POSITIVE ELECTRODE MATERIAL USED FOR LITHIUM ION BATTERY, PREPARATION METHOD THEREFOR, AND LITHIUM ION BATTERY

Abstract

Provided in the present disclosure are a positive electrode material used for a lithium ion battery. The positive electrode material comprises substrate particles, a first cladding layer that covers the substrate particles, and a second cladding layer that covers the first cladding layer; the substrate particles contain LiNi.sub.xMn.sub.y Co.sub.zM.sub.1-x-y-zO.sub.2; the first cladding layer contains lithium cobalt oxide; and the second cladding layer contains an oxide of a transition metal.

Claims

1. A positive electrode material for a lithium-ion battery, comprising: a matrix particle, a first coating layer coated on the matrix particle, and a second coating layer coated on the first coating layer; the matrix particle contains LiNixMnyCozM1-x-y-zO2, wherein x is greater than or equal to 0.80 and less than or equal to 0.90, y is greater than or equal to 0.02 and less than or equal to 0.05, z is greater than or equal to 0.05 and less than or equal to 0.1, and M is at least one of Mg, Ba, B, Al, Si, P, Ti, Zr or Nb; and the first coating layer contains lithium cobaltate, and the second coating layer contains an oxide of a transition metal.

2. The positive electrode material according to claim 1, wherein the content of the first coating layer is 0.1 to 1.5 parts by weight relative to 100 parts by weight of the matrix particle, and the content of the second coating layer is 0.1 to 1.0 parts by weight relative to 100 parts by weight of the matrix particle coated by the first coating layer.

3. (canceled)

4. The positive electrode material according to claim 1, wherein the total thickness of the first coating layer and the second coating layer is 0.1 nm to 500 nm.

5. (canceled)

6. The positive electrode material according to claim 1, wherein the matrix particle is at least one of a single crystal particle or a polycrystalline particle.

7. The positive electrode material according to claim 6, wherein the single crystal particle has a particle size of 0.1 μm to 5 μm; the polycrystalline particle has a particle size of 5 μm to 15 μm.

8-10. (canceled)

11. The positive electrode material according to claim 1, wherein the transition metal is at least one of ruthenium, rhodium, palladium, copper or molybdenum.

12. (canceled)

13. The positive electrode material according to claim 1, wherein the oxide of a transition metal is nanometer ruthenium oxide having a particle size of 10 nm to 50 nm.

14. The positive electrode material according to claim 1, wherein the positive electrode material has a specific surface area of 0.3 m2/g to 1.5 m2/g.

15. (canceled)

16. A method of preparing the positive electrode material for a lithium-ion battery according to claim 1, comprising the following steps: S1, performing second mixing on a matrix particle and a first coating agent to obtain a second mixture; S2, performing third mixing on the second mixture and a second coating agent to obtain a third mixture; and S3, performing second calcination on the third mixture; the matrix particle contains LiNixMnyCozM1-x-y-zO2, wherein x is greater than or equal to 0.80 and less than or equal to 0.90, y is greater than or equal to 0.02 and less than or equal to 0.05, z is greater than or equal to 0.05 and less than or equal to 0.1, and M is at least one of Mg, Ba, B, Al, Si, P, Ti, Zr or Nb; and the first coating agent contains at least one of Co(OH)2, Co3O4, Co2O3, CoO or CoCO3, and the second coating agent contains an oxide of a transition metal.

17. The method according to claim 16, wherein the first coating agent is used in an amount of 0.1 to 1.5 parts by weight relative to 100 parts by weight of the matrix particle, and the second coating agent is used in an amount of 0.1 to 1.0 parts by weight relative to 100 parts by weight of the second mixture.

18. (canceled)

19. The method according to claim 16, wherein in step S1, conditions for the second mixing comprise: a device for the mixing is a high-speed mixer, the mixing is performed at a rotational speed of 2000 rpm to 3000 rpm, the mixing is performed at a temperature of 20° C. to 30° C., and the mixing lasts for 15 minutes to 30 minutes; in step S2, conditions for the third mixing comprise: a device for the mixing is a high-speed mixer, the mixing is performed at a rotational speed of 2000 rpm to 3000 rpm, the mixing is performed at a temperature of 20° C. to 30° C., and the mixing lasts for 15 minutes to 30 minutes; and in step S3, conditions of the second calcination comprise: the calcination is performed at a temperature of 450° C. to 650° C., the calcination lasts for 4 hours to 15 hours, and the calcination is performed in an atmosphere containing 20 volume % to 100 volume % oxygen.

