CN214706019U - Lithium ion battery cell and lithium ion battery - Google Patents

Lithium ion battery cell and lithium ion battery Download PDF

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CN214706019U
CN214706019U CN202121212830.2U CN202121212830U CN214706019U CN 214706019 U CN214706019 U CN 214706019U CN 202121212830 U CN202121212830 U CN 202121212830U CN 214706019 U CN214706019 U CN 214706019U
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lithium
ion battery
lithium ion
negative electrode
ribbon
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徐雄文
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Hunan Lifang New Energy Science and Technology Co Ltd
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    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50—Manufacturing or production processes characterised by the final manufactured product

Abstract

The utility model provides a lithium ion battery cell, including anodal, negative pole, diaphragm and lithium area, anodal the negative pole diaphragm and the lithium area is according to the order of "diaphragm lithium area/negative pole lithium area/diaphragm/anodal in proper order together laminated. This lithium ion battery electricity core is through mending the lithium to the negative pole, can effectively promote the first coulomb efficiency of negative pole, promotes the cyclicity ability of electric core simultaneously. In addition, the utility model provides a lithium ion battery who contains this lithium ion battery electricity core still, above-mentioned technological effect has equally.

Description

Lithium ion battery cell and lithium ion battery
Technical Field
The utility model belongs to the technical field of the electrochemistry energy storage, especially, relate to a lithium ion battery electricity core and lithium ion battery.
Background
The lithium ion battery has the characteristics of high energy density, good cycle performance, good safety, environmental friendliness and the like, and is widely applied to consumer electronics products and power energy storage products. At present, graphite is taken as a main negative electrode material of the lithium ion battery, the theoretical specific capacity of the graphite is only 372mAh/g, and in order to further improve the energy density of the battery, a silicon material gradually becomes the first choice of the negative electrode material of the next generation of lithium ion battery.
The theoretical specific capacity of the silicon negative electrode can reach more than 4000mAh/g, and the silicon negative electrode has lower discharge potential and is a negative electrode material with great potential. However, the volume change of the silicon material is large in the process of lithium intercalation/lithium deintercalation, and reaches up to 300%, and the large volume change often causes the phenomena of active material particles such as crushing, slippage and the like, and finally causes electrode pulverization, capacity reduction and cycle life shortening. In addition, the silicon cathode has the defect of low coulombic efficiency for the first time, and generally can only reach about 70%. In order to apply a silicon negative electrode to a lithium ion battery, lithium is usually required to be supplemented to the silicon negative electrode, and the first coulombic efficiency of the silicon negative electrode is improved to a level close to that of graphite, so that the purpose of improving the energy density is achieved.
At present, a layer of lithium powder is plated on the surface of a negative electrode in a conventional lithium supplementing mode through modes of sputtering, spraying and the like, the risk that the lithium powder is easy to splash and remain exists in the conventional lithium supplementing mode, safety accidents are easy to cause, the operation process is complex, and the process requirement is high.
Therefore, how to provide a lithium ion battery cell with high energy density and good cycle performance becomes a technical problem to be solved urgently by the technical personnel in the field.
SUMMERY OF THE UTILITY MODEL
In order to solve the technical problem, the utility model provides a lithium ion battery cell, this lithium ion battery cell can effectively promote the first coulomb efficiency of negative pole through mending the lithium to the negative pole, promotes the cyclicity ability of electric core simultaneously. In addition, the utility model provides a lithium ion battery who contains this lithium ion battery electricity core still, above-mentioned technological effect has equally.
The utility model provides a lithium ion battery cell, including anodal, negative pole, diaphragm and lithium area, anodal the negative pole diaphragm and the lithium area is according to the order of "diaphragm lithium area/negative pole lithium area/diaphragm/anodal in proper order together laminated.
Preferably, the width of the lithium ribbon is equal to or less than the width of the negative electrode, the length of the lithium ribbon is equal to or less than the length of the negative electrode, and the thickness of the lithium ribbon is equal to or less than 10 μm.
