Patent Application
20220093921
The present application belongs to the field of electrochemical technology. More specifically, the present application relates to a secondary battery and a battery module, battery pack, and apparatus containing the same.
As a new type of high-voltage, high-energy density rechargeable battery, secondary batteries have outstanding characteristics such as light weight, high energy density, no pollution, no memory effect, and long service life, which is a major trend in the development of new energy batteries.
At present, the use of silicon-based materials with a higher gram capacity as a negative electrode active material has great advantages in increasing the energy density of secondary batteries. However, during charging and discharging, the silicon-based materials as the negative electrode active material has a large volume expansion and contraction issue, which is likely to cause damage to the electrode plate structure, especially when the maximum expansion occurs at full charged state, thereby deteriorating the cycling performance of the battery.
A first aspect of the present application provides a secondary battery, which aims to enable the secondary battery to have not only a higher energy density but also a better cycling performance.
In order to achieve above object, the first aspect of the present application provides a secondary battery comprising a positive electrode plate, a negative electrode plate, a separator and an electrolyte, the positive electrode plate comprises a positive electrode current collector and a positive electrode film layer, the positive electrode film layer is coated on at least one surface of the positive electrode current collector and contains a positive electrode active material, the negative electrode plate comprising a negative electrode current collector and a negative electrode film layer, the negative electrode film layer is coated on at least one surface of the negative electrode current collector and contains a negative electrode active material, the positive electrode active material comprises one or more of lithium nickel cobalt manganese oxides and lithium nickel cobalt aluminum oxides; the negative active material comprises a silicon-based material; wherein the secondary battery satisfies the following formula I:
2≤|(AF/AE−1)/(CE/CF−1)|≤7 (Formula I)
in which
CF represents a unit cell volume as measured when the positive electrode active material is prepared into a button battery and the button battery is charged to 100% SOC at a rate of 0.05 C;
CE represents a unit cell volume as measured when the positive electrode active material is prepared into a button battery and the button battery is discharged to 0% SOC at a rate of 0.05 C;
AF represents a volume of the negative electrode active material particles as measured when the silicon-based material is prepared into a single-particle battery, and the single-particle battery is charged to 100% SOC at a rate of 0.5 C; and
AE represents a volume of the negative electrode active material particles as measured when the silicon-based material is prepared into a single-particle battery, and the single-particle battery is discharged to 0% SOC at a rate of 0.5 C.
In the above-mentioned secondary battery, by reasonably matching the positive and negative active materials, the excessive internal stress will not occur with battery cycling, the internal expansion force of the battery will not increase sharply, and the interface integrity of the positive and negative electrode plate has been greatly improved. Further, reasonably matching the positive and negative active materials can also maintain good electrolyte wettability, and avoid the deterioration of battery dynamic performance and cycling performance due to the hindrance of lithium intercalation and deintercalation between the positive and negative electrodes caused by the increase of interface contact resistance. The secondary battery thus obtained has good cycling performance.
In the secondary battery according to the first aspect of the present application, the silicon-based material is present in the negative electrode active material in a mass percentage of 40% or less, optionally from 15% to 30%. The negative electrode active material with the silicon-based material content within the above range enables the secondary battery higher energy density and better cycling performance.
In the secondary battery according to the first aspect of the present application, the positive electrode active material comprises one or more of LiaNibCocMdM′eOfAg and a coating layer modified LiaNibCocMdM′eOfAg on at least a part of surface thereof, wherein 0.8≤a≤1.2, 0.8≤b<1, 0<c<1, 0<d<1, 0≤e≤0.1, 1≤f≤2, 0≤g≤1, M is one or more selected from Mn and Al, M′ is one or more selected from Zr, Al, Zn, Cu, Cr, Mg, Fe, V, Ti and B, and A is one or more selected from N, F, S and Cl. The use of the above-mentioned positive electrode active materials enable the secondary battery higher energy density and better cycling performance.
In the secondary battery according to the first aspect of the present application, the positive electrode active material satisfies: 1.0≤CE/CF≤1.05; optionally 1.038≤CE/CF≤1.04. Using the above mentioned positive electrode active material can provide the secondary battery with higher energy density and better cycling performance.
In the secondary battery according to the first aspect of the present application, the negative electrode active material satisfies: 1.05≤AF/AE≤1.30; optionally 1.08≤AF/AE≤1.27. Using the above mentioned negative electrode active material can provide the secondary battery with higher energy density and better cycling performance.
In the secondary battery according to the first aspect of the present application, the negative active material further comprises carbon materials, and the carbon materials comprises one or more of artificial graphite, natural graphite, soft carbon, and hard carbon, optionally, the negative electrode active material further comprises one or more of artificial graphite and natural graphite. The inclusion of the carbon material in the negative electrode active material increases the structural stability of the negative electrode active material.