20. The method according to claim 16, wherein the matrix particle is at least one of a single crystal particle or a polycrystalline particle.

21. The method according to claim 20, wherein the single crystal particle has a particle size of 0.1 μm to 5 μm; the polycrystalline particle has a particle size of 5 μm to 15 μm.

22-24. (canceled)

25. The method according to claim 16, wherein the transition metal in the oxide of a transition metal in the second coating agent is at least one of ruthenium, rhodium, palladium, copper or molybdenum.

26. (canceled)

27. The method according to claim 16, wherein the second coating agent contains nanometer ruthenium oxide having a particle size of 10 nm to 50 nm.

28. The method according to claim 16, further comprising: crushing and sieving a material obtained from the second calcination.

29. The method according to claim 28, wherein the sieving is performed by using a sieve with a sieve mesh of 300 to 400.

30. The method according to claim 16, further comprising: preparing the matrix particle through the following steps: SS1, performing first mixing on a lithium source and a precursor to obtain a first mixture; and SS2, performing first calcination on the first mixture, and crushing and sieving a material obtained from the first calcination.

31. The method according to claim 30, wherein the lithium source is lithium hydroxide and the precursor contains NixMnyCozM1-x-y-z(OH)2, wherein x is greater than or equal to 0.80 and less than or equal to 0.90, y is greater than or equal to 0.02 and less than or equal to 0.05, z is greater than or equal to 0.05 and less than or equal to 0.1, and M is at least one of Mg, Ba, B, Al, Si, P, Ti, Zr or Nb.

32. A lithium-ion battery, comprising the positive electrode material according to claim 1.

Description

DETAILED DESCRIPTION

[0046] The technical solutions of the present disclosure are further described below through the specific embodiment.

[0047] The present disclosure provides a positive electrode material for a lithium-ion battery in an embodiment. The positive electrode material includes a matrix particle, a first coating layer coated on the matrix particle, and a second coating layer coated on the first coating layer; where the matrix particle contains LiNi.sub.xMn.sub.y Co.sub.zM.sub.1-x-y-zO.sub.2, where x is greater than or equal to 0.80 and less than or equal to 0.90, y is greater than or equal to 0.02 and less than or equal to 0.05, z is greater than or equal to 0.05 and less than or equal to 0.1, and M is at least one of Mg, Ba, B, Al, Si, P, Ti, Zr or Nb; the first coating layer contains lithium cobaltate; the second coating layer contains an oxide of a transition metal. The positive electrode material for a lithium-ion battery provided by the present disclosure can effectively reduce the alkali content on the surface of the positive electrode material, reduce the specific surface area of the positive electrode material, and improve the thermal stability of the positive electrode material, thereby improving the structural stability and electrochemical performance of the positive electrode material.

[0048] In an embodiment, the content of the first coating layer may be 0.1 to 1.5 parts by weight relative to 100 parts by weight of the matrix particle, and the content of the second coating layer may be 0.1 to 1.0 parts by weight relative to 100 parts by weight of the matrix particle coated by the first coating layer. In an embodiment, the content of the first coating layer may be 0.3 to 0.9 parts by weight relative to 100 parts by weight of the matrix particle; the content of the second coating layer may be 0.3 to 0.6 parts by weight relative to 100 parts by weight of the matrix particle coated by the first coating layer; the total thickness of the first coating layer and the second coating layer may be 0.1 nm to 500 nm and is 1 nm to 200 nm in an embodiment.

[0049] In an embodiment, the matrix particle may be at least one of a single crystal particle or a polycrystalline particle.

[0050] In an embodiment, the single crystal particle may have a particle size of 0.1 μm to 5 μm.

[0051] In an embodiment, the single crystal particle may have a particle size of 2 μm to 3 μm.

[0052] In an embodiment, the polycrystalline particle may have a particle size of 5 μm to 15 μm.