The lithium belt is too thick, so that the lithium belt cannot be completely consumed before formation, on one hand, the thickness of a lithium ion battery cell is increased, and the volume energy density of the battery is reduced; on the other hand, the presence of the lithium ribbon hinders the insertion of lithium ions desorbed from the positive electrode into the negative electrode, thereby causing lithium precipitation of the lithium ion battery, lowering the battery capacity, and deteriorating the cycle performance and safety performance of the battery. However, if lithium is not supplemented by a lithium band, the first coulombic efficiency of the lithium ion battery is not high, and active lithium is lost, so that the gram capacity of the battery is low, and the energy density and the cycle performance of the battery are reduced. Therefore, reasonable control of the thickness of the lithium ribbon is required.
Preferably, the thickness of the lithium ribbon is 5 μm or less.
Preferably, the thickness of the lithium ribbon is 2 to 5 μm.
Preferably, the area of the lithium ribbon is 50% to 100% of the area of the negative electrode.
Preferably, the total lithium amount of one lithium ribbon is less than or equal to half of the lithium supplement amount of one negative electrode. Specifically, the total lithium content of a single lithium ribbon should be equal to or slightly less than half of the lithium supplement content of a single negative electrode (double-sided), so as to ensure that the negative electrode does not precipitate lithium.
Preferably, the negative electrode is a silicon carbon negative electrode. The gram capacity of the silicon-carbon cathode is far higher than that of graphite, so that the energy density of a lithium ion battery cell can be remarkably improved by applying the silicon-carbon cathode.
Preferably, the negative active material of the silicon-carbon negative electrode comprises graphite and at least one of nano-silicon, SiOx and silicon alloy.
Preferably, in the silicon-carbon negative electrode, the silicon negative electrode (at least one of nano-silicon, SiOx, and silicon alloy) accounts for 5 to 50 mass% of the active material in the entire silicon-carbon negative electrode.
Preferably, the negative electrode current collector is a copper foil.
Preferably, the positive current collector is an aluminum foil, and the positive active material is one or more of lithium cobaltate, lithium nickel cobalt manganese oxide, lithium iron phosphate, lithium nickel cobalt aluminate, lithium manganese oxide, lithium manganese rich manganese base, lithium nickel manganese oxide, lithium manganese iron phosphate, and lithium cobalt phosphate.
Preferably, the density of the single-side coating surface of the positive electrode is 12-30 mg/cm2。
Preferably, the percentage of the positive electrode active material is 95% to 99%. Here, the positive electrode active percentage refers to a ratio of the positive electrode active material to the total positive electrode material (including the positive electrode active material, the conductive agent, and the binder).
Preferably, the thickness of the lithium ribbon is calculated as follows:
a. calculating the charge gram capacity, the discharge gram capacity and the first coulombic efficiency of the negative electrode;
b. the gram capacity C0 of lithium supplement is equal to the gram capacity of positive electrode discharge/the first coulombic efficiency of negative electrode-gram capacity of positive electrode charge;
c. the lithium supplement capacity per unit area C1 ═ positive electrode coating surface density ═ C0 ═ positive electrode active material percentage;
d. according to the lithium supplement capacity of the unit area and the gram capacity of the lithium metal, the weight of the lithium metal required by the unit area can be obtained;
e. the required lithium ribbon thickness can be calculated from the required lithium metal weight per unit area and the lithium metal density.
The thickness of the lithium strip is calculated through the method (the calculated thickness of the lithium strip is the thickness of the lithium strip required by the unit area of the single side of the negative electrode), the lithium supplement amount of the negative electrode can be accurately controlled, the lithium strip can be completely consumed before formation, the increase of the thickness of the battery cell and the deterioration of an interface caused by lithium metal residue are avoided, and the volume density, the cycle performance and the safety performance of the battery cell are ensured.
Specifically, the gram charge capacity, the gram discharge capacity and the first coulombic efficiency of a single material can be obtained through a button type half cell test. The charge gram capacity, the discharge gram capacity and the first coulombic efficiency of the mixed material can be calculated by weighting the mixed components in proportion.
Preferably, in step a, when the negative electrode is a silicon-carbon negative electrode, the gram-charged capacity, the gram-discharged capacity and the first coulombic efficiency of the negative electrode are calculated in the following manner: the charge gram capacity, the discharge gram capacity and the first effect of the silicon negative electrode and the graphite and the mixing ratio of the silicon negative electrode and the graphite are obtained through weighted calculation.