In the secondary battery according to the first aspect of the present application, the negative active material has an average particle size Dv50 in the range of 10 μm to 23 μm, more optionally, in the range of 12 μm to 16 μm. The average particle size Dv50 of the negative electrode active material falling within the above range provides a secondary battery with a good electrical performance.
In the secondary battery according to the first aspect of the present application, at least a part of the positive electrode active material comprises single crystal particles. The use of such a positive electrode active material can improve the cycling performance of the secondary battery.
In the secondary battery according to the first aspect of the present application, the positive electrode film layer in a single side has a thickness Tc satisfying 46 μm≤Tc≤56 μm; more optionally, 48.5 μm≤Tc≤53.5 μm; and/or, the negative electrode film layer in a single side has a thickness Ta satisfying 66 μm≤Ta≤86 μm; more optionally, 68.5 μm≤Ta≤83.5 μm. The use of such a positive electrode film layer and/or a negative electrode film layer improves the electrical performance of the secondary battery.
In the secondary battery according to the first aspect of the present application, the positive electrode film layer has a compaction density PDpositive satisfying: 3.0 g/cm3≤PDpositive≤3.55 g/cm3; more optionally 3.4 g/cm3≤PDpositive≤3.5 g/cm3; and/or, the negative electrode film layer has a compaction density PDnegative satisfying: 1.5 g/cm3≤PDnegative≤1.8 g/cm3; more optionally 1.6 g/cm3≤PDnegative≤1.7 g/cm3. The compaction density falling within the above range improves the integrity of the active material and maintains good contact between the particles.
The present application in the second aspect provides a battery module, characterized by comprising the secondary battery according to the first aspect of the present application.
The present application in a third aspect provides a battery pack, comprising the battery module according to the second aspect of the present application.
The present application in a fourth aspect provides an apparatus, comprising the secondary battery according to the first aspect of the present application.
The battery module, battery pack, and apparatus of the present application comprise the secondary battery provided by the present application, and thus have at least the same advantages as the secondary battery.
In order to explain the technical solutions of the embodiments of the present application more clearly, the following will briefly introduce the drawings that need to be used in the embodiments of the present application. Obviously, the drawings described below are only some embodiments of the present application. A person of ordinary skill in the art can obtain other drawings based on the drawings without creative work.
In above figures, the reference numerals are defined as follows: 1—battery pack; 2—upper battery box; 3—lower battery box; 4—battery module; 5—secondary battery.
The features, advantages, and technical effects of the exemplary embodiments of the present application will be described below with reference to the accompanying drawings.
In the context of this application, “a”, “an”, “the” as used (especially in the content of the claims) should be interpreted as covering both the singular and the plural, unless otherwise stated or clearly contradictory to the context.
Throughout the present application, where compositions are described as having, including, or comprising specific components or fractions, or where processes are described as having, including, or comprising specific process steps, it is contemplated that the compositions or processes as disclosed herein may further comprise other components or fractions or steps, whether or not, specifically mentioned in this application, as along as such components or steps do not affect the basic and novel characteristics of the present application, but it is also contemplated that the compositions or processes may consist essentially of, or consist of, the recited components or steps.
For the sake of simplicity, only certain ranges are explicitly disclosed herein. However, ranges from any lower limit may be combined with any upper limit to recite a range not explicitly recited, as well as, ranges from any lower limit may be combined with any other lower limit to recite a range not explicitly recited, in the same way, ranges from any upper limit may be combined with any other upper limit to recite a range not explicitly recited. Additionally, within a range includes every point or individual value between its end points even though not explicitly recited. Thus, every point or individual value may serve as its own lower or upper limit combined with any other point or individual value or any other lower or upper limit, to recite a range not explicitly recited.
As used herein, |(AF/AE−1)/(CE/CF−1)| represents the absolute value of (AF/AE−1)/(CE/CF−1).
The terms “optional” and “optionally” refer to embodiments of the present application that may afford certain benefits, under certain circumstances. However, other embodiments may also be optional, under the same or other circumstances. Furthermore, the recitation of one or more optional embodiments does not imply that other embodiments are not useful, and is not intended to exclude other embodiments from the scope of the present application.
In the description herein, it should be noted that, unless otherwise stated, the recitation of numerical ranges by “above” and “below” include all numbers within that range including the endpoints. As used herein, the recitation of “more” in the phrase “one or more” includes two or more.
The secondary battery according to the present application will be described in detail below.
