrogen, a halogen, a C1 to C10 alkyl group, a haloalkyl group, and a combination thereof.)
Specific examples of the aromatic hydrocarbon-based organic 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 combinations thereof.
The electrolyte may further include vinyl ethyl carbonate, vinylene carbonate, or an ethylene carbonate-based compound represented by Chemical Formula 4, as an additive for improving cycle life.
(In Chemical Formula 4, R15 and R16 are the same or different and may each independently be hydrogen, a halogen, a cyano group (CN), a nitro group (NO2), or a C1 to C5 fluoroalkyl group, provided that at least one of R7 and R8 is a halogen, a cyano group (CN), a nitro group (NO2), or a C1 to C5 fluoroalkyl group, and R7 and R8 are not simultaneously hydrogen.)
Examples of the ethylene carbonate-based compound may be difluoro ethylene carbonate, chloroethylene carbonate, dichloroethylene carbonate, bromoethylene carbonate, dibromoethylene carbonate, nitroethylene carbonate, cyanoethylene carbonate, or fluoroethylene carbonate, and the like. An amount of the additive for improving the cycle-life characteristics may be used within an appropriate range.
The lithium salt dissolved in an organic solvent supplies a battery with lithium ions, basically operates the rechargeable lithium battery, and improves transportation of the lithium ions between a positive electrode and a negative electrode. Examples of the lithium salt include at least one or two supporting salts selected from LiPF6, LiSbF6, LiAsF6, LiPO2F2, LiN(SO2C2F5)2, Li(CF3SO2)2N, LiN(SO3C2F5)2, Li(FSO2)2N (lithium bis(fluorosulfonyl)imide: LiFSI), LiC4F9SO3, LiCIO4, LiAlO2, LiAlCl4, LiPO2F2, LiN(CxF2x+1SO2)(CyF2y+1SO2), wherein x and y are natural numbers, for example, an integer of 1 to 20), lithium difluoro(bisoxolato) phosphate), LiCl, Lil, LiB(2O4)2 (lithium bis(oxalato) borate: LiBOB), and lithium difluoro(oxalato)borate (LiDFOB). A concentration of the lithium salt may range 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 excellent performance and lithium ion mobility due to optimal electrolyte conductivity and viscosity.
One embodiment provides a lithium secondary battery including the non-aqueous electrolyte.
The lithium secondary battery includes the non-aqueous electrolyte, a negative electrode, and a positive electrode.
In one embodiment, the negative electrode includes a negative active material layer including a negative active material and a current collector supported thereon.
The negative active material includes a material that reversibly intercalates/deintercalates lithium ions, a lithium metal, a lithium metal alloy, a material capable of doping/dedoping lithium, or a transition metal oxide.
The material that reversibly intercalates/deintercalates lithium ions may be a carbon material that may be any generally-used carbon-based negative active material used in a lithium secondary battery. Examples thereof may be crystalline carbon, amorphous carbon, or a combination thereof. The crystalline carbon may be shapeless (unspecified shape), or may be sheet, flake, spherical, or fiber shaped natural graphite or artificial graphite, and the amorphous carbon may be soft carbon or hard carbon, a mesophase pitch carbonized product, fired cokes, and the like.
The lithium metal alloy may be an alloy of 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/dedoping lithium may be Si, SiOx (0<x<2), a Si-Q alloy (wherein Q is an element 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, and a combination thereof, and not Si), Sn, SnO2, a Sn—R alloy (wherein R is an element 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, and a combination thereof, and not Sn), and the like, and at least one of these materials may be mixed with SiO2. The elements Q and R may be 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 a combination thereof.
The transition elements oxide may be a lithium titanium oxide.
The negative active material according to one embodiment may include a Si—C composite including a Si-based active material and a carbon-based active material.
The Si-based active material is Si, SiOx (0<x<2), or a Si-Q alloy (wherein Q is an element 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, and a combination thereof thereof, and not Si).