Additionally, the utility model provides a lithium ion battery, this lithium ion battery include the battery case, and the above arbitrary lithium ion battery electricity core.
Further, the preparation method of the lithium ion battery comprises the following steps:
s1. preparing anode and cathode by stirring, coating, rolling and die cutting, and drying the anode, cathode and diaphragm;
s2, preparing lithium metal into a lithium belt according to a required specification in a dry environment;
s3. in a dry environment, sequentially laminating the positive electrode, the negative electrode, the diaphragm and the lithium tape according to the sequence of diaphragm/lithium tape/negative electrode/lithium tape/diaphragm/positive electrode to obtain a coiled core, carrying out hot pressing treatment on the coiled core, then loading the coiled core into a battery shell, carrying out standing at room temperature and high temperature after liquid injection, and keeping the standing time for more than or equal to 48 h;
s4., the packaged battery is formed and degassed to obtain the lithium ion battery.
The utility model provides a lithium ion battery's preparation method makes lithium piece and negative pole contact together through the hot pressing of short time, and simple process realizes easily, compares with current lithium ion battery technology, need not to increase extra process, can effectively save resource and energy, and does not influence the energy consumption.
Preferably, the technological parameters of the hot pressing treatment are as follows: hot pressing the core at 60-100 deg.c and 0.6-1.2MPa for 1-10 min.
Preferably, the technological parameters of the hot pressing treatment are as follows: and hot-pressing the coiled core for 1-10 minutes at 80 ℃ and under the pressure of 0.8 MPa.
Besides the preparation method, the middle diaphragm of the utility model can also adopt a solid electrolyte membrane to make the lithium ion battery into a solid battery.
The beneficial effects of the utility model reside in that:
the lithium belt is arranged on two sides of the negative electrode, so that the lithium supplementing efficiency is high and the lithium supplementing uniformity is good; the lithium band is used for supplementing lithium to the negative electrode, so that the first coulombic efficiency of the negative electrode can be effectively improved and is equivalent to that of pure graphite; and the improvement of the first coulombic efficiency of the negative electrode can also improve the cycle life of the lithium ion battery core and the cycle life of the lithium ion battery to a certain extent. And simultaneously, the utility model discloses a lithium area realizes the benefit lithium of negative pole, can not produce lithium powder in the air, and environmental protection and security are high.
Drawings
Fig. 1 is a schematic structural diagram of a lithium ion battery cell according to the present invention;
1-positive electrode, 2-negative electrode, 3-diaphragm. 4-lithium tape.
Detailed Description
In order to make those skilled in the art better understand the technical solutions in the present application, the present application will be clearly and completely described below with reference to specific embodiments, and it is obvious that the described embodiments are only a part of the embodiments of the present application, and not all embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present application.
The utility model provides a lithium ion battery cell, including anodal 1, negative pole 2, diaphragm 3 and lithium area 4, anodal 1, negative pole 2, diaphragm 3 and lithium area 4 are according to the order of "diaphragm 3 lithium area 4/negative pole 2 lithium area 4/diaphragm 3/anodal 1" in proper order and are together laminated together.
Preferably, the width of the lithium ribbon 4 is equal to or less than the width of the negative electrode 2, the length of the lithium ribbon 4 is equal to or less than the length of the negative electrode 2, and the thickness of the lithium ribbon 4 is equal to or less than 10 μm.
Preferably, the thickness of the lithium ribbon 4 is 5 μm or less.
Preferably, the thickness of the lithium ribbon 4 is 2 to 5 μm.
Preferably, the area of the lithium ribbon 4 is 50% to 100% of the area of the negative electrode 2.
Preferably, the total lithium content of a lithium strip 4 is less than or equal to half the lithium supplement content of a negative electrode 2.
Specifically, the total amount of lithium in a single lithium ribbon 4 should be equal to or slightly less than half of the amount of lithium supplement in a single negative electrode 2 (double-sided), so as to ensure that the negative electrode 2 does not precipitate lithium.