According to the present application, the secondary battery comprises a positive electrode plate, a negative electrode plate, a separator and an electrolyte, the positive electrode plate comprises a positive electrode current collector and a positive electrode film layer, the positive electrode film layer was coated on at least one surface of the positive electrode current collector and contains a positive electrode active material, the negative electrode plate comprises a negative electrode current collector and a negative electrode film layer, the negative electrode film layer was coated on at least one surface of the negative electrode current collector and contains a negative electrode active material, the positive electrode active material comprises one or more of lithium nickel cobalt manganese oxide and lithium nickel cobalt aluminum oxide; the negative active material comprises a silicon-based material; wherein the secondary battery satisfies the following formula I:
2≤|(AF/AE−1)/(CE/CF−1)|≤7 (Formula I)
in which
CF represents a unit cell volume as measured when the positive electrode active material is prepared into a button battery and the button battery is charged to 100% SOC at a rate of 0.05 C;
CE represents a unit cell volume as measured when the positive electrode active material is prepared into a button battery and the button battery is discharged to 0% SOC at a rate of 0.05 C;
AF represents a volume of the negative electrode active material particles as measured when the silicon-based material is prepared into a single-particle battery, and the single-particle battery is charged to 100% SOC at a rate of 0.5 C; and
AE represents a volume of the negative electrode active material particles as measured when the silicon-based material is prepared into a single-particle battery, and the single-particle battery is discharged to 0% SOC at a rate of 0.5 C.
During the charging and discharging process of the secondary battery, the following electrochemical process generally occurs. During charging, the potential applied to the two electrodes of the battery forces the active compound of the positive electrode to release active ions and the released active ions are intercalated into the negative active material molecules arranged in a layered structure. During discharging, the active ions are deintercalated from the negative electrode active material and recombine with the positive electrode active compound.
As mentioned above, a secondary battery, such as a lithium ion secondary battery will undergo a significant intercalation-deintercalation of active ions during the above charging and discharging process. Therefore, there will be obvious changes of increasing and decreasing in the thickness of the electrode plate, which is the so-called “breathing effect”. Especially when the negative electrode plate contains a silicon-based material with a relatively large volume expansion, this phenomenon is more obvious.
The inventor found through a lot of research that when the selected positive and negative active materials meet the above-mentioned specific conditions, the volume of the positive electrode plate can change in such a manner that it may match the change in the volume of the negative electrode plate during the charging and discharging process of the battery, which will control the overall volume change of the battery cell well, and to a large extent alleviate the adverse effects of the “breathing effect”, thereby effectively improving the cycling performance of the battery.
When the value of formula I is too large, such as greater than 7, the expansion effect of the negative electrode plate is significantly larger than the contraction effect of the positive electrode plate, and the battery will expand greatly, which will cause the electrolyte inside the battery cell to be squeezed and deteriorate the cycling performance of the battery. At the same time, it easily causes the fracturing of the active material particles in the positive and negative electrode plates, and causes performance deterioration at the material level. The superposition of the two results can easily cause a significant increase of the DC internal resistance (DCR) of battery and a drastic capacity decrease during cycling. Particularly serious situations, such as lithium precipitation, may also cause thermal runaway of the battery, thereby posing safety hazards.
When the value of Formula I is too small, e.g. less than 2, the expansion effect of the negative electrode plate is significantly weaker than the contraction effect of the positive electrode. In such a situation, the contact between the positive and negative electrode plate may become worse, and there are some regions in which electrolyte distributes non-continuously, which reduces the effective reaction area, and is likely to cause lithium precipitation. In addition, the surface of the negative electrode active material has a high concentration of lithium ions at the beginning of charging, and lithium ions gradually diffuse within the entire negative electrode active material particles with battery charging. If the positive electrode shrinks significantly, it will restrain the negative electrode less during the initial stage of charging, at which the stress of the negative electrode active material particles is concentrated on the surface. Without the restraint of external force, the stress will cause the surface layer to crack and shatter and the active material to lose while a large amount of electrolyte is also consumed for a new film-forming reaction.
Therefore, too big or too small value of |(AF/AE−1)/(CE/CF−1)| will deteriorate the battery performance and adversely affect the battery life. Optionally, 2|(AF/AE−1)/(CE/CF−1)|≤4.
It should be noted that the preparation process of the “button cell” in this application can refer to national standards or industry specifications. For example, the positive electrode active material and the customary binder and conductive agent in the industry can be used to prepare electrode plates, and then small metal discs such as lithium plate or sodium plates and the like can be used as a counter electrode to prepare a button battery.
Specifically, the “button cell” can be prepared by the following steps. The selected positive electrode active material is mixed with Super P and PVDF in a certain mass ratio (which can be 92:3:5) and then dissolved in the solvent NMP to make a slurry. Then, the slurry is coated on aluminum foil, and dried to remove the solvent. The obtained plate is cut and pressed to make a round electrode plate, which is assembled with a round small lithium plate as a counter electrode into a button cell in the glove box. The electrolyte salt may be LiPF6 at a concentration of 1 mol/L, and the organic solvent may be a mixture of ethylene carbonate and ethyl methyl carbonate in a volume ratio of 1:1.