[0053] In an embodiment, the polycrystalline particle has a particle size of 6 μm to 12 μm.

[0054] In an embodiment, the transition metal may be at least one of ruthenium, rhodium, palladium, copper or molybdenum.

[0055] In an embodiment, the transition metal is ruthenium.

[0056] In an embodiment, the oxide of a transition metal is nanometer ruthenium oxide having a particle size of 10 nm to 50 nm.

[0057] In an embodiment, the positive electrode material has a specific surface area of 0.3 m.sup.2/g to 1.5 m.sup.2/g.

[0058] In an embodiment, the positive electrode material has a specific surface area of 0.35 m.sup.2/g to 0.7 m.sup.2/g.

[0059] The present disclosure provides a method for preparing a positive electrode material for a lithium-ion battery in an embodiment. The method includes the following steps.

[0060] In S1, second mixing is performed on a matrix particle and a first coating agent to obtain a second mixture.

[0061] In S2, third mixing is performed on the second mixture and a second coating agent to obtain a third mixture.

[0062] In S3, second calcination is performed on the third mixture.

[0063] The matrix particle contains LiNi.sub.xMn.sub.y Co.sub.zM.sub.1-x-y-zO.sub.2, where x is greater than or equal to 0.80 and less than or equal to 0.90, y is greater than or equal to 0.02 and less than or equal to 0.05, z is greater than or equal to 0.05 and less than or equal to 0.1, and M is at least one of Mg, Ba, B, Al, Si, P, Ti, Zr or Nb; the first coating agent contains at least one of Co(OH).sub.2, Co.sub.3O.sub.4, Co.sub.2O.sub.3, CoO or CoCO.sub.3; the second coating agent contains an oxide of a transition metal.

[0064] In an embodiment, the first coating agent containing cobalt can react with residual lithium on the surface of the matrix particle, which on the one hand, can reduce the residual lithium content on the surface of the matrix particle and ensure the capacity of the matrix particle, and on the other hand, save the water-washing process and reduce the cost. The second coating agent containing a transition metal can effectively reduce the specific surface area of the material, reduce the side reaction between an electrolyte and the matrix material at the interface, and improve the thermal stability and structural stability of the material.

[0065] In an embodiment, the first coating agent may be used in an amount of 0.1 to 1.5 parts by weight relative to 100 parts by weight of the matrix particle, and the second coating agent may be used in an amount of 0.1 to 1.0 parts by weight relative to 100 parts by weight of the second mixture. In an embodiment, the first coating agent may be used in an amount of 0.3 to 0.9 parts by weight relative to 100 parts by weight of the matrix particle, and the second coating agent may be used in an amount of 0.3 to 0.6 parts by weight relative to 100 parts by weight of the second mixture.

[0066] In an embodiment, in step S1, conditions for the second mixing may include: a device for the mixing is a high-speed mixer, the mixing is performed at a rotational speed of 2000 rpm to 3000 rpm, the mixing is performed at a temperature of 20° C. to 30° C., and the mixing lasts for 15 minutes to 30 minutes; in step S2, conditions for the third mixing may include: a device for the mixing is a high-speed mixer, the mixing is performed at a rotational speed of 2000 rpm to 3000 rpm, the mixing is performed at a temperature of 20° C. to 30° C., and the mixing lasts for 15 minutes to 30 minutes; in step S3, conditions of the second calcination may include: the calcination is performed at a temperature of 450° C. to 650° C., the calcination lasts for 4 hours to 15 hours, and the calcination is performed in an atmosphere containing 20 volume % to 100 volume % oxygen.

[0067] In an embodiment, the matrix particle may be at least one of a single crystal particle or a polycrystalline particle.

[0068] In an embodiment, the single crystal particle may have a particle size of 0.1 μm to 5 μm.

[0069] In an embodiment, the single crystal particle has a particle size of 2 μm to 3 μm.

[0070] In an embodiment, the polycrystalline particle may have a particle size of 5 μm to 15 μm.

[0071] In an embodiment, the polycrystalline particle has a particle size of 6 μm to 12 μm.

[0072] In an embodiment, the transition metal in the oxide of a transition metal in the second coating agent may be at least one of ruthenium, rhodium, palladium, copper or molybdenum.

