Silicon dioxide composite negative electrode material and its preparation method and application

Abstract

The present invention relates to a silicon oxide composite negative electrode material, a preparation method thereof, and an application thereof. The preparation method of the silicon oxide composite negative electrode material comprises the following steps: grading silicon oxide powder according to particle size to obtain multiple levels of silicon oxide powder; treating each level of silicon oxide powder with an amide solvent to obtain silicon oxide powder with the amide solvent coated on the surface; treating a porous skeleton material with a ketone solvent to obtain a porous skeleton material containing the ketone solvent in the pores; compounding the silicon oxide powder with the amide solvent coated on the surface with the porous skeleton material containing the ketone solvent in the pores according to the level to obtain a composite; and carbon-coating the composite to obtain a silicon oxide composite negative electrode material. The silicon oxide composite negative electrode material prepared by this preparation method not only has the characteristics of high initial efficiency and long cycle stability, but also has low preparation cost.

Description

Technical Field

[0001] The present invention relates to the technical field of batteries, and in particular to a silicon oxide composite negative electrode material and a preparation method and application thereof. Background Art

[0002] Silicon oxide (SiO) materials have a high theoretical specific capacity (>2000mAh / g), a low lithium storage reaction voltage platform, and low preparation cost, making them a highly promising anode material to replace graphite. However, during repeated ion insertion and removal, SiO materials still experience cracking and pulverization due to their large volume expansion, which greatly affects their cyclic stability. Furthermore, during the initial lithium insertion, SiO materials form irreversibly inert substances such as Li2O and Li4SiO4, resulting in a low initial coulombic efficiency. Furthermore, during the preparation of SiO anode materials, the airflow milling process produces a large amount of fine powder that cannot be effectively utilized, resulting in a significant waste of resources and increased preparation costs.

[0003] Therefore, there is an urgent need to provide a method for preparing silicon monoxide composite negative electrode materials with high initial efficiency and long cycle stability in a low-cost manner. Summary of the Invention

[0004] Based on this, it is necessary to provide a silicon oxide composite negative electrode material and its preparation method and application to address the above problems. The silicon oxide composite negative electrode material prepared by this preparation method not only has the characteristics of high initial efficiency and long cycle stability, but also has low preparation cost.

[0005] A method for preparing a silicon oxide composite negative electrode material comprises the following steps:

[0006] The silicon oxide powder is graded according to the particle size to obtain silicon oxide powder of multiple grades;

[0007] Each level of silicon oxide powder is treated with an amide solvent to obtain silicon oxide powder with the surface coated with the amide solvent;

[0008] treating the porous skeleton material with a ketone solvent to obtain a porous skeleton material containing the ketone solvent in the pores;

[0009] The silicon oxide powder coated with an amide solvent is compounded in order of grade with a porous skeleton material containing a ketone solvent in its pores to obtain a composite;

[0010] The composite is carbon-coated to obtain a silicon 2 oxide composite negative electrode material.

[0011] In one embodiment, the step of grading the silicon oxide powder to obtain multiple grades of silicon oxide powder satisfies at least one of the following conditions:

[0012] (1) The median particle size of the silicon oxide powder is 20 nm to 500 nm;

[0013] (2) Among the multiple levels of silicon oxide powder, the median particle size ratio of adjacent levels of silicon oxide powder is 1:1.5-1:3;

[0014] (3) The silicon iodide powder is silicon iodide fine powder produced during the air flow milling process.

[0015] In one embodiment, when the multiple levels of silicon oxide powder include first-level silicon oxide powder, second-level silicon oxide powder, and third-level silicon oxide powder, at least one of the following conditions is met:

[0016] (1) The median particle size of the first-stage silicon oxide powder is 20 nm to 50 nm;

[0017] (2) The median particle size of the second-stage silicon oxide powder is 50 nm to 100 nm;

[0018] (3) The median particle size of the third-grade silicon oxide powder is 100 nm to 500 nm;

[0019] (4) The mass ratio of the porous skeleton material to the first-stage silicon oxide powder is 1:0.5-1:0.7;

[0020] (5) The mass ratio of the porous skeleton material to the second-stage silicon oxide powder is 1:0.1-1:0.2;

[0021] (6) The mass ratio of the porous skeleton material to the third-level silicon oxide powder is 1:0.05-1:0.1.

[0022] In one embodiment, silicon dioxide powder coated with an amide solvent on its surface is compounded with the treated porous skeleton material in ascending order of level.

[0023] In one embodiment, in the step of treating the porous framework material with a ketone solvent, at least one of the following conditions is met:

[0024] (1) The pore structure of the porous skeleton material gradually decreases from the outer surface of the porous skeleton material inward;

[0025] (2) The average pore size of the porous framework material is 10 nm to 500 nm;

[0026] (3) The specific surface area of ​​the porous skeleton material is 190m 2 / g-210m 2 / g;

[0027] (4) The porosity of the porous skeleton material is 50%-60%;

[0028] (5) The porous skeleton material is selected from porous carbon-nitrogen materials.