It should be noted that the preparation process of the “single-particle battery” of the present application can be prepared by the following steps. Under a microscope, a complete silicon-based material particle is selected from the negative electrode active material and sandwiched by two metal lithium electrodes for fixing, which is immersed in the electrolyte in which the electrolyte salt can be LiPF6 at a concentration of 1 mol/L, and the organic solvent can be a mixture of ethylene carbonate and ethyl methyl carbonate in a volume ratio of 1:1) and subjected to charging and discharging tests.
In the secondary battery of the present application, optionally the positive electrode active material comprises one or more of LiaNibCocMdM′eOfAg and a coating layer modified LiaNibCocMdM′eOfAg on at least a part of surface thereof, wherein 0.8≤a≤1.2, 0.8≤b<1, 0<c<1, 0<d<1, 0≤e≤0.1, 1≤f≤2, 0≤g≤1, M is one or more selected from Mn and Al, M′ is one or more selected from Zr, Al, Zn, Cu, Cr, Mg, Fe, V, Ti and B, and A is one or more selected from N, F, S and Cl. The use of the above-mentioned positive electrode active material enables the secondary battery higher energy density and better cycling performance.
In the secondary battery of the present application, optionally, at least a part of the positive electrode active material comprises single crystal particles. The positive electrode active material having single crystal particles can improve the overall compaction density and ductility of the positive electrode film layer, while reducing the contact area between the positive electrode active material and the electrolyte, reducing the occurrence of interface side reactions, and reducing gas production, thereby further improving the cycling performance of batteries. The use of the positive active material improves the cycling performance of the secondary battery.
In the secondary battery of the present application, optionally, the CF of the positive electrode active material satisfies: 0.096 nm3≤CF≤0.098 nm3, more optionally CF=0.097 nm3.
In the secondary battery of the present application, optionally, the CE of the positive electrode active material satisfies: 0.100 nm3≤CE≤0.102 nm3.
In the secondary battery of the present application, optionally, the positive electrode active material satisfies: 1.0≤CE/CF≤1.05; optionally 1.038≤CE/CF≤1.04. The use of the positive electrode active material enables the secondary battery higher energy density and better cycling performance.
In the secondary battery of the present application, optionally, the volume average particle size Dv50 of the positive electrode active material is from 5 μm to 12 μm, more optionally from 6 μm to 10 μm. If the average particle size is too small, the specific surface area of the positive electrode active material is often larger. In such a situation, the oxidation activity becomes higher, the surface side reactions will increase, and the gas generation problem caused by the decomposition of the electrolyte is prominent. If the average particle size is too large, the diffusion path of lithium ions in the large size particles is longer, and the resistance to be overcome for diffusion is greater. Thus, the crystal deformation and volume expansion of the positive electrode active material caused by the intercalation process will continue to accumulate, so that the intercalation process will gradually become difficult to proceed. When the particle size of the positive electrode active material falls within the above-mentioned optional range, the uniformity of the positive electrode plates will be higher, which can avoid not only the deterioration of the performance of the lithium-ion battery caused by more side reactions with the electrolyte due to the too small particle size, but also the deterioration of the performance of the lithium ion battery due to the large particle size hindering the transport of lithium ions inside the particles.
In the secondary battery of the present application, optionally, the thickness T of the positive electrode film layer in a single side satisfies: 46 μm≤Tpositive≤56 μm; more optionally, 48.5 μm≤Tpositive≤53.5 μm. If the thickness is too large, the discharge power performance will deteriorate, and the battery power will decrease; if it is too small, the proportion of the active material will decrease, and the energy density of the battery will decrease. The use of such a positive electrode film layer can improve the electrical performance of the secondary battery.
In the secondary battery of the present application, optionally, the compaction density PD of the positive electrode film layer satisfies: 3.0 g/cm3≤PDpositive≤3.55 g/cm3; more optionally, 3.4 g/cm3≤PDpositive≤3.5 g/cm3. Controlling the compaction density within the range can ensure the integrity of the positive electrode active material particles and maintain good electrical contact between the particles.
In the secondary battery of the present application, the type of the positive electrode current collector is not specifically limited, and can be selected according to actual needs. For example, the positive electrode current collector can be an aluminum foil, a nickel foil or a polymer conductive film. Optionally, the positive electrode current collector is an aluminum foil.
In the secondary battery of the present application, the positive electrode film layer further includes a conductive agent and a bonding agent. The type and content of the conductive agent and the bonding agent are not specifically limited, and can be selected according to actual needs.
In the secondary battery of the present application, optionally, the silicon-based material is one or more selected from elemental silicon, silicon-oxygen compounds, silicon-carbon composites, silicon-nitrogen compounds, and silicon alloys. More desirably, the silicon-based material is selected from silicon-oxygen compounds, such as SiOx, where 0<X<2.
In the secondary battery of the present application, optionally, the AF/AE of the silicon-based material satisfies the following relationship: 1.05<AF/AE<1.30, more optionally 1.08<AF/AE<1.27, which provides a secondary battery with higher energy density and better cycling performance.
