• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The present invention relates to a method for producing an active material for a negative electrode of a lithium-based secondary battery, wherein a coal tar pitch or a petroleum pitch is treated with an organic solvent to remove an organic solvent insoluble component, and the pitch from which the organic solvent insoluble component is removed is 400 to 400 in an inert gas atmosphere. Heat treatment at 450 DEG C for at least 4 hours to form at least 50% by weight of the pitch from which the organic solvent insoluble component has been removed into anisotropic spheres, and to heat the pitch including the anisotropic spheres to coke and carbonize the coke. Thereafter, the carbide is pulverized, and a method of manufacturing a negative electrode active material for a lithium-based secondary battery including the step of graphitizing the pulverized product is provided.
    公开号:KR19990074333A
    申请号:KR1019980007854
    申请日:1998-03-10
    公开日:1999-10-05
    发明作者:최완욱；심규윤；윤상영
    申请人:손욱；삼성전관 주식회사；
    IPC主号:
    专利说明:

    Method for manufacturing active material for negative electrode of lithium series secondary battery
    [Industrial use]
    The present invention relates to a method for producing an active material for negative electrodes of a lithium-based secondary battery, and more particularly, to a method for producing an active material for negative electrodes of a lithium-based secondary battery capable of producing a high capacity battery.
    [Prior art]
    Recently, with the trend toward miniaturization and lightening of new portable electronic devices such as camera-integrated VTRs, audio, laptop personal computers, portable telephones, and the like, there is a need for a technology for increasing the performance and capacity of batteries used as power sources for these devices. In particular, efforts are being made to develop technologies that reduce manufacturing costs of these batteries, particularly in economic terms. In general, batteries include primary batteries used for single use, such as manganese batteries, alkaline batteries, mercury batteries and silver oxide batteries, Ni-MH (nickel-metal hydride) batteries using lead-acid batteries and metal hydrides as negative active materials, and sealed nickel. Rechargeable secondary batteries such as cadmium batteries, lithium-metal batteries, lithium-ion batteries (LIB), lithium-ion batteries such as lithium polymer batteries (LPB), and fuel cells , Solar cells and the like.
    Among them, primary batteries have a small capacity, short lifespan, and are not recycled, causing environmental pollution. On the other hand, secondary batteries can be recharged and used for a long time, and voltage is much higher than that of primary batteries. It is excellent in terms of efficiency, and generates less waste, which is also excellent in environmental protection.
    A schematic structure of a typical lithium-based secondary coin battery among the above batteries is shown in FIG. 1. As shown in FIG. 1, a lithium-based secondary coin battery includes a positive electrode active material 10 coated on a positive electrode current collector Ni and 1, a negative electrode active material 30 coated on a negative electrode current collector Cu and 1 ′, The electrolyte 15 and the separator 25, and the can 5, the cap 35 and the gasket 20 constituting the body of the battery. In addition, the schematic structure of the lithium-based secondary cylindrical battery is shown in FIG. As shown in FIG. 2, the lithium-based secondary cylindrical battery includes a positive electrode 50, a negative electrode 55, a separator 60 disposed between the positive electrode and the negative electrode, a mandrel 65 forming a body of the battery, a positive electrode lead 70, The negative lead 75, the upper insulating plate 80, the lower insulating plate 80 ', and the can buttons 85 and-are formed.
    Lithium metal or a lithium transition metal oxide (LiCoO 2 , LiNiO 2 , LiMn 2 O 4 , LiNi x Co 1-x O y ) is used as the cathode active material, and a polyethylene-based porous polymer is used as the separator. In addition, lithium metal was initially used as a negative electrode active material, and in the process of charging and discharging, the capacity is greatly reduced, and lithium ions are precipitated to form a dendrite phase, which causes the separator to be destroyed, resulting in a shorter battery life. It was. In order to solve this problem, a lithium alloy was used, but the above-described problems caused when using lithium metal did not greatly improve.
    In order to solve this problem, the principle of storing and releasing electric energy in the process of repeating the process of intercalating and deintercalating Li ions in the electrolyte into the carbon material is used. Recently, carbon materials are used as negative electrode active materials.
