Patent Application
20240356023
This application relates to the field of energy storage, and in particular, to an electrochemical device and an electronic device, especially a lithium-ion battery.
In recent years, with the rapid development of electronic products such as smartphones, tablet computers, and smart wearables, consumers are requiring a higher energy density of lithium-ion batteries to adapt to different service durations and operating environments of the electronic products. Currently, the energy density of a lithium-ion battery is typically improved by using high-voltage lithium cobalt oxide (4.4 V or above) as a positive active material and using graphite of a high capacity and a high compaction density as a negative electrode material. However, the cycle performance and safety of such lithium-ion batteries deteriorate significantly with the increase of the temperature and voltage. In addition, with the intensification of the harsh environment caused by global warming (for example, in special operating environments in India, Africa, and the like), higher requirements are imposed on the high-temperature performance of batteries.
In view of this, it is necessary to provide an electrochemical device and electronic device of improved high-temperature performance.
Some embodiments of this application provide an electrochemical device and an electronic device that exhibit improved high-temperature cycle performance and safety to solve some problems in the prior art to some extent.
According to one aspect of this application, this application provides an electrochemical device. The electrochemical device includes: a positive electrode, a negative electrode, and an electrolyte solution. The positive electrode includes a positive current collector and a positive active material layer formed on the positive current collector. The positive active material layer includes a positive active material and a binder. The positive active material includes a first element. The first element includes at least one of aluminum, magnesium, titanium, zirconium, or tungsten. A density of the binder is a g/cm3, where a ranges from 0.6 to 1.5.
According to an embodiment of this application, a ranges from 0.6 to 1.2, 0.7 to 1.0, or 0.7 to 0.9.
According to an embodiment of this application, a porosity of the binder is b %, b ranges from 20 to 50, and a and b satisfy: 17≤a×b≤60.
According to an embodiment of this application, the binder includes a fluorine-containing polymer, preferably polyvinylidene difluoride.
According to an embodiment of this application, the electrochemical device satisfies at least one of the following conditions:
According to an embodiment of this application, the first element includes aluminum. Based on a mass of the positive active material, a mass percentage of aluminum is x %, and x and a satisfy: 0.2≤x/a≤1.
According to an embodiment of this application, the electrolyte solution includes a sulfur-oxygen double bond-containing compound. Based on a mass of the electrolyte solution, a mass percentage of the sulfur-oxygen double bond-containing compound is c %, and c ranges from 0.01 to 5.
According to an embodiment of this application, c and a satisfy: 0.5≤c/a≤3.
According to an embodiment of this application, the electrolyte solution includes a trinitrile compound. Based on a mass of the electrolyte solution, a mass percentage of the trinitrile compound is d %, and d ranges from 0.01 to 5.
According to an embodiment of this application, d and a satisfy: 0.2≤d/a≤4.
According to an embodiment of this application, the electrolyte solution includes at least one of succinonitrile, adiponitrile, ethylene glycol bis(2-cyanoethyl)ether, fluoroethylene carbonate, vinylene carbonate, or 1-propyl phosphate cyclic anhydride.
According to another aspect of this application, this application provides an electronic device. The electronic device includes the electrochemical device according to this application.
The doping element-containing positive active material and a low-density binder are used in combination in this application to effectively improve the interfacial stability of the positive electrode, thereby significantly improving the high-temperature cycle performance and safety of the electrochemical device.
Additional aspects and advantages of some embodiments of this application will be partly described or illustrated herein later or expounded through implementation of an embodiment of this application.
Some embodiments of this application will be described in detail below. No embodiment of this application is to be construed as a limitation on this application.
Unless otherwise expressly specified, the following terms used herein have the meanings defined below.
In the detailed description of embodiments and claims, a list of items recited by using the term “at least one of” may mean any combination of the recited items. For example, if items A and B are listed, the phrases “at least one of A and B” and “at least one of A or B” mean: A alone; B alone; or both A and B. In another example, if items A, B, and C are listed, the phrases “at least one of A, B, and C” and “at least one of A, B, or C” mean: A alone; B alone; C alone; A and B (excluding C); A and C (excluding B); B and C (excluding A); or all of A, B, and C. The item A may include a single element or a plurality of elements. The item B may include a single element or a plurality of elements. The item C may include a single element or a plurality of elements. The term “at least one type of” has the same meaning as the term “at least one of”.
The energy density of an electrochemical device (such as a lithium-ion battery) is typically improved by using high-voltage lithium cobalt oxide (4.4 V or above) as a positive active material and using graphite of a high capacity and a high compaction density as a negative electrode material. However, with the increase of the temperature and voltage, the structural stability of the lithium cobalt oxide deteriorates, and metal ions are prone to dissolve out of a positive electrode and reductively deposit on the surface of a negative electrode, thereby disrupting the structure of the solid electrolyte interphase (SEI) film of the negative electrode, leading to a continuous increase in the negative electrode impedance and the thickness of the battery, and in turn, resulting capacity loss of the lithium-ion battery and deterioration of the cycle performance. In addition, at high temperature and high voltage, the electrolyte solution is prone to oxidative decomposition on the surface of the positive electrode to generate a large amount of gas, thereby leading to swelling of the lithium-ion battery and disruption of the electrode interface, and in turn, deteriorating the performance of the lithium-ion battery. Meanwhile, at high temperature and high voltage, because the oxidation activity of the lithium cobalt oxide is high, the side reactions between the lithium cobalt oxide and the electrolyte solution intensify, thereby resulting in continuous deposition of the decomposition product of the electrolyte solution on the surface of the positive electrode. This further increases the internal resistance of the lithium-ion battery, thereby adversely affecting the high-temperature cycle performance of the lithium-ion battery. These factors pose great safety hazards to the lithium-ion battery.
In the industry, the positive active material (such as lithium cobalt oxide or ternary material) is typically doped with aluminum, magnesium, titanium, zirconium, or tungsten. The doping aluminum and magnesium can more easily enter the crystalline structure of the material while the doping titanium and zirconium tend to concentrate richly on the surface of the particles. Tungsten is used for improving electrical conductivity. However, no reports have been found on the use of such elements for improving the safety of an electrochemical device. In addition, the density of most binders currently used in a positive electrode slurry is 1.7 g/cm3 or above. Based on what is already known, it is not anticipated that a positive active material containing at least one of aluminum, magnesium, titanium, zirconium, or tungsten can be used together with a low-density binder to substantially improve the high-temperature cycle performance and safety performance of the electrochemical device.
In this application, the positive active material containing at least one of aluminum, magnesium, titanium, zirconium, or tungsten is used together with a low-density binder to unexpectedly solve the problems related to high-temperature cycling and safety performance of the electrochemical device. Doping the positive active material with at least one of aluminum, magnesium, titanium, zirconium, or tungsten can effectively improve the stability of a crystal lattice, thereby suppressing the volume change of the particles during charge-discharge cycling at high or low temperature, and in turn, reducing particle cracks and fragmentation and improving the interfacial stability of the positive electrode. The low-density binder can achieve a good bonding effect. In addition, during the preparation of the positive electrode, the low-density binder is little affected by the compaction density, and helps to improve the surface performance of the positive electrode. The specified combination of the positive active material and the binder in this application not only effectively improves the high-temperature cycle performance of the electrochemical device, but also significantly improves the safety (for example, short-circuit safety and thermal abuse safety) of the electrochemical device.
The positive electrode includes a positive current collector and a positive active material layer formed on the positive current collector. The positive active material layer may be a single layer or a plurality of layers. The positive active material layer includes a positive active material. Each layer in the plurality of positive active material layers may include the same or different positive active materials.