In the secondary battery of the present application, optionally, the AE of the silicon-based material satisfies: 700 μm3≤AE≤1100 μm3, more optionally 800 μm3≤AE≤1000 μm3.
In the secondary battery of the present application, optionally, the mass percentage of the silicon-based material in the negative electrode active material is <40%, and more optionally 15%-30%. The negative electrode active material with the silicon-based material content within the above range enables the secondary battery higher energy density and better cycling performance.
In the secondary battery of the present application, the negative electrode active material further includes a carbon material. The carbon material is one or more selected from of graphite, soft carbon, and hard carbon; optionally, the carbon material is selected from graphite, and the graphite is selected one or more from artificial graphite and natural graphite. Such negative electrode active materials have improved structural stability.
In the secondary battery of the present application, optionally, the volume average particle size Dv50 of the negative electrode active material is from 10 μm to 23 μm, and more optionally, from 12 μm to 16 μm. Too small particle size may be due to the high content of silicon-based materials, the binding force between the negative electrode active material particles is weak, and the binding force between the negative electrode film and the negative electrode current collector is weaken. During use, the negative electrode film is prone to peel off, thereby causing capacity degradation. If the average particle size is too large, the diffusion path of lithium ions in the large particle size particles is longer, which makes the intercalation process slower. Thus, the average particle diameter Dv50 of the negative electrode active material falling within the above range provides a secondary battery with good electrical performance.
In the secondary battery of the present application, optionally, the thickness T negative of the negative electrode film in a single side satisfies: 66 μm≤=Tnegative≤=86 μm; more optionally, 68.5 μm≤Tnegative≤=83.5 μm. If the negative electrode film is too thick, the charging polarization becomes larger, the lithium-precipitation window becomes narrower, and the performance becomes worse. In addition, the active material is likely to fall off and delaminate during the charging and discharging of the battery, which affects the cycling performance of the battery. For the thick electrodes, the migration path of lithium ions within small material particles is shorter, and the charging performance is better. At the same time, the volume change of the single particle during charging and discharging is small, and the electrode plate structure is easy to maintain. Otherwise, with large material particles, the charging performance will deteriorate and the structure is easily destroyed. If the negative electrode film is too thin, it will affect the energy density of the battery. The thickness of the negative electrode film in a single side falling within the above range can improve the electrical performance of the secondary battery.
In the secondary battery of the present application, optionally, the compaction density PD negative of the negative electrode film layer satisfies: 1.5 g/cm3≤PDnegative≤1.8 g/cm3; more optionally, 1.6 g/cm3≤PDnegative≤1.7 g/cm3. Controlling the compaction density within the above range can ensure the integrity of the negative electrode active material particles and maintain good electrical contact between the particles.
In the secondary battery of the present application, the type of the negative electrode current collector is not specifically limited, and can be selected according to actual needs. For example, the negative electrode current collector can be a copper foil, a carbon-coated copper foil or a polymer conductive film. Optionally, the negative electrode current collector is a copper foil.
In the secondary battery of the present application, the negative electrode film further includes a conductive agent and a bonding agent. The type and content of the conductive agent and the bonding agent are not specifically limited, and can be selected according to actual needs.
In the secondary battery of the present application, the positive electrode film can be provided on one surface of the positive electrode current collector, or can be provided on both surfaces of the positive electrode current collector; the negative electrode film can be provided on one surface of the negative electrode current collector, or can be provided on both surfaces of the negative electrode current collector. It should be noted that when the above-mentioned positive and negative electrode films are simultaneously disposed on both surfaces of the current collector, the parameter ranges of the positive and negative electrode film given in the present application refer to the parameter ranges of the positive and negative electrode film on either side such as thickness, compaction density and the like. In addition, the thickness of the positive and negative electrode films, mentioned in the present application, refers to the thickness of the positive and negative electrode plates and these plates have been cold-pressed and compacted and used to assemble the battery.
In the secondary battery of the present application, the type of the separator is not specifically limited, and can be any separator material used in the existing batteries, such as polyethylene, polypropylene, polyvinylidene fluoride and their multi-layer composite film, but not limited thereto.
In the secondary battery of the present application, the electrolyte includes a lithium salt and an organic solvent, wherein the specific types and compositions of the lithium salt and the organic solvent are not specifically limited, and can be selected according to actual needs. Optionally, the lithium salt may be one or more selected from lithium hexafluorophosphate, lithium tetrafluoroborate, and lithium perchlorate, and the organic solvent may include one or more of cyclic carbonate, chain carbonate, and carboxylate ester. The electrolyte may also contain a functional additive, such as vinylene carbonate, vinyl sulfate, propane sultone, fluoroethylene carbonate and the like.
The various parameters involved in this application have general meanings known in the art, and can be measured according to methods known in the art. For example, they can be tested according to the method given in the embodiment of the present application.