    Conventionally, a spherical or fibrous carbon material was used as a negative electrode active material. One method for producing such spherical carbon materials mesocarbon microbeads is described in Japanese Patent Laid-Open No. 1-27968. The method described in the Japanese patent is as follows. Coal tar was heat-treated and centrifuged to separate mesophase spherical particles as solids, or the coal tar was centrifuged to obtain supernatants. Prepare the beads. However, the above-described method has a problem in that the manufacturing process is complicated because the manufacturing cost is high and the centrifugation process is required to separate only the mesophase spherical particles which are solids. In addition, since only the mesophase spherical particles are separated to prepare a desired product, there is a problem in that the yield of the final product is low.
    The present invention is to solve the above problems, an object of the present invention is to provide a method for producing a negative electrode active material for a lithium-based secondary battery capable of producing a battery having a high charge and discharge capacity and efficiency.
    Another object of the present invention is to provide a method for producing a negative electrode active material for a lithium-based secondary battery which can produce the active material having the above-described physical properties in a high yield using a simple process.
    1 is a schematic cross-sectional view of a 2016 type coin battery of a lithium-based secondary battery.
    Figure 2 is a schematic cross-sectional view of a cylindrical battery of the 18650 form of the lithium-based secondary battery.
    Explanation of symbols on the main parts of the drawings
    1: Current collector for positive electrode 1 ': Current collector for negative electrode 5: Can
    10: positive electrode active material or counter electrode 15: electrolyte 20: gasket
    25 separator 30 negative electrode active material 35 cap
    50: anode 55: cathode 60: separator
    65 mandrel 70 positive lead 75 negative lead
    80: upper insulation plate 80 ': lower insulation plate 85: can button
    [Means for solving the problem]
    In order to achieve the above object, the present invention is to treat the coal tar pitch or petroleum pitch with an organic solvent to remove the organic solvent insoluble component; Heat-treating the pitch from which the organic solvent insoluble component is removed at 400 to 450 ° C. for 4 hours or more in an inert gas atmosphere to form at least 50% by weight of the pitch from which the organic solvent insoluble component is removed into an anisotropic sphere; Heat treating the pitch comprising the anisotropic spheres to coke; Carbonizing the coke; It provides a method for producing an active material for a negative electrode of a lithium-based secondary battery comprising the step of graphitizing the carbide.
    Hereinafter, the present invention will be described in more detail.
    Method for producing an active material for a negative electrode of the lithium-based secondary battery of the present invention is as follows.
    Coal tar pitch or petroleum pitch is treated with an organic solvent to remove organic solvent insoluble components. The organic solvent may be selected from the group consisting of tetrahydrofuran, quinoline, benzene, toluene and the like. The pitch from which the organic solvent insoluble component is removed is heat-treated at 400 to 450 ° C. for at least 4 hours under an inert gas atmosphere of nitrogen or argon gas to form at least 50 wt% of the pitch from which the organic solvent insoluble component is removed to form an anisotropic sphere. do. As for the quantity of the anisotropic sphere contained in the said pitch, 50-98 weight% is more preferable. The production of a negative electrode active material using a pitch containing anisotropic spheres in an amount in the above range is preferable because a high capacity battery can be produced. The pitch containing the anisotropic sphere is heat-treated under an inert gas atmosphere of nitrogen or argon gas while gradually raising the temperature to 600 ° C to coke. The coke is carbonized at a temperature of at least 900 ° C, in particular at a temperature of 1000 to 1300 ° C. The carbonization process is a process of removing components such as H, N, and O from the components of the coked sample. If the temperature is lower than the above range, the above components are hardly removed. In addition, when the temperature is higher than the above temperature, the charge / discharge capacity is decreased, which is not preferable. The carbide is ground to form amorphous particles. The amorphous particles are graphitized at a temperature of 2000 ° C. or higher, preferably 2500 to 3000 ° C. to prepare a negative active material for a lithium-based secondary battery. The graphitization process is a process of aligning the microstructure of the carbonized sample. If the temperature is lower than the temperature in the above-described range, the crystal structure is not well formed, and thus the characteristics of amorphous carbon are not preferable. In addition, when the temperature is higher than the above range, the charge / discharge capacity becomes small, which is not preferable.
    In the present invention, the anisotropic spheres were introduced into the carbon material and the electrochemical properties were measured while varying the content thereof to set the optimum anisotropic spheres content and optimize the process. In the manufacturing process of the present invention, the amorphous particles were produced without using conventional grinding of spherical anisotropic spheres or carbonaceous carbon materials. Therefore, a high capacity active material could be manufactured by a simple manufacturing process. In the carbon material used in the present invention, the graphite-based carbon used in the present invention has a grain size of about 10 to 100 nm, a La size of about 20 to 200 nm, and a specific surface area of about 3 to 20 m 2 / g. Had
    EXAMPLE
    Hereinafter, preferred examples and comparative examples of the present invention are described. However, the following examples are only one preferred embodiment of the present invention and the present invention is not limited to the following examples.
