• 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:
    PURPOSE: A method for manufacturing LiCoO2 which is an active material is provided to have a high pyrolysis temperature and to secure an excellent temperature stability. CONSTITUTION: A method for manufacturing LiCoO2 which is active material comprises the steps of: manufacturing LiMn2O4 which is an active material for a lithium secondary battery of a formula 1 LiCoO2, which LiMn2O4 is coated on the surface in a sol and a gel state; mixing the LiMn2O4 in the sol and the gel state and the LiCoO2 in a powder state; and heating the mixture. A weight percent of the LiMn2O4 in the sol and the gel state and the LiCoO2 in the powder state are 1-5 weight percents to 95-99 weight percents. The heating process operates 600 to 700°C.
    公开号:KR20000028033A
    申请号:KR1019980046151
    申请日:1998-10-30
    公开日:2000-05-15
    发明作者:조재필；김근배；박용철
    申请人:손욱；삼성에스디아이 주식회사；
    IPC主号:
    专利说明:

    Cathode active material for lithium secondary battery and manufacturing method thereof
    Industrial use field
    The present invention relates to a positive electrode active material for a lithium secondary battery and a method of manufacturing the same, and more particularly, to a positive electrode active material for a lithium secondary battery excellent in thermal stability.
    Prior art
    Lithium transition metal oxides such as LiCoO 2 , LiMn 2 O 4 , LiMnO 2 , LiNiO 2 are mainly used as positive electrode active materials of lithium secondary batteries.
    LiCoO 2 has advantages of relatively easy synthesis and easy diffusion of lithium ions, but has a disadvantage of low thermal stability. LiCoO 2 has different thermal stability depending on the charging voltage band, and the thermal stability is lower at 4.3V than at 4.2V. When the charging voltage is 4.3V as compared with the case where the charging voltage is 4.2V, the amount of lithium present in the active material in the charged state is small, so that the active material structure is more unstable. This unstable active material easily reacts with the electrolyte at high temperatures and is easily decomposed. In addition, heat generated when the active material is decomposed may increase the internal temperature of the battery, thereby impairing the safety of the battery.
    In order to solve the above problems, an object of the present invention is to provide a LiCoO 2 cathode active material having a high thermal decomposition temperature, that is, excellent thermal stability.
    Another object of the present invention is to provide a method for producing a LiCoO 2 positive electrode active material having excellent thermal stability.
    1 is a SEM photograph of a positive electrode active material according to an embodiment of the present invention.
    2 is a SEM photograph of a positive electrode active material according to the prior art.
    Figure 3 is a graph showing the results of DSC analysis of the positive electrode active material according to an embodiment of the present invention and the prior art.
    Figure 4 is a graph showing the DSC results of the positive electrode active material according to the prior art.
    In order to achieve the object of the present invention, the present invention is a process for preparing LiMn 2 O 4 in a sol or gel state, a process of mixing LiMn 2 O 4 and powdered LiCoO 2 in the sol or gel state, and the Provided is a method for preparing a cathode active material for a lithium secondary battery including a process of heat treating the mixture, and a cathode active material for lithium secondary battery of Formula 1 having LiMn 2 O 4 coated on the surface thereof.
    [Formula 1]
    LiCoO 2
    Hereinafter, the present invention will be described in more detail.
    In order to prepare LiMn 2 O 4 in a sol state, lithium acetate and manganese acetate may be quantified in a molar ratio of 1: 2, and then mixed with ethanol or methanol. At this time, glycine may be further added to ethanol or methanol.
    In order to prepare LiMn 2 O 4 in a gel state, lithium acetate and manganese acetate can be quantified in a molar ratio of 1: 2, and then mixed with ethanol or methanol in which a chelating agent is dissolved. In this case, the chelating agent may be gelatin, oxalic acid or citric acid.
    LiCoO 2 powder is mixed with LiMn 2 O 4 in the sol or gel state thus prepared. At this time, the mixing weight ratio of LiMn 2 O 4 and LiCoO 2 is preferably 1-5% by weight: 95-99% by weight. When LiMn 2 O 4 is used in excess of 5% by weight, the LiMn 2 O 4 thin film is formed too thick on the LiCoO 2 surface, which is not preferable. When LiMn 2 O 4 is used in less than 1% by weight, the LiMn 2 O 4 thin film is formed too thin on the LiCoO 2 surface, so that the thermal stability of the final active material is not satisfactory. LiCoO 2 powder as can be commercial LiCoO 2 powder, Alternatively, the cobalt salt of a lithium salt and a cobalt hydroxide such as lithium hydroxide in 1: Direct LiCoO 2 by firing were mixed in a molar ratio of 1 Powders may also be prepared and used.