[0029] In one embodiment, when the pore structure of the porous skeleton material gradually decreases from the outer surface of the porous skeleton material inward, silicon dioxide powder coated with an amide solvent on the surface is compounded with the treated porous skeleton material in order from small to large levels.

[0030] A silicon oxide composite negative electrode material comprises a core and a carbon coating layer coated on the surface of the core, wherein the core comprises a porous skeleton material, the pores of the porous skeleton material are filled with multiple silicon oxide particle layers, and the particle size level of the silicon oxide particles in each silicon oxide particle layer is different.

[0031] In one embodiment, the silicon 2 Oxide composite negative electrode material satisfies at least one of the following conditions:

[0032] (1) The filling amount of the silicon oxide particles is 65%-90% of the total mass of the core;

[0033] (2) The pore structure of the porous skeleton material gradually decreases from the outer surface of the porous skeleton material inward;

[0034] (3) multiple silicon oxide particle layers are sequentially filled into the pores of the porous framework material in order of particle size from small to large;

[0035] (4) The thickness of the carbon coating layer is 3nm-5nm.

[0036] A negative electrode sheet prepared using the silicon monoxide composite negative electrode material as described above.

[0037] A secondary battery prepared using the negative electrode sheet as described above.

[0038] In the preparation method of the silicon dioxide composite negative electrode material of the present invention, silicon dioxide powder with an amide solvent coated on its surface and a porous skeleton material containing a ketone solvent in its pores are provided, and hydrogen bonds are formed between the ketone solvent and the amide solvent with strong binding force, so that the silicon dioxide powder can be accurately anchored in the pores of the porous skeleton material, so that the silicon dioxide can fully utilize the buffer space provided by the pores of the porous skeleton material, reduce the expansion coefficient and agglomeration risk of silicon dioxide, and improve the first coulombic efficiency of the silicon dioxide composite negative electrode material; moreover, since the silicon dioxide powder is compounded with the porous skeleton material in sequence according to the level, the filling amount of the silicon dioxide powder can be increased, thereby achieving the purpose of fully recycling and utilizing the silicon dioxide powder and reducing the preparation cost; at the same time, through carbon coating, the structural stability and conductivity of the porous skeleton material can be improved, and the contact between the electrolyte and the silicon dioxide powder can also be reduced, thereby improving the cycle stability of the silicon dioxide composite negative electrode material.

[0039] In addition, in the present invention, the silicon oxide powder can be silicon oxide fine powder produced in the process of air flow milling, thereby achieving the purpose of saving resources and reducing preparation costs.

[0040] Therefore, the silicon 2 Oxide composite negative electrode material prepared by the method for preparing the silicon 2 Oxide composite negative electrode material of the present invention not only has the characteristics of high initial efficiency and long cycle stability, but also has low preparation cost. DETAILED DESCRIPTION

[0041] To facilitate understanding of the present invention, the present invention will be described in more detail below. However, it should be understood that the present invention can be implemented in many different forms and is not limited to the embodiments or examples described herein. On the contrary, the purpose of providing these embodiments or examples is to make the understanding of the disclosure of the present invention more thorough and comprehensive.

[0042] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as those generally understood by those skilled in the art of the technical field of the present invention. The terms used herein in the specification of the present invention are only for the purpose of describing specific embodiments or embodiments and are not intended to limit the present invention. The optional scope of the term "and / or" used herein includes any one of two or more related listed items, and also includes any and all combinations of related listed items, including any two related listed items, any more related listed items, or the combination of all related listed items.

[0043] The method for preparing the silicon monoxide composite negative electrode material provided by the present invention comprises the following steps:

[0044] S1, classifying silicon oxide powder according to particle size to obtain silicon oxide powder of multiple grades;

[0045] S2, treating each level of silicon oxide powder with an amide solvent to obtain silicon oxide powder with the surface coated with the amide solvent;

[0046] S3, treating the porous skeleton material with a ketone solvent to obtain a porous skeleton material containing the ketone solvent in the pores;

[0047] S4, compounding the silicon oxide powder coated with an amide solvent on the surface with the porous skeleton material containing a ketone solvent in the pores in order of grade to obtain a composite;

[0048] S5, carbon-coating the composite to obtain a silicon 2 Oxide composite negative electrode material.

[0049] In the preparation method of the silicon iodine composite negative electrode material of the present invention, each level of silicon iodine powder is treated with an amide solvent so that the surface of each level of silicon iodine powder is coated with an amide solvent, that is, silicon iodine powder with an amide solvent coated on the surface is obtained, and at the same time, the porous skeleton material is treated with a ketone solvent to obtain a porous skeleton material with the ketone solvent adsorbed in the pores.