Preferably, the negative electrode 2 is a silicon carbon negative electrode. The gram capacity of the silicon-carbon cathode is far higher than that of graphite, so that the energy density of a lithium ion battery cell can be remarkably improved by applying the silicon-carbon cathode.
Preferably, the negative active material of the silicon-carbon negative electrode comprises graphite and at least one of nano-silicon, SiOx and silicon alloy.
Preferably, in the silicon-carbon negative electrode, the silicon negative electrode (at least one of nano-silicon, SiOx, and silicon alloy) accounts for 5 to 50 mass% of the active material in the entire silicon-carbon negative electrode.
Preferably, the negative electrode current collector is a copper foil.
Preferably, the positive current collector is an aluminum foil, and the positive active material is one or more of lithium cobaltate, lithium nickel cobalt manganese oxide, lithium iron phosphate, lithium nickel cobalt aluminate, lithium manganese oxide, lithium manganese rich manganese base, lithium nickel manganese oxide, lithium manganese iron phosphate, and lithium cobalt phosphate.
Preferably, the density of the single-side coating surface of the positive electrode is 12-30 mg/cm2。
Preferably, the percentage of the positive electrode active material is 95% to 99%. Here, the positive electrode active percentage refers to a ratio of the positive electrode active material to the total positive electrode material (including the positive electrode active material, the conductive agent, and the binder).
Preferably, the thickness of the lithium strip 4 is calculated as follows:
a. calculating the charge gram capacity, the discharge gram capacity and the first coulombic efficiency of the negative electrode;
b. the gram capacity C0 of lithium supplement is equal to the gram capacity of positive electrode discharge/the first coulombic efficiency of negative electrode-gram capacity of positive electrode charge;
c. the lithium supplement capacity per unit area C1 ═ positive electrode coating surface density ═ C0 ═ positive electrode active material percentage;
d. according to the lithium supplement capacity of the unit area and the gram capacity of the lithium metal, the weight of the lithium metal required by the unit area can be obtained;
e. the required lithium ribbon thickness (calculated here is the required lithium ribbon thickness per unit area of the negative electrode) can be calculated from the required lithium metal weight per unit area and the lithium metal density.
Specifically, the gram charge capacity, the gram discharge capacity and the first coulombic efficiency of a single material can be obtained through a button type half cell test. The charge gram capacity, the discharge gram capacity and the first coulombic efficiency of the mixed material can be calculated by weighting the mixed components in proportion.
Preferably, in step a, when the negative electrode 2 is a silicon-carbon negative electrode, the gram-charged capacity, the gram-discharged capacity, and the first coulombic efficiency of the negative electrode 2 are calculated in the following manner: the charge gram capacity, the discharge gram capacity and the first effect of the silicon negative electrode and the graphite and the mixing ratio of the silicon negative electrode and the graphite are obtained through weighted calculation.
Additionally, the utility model provides a lithium ion battery, this lithium ion battery include the battery case to and an arbitrary lithium ion battery electricity core of above.
Further, the preparation method of the lithium ion battery comprises the following steps:
s1. preparing anode and cathode by stirring, coating, rolling and die cutting, and drying the anode, cathode and diaphragm;
s2, preparing lithium metal into a lithium belt according to a required specification in a dry environment;
s3. in a dry environment, sequentially laminating the positive electrode, the negative electrode, the diaphragm and the lithium tape according to the sequence of diaphragm/lithium tape/negative electrode/lithium tape/diaphragm/positive electrode to obtain a coiled core, carrying out hot pressing treatment on the coiled core, then loading the coiled core into a battery shell, carrying out standing at room temperature and high temperature after liquid injection, and keeping the standing time for more than or equal to 48 h;
s4., the packaged battery is formed and degassed to obtain the lithium ion battery.
Preferably, the technological parameters of the hot pressing treatment are as follows: hot pressing the core at 60-100 deg.c and 0.6-1.2MPa for 1-10 min.
Preferably, the technological parameters of the hot pressing treatment are as follows: and hot-pressing the coiled core for 1-10 minutes at 80 ℃ and under the pressure of 0.8 MPa.