A main characteristic of the electrochemical device of this application is: the positive active material layer includes a positive active material and a binder; the positive active material includes a first element; the first element includes at least one of aluminum, magnesium, titanium, zirconium, or tungsten; and a density of the binder is a g/cm3, where a ranges from 0.6 to 1.5. In some embodiments, a ranges from 0.6 to 1.2. In some embodiments, a ranges from 0.7 to 1.0. In some embodiments, a ranges from 0.7 to 0.9.
The density of a positive binder commonly used in the battery field is typically greater than 1.7 g/cm3 to ensure a sufficient bonding force. However, the applicant hereof unexpectedly finds that when the density of the positive binder is greater than 1.5 g/cm3, the flexibility of the positive electrode is affected to some extent, the positive binder is prone to fracture during winding. When the density of the positive binder is less than 0.6 g/cm3, the bonding force of the binder is insufficient, thereby adversely affecting the electrochemical stability of the electrochemical device. Moreover, the positive binder includes a relatively large number of porous structures, thereby improving the strength of the electrode and accelerating the infiltration of the electrolyte solution. When the density of the positive binder is controlled to fall within the above range, not only the adhesiveness is high, but also the high-temperature cycle performance and safety of the electrochemical device are improved significantly.
In some embodiments, the porosity of the binder is b %, and b ranges from 20 to 50. In some embodiments, b ranges from 25 to 45. In some embodiments, b is 20, 22, 25, 30, 35, 40, 45, 50, or a value falling within a range formed by any two thereof. When the porosity of the binder is controlled to fall within the above range, the high-temperature cycle performance and safety of the electrochemical device are further improved.
In some embodiments, a and b satisfy: 17≤a×b≤60. In some embodiments, a and b satisfy the following relationship: 20≤a×b≤50. In some embodiments, a×b is 17, 18, 19, 20, 25, 30, 35, 40, 45, 50, 55, 60, or a value falling within a range formed by any two thereof. When the density and porosity of the binder satisfy the above relationship, the high-temperature cycle performance and safety of the electrochemical device are further improved.
In some embodiments, the binder includes a fluorine-containing polymer. In some embodiments, the fluorine-containing polymer includes polyvinylidene difluoride.
In some embodiments, based on the mass of the positive active material, the mass percentage of the first element is 0.01% to 2%. In some embodiments, based on the mass of the positive active material, the mass percentage of the first element is 0.05% to 1%. In some embodiments, based on the mass of the positive active material, the mass percentage of the first element is 0.1% to 0.5%. In some embodiments, based on the mass of the positive active material, the mass percentage of the first element is 0.01%, 0.05%, 0.1%, 0.5%, 1%, 2%, or a value falling within a range formed by any two thereof. When the mass percentage of the first element in the positive active material satisfies the above relationship, the surface defects of the crystal structure of the positive active material can be reduced, thereby effectively suppressing the continuous disruption of the passivation layer on the surface of the positive electrode during the charge-discharge cycles of the electrochemical device, reducing the number of repairs, sufficiently improving the interfacial stability of the positive active material layer, and in turn, further improving the high-temperature cycle performance and safety of the electrochemical device.
In some embodiments, the first element includes at least two of aluminum, magnesium, titanium, zirconium, or tungsten. In this case, the positive active material is more stable at high temperature and high pressure. Combining the positive active material with a low-density binder can further improve the high-temperature cycle performance and safety of the electrochemical device.
In some embodiments, the first element further includes aluminum and at least one of magnesium, titanium, zirconium, or tungsten.
In some embodiments, the first element further includes tungsten and at least one of magnesium, titanium, zirconium, or aluminum.
In some embodiments, the first element includes aluminum and tungsten. Based on the mass of the positive active material, the mass percentage of aluminum and the mass percentage of tungsten are x % and y % respectively, and x and y satisfy: 1≤x/y≤5. In some embodiments, x and y satisfy the following relationship: 1.5≤x/y≤4.5. In some embodiments, x/y is 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, or a value falling within a range formed by any two thereof. When the mass percentages of aluminum and tungsten in the positive active material satisfy the above relationship, the decomposition and regeneration of the passivation layer on the surface of the positive electrode during the cycling of the electrochemical device can be reduced, thereby sufficiently improving the interfacial stability of the positive active material layer, and in turn, further improving the high-temperature cycle performance and safety of the electrochemical device.
In some embodiments, the first element includes aluminum. Based on the mass of the positive active material, the mass percentage of aluminum is x %, and x and a satisfy: 0.2≤x/a≤1. In some embodiments, x/a is 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, or a value falling within a range formed by any two thereof. When the mass percentage of aluminum and the density of the binder in the positive active material satisfy the above relationship, the decomposition and regeneration of the passivation layer on the surface of the positive electrode during the cycling of the electrochemical device can be reduced, thereby sufficiently improving the interfacial stability of the positive active material layer, and in turn, further improving the high-temperature cycle performance and safety of the electrochemical device.
In some embodiments, x ranges from 0.01 to 1. In some embodiments, x ranges from 0.05 to 0.5. In some embodiments, x ranges from 0.1 to 0.3. In some embodiments, x is 0.01, 0.05, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, or a value falling within a range formed by any two thereof.
In some embodiments, y ranges from 0.01 to 1. In some embodiments, y ranges from 0.05 to 0.5. In some embodiments, y ranges from 0.1 to 0.3. In some embodiments, y is 0.01, 0.05, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, or a value falling within a range formed by any two thereof.
The type of the positive active material is not particularly limited, as long as the material can electrochemically occlude and release metal ions (such as lithium ions). In some embodiments, the positive active material is a material containing lithium and at least one transition metal. Examples of the positive active material may include, but are not limited to, a lithium transition metal composite oxide, and a lithium-containing transition metal phosphate compound.
In some embodiments, a material different from the constituents of the above positive active material may be attached to the surface of the positive active material. Examples of materials attached to the surface may include, but are not limited to: oxides such as aluminum oxide, silicon dioxide, titanium dioxide, zirconium oxide, magnesium oxide, calcium oxide, boron oxide, antimony oxide, and bismuth oxide; sulfates such as lithium sulfate, sodium sulfate, potassium sulfate, magnesium sulfate, calcium sulfate, and aluminum sulfate; carbonates such as lithium carbonate, calcium carbonate, and magnesium carbonate; carbon; and the like. The attachment of the material onto the surface of the positive active material can suppress oxidation reactions of the electrolyte solution on the surface of the positive active material, and increase the lifespan of the electrochemical device. When the amount of the material attached to the surface is too small, the effect of the material is not fully exhibited. When the amount of the material attached to the surface is too large, the material will hinder movement of lithium ions, and thereby sometimes increase an electrical resistance. In this application, the material whose composition is different from that of the positive active material, which is attached onto the surface of the positive active material, is also referred to as a “positive active material”.
In some embodiments, the positive active material includes at least one of lithium cobalt oxide or lithium nickel cobalt manganese oxide.
In some embodiments, a shape of a particle of the positive active material includes, but is not limited to, a block shape, a polyhedron shape, a spherical shape, an elliptical spherical shape, a plate shape, a needle shape, a column shape, and the like. In some embodiments, particles of the positive active material include primary particles, secondary particles, or a combination thereof. In some embodiments, the primary particles may coalesce into the secondary particles.