[0073] In an embodiment, the transition metal in the oxide of a transition metal in the second coating agent is ruthenium.

[0074] In an embodiment, the second coating agent contains nanometer ruthenium oxide having a particle size of 10 nm to 50 nm.

[0075] In an embodiment, the method further includes: crushing and sieving a material obtained from the second calcination. In an embodiment, sieving is performed by using a sieve with a sieve mesh of 300 to 400.

[0076] In an embodiment, the method may further include: preparing the matrix particle through the following steps.

[0077] In SS1, first mixing is performed on a lithium source and a precursor to obtain a first mixture.

[0078] In SS2, first calcination is performed on the first mixture, and a material obtained from the first calcination is crushed and sieved.

[0079] In an embodiment, the lithium source may be lithium hydroxide and the precursor may contain Ni.sub.xMn.sub.y Co.sub.zM.sub.1-x-y-z(OH).sub.2, where x is greater than or equal to 0.80 and less than or equal to 0.90, y is greater than or equal to 0.02 and less than or equal to 0.05, z is greater than or equal to 0.05 and less than or equal to 0.1, and M is at least one of Mg, Ba, B, Al, Si, P, Ti, Zr or Nb.

[0080] The present disclosure provides a lithium-ion battery in an embodiment. The lithium-ion battery contains the preceding positive electrode material or a positive electrode material prepared by the preceding method.

[0081] In the present disclosure, the coating layers of the double-layer coating are relatively uniform and complete, which can reduce the residual alkali amount, facilitate the inhibition of the gas production of the material, and improve the cycle stability and safety. The specific surface area of the positive electrode material is significantly reduced, which facilitates the reduction of the side reaction between the electrolyte and the matrix material at the interface, reduces particle breakage, and improves thermal stability.

[0082] The present disclosure is further described below through specific examples, but the examples described below are not intended to limit the technical solutions of the present disclosure. All the raw materials used in the following examples are commercially available.

Example 1

[0083] A precursor Ni.sub.a Co.sub.bMn.sub.cAl.sub.d(OH).sub.2 (a=0.88, b=0.06, c=0.03, and d=0.03) and LiOH were mixed in a molar ratio of 1:1.03 to obtain a first mixture. First calcination was performed on the first mixture, and a material obtained from the first calcination was cooled and then crushed and sieved to obtain a matrix particle. The conditions of the first calcination were as follows: sintering was performed at 840° C. for 8 hours in an oxygen atmosphere, and then sintering was performed at 750° C. for 6 hours.

[0084] Second mixing was performed on the matrix particle and Co(OH).sub.2 in a mass ratio of 100:0.9 to obtain a second mixture. Third mixing was performed on the second mixture and nano RuO.sub.2 in a mass ratio of 100:0.3 to obtain a third mixture. Second calcination was performed on the third mixture, and a product of the second calcination was cooled and then crushed and sieved to obtain the positive electrode material of this example. The conditions of the second mixing were as follows: the mixing was performed by using a high-speed mixer at a rotational speed of 2000 rpm at 25±5° C. for 15 minutes. The conditions of the third mixing were as follows: the mixing was performed by using a high-speed mixer at a rotational speed of 2000 rpm at 25±5° C. for 15 minutes. The conditions of the second calcination were as follows: sintering was performed in an oxygen atmosphere at 600° C. for 10 hours.

Example 2

[0085] The method of preparing the positive electrode material in this example is the same as the method in Example 1, except that in this example, the mass ratio of the matrix particle to Co(OH).sub.2 in the second mixing was 100:0.2 and the mass ratio of the second mixture to nano RuO.sub.2 in the third mixing was 100:0.1.

Example 3

[0086] The method of preparing the positive electrode material in this example is the same as the method in Example 1, except that in this example, the mass ratio of the matrix particle to Co(OH).sub.2 in the second mixing was 100:0.3 and the mass ratio of the second mixture to nano RuO.sub.2 in the third mixing was 100:0.2.

Example 4

[0087] The method of preparing the positive electrode material in this example is the same as the method in Example 1, except that in this example, the mass ratio of the matrix particle to Co(OH).sub.2 in the second mixing was 100:0.7 and the mass ratio of the second mixture to nano RuO.sub.2 in the third mixing was 100:0.5.