The secondary battery can be prepared by a method known in the art. As an example, the positive electrode plate, the separator, and the negative electrode plate are wound (or laminated) in order, so that the separator is located between the positive electrode plate and the negative electrode plate for isolation to obtain an electrode assembly. The electrode assembly is placed in an outer package in which an electrolyte is injected and then sealed to obtain a secondary battery.
In the secondary battery of the present application, the outer package may be a hard shell (such as an aluminum shell) or a soft package (such as a bag).
The present application in a second aspect provides a battery module, comprising any one or more of the secondary battery according to the first aspect of the present application. The number of the secondary battery in the battery module can be adjusted according to the application and capacity of the battery module.
In some embodiments, referring to
Optionally, the battery module 4 may further include a housing having a receiving space, in which a plurality of lithium ion batteries 5 are received.
The present application in a third aspect provides a battery pack, comprising any one or more of the battery module according to the second aspect of the present application. That is to say, the battery pack comprises any one or more of the secondary battery according to the first aspect of the present application.
The number of battery modules included in the battery pack can be adjusted according to the application and capacity of the battery pack.
In some embodiments, with reference to
The present application in a fourth aspect provides an apparatus, comprising any one or more of the secondary battery according to the first aspect of the present application. The secondary battery may be used as a power source of the apparatus or as an energy storage unit of the apparatus. Optionally, the apparatus may be, but is not limited to, a mobile apparatus (such as a mobile phone, a notebook computer, and the like), an electric vehicle (such as a pure electric vehicle, a hybrid electric vehicle, a plug-in hybrid electric vehicle, an electric bicycle, an electric scooter, and an electric golf vehicles, electric trucks, and the like), electric trains, ships and satellites, energy storage systems, or the like.
For example,
In order to make the purpose of the application, technical solutions, and beneficial technical effects of the present application clearer, the following further describes the present application in detail with reference to embodiments. However, it should be understood that the embodiments of the application are only for explaining the application, not for limiting the application, and the embodiments of the application are not limited to the embodiments given in the specification. The specific experimental conditions or operating conditions that are not specified in the examples are manufactured under conventional conditions, or manufactured under the conditions recommended by the material supplier.
The batteries of Examples 1-11 and Comparative Examples 1-2 were prepared according to the following methods.
A) Preparation of Positive Electrode Plate:
A positive electrode active material (see Table 1 for details), a conductive agent (Super P), and a bonding agent bonding agent (PVDF) were mixed in a ratio of 96:2:2, a solvent (NMP) was added. The resulting mixture was stirred under the action of a vacuum mixer until the system become uniform and transparent, and a positive electrode slurry was obtained. The positive electrode slurry was evenly applied on an aluminum foil as a positive electrode current collector. The positive electrode current collector coated with the positive electrode slurry was dried at room temperature and then transferred to an oven for drying followed by cold pressing, slitting and other processes to obtain the positive electrode plate.
B) Preparation of Negative Electrode Plate:
A negative active material (see Table 1 for details), a conductive agent (Super P), CMC (carboxymethyl cellulose), and a bonding agent (styrene butadiene rubber) were mixed in a mass ratio of 94.5:1.5:1.5:2.5 and then mixed with a solvent (deionized water) uniformly under the action of a vacuum mixer to prepare a negative electrode slurry. The negative electrode slurry was evenly coated on the negative electrode collector copper foil. The negative electrode current collector coated with the negative electrode slurry was dried at room temperature and then transferred to an oven for drying followed by cold pressing, slitting and other processes to obtain the negative electrode plate.
C) Preparation of Electrolyte:
Ethylene carbonate (EC), ethyl methyl carbonate (EMC), and diethyl carbonate (DEC) were mixed in a volume ratio of 1:1:1, and fluoroethylene carbonate (FEC) was added. After that, LiPF6 was uniformly dissolved in the above solution to obtain an electrolyte, wherein the concentration of LiPF6 was 1 mol/L, and the mass fraction of FEC in the electrolyte was 6%.
D) Separator: A Polyethylene Film was Used.
E) Assembly of the Battery:
The above-mentioned positive electrode film, separator, and negative electrode film were stacked in order, so that the separator was located between the positive electrode and negative electrode films for isolation, which was then wound to obtain an electrode assembly. The electrode assembly was placed into an outer package, in which the electrolyte prepared above was injected, thereby obtaining a lithium ion secondary battery through the steps of vacuum packaging, standing, chemical conversion, and shaping.
The preparation process of Example 2-11 and Comparative Example 1-2 were similar to that of Example 1, with the differences as shown in Table 1.
In the secondary battery of the present application, the parameters of the positive and negative electrode active materials and the positive and negative electrode films can be tested according to the following methods, or can be tested according to other known methods in the art, and the test results as obtained are all within the margin of error.