The positive conductive material is not limited in type, and may be any known conductive material. Examples of the positive conductive material may include, but are not limited to, graphite such as natural graphite and artificial graphite; carbon black such as acetylene black; carbon materials such as amorphous carbon (for example, needle coke); carbon nanotubes; graphene, and the like. The foregoing positive conductive materials may be used alone or combined arbitrarily.
The solvent used to form a positive electrode slurry is not limited in type, and any solvent is appropriate as long as it can dissolve or disperse the positive active material, the conductive material, the positive binder, and a thickener used as needed. Examples of the solvent used to form the positive electrode slurry may include any one of an aqueous solvent or an organic solvent. Examples of the aqueous medium solvent may include, but are not limited to, water, and a mixed medium of alcohol and water, and the like. Examples of the organic media solvent include, but are not limited to, aliphatic hydrocarbons such as hexane; aromatic hydrocarbons such as benzene, toluene, xylene, and methyl naphthalene; heterocyclic compounds such as quinoline and pyridine; ketones such as acetone, methyl ethyl ketone, and cyclohexanone; esters such as methyl acetate and methyl acrylate; amines such as diethylene triamine, and N,N-dimethylaminopropylamine; ethers such as diethyl ether, propylene oxide, and tetrahydrofuran (THF); amides such as N-methyl-pyrrolidone (NMP), dimethylformamide, and dimethylacetamide; and aprotic polar solvents such as hexamethylphosphoramide, and dimethylsulfoxide.
A thickener is usually used to adjust viscosity of a slurry. In a case that an aqueous medium is used, a thickener and a styrene butadiene rubber (SBR) emulsion may be added to make a slurry. The thickener is not particularly limited in type. Examples of the thickener may include, but are not limited to, carboxymethyl cellulose, methyl cellulose, hydroxymethyl cellulose, ethyl cellulose, polyvinyl alcohol, oxidized starch, phosphorylated starch, casein, and a salt thereof, and the like. The foregoing thickeners may be used alone or combined arbitrarily.
The positive current collector is not particularly limited in type, and may be made of any material known as suitable for use in a positive current collector. Examples of the positive current collector may include, but are not limited to, metal materials such as aluminum, stainless steel, nickel plating, titanium, and tantalum; and carbon materials such as carbon cloth and carbon paper. In some embodiments, the positive current collector is made of a metal material. In some embodiments, the positive current collector is made of aluminum.
To reduce an electronic contact resistance of the positive current collector and the positive active material layer, a conductive agent may be contained on a surface of the positive current collector. Examples of the conductive agent may include, but are not limited to, carbon and noble metals such as gold, platinum, and silver.
A positive electrode may be prepared by forming a positive active material layer on a current collector, where the positive active material layer contains a positive active material and a binder. The positive electrode that contains a positive active material may be prepared by a conventional method. To be specific, the method may include: dry-mixing a positive active material, a binder, and, as appropriate, a conductive material and a thickener and the like, so as to form a sheet; and crimping the obtained sheet onto the positive current collector; or dissolving or dispersing such materials into a liquid medium to form a slurry, coating the positive current collector with the slurry, and drying to form a positive active material layer on the current collector, thereby obtaining a positive electrode.
In some embodiments, the mass percentage of the positive active material in the positive active material layer is 95%, preferably 96%, and more preferably 97%. In some embodiments, the mass percentage of the positive active material in the positive active material layer is 98%. In some embodiments, the mass percentage of the positive active material in the positive active material layer is 99%. When the mass percentage of the positive active material in the positive active material layer falls within the above range, the energy density of the electrochemical device can be increased significantly.
When the positive active material is primary particles, the average particle size of the positive active material means a primary particle size of the particles of the positive active material. When the primary particles of the positive active material particles coalesce to form secondary particles, the average particle size of the positive active material particles means a secondary particle size of the positive active material particles.
In some embodiments, an average particle size of the positive active material is D μm, and D ranges from 5 to 30. In some embodiments, D ranges from 10 to 25. In some embodiments, D ranges from 12 to 20. In some embodiments, D is 5, 7, 9, 10, 12, 15, 18, 20, 25, or 30, or a value falling within a range formed by any two thereof.
When the average particle size of the positive active material falls within the above range, the positive active material of a high tap density can be obtained, the deterioration of the performance of the electrochemical device can be suppressed, and problems such as occurrence of streaks can be avoided in a process of preparing the positive electrode of the electrochemical device (that is, mixing the positive active material, the conductive material, the binder, and the like with a solvent to form a slurry, and applying the slurry as a thin-film coating). In this way, packability of the positive active materials during preparation of the positive electrode can be further increased by mixing two or more types of positive active materials of different average particle sizes.
The average particle size of the positive active material may be determined with a laser diffraction/scattering particle size distribution analyzer. An exemplary measurement method includes: using a HORIBA LA-920 instrument as a particle size distribution analyzer, using a sodium hexametaphosphate aqueous solution of a 0.1% concentration as a dispersion medium for the measurement, ultrasonically dispersing the dispersion medium for 5 minutes, and then setting a measurement refractive index to 1.24 to determine the average particle size. Alternatively, the average particle size of the positive active material may be determined by a laser diffraction particle size analyzer (Shimadzu SALD-2300) and a scanning electron microscope (ZEISS EVO18, with at least 100 specimens selected).
The electrolyte solution used in the electrochemical device of this application includes an electrolyte and a solvent that dissolves the electrolyte.
In some embodiments, the electrolyte solution further includes a sulfur-oxygen double bond-containing compound.
In some embodiments, the sulfur-oxygen double bond-containing compound includes at least one of: a cyclic sulfate ester, a chain sulfate ester, a chain sulfonate ester, a cyclic sulfonate ester, a chain sulfite ester, or a cyclic sulfite ester.
In some embodiments, the cyclic sulfate ester includes, but is not limited to, one or more of: 1,2-ethylene glycol sulfate, 1,2-propylene glycol sulfate, 1,3-propylene glycol sulfate, 1,2-butylene glycol sulfate, 1,3-butylene glycol sulfate, 1,4-butylene glycol sulfate, 1,2-pentanediol sulfate, 1,3-pentanediol sulfate, 1,4-pentanediol sulfate, 1,5 pentanediol sulfate, or the like.
In some embodiments, the chain sulfate ester includes, but is not limited to, one or more of: dimethyl sulfate, ethyl methyl sulfate, diethyl sulfate, or the like.
In some embodiments, the chain sulfonate ester includes, but is not limited to, one or more of: a fluorosulfonate ester such as methyl fluorosulfonate and ethyl fluorosulfonate; methyl methanesulfonate; ethyl methanesulfonate; butyl dimethanesulfonate; 2-(methylsulfonyloxy) methyl propionate; 2-(methylsulfonyloxy) ethyl propionate, or the like.
In some embodiments, the cyclic sulfonate ester includes, but is not limited to, one or more of: 1,3-propane sultone, 1-fluoro-1,3-propane sultone, 2-fluoro-1,3-propane sultone, 3-fluoro-1,3-propane sultone, 1-methyl-1,3-propane sultone, 2-methyl-1,3-propane sultone, 3-methyl-1,3-propane sultone, 1-propene-1,3-sultone, 2-propene-1,3-sultone, 1-fluoro-1-propene-1,3-sultone, 2-fluoro-1-propene-1,3-sultone, 3-fluoro-1-propene-1,3-sultone, 1-fluoro-2-propene-1,3-sultone, 2-fluoro-2-propene-1,3-sultone, 3-fluoro-2-propene-1,3-sultone, 1-methyl-1-propene-1,3-sultone, 2-methyl-1-propene-1,3-sultone, 3-methyl-1-propene-1,3-sultone, 1-methyl-2-propene-1,3-sultone, 2-methyl-2-propene-1,3-sultone, 3-methyl-2-propene-1,3-sultone, 1,4-butane sultone, 1,5-pentane sultone, methylene methane disulfonate, ethylene methane disulfonate, or the like.