Example 5

[0088] The method of preparing the positive electrode material in this example is the same as the method in Example 1, except that in this example, the mass ratio of the matrix particle to Co(OH).sub.2 in the second mixing was 100:1.0; the mass ratio of the second mixture to nano RuO.sub.2 in the third mixing was 100:0.7; the conditions of the second mixing were as follows: the mixing was performed by using a high-speed mixer at a rotational speed of 2500 rpm at 25±5° C. for 20 minutes; the conditions of the third mixing were as follows: the mixing was performed by using a high-speed mixer at a rotational speed of 2500 rpm at 25±5° C. for 20 minutes; the conditions of the second calcination were as follows: sintering was performed in an oxygen atmosphere at 600° C. for 10 hours.

Example 6

[0089] The method of preparing the positive electrode material in this example is the same as the method in Example 1, except that in this example, the mass ratio of the matrix particle to Co(OH).sub.2 in the second mixing was 100:1.2; the mass ratio of the second mixture to nano RuO.sub.2 in the third mixing was 100:1.0; the conditions of the second mixing were as follows: the mixing was performed by using a high-speed mixer at a rotational speed of 2500 rpm at 25±5° C. for 20 minutes; the conditions of the third mixing were as follows: the mixing was performed by using a high-speed mixer at a rotational speed of 2500 rpm at 25±5° C. for 20 minutes; the conditions of the second calcination were as follows: sintering was performed in an oxygen atmosphere at 600° C. for 10 hours.

Example 7

[0090] The method of preparing the positive electrode material in this example is the same as the method in Example 1, except that in this example, the precursor was Ni.sub.a Co.sub.bMn.sub.cAl.sub.d(OH).sub.2 (a=0.90, b=0.07, c=0.02, and d=0.03) and the precursor and LiOH were mixed in a molar ratio of 1:1.03 to prepare the matrix particle. The conditions of the first calcination were as follows: sintering was performed at 840° C. for 8 hours in an oxygen atmosphere, and then sintering was performed at 750° C. for 6 hours.

[0091] Second mixing was performed on the matrix particle and Co(OH).sub.2 in a mass ratio of 100:0.9 to obtain a second mixture. Third mixing was performed on the second mixture and nano RuO.sub.2 in a mass ratio of 100:0.3 to obtain a third mixture. Second calcination was performed on the third mixture, and a product of the second calcination was cooled and then crushed and sieved to obtain the positive electrode material of this example. The conditions of the second mixing were as follows: the mixing was performed by using a high-speed mixer at a rotational speed of 2000 rpm at 25±5° C. for 15 minutes. The conditions of the third mixing were as follows: the mixing was performed by using a high-speed mixer at a rotational speed of 2000 rpm at 25±5° C. for 15 minutes. The conditions of the second calcination were as follows: sintering was performed in an oxygen atmosphere at 600° C. for 10 hours.

Comparative Example 1

[0092] A precursor Ni.sub.a Co.sub.bMn.sub.cAl.sub.d(OH).sub.2 (a=0.88, b=0.06, c=0.03, and d=0.03) and LiOH were mixed in a molar ratio of 1:1.03 to obtain a first mixture. First calcination was performed on the first mixture, and a material obtained from the first calcination was cooled and then crushed and sieved to obtain the positive electrode material of this comparative example. The conditions of the first calcination were as follows: sintering was performed at 840° C. for 8 hours in an oxygen atmosphere, and then sintering was performed at 750° C. for 6 hours.

Comparative Example 2

[0093] A precursor Ni.sub.a Co.sub.bMn.sub.cAl.sub.d(OH).sub.2 (a=0.88, b=0.06, c=0.03, and d=0.03) and LiOH were mixed in a molar ratio of 1:1.03 to obtain a first mixture. First calcination was performed on the first mixture, and a material obtained from the first calcination was cooled and then crushed and sieved to obtain a matrix particle. The conditions of the first calcination were as follows: sintering was performed at 840° C. for 8 hours in an oxygen atmosphere, and then sintering was performed at 750° C. for 6 hours.