(1) Unit Cell Volume of Positive Electrode Active Material
A button battery was prepared according to the aforementioned preparation method and the prepared button battery was charged to 100% SOC at a rate of 0.05 C. After that, the button battery was disassembled in the glove box for the electrode plate and the obtained electrode plate was subjected to XRD test. The cell volume was obtained by calculation, which was marked as CF. Another prepared button battery was discharged to 0% SOC at a rate of 0.05 C. After that, the button battery was disassembled in the glove box for the electrode plate and the obtained electrode plate was subjected to XRD test. The cell volume was obtained by calculation, which was marked as CE.
(2) Volume of Silicon-Based Material Particles
A single-particle battery was prepared according to the aforementioned method, and then a microscope was used in situ to take pictures of several particles in the charged state and the discharged state, and the volumes in the charged state and the discharged state were calculated according to the pictures. Test 20 Ea single-particle batteries separately, and average the volume expansion rate of charge and discharge.
(3) Volume Average Particle Size Dv50 of the Positive and Negative Electrode Active Materials
The average particle size Dv50 of the positive and negative electrode active materials were measured by using a laser diffraction particle size distribution measuring instrument such as Mastersizer 3000. Dv50 represents the particle size at which the positive and negative electrode active material particles reaches 50% of cumulative volume distribution percentage, i.e. an average particle size of volume distribution.
(4) The Compaction Density of the Positive and Negative Electrode Film in a Single Side
The compaction density of the positive and negative electrode films in a single side represented as PD=m/V, in which m represented the weight of the membrane, and V represented the volume of the membrane, m of the electrode film was obtained by weighing the film using an electronic balance with an accuracy of 0.01 g or more and V of the electrode film was obtained by the product of the surface area of the film and the thickness of the film, where the thickness of the film was measured using a spiral micrometer with an accuracy of 0.5 μm.
The above-mentioned Examples 1-11 and Comparative Examples 1-2 were tested for various properties according to the following methods.
At 25° C., the obtained secondary battery was charged at a constant current of 0.7 C to a voltage of 4.35V, then charged at a constant voltage of 4.35V to a current of 0.05 C, and afterwards discharged at a constant current of 1 C to a voltage of 3.0V, which is a charge-discharge cycle process. The process was repeated for 300 times.
Capacity retention rate after 300 cycles=discharge capacity after the 300th cycle/discharge capacity after the first cycle×100%.
The above test results were shown in Table 1.
It can be seen from the test results in Table 1 that:
Examples 1-11 and Comparative Examples 1-2 examined the effect of |(AF/AE−1)/(CE/CF−1)| on battery performance when a high nickel positive electrode active material was as a positive electrode active material, and a mixture of silicon-based material and graphite material was as a negative electrode active material. From the data of these Examples 1-10 and Comparative Examples 1-2, it can be seen that when 2≤|(AF/AE−1)/(CE/CF−1)|≤7, the battery had good cycling performance. When |(AF/AE−1)/(CE/CF−1)|>7 or |(AF/AE−1)/(CE/CF−1)|<2, the DC impedance of the battery was greatly increased, and the cycling performance was significantly reduced, as shown in Comparative Examples 1 and 2. Therefore, in order to ensure the electrical performance of batteries, especially the DC impedance and cycling performance of batteries, it was necessary to ensure that 2≤|(AF/AE−1)/(CE/CF−1)|≤7, and the best performance was obtained.
Below are some exemplary embodiments of the present application.
Embodiment 1. A secondary battery comprising a positive electrode plate, a negative electrode plate, a separator and an electrolyte, the positive electrode plate comprising a positive electrode current collector and a positive electrode film layer coated on at least one surface of the positive electrode current collector and containing a positive electrode active material, the negative electrode plate comprising a negative electrode current collector and a negative electrode film layer coated on at least one surface of the negative electrode current collector and containing a negative electrode active material, characterized in that:
the positive electrode active material comprises one or more of lithium nickel cobalt manganese oxide and lithium nickel cobalt aluminum oxide;
the negative active material comprises a silicon-based material; and
the secondary battery satisfies the following formula I:
2≤|(AF/AE−1)/(CE/CF−1)|≤7 (Formula I)
in which
CF represents a unit cell volume as measured when the positive electrode active material is prepared into a button battery and the button battery is charged to 100% SOC at a rate of 0.05 C;
CE represents a unit cell volume as measured when the positive electrode active material is prepared into a button battery and the button battery is discharged to 0% SOC at a rate of 0.05 C;
AF represents a volume of the negative electrode active material particles as measured when the silicon-based material is prepared into a single-particle battery, and the single-particle battery is charged to 100% SOC at a rate of 0.5 C; and
AE represents a volume of the negative electrode active material particles as measured when the silicon-based material is prepared into a single-particle battery, and the single-particle battery is discharged to 0% SOC at a rate of 0.5 C.