In some embodiments, the chain sulfite ester includes, but is not limited to, one or more of: dimethyl sulfite, ethyl methyl sulfite, diethyl sulfite, or the like.
In some embodiments, the cyclic sulfite ester includes, but is not limited to, one or more of: 1,2-ethylene glycol sulfite, 1,2-propylene glycol sulfite, 1,3-propylene glycol sulfite, 1,2-butylene glycol sulfite, 1,3-butylene glycol sulfite, 1,4-butylene glycol sulfite, 1,2-pentanediol sulfite, 1,3-pentanediol sulfite, 1,4-pentanediol sulfite, 1,5 pentanediol sulfite, or the like.
In some embodiments, the sulfur-oxygen double bond-containing compound includes the compound represented by Formula I:
In the formula above, W is selected from
In some embodiments, the compound represented by Formula I includes at least one of the following compounds:
In some embodiments, the bicyclic sultone includes a compound represented by Formula II:
In Formula II, A1, A2, A3, and A4 each are independently selected from substituted or unsubstituted C1 to C3 alkylidene, in which a substituent for substitution is selected from C1 to C5 alkyl, halogen, or halogenated C1 to C5 alkyl.
In some embodiments, the compound represented by Formula II includes at least one of the following compounds:
In some embodiments, based on the mass of the electrolyte solution, the mass percentage of the sulfur-oxygen double bond-containing compound is c %, and c ranges from 0.01 to 5. In some embodiments, c falls within a range of 0.01 to 3. In some embodiments, c falls within a range of 0.1 to 2. In some embodiments, c is 0.01, 0.05, 0.1, 0.2, 0.3, 0.4, 0.5, 0.8, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, or a value falling within a range formed by any two thereof. When the mass percentage of the sulfur-oxygen double bond-containing compound in the electrolyte solution falls within the above range, the high-temperature cycle performance and safety of the electrochemical device are further improved.
In some embodiments, c and a satisfy: 0.5≤c/a≤3. In some embodiments, c and a satisfy: 0.8≤c/a≤2. In some embodiments, c and a satisfy: 1≤c/a≤2.5. In some embodiments, c/a is 0.5, 0.6, 07, 0.8, 1, 1.2, 1.5, 2, 2.5, 3, or a value falling within a range formed by any two thereof. When the mass percentage of the sulfur-oxygen double bond-containing compound and the density of the binder in the electrolyte solution satisfy the above relationship, the high-temperature cycle performance and safety of the electrochemical device are further improved.
In some embodiments, the electrolyte solution further includes a trinitrile compound.
In some embodiments, the polynitrile compound includes at least one of 1,3,5-pentanetricarbonitrile, 1,2,3-propanetricarbonitrile, 1,3,6-hexanetricarbonitrile, 1,2,6-hexanetricarbonitrile, 1,2,3-tris(2-cyanoethoxy)propane, 1,2,4-tris(2-cyanoethoxy)butane, 1,1,1-tris(cyanoethoxymethylene)ethane, 1,1,1-tris(cyanoethoxymethylene)propane, 3-methyl 1,3,5-tris(cyanoethoxy)pentane, 1,2,7-tris(cyanoethoxy)heptane, 1,2,6-tris(cyanoethoxy)hexane, or 1,2,5-tris(cyanoethoxy)pentane.
In some embodiments, based on the mass of the electrolyte solution, the mass percentage of the trinitrile compound is d %, and d ranges from 0.01 to 5. In some embodiments, d falls within a range of 0.01 to 3. In some embodiments, d falls within a range of 0.1 to 2. In some embodiments, d is 0.01, 0.05, 0.1, 0.2, 0.3, 0.4, 0.5, 0.8, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, or a value falling within a range formed by any two thereof. When the mass percentage of the trinitrile compound in the electrolyte solution falls within the above range, the high-temperature cycle performance and safety of the electrochemical device are further improved.
In some embodiments, d and a satisfy: 0.2≤d/a≤4. In some embodiments, d and a satisfy: 0.5≤d/a≤3.5. In some embodiments, d and a satisfy: 1≤d/a≤3.5. In some embodiments, d/a is 0.2, 0.3, 0.5, 0.6, 07, 0.8, 1, 1.2, 1.5, 2, 2.5, 3, 3.5, 4, or a value falling within a range formed by any two thereof. When the mass percentage of the trinitrile compound and the density of the binder in the electrolyte solution satisfy the above relationship, the high-temperature cycle performance and safety of the electrochemical device are further improved.
In some embodiments, the electrolyte solution further includes at least one of succinonitrile, adiponitrile, ethylene glycol bis(2-cyanoethyl)ether, fluoroethylene carbonate, vinylene carbonate, or 1-propyl phosphate cyclic anhydride. In some embodiments, based on the mass of the electrolyte solution, the mass percentage of the above compound is 0.1% to 6%. In some embodiments, based on the mass of the electrolyte solution, the mass percentage of the above compound is 0.5% to 5%. In some embodiments, based on the mass of the electrolyte solution, the mass percentage of the above compound is 1% to 3%. Such compounds can stabilize the interface between the positive electrode and the electrolyte solution, thereby further improving the cycle performance and safety of the electrochemical device at high temperature and high voltage.
In some embodiments, the electrolyte solution further includes any nonaqueous solvent known in the prior art for use as a solvent in the electrolyte solution.
In some embodiments, the nonaqueous solvent includes, but is not limited to, one or more of: cyclic carbonate, chain carbonate, cyclic carboxylate, chain carboxylate, cyclic ether, chain ether, a phosphorus-containing organic solvent, a sulfur-containing organic solvent, or an aromatic fluorine-containing solvent.
In some embodiments, examples of the cyclic carbonate may include, but are not limited to, one or more of: ethylene carbonate (EC), propylene carbonate (PC), or butylene carbonate. In some embodiments, the cyclic carbonate contains 3 to 6 carbon atoms.
In some embodiments, examples of the chain carbonate may include, but are not limited to, one or more of: dimethyl carbonate, ethyl methyl carbonate, diethyl carbonate (DEC), methyl n-propyl carbonate, ethyl n-propyl carbonate, di-n-propyl carbonate, or the like. Examples of a fluorinated chain carbonate may include, but are not limited to, one or more of: bis(fluoromethyl)carbonate, bis(difluoromethyl)carbonate, bis(trifluoromethyl)carbonate, bis(2-fluoroethyl)carbonate, bis(2,2-difluoroethyl)carbonate, bis(2,2,2-trifluoroethyl)carbonate, 2-fluoroethyl methyl carbonate, 2,2-difluoroethyl methyl carbonate, 2,2,2-trifluoroethyl methyl carbonate, or the like.
In some embodiments, examples of the cyclic carboxylate may include, but are not limited to, one or more of: gamma-butyrolactone and gamma-valerolactone. In some embodiments, a part of hydrogen atoms of the cyclic carboxylate may be substituted by fluorine.