    (Example 1)
    Coal tar pitch is treated with tetrahydrofuran to remove the tetrahydrofuran insoluble component. The remaining components were heat-treated for 4 hours at a temperature of 430 ° C. in a nitrogen atmosphere to form about 50% of the pitch from which the tetrahydrofuran insoluble component was removed as mesophase micro beads. Subsequently, the pitch containing the anisotropic sphere was heat treated in a nitrogen atmosphere while gradually raising the temperature to 600 ° C. to coke. This coke was carbonized in 1000 degreeC nitrogen atmosphere. The resulting carbide was ground to form amorphous particles. The amorphous particles were graphitized for 30 minutes under an inert atmosphere of argon gas and nitrogen gas at a temperature of 2800 ° C. to produce graphite carbon.
    After dissolving polyvinylidene fluoride as a binder in a solvent of N-methylpyrrolidone, carbon prepared by the method of Example 1 was added to form a slurry, and the negative electrode was cast (coated) on a Cu foil current collector. Prepared. Coin form as shown in FIG. 1 under the condition that the inert atmosphere and humidity of Ar gas are controlled by using the anode and the lithium flake as the anode and using an electrolyte in which alkali carbonates (LiPF 6 , LClO 4 ) are dissolved in an organic solvent The battery of was prepared. The charge / discharge test of this battery was carried out to measure the discharge efficiency (discharge capacity / charge capacity) indicating the ratio of the capacity, initial charged capacity and discharged capacity, and the results are shown in Table 1 below.
    (Example 2)
    Coal tar pitch was treated with tetrahydrofuran to remove the tetrahydrofuran insoluble component. The remaining components were heat-treated in a nitrogen atmosphere at a temperature of 430 ° C. for 8 hours to form about 70% of the pitch from which the tetrahydrofuran insoluble component was removed as mesophase micro beads. Subsequently, the pitch containing the anisotropic sphere was heat treated in a nitrogen atmosphere while gradually raising the temperature to 600 ° C. to coke. This coke was carbonized in 1000 degreeC nitrogen atmosphere. This carbide was ground to form amorphous particles. The amorphous particles were graphitized for 30 minutes under an inert atmosphere of argon gas and nitrogen gas at a temperature of 2800 ° C. to produce graphite carbon.
    After dissolving polyvinylidene fluoride as a binder in N-methylpyrrolidone solvent, carbon prepared by the method of Example 2 was added to form a slurry, and the slurry was cast (coated) on a Cu foil current collector. To prepare a negative electrode. After dissolving polyvinylidene fluoride as a binder in an N-methylpyrrolidone solvent, LiCoO 2 was added to form a slurry, and the slurry was cast (coated) to a Ni foil current collector to prepare a positive electrode. Coin-type battery as shown in FIG. 1 under the condition that the inert atmosphere and humidity of Ar gas are controlled using the above-described negative electrode and positive electrode, and an electrolyte in which alkali carbonates (LiPF 6 , LClO 4 ) are dissolved in an organic solvent Was prepared. A charge and discharge test of this battery was carried out to measure capacity and discharge efficiency, and the results are shown in Table 1 below.
    (Example 3)
    Coal tar pitch was treated with tetrahydrofuran to remove the tetrahydrofuran insoluble component. The remaining components were heat-treated in a nitrogen atmosphere at a temperature of 430 ° C. for 15 hours to form about 98% of the pitch from which the tetrahydrofuran insoluble component was removed as mesophase micro beads. Subsequently, the pitch containing the anisotropic sphere was heat treated in a nitrogen atmosphere while gradually raising the temperature to 600 ° C. to coke. This coke was carbonized in 1000 degreeC nitrogen atmosphere. This carbide was ground to form amorphous particles. The amorphous particles were graphitized for 30 minutes under an inert atmosphere of argon gas or nitrogen gas at a temperature of 2800 ° C. to produce graphite carbon.