[0094] Second mixing was performed on the matrix particle and Co(OH).sub.2 in a mass ratio of 100:0.9 to obtain a second mixture. Second calcination was performed on the second mixture, and a product of the second calcination was cooled and then crushed and sieved to obtain the positive electrode material of this example. The conditions of the second mixing were as follows: the mixing was performed by using a high-speed mixer at a rotational speed of 2000 rpm at 25±5° C. for 15 minutes. The conditions of the second calcination were as follows: sintering was performed in an oxygen atmosphere at 600° C. for 10 hours.

Comparative Example 3

[0095] A precursor Ni.sub.a Co.sub.bMn.sub.cAl.sub.d(OH).sub.2 (a=0.88, b=0.06, c=0.03, and d=0.03) and LiOH were mixed in a molar ratio of 1:1.03 to obtain a first mixture. First calcination was performed on the first mixture, and a material obtained from the first calcination was cooled and then crushed and sieved to obtain a matrix particle. The conditions of the first calcination were as follows: sintering was performed at 840° C. for 8 hours in an oxygen atmosphere, and then sintering was performed at 750° C. for 6 hours.

[0096] Second mixing was performed on the matrix particle and RuO.sub.2 in a mass ratio of 100:0.3 to obtain a second mixture. Second calcination was performed on the second mixture, and a product of the second calcination was cooled and then crushed and sieved to obtain the positive electrode material of this example. The conditions of the second mixing were as follows: the mixing was performed by using a high-speed mixer at a rotational speed of 2000 rpm at 25±5° C. for 15 minutes. The conditions of the second calcination were as follows: sintering was performed in an oxygen atmosphere at 600° C. for 10 hours.

Test Example 1

[0097] The crystalline form and particle size of the matrix particles in the positive electrode materials prepared in Examples 1 to 7 and Comparative Examples 1 to 3, the part by weight of the first coating layer relative to 100 parts by weight of the matrix particle, the part by weight of the second coating layer relative to 100 parts by weight of the matrix particle coated by the first coating layer, the total thickness of the first coating layer and the second coating layer, and the specific surface area of the positive electrode material were measured by specifically using an X-ray diffractometer (XRD) and a high resolution scanning electron microscope (SEM). The measurement results are shown in Table 1.

TABLE-US-00001 TABLE 1 Particle Part by Part by Total thickness size weight weight of the first Crystalline of the of the of the coating layer and form of matrix first second the second the matrix particle coating coating coating layer Group No. particle (μm) layer layer (nm) Example 1 crystal 2.5 ± 0.2 0.9 0.3 2.1 Example 2 crystal 2.5 ± 0.2 0.2 0.1 1.3 Example 3 crystal 2.5 ± 0.2 0.3 0.2 1.5 Example 4 crystal 2.5 ± 0.2 0.7 0.5 2.3 Example 5 crystal 2.5 ± 0.2 1.0 0.7 3.2 Example 6 crystal 2.5 ± 0.2 1.2 1.0 4.5 Example 7 crystal 3.0 ± 0.2 0.9 0.3 2.5 Comparative crystal 2.5 ± 0.2 0 0 0 Example 1 Comparative crystal 2.5 ± 0.2 0.9 0 1.1 Example 2 Comparative crystal 2.5 ± 0.2 0 0.3 0.6 Example 3

[0098] As can be seen from Table 1, the thickness of the coating layers was between 0.5 nm and 4.5 nm.

Test Example 2

[0099] The amount of residual alkali (Li.sub.2 CO.sub.3 and LiOH) in the positive electrode materials prepared in Examples 1 to 7 and Comparative Examples 1 to 3 and the specific surface area of the positive electrode materials were measured by chemical titration analysis and specific surface area analysis. The specific results are shown in Table 2.

TABLE-US-00002 TABLE 2 Content of Specific surface area Li.sub.2CO.sub.3 LiOH Li.sub.2CO.sub.3 and of the positive Group No. content content LiOH electrode material Example 1 0.22 0.16 0.38 0.37 Example 2 0.35 0.36 0.71 0.39 Example 3 0.31 0.32 0.62 0.40 Example 4 0.26 0.26 0.52 0.42 Example 5 0.19 0.15 0.34 0.43 Example 6 0.17 0.14 0.31 0.46 Example 7 0.26 0.28 0.44 0.50 Comparative 0.41 1.81 2.22 1.23 Example 1 Comparative 0.33 0.40 0.73 0.65 Example 2 Comparative 0.45 0.56 1.01 0.7 Example 3

[0100] As can be seen from Table 2, the residual alkali content and specific surface area of positive electrode materials after coated were significantly reduced compared with that of Comparative Example 1.