In some embodiments, examples of the chain carboxylate may include, but are not limited to, one or more of: methyl acetate, ethyl acetate, propyl acetate, isopropyl acetate, butyl acetate, sec-butyl acetate, isobutyl acetate, tert-butyl acetate, methyl propionate, ethyl propionate, propyl propionate, isopropyl propionate, methyl butyrate, ethyl butyrate, propyl butyrate, methyl isobutyrate, ethyl isobutyrate, methyl valerate, ethyl valerate, methyl pivalate, ethyl pivalate, or the like. In some embodiments, a part of hydrogen atoms of the chain carboxylate may be substituted by fluorine. In some embodiments, examples of a fluorinated chain carboxylate may include, but are not limited to, methyl trifluoroacetate, ethyl trifluoroacetate, propyl trifluoroacetate, butyl trifluoroacetate, 2,2,2-trifluoroethyl trifluoroacetate, or the like.
In some embodiments, examples of the cyclic ether may include, but are not limited to, one or more of: tetrahydrofuran, 2-methyl tetrahydrofuran, 1,3-dioxolane, 2-methyl1,3-dioxolane, 4-methyl 1,3-dioxolane, 1,3-dioxane, 1,4-dioxane, or dimethoxypropane.
In some embodiments, examples of the chain ether may include, but are not limited to, one or more of: dimethoxymethane, 1,1-dimethoxyethane, 1,2-dimethoxyethane, diethoxymethane, 1,1-diethoxyethane, 1,2-diethoxyethane, ethoxymethoxymethane, 1,1-ethoxymethoxyethane, 1,2-ethoxymethoxyethane, or the like.
In some embodiments, examples of the phosphorus-containing organic solvent may include, but are not limited to, one or more of: trimethyl phosphate, triethyl phosphate, dimethyl ethyl phosphate, methyl diethyl phosphate, ethylene methyl phosphate, ethylene ethyl phosphate, triphenyl phosphate, trimethyl phosphite, triethyl phosphite, triphenyl phosphite, tris(2,2,2-trifluoroethyl) phosphate, tris(2,2,3,3,3-pentafluoropropyl) phosphate, or the like.
In some embodiments, examples of the sulfur-containing organic solvent may include, but are not limited to, one or more of: sulfolane, 2-methyl sulfolane, 3-methyl sulfolane, dimethyl sulfone, diethyl sulfone, ethyl methyl sulfone, methyl propyl sulfone, dimethyl sulfoxide, methyl methanesulfonate, ethyl methanesulfonate, methyl ethanesulfonate, ethyl ethanesulfonate, dimethyl sulfate, diethyl sulfate, or dibutyl sulfate. In some embodiments, a part of hydrogen atoms of the sulfur-containing organic solvent may be substituted by fluorine.
In some embodiments, the aromatic fluorine-containing solvent includes, but is not limited to, one or more of: fluorobenzene, difluorobenzene, trifluorobenzene, tetrafluorobenzene, pentafluorobenzene, hexafluorobenzene, or trifluoromethylbenzene.
In some embodiments, the solvent used in the electrolyte solution in this application includes cyclic carbonate, chain carbonate, cyclic carboxylate, chain carboxylate, and any combination thereof. In some embodiments, the solvent used in the electrolyte solution in this application includes an organic solvent containing a material selected from: ethylene carbonate, propylene carbonate, diethyl carbonate, ethyl propionate, propyl propionate, n-propyl acetate, ethyl acetate, or any combination thereof. In some embodiments, the solvent used in the electrolyte solution according to this application includes: ethylene carbonate, propylene carbonate, diethyl carbonate, ethyl propionate, propyl propionate, gamma-butyrolactone, and any combination thereof.
In some embodiments, the electrolyte is not particularly limited, and may be any material well-known for use as an electrolyte. In a case of a lithium secondary battery, a lithium salt is generally used as the electrolyte. Examples of the electrolyte may include, but are not limited to, inorganic lithium salts such as LiPF6, LiBF4, LiClO4, LiAlF4, LiSbF6, and LiWF7; lithium tungstate such as LiWOF5, carboxylic lithium salts such as HCO2Li, CH3CO2Li, CH2FCO2Li, CHF2CO2Li, CF3CO2Li, CF3CH2CO2Li, CF3CF2CO2Li, CF3CF2CF2CO2Li, and CF3CF2CF2CF2CO2Li; lithium sulfonate salts such as FSO3Li, CH3SO3Li, CH2FSO3Li, CHF2SO3Li, CF3SO3Li, CF3CF2SO3Li, CF3CF2CF2SO3Li, and CF3CF2CF2CF2SO3Li; lithium imide salts such as LiN(FCO)2, LiN(FCO)(FSO2), LiN(FSO2)2, LiN(FSO2)(CF3SO2), LiN(CF3SO2)2, LiN(C2F5SO2)2, cyclic lithium 1,2-perfluoroethane bissulfonimide, cyclic lithium 1,3-perfluoropropane bissulfonimide, and LiN(CF3SO2)(C4F9SO2); methylated lithium salts such as LiC(FSO2)3, LiC(CF3SO2)3, and LiC(C2F5SO2)3; (malonato)lithium borate salts such as lithium bis(malonato)borate, and lithium difluoro(malonato)borate; (malonato) lithium phosphate salts such as lithium tris(malonato)phosphate, lithium difluorobis(malonato)phosphate, and lithium tetrafluoro(malonato)phosphate; fluorine-containing organic lithium salts such as LiPF4(CF3)2, LiPF4(C2F5)2, LiPF4(CF3SO2)2, LiPF4(C2F5SO2)2, LiBF3CF3, LiBF3C2F5, LiBF3C3F7, LiBF2(CF3)2, LiBF2(C2F5)2, LiBF2(CF3SO2)2, and LiBF2(C2F5SO2)2; (oxalato) lithium borate salts such as lithium difluoro(oxalato)borate and lithium bis(oxalato)borate; and (oxalato) lithium phosphate salts such as lithium tetrafluoro(oxalato)phosphate, lithium difluorobis(oxalato)phosphate, lithium tris(oxalato)phosphate, and the like.
In some embodiments, the electrolyte is selected from LiPF6, LiSbF6, FSO3Li, CF3SO3Li, LiN(FSO2)2, LiN(FSO2)(CF3SO2), LiN(CF3SO2)2, LiN(C2F5SO2)2, cyclic lithium 1,2-perfluoroethane bissulfonimide, cyclic lithium 1,3-perfluoropropane bissulfonimide, LiC(FSO2)3, LiC(CF3SO2)3, LiC(C2F5SO2)3, LiBF3CF3, LiBF3C2F5, LiPF3(CF3)3, LiPF3(C2F5)3, lithium difluoro(oxalato)borate, lithium bis(oxalato)borate, or lithium difluorobis(oxalato)phosphate. Such electrolytes improve the output power feature, high-rate charge-discharge feature, high-temperature storage feature, cycling feature, and the like of the electrochemical device.
A content of the electrolyte is not particularly limited as long as effects of this application are not impaired. In some embodiments, a total molar concentration of lithium in the electrolyte solution is greater than 0.3 mol/L, greater than 0.4 mol/L, or greater than 0.5 mol/L. In some embodiments, the total molar concentration of lithium in the electrolyte solution is less than 3 mol/L, less than 2.5 mol/L, or less than 2.0 mol/L. In some embodiments, the total molar concentration of lithium in the electrolyte solution falls within a range formed by any two of the foregoing values. When the concentration of the electrolyte is within the foregoing ranges, lithium as charged particles will not be deficient, and a viscosity of the lithium will be in an appropriate range, thereby ensuring a high electrical conductivity easily.