    The mixture of LiMn 2 O 4 and LiCoO 2 prepared as described above was subjected to a first heat treatment at 300-500 ° C., followed by a second heat treatment at 600-800 ° C. to form LiCoO 2 coated on the surface of the spinel LiMn 2 O 4. Obtain an active material.
    Those skilled in the art will be able to easily manufacture a lithium secondary battery according to a known battery manufacturing method using the cathode active material of the present invention.
    In the lithium secondary battery, a negative electrode active material such as crystalline carbon or amorphous carbon may be used as a negative electrode active material, and a separator may use a polypropylene-based porous polymer, and as an electrolyte, LiPF 6 And propylene carbonate and ethylene carbonate in which lithium salts such as LiClO 4 and the like are dissolved can be used.
    The following presents a preferred embodiment to aid the understanding of the present invention. However, the following examples are merely provided to more easily understand the present invention, and the present invention is not limited to the following examples.
    Example 1
    Lithium acetate and manganese acetate were quantified in a molar ratio of 1: 2 (10.2 g of lithium acetate, 49.01 g of manganese acetate). This was slowly added to 50 ml of methanol and mixed using a magnetic bar. At this time, ethanol may be used instead of methanol. At this time, the temperature was maintained at 50 ℃ and after some time a sticky sol was formed. 4 g of the sol and 14 g of LiCoO 2 powder having an average particle size of 5 microns were mixed in a mortar and pestle. The mixture was subjected to primary heat treatment at 300 ° C. for 3 hours, and then mixed lightly, and subjected to secondary heat treatment at 700 ° C. for 7 hours.
    The powder prepared by the second heat treatment, polyvinylidene fluoride and carbon black were mixed in a weight ratio of 92: 4: 4 and then mixed until a uniform paste was added while adding an amount of N-methyl pyrrolidone. The paste was coated on aluminum foil with a doctor blade machine to a thickness of 300 microns and then completely blown N-methyl pyrrolidone at 150 ° C. and compressed under constant pressure. This was cut into circles and welded to coin cell cans. Lithium foil, a negative electrode, was also cut to the same size as the positive electrode and then pressed into a nickel foil of a coin cell cap. A separator manufactured by Celgard was used, and a battery was manufactured using a mixture of ethylene carbonate and diethyl carbonate in which LiPF 6 was dissolved as an electrolyte.
    Example 2
    Lithium acetate and manganese acetate were quantified in a molar ratio of 1: 2 (10.2 g of lithium acetate, 49.01 g of manganese acetate). This was slowly added to 50 ml of methanol in which gelatine, a chelating agent, was dissolved, and mixed using a magnetic bar. In this case, ethanol may be used instead of methanol, and oxalic acid or citric acid may be used instead of gelatin as a chelating agent. At this time, the temperature was maintained at 50 ℃ and after some time a sticky gel was formed. 4 g of the gel and 14 g of LiCoO 2 powder having an average particle size of 5 microns were mixed in a mortar and pestle. The mixture was subjected to primary heat treatment at 300 ° C. for 3 hours, and then mixed lightly, and subjected to secondary heat treatment at 700 ° C. for 7 hours.
    Thereafter, a battery was manufactured using the same method as in Example 1.
    Example 3
    Lithium hydroxide and manganese acetate were quantified in a molar ratio of 1: 2 (10.2 g of lithium hydroxide, 49.01 g of manganese acetate). This was mixed using a magnetic bar while slowly adding to 50 ml of methanol in which 5 g of glycine was dissolved. At this time, ethanol may be used instead of methanol. At this time, the temperature was maintained at 50 ℃ and after some time a sticky sol was formed. 3 g of the sol and 12 g of LiCoO 2 powder having an average particle size of 5 microns were mixed in a mortar and pestle. The mixture was subjected to primary heat treatment at 300 ° C. for 3 hours, and then mixed lightly, and subjected to secondary heat treatment at 800 ° C. for 7 hours.
    Thereafter, a battery was manufactured using the same method as in Example 1.
    Comparative Example 1
    Li 2 CO 3 and CoCO 3 were mixed in mortar at a molar ratio of 1: 1, and then calcined at 800 ° C. for 24 hours in an oxygen atmosphere and then cooled. This powder was classified to obtain a LiCoO 2 positive electrode active material having an average particle size of 25 microns.
    Thereafter, a battery was manufactured using the same method as in Example 1.