An average particle diameter of the Si-based active material may be 50 nm to 200 nm.
When the particle diameter of the Si particle is within the range, the volume expansion caused during charge and discharge may be suppressed, and breakage of the conductive path due to crushing of particles may be prevented.
The Si-based active material may be included in an amount of 1 wt % to 60 wt % based on the total weight of the Si—C composite, and for example, 3 wt % to 60 wt %.
The negative active material according to another embodiment may further include a crystalline carbon in addition to the Si—C composite.
If the negative active material includes both the Si—C composite and crystalline carbon, the Si—C composite and the crystalline carbon may be included in the form of a mixture, and herein, the Si—C composite and the crystalline carbon may be included at a weight ratio of 1:99 to 50:50. More specifically, the Si—C composite and the crystalline carbon may be included in a weight ratio of 5:95 to 20:80.
The crystalline carbon, may, for example, include graphite, and more specifically, may include natural graphite, artificial graphite, or mixtures thereof.
The crystalline carbon may have an average particle diameter of 5 μm to 30 μm.
In the specification, the average a particle diameter refers to a particle size (D50) where a cumulative volume is 50 volume % in a cumulative size-distribution curve.
The Si—C composite may further include a shell surrounded on a surface of the Si—C composite, and the shell may include amorphous carbon. A thickness of the shell may be 5 nm to 100 nm.
The amorphous carbon may be soft carbon, hard carbon, mesophase pitch carbide, a sintered coke, or a mixture thereof.
The amorphous carbon may be included at an amount of 1 part by weight to 50 parts by weight based on 100 parts by weight of the carbon-based active material, for example, 5 parts by weight to 50 parts by weight, or 10 parts by weight to 50 parts by weight.
The negative active material layer may further include a conductive material.
In the negative active material layer, an amount of the negative active material may be about 95 wt % to about 99 wt % based on the negative active material layer. An amount of the binder may be about 1 wt % to about 5 wt % based on the total, 100 wt %, of the negative active material layer. Further, when the negative active material layer includes a conductive material, the negative active material layer includes about 90 wt % to about 98 wt % of the negative 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 active material particles with one another and with a current collector. The binder includes a non-aqueous binder, an aqueous binder, or a combination thereof.
The non-aqueous binder may be an ethylene propylene copolymer, polyacrylonitrile, polystyrene, polyvinylchloride, carboxylated polyvinylchloride, polyvinyl fluoride, polyurethane, polytetrafluoroethylene, polyvinylidene fluoride, polyethylene, polypropylene, polyamideimide, polyimide, or combinations thereof.
The aqueous binder may include styrene-butadiene rubber, an acrylated styrene-butadiene rubber, an acrylonitrile-butadiene rubber, an acrylic rubber, a butyl rubber, a fluorine rubber, an ethylene oxide-containing polymer, polyvinylpyrrolidone, polyepichlorohydrin, polyphosphazene, an ethylene propylene diene copolymer, polyvinylpyridine, chlorosulfonated polyethylene, latex, a polyester resin, an acrylic resin, a phenolic resin, an epoxy resin, polyvinyl alcohol, or combinations thereof.
When the aqueous binder is used as a 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 carboxymethyl cellulose, hydroxypropyl methyl cellulose, methyl cellulose, or alkali metal salts thereof. The alkali metal may be Na, K, or L. The thickener may be included in an amount of about 0.1 parts by weight to about 3 parts by weight based on 100 parts by weight of the negative active material.
The conductive material is included to provide electrode conductivity, and any electrically conductive material may be used as a conductive material unless it causes a chemical change. Examples of the conductive material may be a carbon-based material such as natural graphite, artificial graphite, carbon black, acetylene black, ketjen black, a 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 current collector may include one 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, and a combination thereof, but is not limited thereto.
In one embodiment, the positive electrode including the positive active material includes a positive active material layer including the positive active material and a current collector supporting the positive active material layer.