When two or more types of electrolytes are in use, the electrolyte includes at least one salt selected from groups consisting of any of monofluorophosphate, borate, oxalate, or fluorosulfonate. In some embodiments, the electrolyte includes a salt selected from groups consisting of any of monofluorophosphate, oxalate, or fluorosulfonate. In some embodiments, the electrolyte includes a lithium salt. In some embodiments, based on a weight of the electrolyte, a content of the salt selected from the groups consisting of any of monofluorophosphate, borate, oxalate, or fluorosulfonate is greater than 0.01% or greater than 0.1%. In some embodiments, based on the weight of the electrolyte, the content of the salt selected from the groups consisting of any of monofluorophosphate, borate, oxalate, or fluorosulfonate is less than 20% or less than 10%. In some embodiments, the content of the salt selected from the groups consisting of any of monofluorophosphate, borate, oxalate, or fluorosulfonate is within a range formed by any two of the foregoing values.
In some embodiments, the electrolyte contains at least one material selected from groups consisting of any of monofluorophosphate, borate, oxalate, or fluorosulfonate, and a least one type of salt other than the material. The salt other than the material may be a lithium salt exemplified above. In some embodiments, the salt other than the material is LiPF6, LiN(FSO2)(CF3SO2), LiN(CF3SO2)2, LiN(C2F5SO2)2, cyclic lithium 1,2-perfluoroethane bissulfonimide, cyclic lithium 1,3-perfluoropropane bissulfonimide, LiC(FSO2)3, LiC(CF3SO2)3, LiC(C2F5SO2)3, LiBF3CF3, LiBF3C2F5, LiPF3(CF3)3, or LiPF3(C2F5)3. In some embodiments, the salt other than the material is LiPF6.
In some embodiments, based on the weight of the electrolyte, a content of the salt other than the material is greater than 0.01% or greater than 0.1%. In some embodiments, based on the weight of the electrolyte, the content of the salt other than the material is less than 20%, less than 15%, or less than 10%. In some embodiments, the content of the salt other than the material is within a range formed by any two of the foregoing values. Added at a mass percentage specified above, the salt other than the material is conducive to balancing the conductivity and viscosity of the electrolyte solution.
The negative electrode includes a negative current collector and a negative active material layer disposed on one or two surfaces of the negative current collector. The negative active material layer includes a negative active material. The negative active material layer may be one layer or a plurality of layers. Each layer in the multilayer negative active material may contain the same or different negative active materials. The negative active material is any material capable of reversibly intercalating and deintercalating metal ions such as lithium ions. In some embodiments, a chargeable capacity of the negative active material is greater than a discharge capacity of the positive active material, so as to prevent unexpected precipitation of lithium metal on the negative electrode during charging.
The current collector that retains the negative active material may be any well-known current collector. Examples of the negative current collector include, but are not limited to, a metal material such as aluminum, copper, nickel, stainless steel, and nickel-plated steel. In some embodiments, the negative current collector is copper.
When the negative current collector is made of a metal material, the form of the negative current collector may include, but is not limited to, a metal foil, a metal cylinder, a metal coil, a metal sheet, a metal thin film, a metal mesh, stamped metal, foamed metal, and the like. In some embodiments, the negative current collector is a metal thin film. In some embodiments, the negative current collector is a copper foil. In some embodiments, the negative current collector is a calendered copper foil prepared by a calendering method or an electrolytic copper foil prepared by an electrolytic method.
In some embodiments, the thickness of the negative current collector is greater than 1 μm or greater than 5 μm. In some embodiments, the thickness of the negative current collector is less than 100 μm or less than 50 μm. In some embodiments, the thickness of the negative current collector falls within a range formed by any two of the foregoing values.
The negative active material is not particularly limited, as long as the material can reversibly occlude and release lithium ions. Examples of the negative active material may include, but are not limited to, carbon materials such as natural graphite and artificial graphite; metals such as silicon (Si) and tin (Sn); oxides of metal elements such as Si and Sn; or the like. The negative active materials may be used alone or used in combination.
The negative active material layer may further include a negative binder. The negative binder can strengthen the bonding between the particles of the negative active material and the bonding between the negative active material and the current collector. The type of the negative binder is not particularly limited, as long as the material of the binder is stable to the electrolyte solution or the solvent used in manufacturing the electrode. In some embodiments, the negative binder includes a resin binder. Examples of the resin binder include, but are not limited to, fluororesin, polyacrylonitrile (PAN), polyimide resin, acrylic resin, polyolefin resin, and the like. When a negative electrode slurry is prepared from an aqueous solvent, the negative binder includes, but is not limited to, carboxymethyl cellulose (CMC) or a salt thereof, styrene-butadiene rubber (SBR), polyacrylic acid (PAA) or a salt thereof, polyvinyl alcohol, and the like.
The negative electrode may be prepared by the following method: coating a negative current collector with a negative electrode slurry that contains a negative active material, a resin binder, and the like; drying the slurry, and then calendering the current collector to form a negative active material layer on both sides of the negative current collector, thereby obtaining a negative electrode.
To prevent short circuits, a separator is generally disposed between the positive electrode and the negative electrode. In this case, the electrolyte solution of this application generally works by penetrating into the separator.
The material and shape of the separator are not particularly limited as long as they do not significantly impair the effects of this application. The material of the separator may be resin, glass fiber, an inorganic compound, or the like that is stable to the electrolyte solution of this application. In some embodiments, the separator contains a highly liquid-retaining porous sheet or non-woven fabric shaped material, and the like. Examples of resin or glass fiber used as the separator may include, but are not limited to, polyolefin, aramid, polytetrafluoroethylene, polyethersulfone, and the like. In some embodiments, the polyolefin is polyethylene or polypropylene. In some embodiments, the polyolefin is polypropylene. The foregoing separator materials may be used alone or combined arbitrarily.
The separator may also be made of a material that is formed by stacking the foregoing materials. Examples of such material include, but are not limited to, a three-layer separator formed by sequentially stacking polypropylene, polyethylene, and polypropylene.
Examples of the inorganic compound used as the material of the separator may include, but are not limited to, an oxide such as aluminum oxide and silicon dioxide; a nitride such as aluminum nitride and silicon nitride; and a sulfate salt (such as barium sulfate and calcium sulfate). The shape of the inorganic compound may include, but is not limited to a particle or fiber shape.
The form of the separator may be a thin film form. Examples include, but are not limited to, a non-woven fabric, a woven fabric, a microporous film, and the like. In a case that the separator is in a thin film form, a pore size of the separator is 0.01 μm to 1 μm, and a thickness of the separator is 5 μm to 50 μm. Other than the stand-alone separator described above, a separator made in the following way is also applicable: a separator made by forming a composite porous layer on the surface of the positive electrode and/or the negative electrode by using a resinous binder, where the composite porous layer contains the foregoing inorganic particles. For example, the separator is made by using a fluororesin as a binder so that aluminum oxide particles with a volume median diameter Dv90 less than 1 μm form a porous layer on both sides of the positive electrode.
The thickness of the separator is arbitrary. In some embodiments, the thickness of the separator is greater than 1 μm, greater than 5 μm, or greater than 8 μm. In some embodiments, the thickness of the separator is less than 50 μm, less than 40 μm, or less than 30 μm. In some embodiments, the thickness of the separator is within a range formed by any two of the foregoing values. When the thickness of the separator falls within the foregoing ranges, high insulation and mechanical strength of the separator are ensured, and high rate performance and energy density of the electrochemical device are ensured.