[0050] Since hydrogen bonds are formed between ketone solvents and amide solvents, and the bonding force is strong, when the silica powder coated with amide solvents on the surface is composited with the porous skeleton material containing ketone solvents in the pores, the silica powder can be precisely anchored in the pores of the porous skeleton material, avoiding the silica powder from being composited on the surface of the porous skeleton material, so that the silica can fully utilize the buffer space provided by the pores of the porous skeleton material, reducing the expansion coefficient and agglomeration risk of silica, and improving the first coulombic efficiency of the silica composite negative electrode material; moreover, since the silica powder coated with amide solvents on the surface is composited with the porous skeleton material containing ketone solvents in the pores in sequence according to the level, it is convenient to better fill silica powder of different particle sizes into the pores of the porous skeleton material, so that silica powder of different particle sizes can be fully combined with the porous skeleton material, thereby increasing the filling amount of silica powder, and then achieving the purpose of fully recycling and utilizing silica powder, and reducing the preparation cost.

[0051] At the same time, by carbon coating the composite, the structural stability and conductivity of the porous skeleton material can be improved, and the contact between the electrolyte and the silicon oxide powder can be reduced, thereby improving the cycle stability of the silicon oxide composite negative electrode material.

[0052] Therefore, the silicon 2 Oxide composite negative electrode material prepared by the method for preparing the silicon 2 Oxide composite negative electrode material of the present invention not only has the characteristics of high initial efficiency and long cycle stability, but also has low preparation cost.

[0053] In step S1, the silicon oxide powder is the silicon oxide fine powder produced in the air flow milling process, or can be the silicon oxide fine powder obtained by further milling silicon oxide micropowder through air flow, thereby achieving the purpose of saving resources and reducing preparation costs.

[0054] The median particle size of the silicon oxide powder is 20 nm to 500 nm. It is understood that the median particle size of the silicon oxide powder includes but is not limited to 20 nm, 80 nm, 100 nm, 120 nm, 180 nm, 200 nm, 220 nm, 250 nm, 280 nm, 300 nm, 400 nm, 450 nm, and 500 nm.

[0055] Optionally, among multiple levels of silica powder, the median particle size ratio of adjacent levels of silica powder is 1:1.5-1:3, preferably 1:2-1:2.5. It can be understood that the median particle size of the silica powder includes but is not limited to 1:1.5, 1:2, 1:2.1, 1:2.2, 1:2.3, 1:2.5, and 1:3.

[0056] In the present invention, the multiple levels of silica powder can be two levels of silica powder, or three levels of silica powder, or four levels of silica powder, etc. Considering the difficulty of grading silica powder and the filling condition of silica powder in the porous skeleton material, in the present invention, three levels of silica powder are preferred.

[0057] Further, when the multiple levels of silicon oxide powder are three levels of silicon oxide powder, the three levels of silicon oxide powder include first-level silicon oxide powder, second-level silicon oxide powder and third-level silicon oxide powder.

[0058] The median particle size of the first-stage silicon monoxide powder is 20 nm-50 nm. It can be understood that the median particle size of the first-stage silicon monoxide powder includes but is not limited to 20 nm, 30 nm, 40 nm, and 50 nm.

[0059] The median particle size of the second-stage silicon monoxide powder is 50 nm-100 nm. It can be understood that the median particle size of the second-stage silicon monoxide powder includes but is not limited to 50 nm, 60 nm, 70 nm, 80 nm, 90 nm, and 100 nm.

[0060] The median particle size of the third-grade silicon 2 oxide powder is 100 nm to 500 nm. It is understood that the median particle size of the third-grade silicon 2 oxide powder includes but is not limited to 100 nm, 150 nm, 200 nm, 250 nm, 300 nm, 350 nm, 400 nm, 450 nm, and 500 nm.

[0061] In the present invention, by controlling the median particle size of silicon oxide powders of different levels, the filling amount of silicon oxide powders of different particle sizes in the pores of the porous skeleton material is increased, and the structural stability of the silicon oxide composite negative electrode material is further improved.

[0062] It should be noted that in step S1 , among the multiple levels of silicon monoxide powder, a higher level represents a higher median particle size of the silicon monoxide powder.

[0063] In step S2, the specific steps of using amide solvents to treat each level of silicon oxide powder are as follows: each level of silicon oxide powder is placed in an amide solvent for treatment, and excess amide solvent is removed by filtering, so that the surface of each level of silicon oxide powder is coated with amide solvent.

[0064] In one embodiment, the amide solvent is selected from at least one of N,N-dimethylformamide (DMF), acetamide, and benzamide, preferably N,N-dimethylformamide.

[0065] In step S3, the porous skeleton material is placed in a ketone solvent for treatment, and the ketone solvent adsorbed on the surface of the porous skeleton material is removed by washing to obtain a porous skeleton material containing the ketone solvent in the pores.