Besides the preparation method, the diaphragm in the embodiment of the present invention can also adopt a solid electrolyte membrane to make a lithium ion battery into a solid battery.
Example 1
The present embodiment provides a lithium ion battery, which includes a lithium ion battery cell, in which a positive electrode, a negative electrode, a diaphragm, and a lithium ribbon are sequentially stacked together according to an order of "diaphragm/lithium ribbon/negative electrode/lithium ribbon/diaphragm/positive electrode".
The negative electrode is a silicon-carbon negative electrode; wherein the proportion of the silicon negative electrode in the silicon-carbon negative electrode active material is 15%, the negative electrode current collector is copper foil, the percentage of the negative electrode active material is 97.3%, and the surface density of the negative electrode is 8.5mg/cm2。
The positive electrode is lithium cobaltate; the positive current collector is aluminum foil, the percentage of positive active substances is 98 percent, and the surface density of the positive electrode is 20.5mg/cm2。
The thickness of the lithium belt is 5 μm, the area of the lithium belt is 86% of the active material coating area of the negative pole piece, the length of the lithium belt is less than that of the negative pole piece, and the width of the lithium belt is less than that of the negative pole piece.
Specifically, the calculation method of the thickness of the lithium strip comprises the following steps:
a. through a button type half cell test, the charging gram capacity of the graphite is 373mAh/g, the discharging gram capacity is 351mAh/g, and the first coulombic efficiency is 94.2%; the charge gram capacity of the silicon material is 2142mAh/g, the discharge gram capacity is 1291mAh/g, and the first coulombic efficiency is 60.3%. According to 15% of the mixing ratio of the graphite and the silicon material, the charge gram capacity of the negative electrode is 638.4mAh/g, the discharge gram capacity is 492.3mAh/g and the first coulombic efficiency is 77.1% through weighted calculation;
b. the gram capacity C0 requiring lithium supplement is the positive electrode discharging gram capacity (186 mAh/g)/negative electrode first coulombic efficiency (77.1%) — positive electrode charging gram capacity (196.8 mAh/g);
c. lithium supplement capacity per unit area C1-positive electrode coating surface density (20.5 mg/cm)2) C0 positive active material percentage (98%);
d. according to the lithium supplement capacity C1 of a unit area and the gram capacity (3860mAh/g) of lithium metal, the weight of the lithium metal required by the unit area can be obtained;
e. the required lithium ribbon thickness (here, the calculated lithium ribbon thickness is the lithium ribbon thickness required for the unit area of the negative electrode) can be calculated from the required lithium metal weight per unit area and the lithium metal density, the thickness of the lithium ribbon actually used is obtained by rounding the calculated thickness of the lithium ribbon per unit area, and the percentage of the lithium ribbon to the negative electrode active material coating area is calculated (here, the percentage of the lithium ribbon to the negative electrode active material coating area is the calculated lithium ribbon thickness/the lithium ribbon thickness actually used after rounding; here, for example, the lithium ribbon thickness required for the unit area is 4.3 μm by calculation according to the above parameters, the lithium ribbon thickness 5 μm is used after rounding, and the percentage of the lithium ribbon to the active material coating area is 4.3/5 — 86%).
The preparation of the lithium ion battery in example 1 was as described above.
Example 2
The embodiment provides a lithium ion battery, which comprises a lithium ion battery cell, wherein the thickness of a lithium ribbon in the embodiment 2 is 8 μm, and the length and the width of the lithium ribbon and the rest of the structure of the lithium ion battery are the same as those in the embodiment 1.
The method for preparing the lithium ion battery in example 2 is the same as that in example 1.
Example 3
The embodiment provides a lithium ion battery, which comprises a lithium ion battery cell, wherein the thickness of a lithium ribbon in embodiment 3 is 2 μm, and the length and width of the lithium ribbon and the rest of the structure of the lithium ion battery are the same as those in embodiment 1.
The method for preparing the lithium ion battery in example 3 is the same as that in example 1.