When a porous material such as a porous sheet or non-woven fabric is used as the separator, a porosity of the separator is arbitrary. In some embodiments, the porosity of the separator is greater than 10%, greater than 15%, or greater than 20%. In some embodiments, the porosity of the separator is less than 60%, less than 50%, or less than 45%. In some embodiments, the porosity of the separator is within a range formed by any two of the foregoing values. When the porosity of the separator falls within the foregoing ranges, high insulation and mechanical strength of the separator are ensured, a separator resistance can be suppressed, and high safety performance of the electrochemical device is ensured.
An average pore size of the separator is also arbitrary. In some embodiments, the average pore size of the separator is less than 0.5 μm or less than 0.2 μm. In some embodiments, the average pore size of the separator is greater than 0.05 μm. In some embodiments, the average pore size of the separator is within a range formed by any two of the foregoing values. If the average pore size of the separator exceeds the foregoing ranges, a short circuit is likely to occur. When the average pore size of the separator falls within the foregoing ranges, high safety performance of the electrochemical device is ensured.
Components of the electrochemical device include an electrode assembly, a current collection structure, an outer housing, and a protection element.
The electrode assembly may be a stacked structure formed by stacking the positive electrode and the negative electrode that are interspaced with the separator, or a jelly-roll structure formed by spirally winding the positive electrode and the negative electrode that are interspaced with the separator. In some embodiments, a percentage of a volume of the electrode assembly in a total volume inside a battery (hereinafter referred to as “electrode assembly volume percentage”) is greater than 40% or greater than 50%. In some embodiments, the electrode assembly volume percentage is less than 90% or less than 80%. In some embodiments, the electrode assembly volume percentage is within a range formed by any two of the foregoing values. When the electrode assembly volume percentage falls within the foregoing range, a high capacity of the electrochemical device is ensured, and deterioration of performance such as charge and discharge cycle performance and high-temperature storage performance is suppressed, where the deterioration of performance is accompanied with an increase of an internal pressure.
The current collection structure is not particularly limited. In some embodiments, the current collection structure is a structure that reduces a resistance of a wiring part and a splicing part. When the electrode assembly is the foregoing stacked structure, it is appropriate to use a structure formed by bundling a metal core part of each electrode layer and welding the bundle to a terminal. When an area of an electrode plate increases, an internal resistance increases. Therefore, it is appropriate to configure at least 2 terminals in the electrode to reduce the resistance. When the electrode assembly is the jelly-roll structure, at least 2 wiring structures are disposed on the positive electrode and the negative electrode separately and are bundled on the terminals, thereby reducing the internal resistance.
The material of the outer housing is not particularly limited as long as the material is stable to the electrolyte solution in use. The material of the outer housing may be, but is not limited to, a metallic material such as nickel-plated steel, stainless steel, aluminum, aluminum alloy, magnesium alloy, or a laminated film of resin and an aluminum foil. In some embodiments, the outer housing is a metal or laminated film of aluminum or aluminum alloy.
The metallic outer housing includes, but is not limited to, a sealed airtight structure formed by fusing metals to each other by means of laser welding, resistance welding, or ultrasonic welding; or the metallic outer housing is a riveted structure formed by using such metals cushioned by a resin gasket. The outer housing made of the laminated film includes, but is not limited to, a sealed airtight structure formed by thermally bonding resin layers. To increase airtightness, the resin layers may be interspaced with a resin different from the resin used in the laminated film. When the airtight structure is formed by thermally bonding the resin layers through a current collection terminal, in view of the bonding between the metal and the resin, the resin between the resin layers may be a resin that contains a polar group or a modified resin into which a polar group is introduced. In addition, the shape of the outer housing is also arbitrary. For example, the outer housing may be any of the shapes such as a cylindrical shape, a square shape, a laminated shape, a button shape, and a bulk shape.
The protection element may be a positive temperature coefficient (PTC) thermistor, a temperature fuse, or a thermistor, which, in each case, increases a resistance when abnormal heat is emitted or an excessive current is passed; or may be a valve (a current cutoff valve) that cuts off the current in a circuit by rapidly increasing the internal pressure or internal temperature of the battery during abnormal heat emission, or the like. The protection element may be an element that remains idle during routine use under a high current, and may also be designed in a form that prevents abnormal heat radiation or thermal runaway even if no protection element exists.
The electrochemical device of this application includes any device in which an electrochemical reaction occurs. Specific examples of the electrochemical device include a lithium metal secondary battery or a lithium-ion secondary battery.
This application further provides an electronic device containing the electrochemical device according to this application.
The uses of the electrochemical device according to this application are not particularly limited, and the electrochemical device may be used in any electronic device known in the prior art. In some embodiments, the electrochemical device according to this application is applicable to, but without being limited to, a notebook computer, pen-inputting computer, mobile computer, e-book player, portable phone, portable fax machine, portable photocopier, portable printer, stereo headset, video recorder, liquid crystal display television set, handheld cleaner, portable CD player, mini CD-ROM, transceiver, electronic notepad, calculator, memory card, portable voice recorder, radio, backup power supply, motor, automobile, motorcycle, power-assisted bicycle, bicycle, lighting appliance, toy, game console, watch, electric tool, flashlight, camera, large household battery, lithium-ion capacitor, and the like.
By using a lithium-ion battery as an example, the following describes a preparation method of a lithium-ion battery with reference to specific embodiments. A person skilled in the art understands that the preparation methods described in this application are merely examples, and any other appropriate preparation methods still fall within the scope of this application.
Mixing artificial graphite, styrene-butadiene rubber, and sodium carboxymethyl cellulose at a mass ratio of 96%:2%:2%, adding deionized water, and stirring well to obtain a negative electrode slurry. Coating a 9 μm-thick copper foil with the negative electrode slurry, drying the slurry, cold-pressing the foil, and then cutting the plate and welding tabs to obtain a negative electrode.
Weighing out a specified amount of Co3O4 and LiOH powder, mixing and grinding the powder well in an agate mortar, and then calcining the mixture at 900° C. for 10 hours. Adding a specified stoichiometric amount of an oxide, sulfate salt, or nitrate salt containing a first element into the calcined mixture, adding alcohol as a solvent, ball-milling the mixture for 10 hours, and then calcining the mixture at 800° C. for 10 hours to obtain lithium cobalt oxide containing the first element.
Mixing the positive active material (lithium cobalt oxide with or without the first element), carbon nanotubes, and polyvinylidene difluoride at a mass ratio of 97:1:2, adding N-methyl-pyrrolidone (NMP), and stirring well to obtain a positive electrode slurry. coating an aluminum foil of 12 μm in thickness with the positive electrode slurry, and performing drying, cold calendering, cutting, and tab welding to obtain a positive electrode.
Mixing ethylene carbonate (EC), propylene carbonate (PC), and diethyl carbonate (DEC) at a mass ratio of 1:1:1 in a dry argon atmosphere, adding LiPF6, and stirring well to form a base electrolyte solution in which the concentration of LiPF6 is 12.5%. Adding additives at different mass percentages into the base electrolyte solution to obtain the electrolyte solutions for different embodiments and comparative embodiments.
The abbreviations and full names of constituents in the electrolyte solution are shown in the following table:
Using a polyethylene porous polymer film as a separator.
Sequentially winding the obtained positive electrode, separator, and negative electrode, putting them into an outer package foil, and leaving an injection hole; Injecting the electrolyte solution through the injection hole, and performing the steps such as sealing, chemical formation, and capacity grading to obtain a lithium-ion battery.
Charging a lithium-ion battery at a constant current of 1 C under 65° C. until the voltage reaches 4.7 V, then charging the battery at a constant voltage of 4.7 V until the current reaches 0.05 C, and then discharging the battery at a constant current of 1 C until the voltage reaches 3.0 V, thereby completing a first cycle. Performing 500 cycles on the lithium-ion battery under the foregoing conditions. “1C” is a current value at which the rated capacity of a battery can be fully discharged within 1 hour.