The positive electrode active material may include lithiated intercalation compounds that reversibly intercalate and deintercalate lithium ions, and specifically, one or more composite oxides of a metal selected from cobalt, manganese, nickel, and a combination thereof, and lithium may be used. More specifically, the compounds represented by one of the following chemical formulae may be used. LiaA1-bXbD2 (0.90≤a≤1.8, 0≤b≤0.5); LiaA1-bXbO2-cDc (0.90≤a≤1.8, 0≤b≤0.5, 0≤c≤0.05); LiaE1-bXbO2-cDc (0.90≤a≤1.8, 0≤b≤0.5, 0≤c≤0.05); LiaE2-bXbO4-cDc (0.90≤a≤1.8, 0≤b≤0.5, 0≤c≤0.05); LiaNi1-b-cCobXcDa (0.90≤a≤1.8, 0≤b≤0.5, 0≤c≤0.5, 0<a≤2); LiaNi1-b-cCObXcO2-aTa (0.90≤a≤1.8, 0≤b≤0.5, 0≤c≤0.5, 0<a<2); LiaNi1-b-cCObXcO2-aT2 (0.90≤a≤1.8, 0≤b≤0.5, 0≤c≤0.5, 0<a<2); LiaNi1-b-cMnbXcDa (0.90≤a≤1.8, 0≤b≤0.5, 0≤c≤0.5, 0<a≤2); LiaNi1-b-cMnbXcO2-aTa (0.90≤a≤1.8, 0≤b≤0.5, 0≤c≤0.5, 0<a<2); LiaNi1-b-cMnbXcO2-aT2 (0.90≤a≤1.8, 0≤b≤0.5, 0≤c≤0.5, 0<a<2); LiaNibEcGdO2 (0.90≤a≤1.8, 0≤b≤0.9, 0≤c≤0.5, 0.001≤d≤0.1); LiaNibCocMndGeO2 (0.90≤a≤1.8, 0≤b≤0.9, 0≤c≤0.5, 0≤d≤0.5, 0.001≤e≤0.1); LiaNiGbO2 (0.90≤a≤1.8, 0.001≤b≤0.1) LiaCoGbO2 (0.90≤a≤1.8, 0.001≤b≤0.1); LiaMn1-bGbO2 (0.90≤a≤1.8, 0.001≤b≤0.1); LiaMn2GbO4 (0.90≤a≤1.8, 0.001≤b≤0.1); LiaMn1-gGgPO4 (0.90≤a≤1.8, 0≤g≤0.5); QO2; QS2; LiQS2; V2O5; LiV2O5; LiZO2; LiNiVO4 Li(3-f)J2(PO4)3 (0≤f≤2); Li(3-f)Fe2(PO4)3 (0≤f≤2); LiaFePO4 (0.90≤a≤1.8)
In the above chemical formulae, A is selected from Ni, Co, Mn, and a combination thereof; X is selected from Al, Ni, Co, Mn, Cr, Fe, Mg, Sr, V, a rare earth element, and a combination thereof; D is selected from O, F, S, P, and a combination thereof; E is selected from Co, Mn, and a combination thereof; T is selected from F, S, P, and a combination thereof; G is selected from Al, Cr, Mn, Fe, Mg, La, Ce, Sr, V, and a combination thereof; Q is selected from Ti, Mo, Mn, and a combination thereof; Z is selected from Cr, V, Fe, Sc, Y, and a combination thereof; and J is selected from V, Cr, Mn, Co, Ni, Cu, and a combination thereof.
Also, the compounds may have a coating layer on the surface, or may be mixed with another compound having a coating layer. The coating layer may include at least one coating element compound selected from the group consisting of an oxide of a coating element, a hydroxide of a coating element, an oxyhydroxide of a coating element, an oxycarbonate of a coating element, and a hydroxyl carbonate of a coating element. The compound for the coating layer may be amorphous or crystalline. The coating element included in the coating layer may include Mg, Al, Co, K, Na, Ca, Si, Ti, V, Sn, Ge, Ga, B, As, Zr, or a mixture thereof. The coating layer may be disposed in a method having no adverse influence on properties of a positive electrode active material by using these elements in the compound, and for example, the method may include any coating method such as spray coating, dipping, and the like, but is not illustrated in more detail since it is well-known in the related field.