Test Example 3

[0101] DSC measurement was performed on the positive electrode materials prepared in Examples 1 to 7 and Comparative Examples 1 to 3 by TG-thermogravimetric analysis. The test results are shown in Table 3.

TABLE-US-00003 TABLE 3 Group No. DSC temperature (° C.) Example 1 235 Example 2 208 Example 3 210 Example 4 213 Example 5 230 Example 6 238 Example 7 223 Comparative Example 1 192 Comparative Example 2 209 Comparative Example 3 198

[0102] As can be seen from Table 3, the DSC temperature value is the exothermic peak temperature of the reaction between the positive electrode material and the electrolyte, and the higher the value, the better the thermal stability and safety of the positive electrode material. As can be seen from the test data in the table, the thermal stability of the positive electrode material after coated was significantly improved compared with that of Comparative Example 1. Example 7 suggested that with the increase of Ni content in the positive electrode material, the structural stability became poor. The double-layer coating of the present disclosure is more beneficial to improving the structural stability of materials.

Test Example 4

[0103] The positive electrode material layers prepared in Examples 1 to 7 and Comparative Examples 1 to 3 were used to prepare positive electrode material layers, and the prepared positive electrode material layers were respectively pressed with an electrolyte and a negative electrode plate to obtain batteries. Ten batteries in each of Examples 1 to 7 and Comparative Examples 1 to 3 were tested at 25° C. on a LAND battery test device at a test voltage ranging from 2.7 V to 4.3 V. The battery was tested for the charge-discharge cycle test at a discharge efficiency of 0.1 C. After two cycles, the battery was tested for the charge-discharge test at 1 C for 50 cycles and then retested for the charge-discharge cycle test at 0.1 C for two cycles. Then the test stopped. The average value of each group of batteries was calculated, and the data of average initial discharge specific capacity, average initial discharge efficiency, and cycle retention rate at room temperature of the battery are shown in Table 4. The specific steps of preparing the battery were as follows: the prepared quaternary positive electrode material, a conductive agent, and a binder were prepared into a slurry according to a certain proportion, the slurry was coated on aluminum foil, vacuum drying and rolling were performed on the aluminum foil to form a positive electrode plate, the negative electrode plate was prepared by using a lithium metal sheet, the electrolyte including lithium hexafluorophosphate (LiPF.sub.6) solution with a concentration of 1.15 M was prepared by using a mixed solvent of ethylene carbonate (EC) and dimethyl carbonate (DMC) at a volume ratio of EC to DMC of 1:1, and a button battery was assembled.

TABLE-US-00004 TABLE 4 Initial discharge specific capacity Initial (based on the overall mass of the discharge 50-cycle positive electrode material, efficiency retention Group No. mAh/g) (%) rate (%) Example 1 215 92.3 97.53 Example 2 198 88.3 88.65 Example 3 201 89.6 88.92 Example 4 205 90.3 95.32 Example 5 210 90.9 97.85 Example 6 216 92.6 96.98 Example 7 216 92.5 89.65 Comparative 185 83.9 86.49 Example 1 Comparative 196 87.4 88.12 Example 2 Comparative 191 86.5 87.07 Example 3

[0104] As can be seen from Table 4, the electrochemical performance of the double-layer coated positive electrode material of the present disclosure is superior to that of the positive electrode material of Comparative Example 1 which is not coated and is also higher than that of the single-layer coated positive electrode materials of Comparative Examples 2 and 3. In a case where the content of the first coating layer is 0.1 to 1.5 parts by weight relative to 100 parts by weight of the matrix particle and the content of the second coating layer is 0.1 to 1.0 parts by weight relative to 100 parts by weight of the matrix particle coated by the first coating layer, the electrochemical performance of the positive electrode material is better.