Calculating the capacity retention rate of the cycled lithium-ion battery by the following formula:
capacity retention rate of a battery cycled for a number of cycles=(discharge capacity at the end of the cycles/discharge capacity at the end of a first cycle)×100%.
Leaving the lithium-ion battery to stand at 25° C. for 30 minutes, charging the battery at a constant current of 0.5 C-rate until the voltage reaches 4.7 V, charging the battery at a constant voltage of 4.7 V until the current reaches 0.05 C, leaving the battery to stand for 60 minutes, and measuring a thickness T1 of the lithium-ion battery; and Subsequently, short-circuiting the lithium-ion battery for 10 seconds by using a resistance of 100 mΩ, and then measuring the thickness T2 of the lithium-ion battery. Calculating the high-temperature short-circuit deformation rate of the lithium-ion battery as:
Table 1 shows how the positive active material and the binder affect the high-temperature cycle performance and safety of the lithium-ion battery. In each embodiment and each comparative embodiment in this table, the positive active material is lithium cobalt oxide with or without the first element.
As shown in Comparative Embodiment 1-1, when the positive active material is undoped, the lithium-ion battery exhibits a relatively low high-temperature cycle capacity retention rate and a relatively high short-circuit deformation rate even if the low-density positive binder of this application is used. As shown in Comparative Embodiments 1-2 and 1-3, when the positive active material is doped with at least one of aluminum, magnesium, titanium, zirconium, or tungsten but the density of the positive binder is overly high (higher than 1.5 g/cm3) or overly low (lower than 0.6 g/cm3), the lithium-ion battery still exhibits a relatively low high-temperature cycle capacity retention rate and a relatively high short-circuit deformation rate.
As shown in Embodiments 1-1 to 1-24, when the positive active material is doped with at least one of aluminum, magnesium, titanium, zirconium, or tungsten and the density of the positive binder is 0.6 to 1.5 g/cm3, the high-temperature cycle capacity retention rate of the lithium-ion battery can be increased significantly, and the short-circuit deformation rate of the lithium-ion battery can be decreased significantly.
Table 2 shows how the porosity of the binder and the relationship between the porosity and the density affect the high-temperature cycle performance and safety of the lithium-ion battery. Except the parameters set out in Table 2, the settings in Embodiments 2-1 to 2-16 are the same as those in Embodiment 1-1.
The results show that when the porosity of the binder is 20% to 50% and the porosity b % of the binder and the density a g/cm3 satisfy 17≤a×b≤60, the high-temperature cycle capacity retention rate of the lithium-ion battery can be further increased and the short-circuit deformation rate of the lithium-ion battery can be further decreased.
Table 3 shows how the mass percentages of aluminum and tungsten in the positive active material affect the high-temperature cycle performance and safety of the lithium-ion battery. Except the parameters set out in Table 3, the settings in Embodiments 3-1 to 3-9 are the same as those in Embodiment 1-1.
The results show that when the positive active material includes aluminum and tungsten and when the mass percentage x % of aluminum and the mass percentage y % of tungsten satisfy 1≤x/y≤5, the high-temperature cycle capacity retention rate of the lithium-ion battery can be further increased and the short-circuit deformation rate of the lithium-ion battery can be further decreased.
Table 4 shows how the relationship between the mass percentage of aluminum and the density of the binder in the positive active material affects the high-temperature cycle performance and safety of the lithium-ion battery. Except the parameters set out in Table 4, the settings in Embodiments 4-1 to 4-10 are the same as those in Embodiment 1-1.
The results show that when the positive active material includes aluminum and the mass percentage x % of aluminum and the density a g/cm3 of the binder satisfy 0.2≤x/a≤1, the high-temperature cycle capacity retention rate of the lithium-ion battery can be further increased and the short-circuit deformation rate of the lithium-ion battery can be further decreased.
Table 5 shows how the sulfur-oxygen double bond-containing compound in the electrolyte solution and the relationship between the compound and the density of the binder affect the high-temperature cycle performance and safety of the lithium-ion battery. Except the parameters set out in Table 5, the settings in Embodiments 5-1 to 5-14 are the same as those in Embodiment 1-1.
The results show that when a sulfur-oxygen double bond-containing compound is further added at a mass percentage of 0.01% to 5% in the electrolyte solution, the high-temperature cycle capacity retention rate of the lithium-ion battery can be further increased and the short-circuit deformation rate of the lithium-ion battery can be further decreased.
When the mass percentage c % of the sulfur-oxygen double bond-containing compound in the electrolyte solution and the density a g/cm3 of the binder satisfy 0.5≤c/a≤3, the high-temperature cycle capacity retention rate of the lithium-ion battery can be further increased and the short-circuit deformation rate of the lithium-ion battery can be further decreased.
Table 6 shows how the trinitrile compound in the electrolyte solution and the relationship between the compound and the density of the binder affect the high-temperature cycle performance and safety of the lithium-ion battery. Except the parameters set out in Table 6, the settings in Embodiments 6-1 to 6-14 are the same as those in Embodiment 1-1.
The results show that when a trinitrile compound is further added at a mass percentage of 0.01% to 5% in the electrolyte solution, the high-temperature cycle capacity retention rate of the lithium-ion battery can be further increased and the short-circuit deformation rate of the lithium-ion battery can be further decreased.
When the mass percentage d % of the trinitrile compound compound in the electrolyte solution and the density a g/cm3 of the positive binder satisfy 0.2≤d/a≤4, the high-temperature cycle capacity retention rate of the lithium-ion battery can be further increased and the short-circuit deformation rate of the lithium-ion battery can be further decreased.
Table 7 shows how the additive in the electrolyte solution affects the high-temperature cycle performance and safety of the lithium-ion battery. Except the parameters set out in Table 7, the settings in Embodiments 7-1 to 7-10 are the same as those in Embodiment 1-1.
The results show that when the electrolyte solution includes at least one of succinonitrile, adiponitrile, ethylene glycol bis(2-cyanoethyl)ether, fluoroethylene carbonate, vinylene carbonate, or 1-propyl phosphate cyclic anhydride, the high-temperature cycle capacity retention rate of the lithium-ion battery can be further increased and the short-circuit deformation rate of the lithium-ion battery can be further decreased.
References to “embodiments”, “some embodiments”, “an embodiment”, “another example”, “example”, “specific example” or “some examples” throughout the specification mean that specified features, structures, materials, or characteristics described in such embodiment(s) or example(s) are included in at least one embodiment or example in this application. Therefore, descriptions throughout the specification, which make references by using expressions such as “in some embodiments”, “in an embodiment”, “in one embodiment”, “in another example”, “in an example”, “in a specific example”, or “example”, do not necessarily refer to the same embodiment(s) or example(s) in this application. In addition, specific features, structures, materials, or characteristics herein may be combined in one or more embodiments or examples in any appropriate manner.
Although illustrative embodiments have been demonstrated and described above, a person skilled in the art understands that the foregoing embodiments are never to be construed as a limitation on this application, and changes, replacements, and modifications may be made to the embodiments without departing from the spirit, principles, and scope of this application.
This application is a continuation application of International Application No. PCT/CN2021/142399, filed on Dec. 29, 2021, the contents of which are incorporated herein by reference in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/CN2021/142399 | Dec 2021 | WO |
| Child | 18758089 | US |