    After dissolving polyvinylidene fluoride as a binder in an N-methylpyrrolidone solvent, carbon prepared by the method of Example 3 was added to form a slurry, and the slurry was cast (coated) onto a Cu foil current collector. To prepare a negative electrode. After dissolving polyvinylidene fluoride as a binder in an N-methylpyrrolidone solvent, LiCoO 2 was added to form a slurry, and the slurry was cast (coated) to a Ni foil current collector to prepare a positive electrode. A coin-type battery as shown in FIG. 1 was prepared under an inert atmosphere and humidity controlled conditions by using an electrolyte in which an alkali carbonate (LiPF 6 , LClO 4 ) was dissolved in an organic solvent using the above-described negative electrode and positive electrode. . A charge and discharge test of this battery was carried out to measure capacity and discharge efficiency, and the results are shown in Table 1 below.
    (Control Example 1)
    After dissolving polyvinylidene fluoride as a binder in an N-methylpyrrolidone solvent, mesocarbon microbeads (Osaka, Japan), which is a carbon material, were added to form a slurry. This slurry was cast (coated) to a Cu foil current collector to prepare a negative electrode. A lithium battery was used as the negative electrode and the positive electrode to prepare a coin-shaped battery as shown in FIG. 1 in an Ar atmosphere. A charge and discharge test of this battery was conducted to measure capacity and discharge efficiency, and the results are shown in Table 1 below.
    Capacity [mAh / g]efficiency Example 129088 Example 230083 Example 331492 Comparative Example 128085
    (Example 4)
    After dissolving polyvinylidene fluoride as a binder in an N-methylpyrrolidone solvent, carbon prepared by the method of Example 3 was added to form a slurry, and the slurry was cast (coated) onto a Cu foil current collector. To prepare a negative electrode. After dissolving polyvinylidene fluoride as a binder in an N-methylpyrrolidone solvent, LiCoO 2 was added to form a slurry, and the slurry was cast (coated) to a Ni foil current collector to prepare a positive electrode. Using the above-described negative electrode and positive electrode to prepare a battery of a cylindrical shape as shown in FIG. The charge and discharge test of this battery was carried out, and the capacity of the cylindrical battery was measured, yielding 1600 mAh.
    As described above, according to the present invention, a carbon material having a different content of anisotropic spheres was prepared, and a negative electrode for a lithium secondary battery having a high capacity could be manufactured using the same.
    In addition, the method was able to increase the yield of the final product in a simple process of carrying out the grinding process to produce an amorphous carbon material.
    权利要求:
    Claims (6)
    [1" claim-type="Currently amended] Treating coal tar pitch or petroleum pitch with an organic solvent to remove organic solvent insoluble components;
    Heat-treating the pitch from which the organic solvent insoluble component is removed at 400 to 450 ° C. for 4 hours or more in an inert gas atmosphere to form at least 50% by weight of the pitch from which the organic solvent insoluble component is removed into an anisotropic sphere;
    Coking the pitch containing the anisotropic sphere by heat treatment;
    Carbonizing the coke;
    Grinding the carbide;
    Graphitizing the milled product;
    The manufacturing method of the active material for negative electrodes of a lithium type secondary battery containing the process.
    [2" claim-type="Currently amended] The method of claim 1, wherein the inert gas atmosphere is a nitrogen or argon gas atmosphere.
    [3" claim-type="Currently amended] The method for producing an active material for a negative electrode of a lithium-based secondary battery according to claim 1, wherein the amount of the anisotropic sphere contained in the pitch is 50 to 98 wt%.
    [4" claim-type="Currently amended] The method of claim 1, wherein the coking step is performed in an inert atmosphere while heating up to 600 ° C. 3.
    [5" claim-type="Currently amended] The method of claim 1, wherein the carbonization is performed at a temperature of 900 ° C. or higher.
    [6" claim-type="Currently amended] The method of claim 1, wherein the graphitization treatment step is performed at a temperature of 2000 ° C. or higher.
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    同族专利:
    公开号 | 公开日
    CN1228619A|1999-09-15|
    US6730135B2|2004-05-04|
    US20020039685A1|2002-04-04|
    JP4107624B2|2008-06-25|
    JPH11317229A|1999-11-16|
    KR100269923B1|2000-10-16|
    CN1181579C|2004-12-22|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    1998-03-10|Application filed by 손욱, 삼성전관 주식회사
    1998-03-10|Priority to KR1019980007854A
    1999-10-05|Publication of KR19990074333A
    2000-10-16|Application granted
    2000-10-16|Publication of KR100269923B1
    优先权:
    申请号 | 申请日 | 专利标题
    KR1019980007854A|KR100269923B1|1998-03-10|1998-03-10|Method for manufacturing active material for negative electrode of lithium series secondary battery|
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