    Comparative Example 2
    A battery was prepared in the same manner as in Example 1 using LiCoO 2 (manufactured by UM Co., Belgium) having an average particle size of 5 microns.
    An SEM photograph of the active material according to Example 1 is shown in FIG. 1, and an SEM photograph of the active material according to Comparative Example 2 is shown in FIG. 2. As shown in FIG. 2, the LiCoO 2 active material having an average particle size of 5 microns according to Comparative Example 2 had a smooth surface, but the active material according to Example 1 was found to have a smooth surface because LiMn 2 O 4 was coated on the surface. have.
    X-ray diffraction analysis of the active materials according to Examples 1-3 and Comparative Example 1 showed nearly the same pattern as that of the 16-0427 pattern of Joint Committe om Powder Diffraction (JCPDS), showing almost the same interlayer structure. It was.
    After charging the battery according to Example 1 and Comparative Example 1 to 4.3V, the positive electrode plate in the state impregnated with the electrolyte was removed and subjected to DSC analysis, the results are shown in FIG. (A) of FIG. 3 is a result of DSC analysis of Example 1, and (b) is a result of DSC analysis of Comparative Example 1. FIG. The decomposition temperature of the active material of Example 1 was about 220 ° C., and the calorific value at this time was about 160 J / g. On the other hand, the active material decomposition temperature of Comparative Example 1 was about 210 ° C, and the calorific value at this time was about 120 J / g. Since the LiCoO 2 active material (Example 1) having an average particle size of 5 microns and the surface coated with LiMn 2 O 4 is higher than the LiCoO 2 active material (Comparative Example 2) having an average particle size of 25 microns, thermal stability is further increased. It can be seen that excellent. This result demonstrates that the thermal stability can be improved by surface coating with LiMn 2 O 4 as in the present invention, even if the average particle size is relatively small and the active material is highly reactive with the electrolyte.
    After charging the battery according to Comparative Example 2 to 4.1V, 4,2V, 4,3V, the positive electrode plate in the state in which the electrolyte was impregnated and subjected to DSC analysis, the results are shown in FIG. (A) of FIG. 4 is a case where it charges to 4.1V, (b) is a case where it charges to 4.2V, and (c) is a case where it charges to 4.3V. When the charge voltage is 4.1V, the calorific value is 320J / g when the active material is decomposed, the calorific value is 350J / g at 4.2V, and the calorific value is 340J / g at 4.3V.
    3 (b) which is a DSC analysis result when the battery of Example 1 was charged to 4.3V and FIG. 4 (c) which is a DSC analysis result when the battery of Comparative Example 2 was charged to 4.3V As a result, it can be seen that Example 1 has a lower calorific value when the active material is decomposed than that of Comparative Example 1, thereby inhibiting the stability of the battery less.
    As described above, the LiCoO 2 active material according to the present invention improves thermal stability by performing surface coating with LiMn 2 O 4 . In particular, the LiCoO 2 active material surface-coated with LiMn 2 O 4 according to the present invention has excellent thermal stability even when charged to 4.3V, thereby improving battery safety.
    权利要求:
    Claims (4)
    [1" claim-type="Currently amended] A cathode active material for a lithium secondary battery of Formula 1 having LiMn 2 O 4 coated on its surface.
    [Formula 1] LiCoO 2
    [2" claim-type="Currently amended] Preparing a LiMn 2 O 4 in a sol or gel state;
    Mixing the LiMn 2 O 4 in a sol or gel state with LiCoO 2 in powder form; And
    A method of manufacturing a cathode active material for a lithium secondary battery, comprising the step of heat treating the mixture.
    [3" claim-type="Currently amended] The method according to claim 2, wherein the weight ratio of LiMn 2 O 4 in the sol or gel state to LiCoO 2 in the powder form is 1-5% by weight: 95-99% by weight.
    [4" claim-type="Currently amended] The method of claim 2, wherein the heat treatment is performed after the first heat treatment at 300-500 ° C. and the second heat treatment at 600-800 ° C. 4.
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    同族专利:
    公开号 | 公开日
    KR100300318B1|2003-08-21|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    1998-10-30|Application filed by 손욱, 삼성에스디아이 주식회사
    1998-10-30|Priority to KR10-1998-0046151A
    2000-05-15|Publication of KR20000028033A
    2003-08-21|Application granted
    2003-08-21|Publication of KR100300318B1
    优先权:
    申请号 | 申请日 | 专利标题
    KR10-1998-0046151A|KR100300318B1|1998-10-30|1998-10-30|Cathode active material for lithium secondary battery and its manufacturing method|
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