In the positive electrode, an amount of the positive active material may be about 90 wt % to about 98 wt % based on the total weight of the positive active material layer.
In one embodiment, the positive active material layer may further include a binder and a conductive material. Herein, the amount of the binder and the conductive material may be 1 wt % to 5 wt %, respectively, based on the total amount of the positive active material layer.
The binder improves binding properties of positive electrode active material particles with one another and with a current collector, and examples of the binder may be polyvinyl alcohol, carboxymethyl cellulose, hydroxypropyl cellulose, diacetyl cellulose, polyvinylchloride, carboxylated polyvinylchloride, polyvinylfluoride, an ethylene oxide-containing polymer, polyvinylpyrrolidone, polyurethane, polytetrafluoroethylene, polyvinylidene fluoride, polyethylene, polypropylene, styrene butadiene rubber, acrylated styrene butadiene rubber, an epoxy resin, nylon, and the like, but are not limited thereto.
The conductive material is included to provide electrode conductivity, and any electrically conductive material may be used as a conductive material unless it causes a chemical change. Examples of the conductive material include a carbon-based material such as natural graphite, artificial graphite, carbon black, acetylene black, ketjen black, a 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 current collector may use aluminum foil, nickel foil, or a combination thereof, but is not limited thereto.
The positive active material layer and the negative active material layer may be formed by mixing an active material, a binder, and optionally a conductive material in a solvent to prepare an active material composition and coating the active material composition on a current collector. Such an active material layer preparation method is well known and thus is not described in detail in the present specification. The solvent includes N-methyl pyrrolidone and the like, but is not limited thereto. In addition, when the binder is a water-soluble binder in the negative active material layer, the solvent used for preparing the negative active material composition may be water.
Furthermore, a separator may be disposed between the positive electrode and the negative electrode depending on a type of a rechargeable lithium battery. The separator may use polyethylene, polypropylene, polyvinylidene fluoride, or multi-layers thereof having two or more layers, and may be a mixed multilayer such as a polyethylene/polypropylene double-layered separator, a polyethylene/polypropylene/polyethylene triple-layered separator, a polypropylene/polyethylene/polypropylene triple-layered separator, and the like.
According to one embodiment, the separator may also be a composite porous separator including a porous substrate and a functional layer positioned on the porous substrate. The functional layer may have additional functions, and for example, may be at least one of a heat-resistance layer and an adhesive layer. The heat-resistance layer may include a heat-resistance resin and optionally a filler. In addition, the adhesive layer may include an adhesive resin and optionally a filler. The filler may be an organic filler, an inorganic filler, or combinations thereof. The heat-resistance resin and the adhesive resin may be any materials which may be used in the separator in the related art.
Referring to
Hereinafter, examples of the present invention and comparative examples are described. These examples, however, are not in any sense to be interpreted as limiting the scope of the invention.
1.5 M LiPF6 was dissolved in a non-aqueous organic solvent in which ethylene carbonate, propylene carbonate, ethyl propionate, and propyl propionate were mixed in a volume % of 20:10:30:40 to prepare an electrolyte for a lithium secondary cell.
1.5 M LiPF6 was dissolved in a non-aqueous organic solvent in which ethylene carbonate, propylene carbonate, ethyl propionate, and propyl propionate were mixed in a volume % of 20:10:30:40, and a sulfolane of Chemical Formula 1a as a first additive and a compound of Chemical Formula 2a as a second additive were added thereto, thereby preparing an electrolyte for a lithium secondary battery. Herein, the amount of sulfolane of Chemical Formula 1a as the first additive was set to be 5 wt % based on the total amount, 100 wt %, of the non-aqueous organic solvent and the lithium salt, the compound of Chemical Formula 2a as the second additive was set to be 0.5 wt % based on the total amount, 100 wt % of the non-aqueous organic solvent and the lithium salt, and thus, the mixing ratio of the first additive and the second additive was 10:1.