Comparative example 1
The embodiment provides a lithium ion battery, which includes a lithium ion battery cell, wherein a positive electrode, a negative electrode, a diaphragm, and a lithium ribbon in the lithium ion battery cell are sequentially laminated together according to the sequence of "diaphragm/negative electrode/lithium ribbon/diaphragm/positive electrode", and the size and the specification of the lithium ribbon, and the rest of the structure of the lithium ion battery are the same as those in embodiment 1.
The method for preparing the lithium ion battery in the comparative example 1 is the same as that of the example 1.
Comparative example 2
The embodiment provides a lithium ion battery, which comprises a lithium ion battery cell, wherein a positive electrode, a negative electrode, a diaphragm and a lithium strip in the lithium ion battery cell are sequentially laminated together according to the sequence of 'diaphragm/negative electrode/lithium strip/diaphragm/positive electrode', the length and width of the lithium strip are the same as those in embodiment 1, but the thickness of the lithium strip is 10 μm, and the rest structure of the lithium ion battery is the same as that in embodiment 1.
The lithium ion battery of comparative example 2 was prepared in the same manner as in example 1.
The lithium ion batteries manufactured in examples 1 to 3 and comparative examples 1 and 2 were subjected to test experiments, respectively, and the test results are shown in table 1.
TABLE 1 lithium ion Battery Performance test results
Figure BDA0003094868470000081
Figure BDA0003094868470000091
It can be seen from the data in table 1 that embodiment 1 ~ 3 show, adopt the utility model discloses a calculation method, can accurate control mend lithium volume, can satisfy the mend lithium demand of negative pole, can not be excessive again, so embodiment 1 battery has high first effect and gram capacity and cyclicity, and embodiment 2 has high first effect and gram capacity, but owing to mend lithium volume excessive, lead to the negative pole to have the lithium of analyzing, has reduced cyclicity on the contrary, embodiment 3 mends lithium volume not enough, lead to first effect and gram capacity very low, and the circulation is relatively poor. It can be seen from comparative examples 1-2 that the effect of single-side lithium supplement is much less than that of double-side lithium supplement, and even though the lithium supplement amount of comparative example 2 is the same as that of example 1, the lithium supplement effect is much worse.
The previous description of the disclosed embodiments is provided to enable any person skilled in the art to make or use the present invention. Various modifications to these embodiments will be readily apparent to those skilled in the art, and the generic principles defined herein may be applied to other embodiments without departing from the spirit or scope of the invention. Thus, the present invention is not intended to be limited to the embodiments shown herein but is to be accorded the widest scope consistent with the principles and novel features disclosed herein.

Claims (9)

1. A lithium ion battery cell is characterized by comprising a positive electrode, a negative electrode, a diaphragm and a lithium belt,
the positive electrode, the negative electrode, the separator, and the lithium ribbon are sequentially laminated in the order of "separator/lithium ribbon/negative electrode/lithium ribbon/separator/positive electrode".
2. The lithium ion battery cell of claim 1, wherein a width of the lithium ribbon is less than or equal to a width of the negative electrode,
the length of the lithium ribbon is less than or equal to the length of the negative electrode,
the thickness of the lithium band is less than or equal to 10 mu m.
3. The lithium ion battery cell of claim 2, wherein the thickness of the lithium ribbon is less than or equal to 5 μ ι η.
4. The lithium ion battery cell of claim 3, wherein the lithium ribbon has a thickness of 2-5 μm.
5. The lithium ion battery cell of any of claims 1 to 4, wherein the area of the lithium ribbon is 50-100% of the area of the negative electrode.
6. The lithium ion battery cell of claim 1, wherein the total amount of lithium of one of the lithium strips is less than or equal to half the amount of lithium replenishment of one of the cathodes.
7. The lithium ion battery cell of claim 1, wherein the negative electrode is a silicon carbon negative electrode.
8. The lithium ion battery cell of claim 7, wherein the negative active material of the silicon-carbon negative electrode comprises graphite and at least one of nano-silicon, SiOx, and silicon alloys.
9. A lithium ion battery comprising a battery case and a lithium ion battery cell disposed in the battery case, wherein the lithium ion battery cell is the lithium ion battery cell of any of claims 1 to 8.
CN202121212830.2U 2021-06-01 2021-06-01 Lithium ion battery cell and lithium ion battery Active CN214706019U (en)

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