Embodiment 2. The secondary battery according to Embodiment 1, wherein the silicon-based material is present in the negative electrode active material in a mass percentage of 40% or less, optionally from 15% to 30%.
Embodiment 3. The secondary battery according to Embodiment 1 or 2, wherein the positive electrode active material comprises one or more of LiaNibCocMdM′eOfAg and a coating layer modified LiaNibCocMdM′eOfAg on at least a part of surface thereof, wherein 0.8≤a≤1.2, 0.8≤b<1, 0<c<1, 0<d<1, 0≤e≤0.1, 1≤f≤2, 0≤g≤1, M is one or more selected from Mn and Al, M′ is one or more selected from Zr, Al, Zn, Cu, Cr, Mg, Fe, V, Ti and B, and A is one or more selected from N, F, S and Cl.
Embodiment 4. The secondary battery according to any one of Embodiments 1 to 3, wherein the positive electrode active material satisfies: 1.0≤CE/CF≤1.05; optionally 1.038≤CE/CF≤1.04.
Embodiment 5. The secondary battery according to any one of Embodiments 1-4, wherein the negative electrode active material satisfies: 1.05≤AF/AE≤1.30; optionally 1.08≤AF/AE≤1.27.
Embodiment 6. The secondary battery according to any one of Embodiments 1-5, wherein the negative active material further comprises a carbon material, and the carbon material comprises one or more of artificial graphite, natural graphite, soft carbon, and hard carbon, optionally, the negative electrode active material further comprises one or more of artificial graphite and natural graphite.
Embodiment 7. The secondary battery according to Embodiments 1-6, wherein the negative active material has an average particle size Dv50 in the range of 10 μm to 23 μm, more optionally, in the range of 12 μm to 16 μm.
Embodiment 8. The secondary battery according to any one of Embodiments 1-7, wherein at least a part of the positive electrode active material is a single crystal particle.
Embodiment 9. The secondary battery according to any one of Embodiments 1-8, wherein the positive electrode film layer in a single side has a thickness Tc satisfying 46 μm≤Tc≤56 μm; more optionally, 48.5 μm≤Tc≤53.5 μm; and/or, the negative electrode film layer in a single side has a thickness Ta satisfying 66 μm≤Ta≤86 μm; more optionally, 68.5 μm≤Ta≤83.5 μm.
Embodiment 10. The secondary battery according to any one of Embodiments 1-9, wherein the positive electrode film layer has a compaction density PD positive satisfying: 3.0 g/cm3≤PDpositive≤3.55 g/cm3; more optionally 3.4 g/cm3≤PDpositive≤3.5 g/cm3; and/or, the negative electrode film layer has a compaction density PD negative satisfies: 1.5 g/cm3≤PDnegative≤1.8 g/cm3; more optionally 1.6 g/cm3≤PDnegative≤1.7 g/cm3.
Embodiment 11. A battery module, characterized by comprising the secondary battery according to any one of Embodiments 1-10.
Embodiment 12. A battery pack, comprising the battery module according to Embodiment 11.
Embodiment 13. An apparatus, comprising the secondary battery according to any one of Embodiments 1-10, the secondary battery being used as a power source or an energy storage unit of the apparatus; optionally, the apparatus comprising mobile equipment, electric vehicles, electric trains, satellites, ships and energy storage systems.
Furthermore, in those instances where a convention analogous to “at least one of A, B, and C, etc.” is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., “a system having at least one of A, B, and C” would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). In those instances where a convention analogous to “at least one of A, B, or C, etc.” is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., “a system having at least one of A, B, or C” would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). It will be further understood by those within the art that virtually any disjunctive word and/or phrase presenting two or more alternative terms, whether in the description, claims, or drawings, should be understood to contemplate the possibilities of including one of the terms, either of the terms, or both terms. For example, the phrase “A or B” will be understood to include the possibilities of “A” or “B” or “A and B.”
In addition, where features or aspects of the disclosure are described in terms of Markush groups, those skilled in the art will recognize that the disclosure is also thereby described in terms of any individual member or subgroup of members of the Markush group.
Based on the application and teaching of the foregoing specification, those skilled in the art can also make changes and modifications to the foregoing embodiments. Therefore, the present application is not limited to the specific embodiments disclosed and described above, and some modifications and changes to the present application should also fall within the protection scope of the claims of the present application. In addition, although some specific terms are used in the present specification, these terms are only for convenience of description and do not constitute any limitation to the present application.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201911075791.3 | Nov 2019 | CN | national |
This application is a continuation of International Application No. PCT/CN2020/124951, filed on Oct. 29, 2020, which claims priority to Chinese Patent Application No. 201911075791.3 filed on Nov. 6, 2019, both of which are incorporated herein by reference in their entireties.
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/CN2020/124951 | Oct 2020 | US |
| Child | 17541152 | US |