97 wt % of an artificial graphite negative active material, 1 wt % of a ketjen black conductive material, 1 wt % of a styrene-butadiene rubber binder, and 1 wt % of a carboxymethyl cellulose thickener were mixed in a distilled water solvent to prepare a negative active material slurry. The negative active material slurry was coated on a copper foil, dried, and pressurized to prepare a negative electrode.
96 wt % of a LiCoO2 positive active material, 2 wt % of a ketjen black conductive material and 2 wt % of polyvinylidene fluoride were mixed in an N-methylpyrrolidone solvent to prepare a positive active material slurry. The positive active material slurry was coated on an aluminum foil and dried followed by pressurizing to prepare a positive electrode.
Using the electrolyte, the positive electrode, and the negative electrode, a 4.4 V grade pouch lithium secondary cell was fabricated according to the convention procedure.
Electrolytes were prepared by the same procedure as in Example 1, except that the used amount of sulfolane of Chemical Formula 1a and the used amount of the compound of Chemical formula 2a were changed as shown in Table 1, and lithium secondary cells were fabricated by the same procedure as in Example 1, except that the electrolyte, and the negative electrode and the positive electrode of Example 1, were used.
The lithium secondary cells the Examples 1 to 11 and Comparative Examples 1 to 5 were constant current-constant voltage charged at 0.7 C, 4.4 V, and 0.05 C cut-off condition at 25° C., and stored at 60° C. for 30 days. Thicknesses of the cells before storage (initial thickness) were measured and thicknesses of the cells after storing for 30 days were measured. From these results, the cell thickness increase ratio, were calculated, and the results, together with the initial thickness, and the thickness after being stored at 60° C. for 30 days are shown in Table 2.
Thickness increase ratio of thickness[%]=[(Cell thickness after 30 days at 60° C.−Cell thickness before storage)/Cell thickness before storage]×100 [Equation 1]
The lithium secondary cells allowed to stand at a high temperature (60° C.) for 30 days according to Experimental Example 1 were discharged at 0.2 C to 3.0 V at room temperature (25° C.) under a constant current condition to measure a discharge capacity.
Thereafter, in order to evaluate capacity recovery, the lithium secondary cells in which discharge capacity test was performed, were recharged at 0.2 C to 4.4 V under a constant current condition and under a constant voltage with an end current of 0.05 C, and discharged at 0.2 C to 3.0 V under a constant current condition to measure a discharge capacity. In addition, capacity recovery was calculated according to Equation 2 and the results are shown in Table 2.
Capacity recovery [%]=[Discharge capacity of the recharged lithium secondary cell after allowing to stand at a high temperature/Initial discharge capacity before allowing to stand at a high temperature]×100 [Equation 2]
As shown in Table 2, Examples 1 to 11 in which the electrolyte with the first and second additives at a 0.5 1 to 10:1 by weight ratio was used, exhibited a surprisingly low thickness increase ratio at high temperature storage, while the good capacity retention and capacity recovery were maintained, and thus, the amount of gas generated at high temperature storage was effectively decreased.
Whereas, Comparative Example 1 using the electrolyte without the first and the second additives exhibited extremely high thickness increase ratio, and Comparative Example 2 and Comparative Example 4 using the electrolytes at a too small amount of the first additive at a mixing ratio of 0.1:1 exhibited insufficiently reduction in thickness increase ratio. Furthermore, Comparative Examples 3 and 5 using the electrolyte with the first additive at a too large
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2020-0148014 | Nov 2020 | KR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2021/013943 | 10/8/2021 | WO |