[0066] Optionally, the pore structure of the porous skeleton material gradually decreases from the outer surface of the porous skeleton material inward, so that the pore structure is wide on the outside and narrow on the inside, which is conducive to the filling of silica powder in the pores of the porous skeleton material, and can ensure the dispersion of silica powder in the pores to a certain extent, and better prevent the agglomeration of silica powder.

[0067] Furthermore, considering the amount of silica powder packed into the porous framework material, when the pore structure of the porous framework material gradually decreases inward from the outer surface of the porous framework material, in step S4, silica powder coated with an amide solvent on its surface is sequentially compounded with the treated porous framework material in ascending order of rank. This arrangement can further increase the amount of silica powder packed into the porous framework material, enabling better recycling of the silica powder.

[0068] Optionally, the average pore size of the porous skeleton material is 10nm-500nm; it can be understood that the average pore size of the porous skeleton material includes but is not limited to 10nm, 50nm, 100nm, 150nm, 200nm, 250nm, 300nm, 350nm, 400nm, 450nm, 500nm.

[0069] Optionally, the specific surface area of ​​the porous skeleton material is 190m 2 / g-210m 2 / g; It can be understood that the specific surface area of ​​the porous skeleton material includes but is not limited to 190m 2 / g、195m 2 / g, 200m 2 / g、205m 2 / g, 210m 2 / g.

[0070] Optionally, the porosity of the porous skeleton material is 50%-60%; understandably, the porosity of the porous skeleton material includes but is not limited to 50%, 55%, and 60%.

[0071] In the present invention, by controlling the average pore size, specific surface area and porosity of the porous skeleton material, the filling amount of silicon oxide powder in the porous skeleton material can be further increased, the recycling of silicon oxide powder can be better realized, the preparation cost can be reduced, and at the same time, the structural stability of the porous skeleton material can be better guaranteed, thereby effectively improving the initial effect and cycle stability of the silicon oxide composite negative electrode material.

[0072] In the present invention, the porous skeleton material is selected from any one of porous carbon-nitrogen material, porous ceramic or porous carbon material, preferably porous carbon-nitrogen material. In this way, the incorporation of nitrogen can bring high electron mobility and higher capacity retention and rate performance to the porous skeleton material.

[0073] The porous carbon-nitrogen material of the present invention can be purchased from the market, or can be prepared by referring to the following method for preparing the porous carbon-nitrogen material.

[0074] Specifically, the preparation method of the porous carbon-nitrogen material comprises the following steps:

[0075] S31, mixing a carbon-nitrogen-containing compound, a pore-forming agent, and deionized water to obtain a mixed solution, and then subjecting the mixed solution to rotary evaporation drying to obtain an intermediate;

[0076] S32, sintering the intermediate at a high temperature under a protective gas atmosphere to obtain a porous carbon-nitrogen material.

[0077] In step S31, the mass ratio of the carbon-nitrogen-containing compound to the pore-forming agent is 25:1-40:1, preferably 30:1.

[0078] Furthermore, the carbon-nitrogen-containing compound is selected from at least one of dicyandiamide, urea or melamine; the pore-forming agent is selected from ammonium bicarbonate, potassium hydroxide or sodium chloride. Since ammonium bicarbonate has a low thermal decomposition temperature, ammonium bicarbonate is preferably used in the present invention.

[0079] In step S32, the high-temperature sintering temperature is 450°C-650°C, preferably 500°C, and the high-temperature sintering time is 5h-8h, preferably 6h.

[0080] In one embodiment, the protective gas atmosphere may be an argon atmosphere.

[0081] It should be noted that the pore structure of the porous carbon-nitrogen material prepared by the above method in the present invention gradually decreases from the outer surface of the porous skeleton material inward, that is, it is wide on the outside and narrow on the inside. The reason is that the carbon dioxide and ammonia gases decomposed by the pore-forming agent (such as ammonium bicarbonate) are released from the inside to the outside. During the process, the outward pressure becomes smaller, resulting in the outward pore diameter becoming larger and larger, thus forming a wide outside and narrow inside.

[0082] In one embodiment, the porous carbonitride material is in the shape of a sheet, and the pores are not multi-level pores that are interconnected. This configuration is beneficial for avoiding the agglomeration of silicon monoxide powder.

[0083] In one embodiment, multiple centrifugal water washings are used to remove ketone solvents on the surface of the porous skeleton material, so that the outer surface of the porous skeleton material containing ketone solvents in the pores contains almost no ketone solvents, thereby better ensuring that the silicon dioxide powder is accurately embedded in the pores of the porous skeleton material.

[0084] In one embodiment, the ketone solvent is selected from at least one of acetone, methyl ethyl ketone, and cyclohexanone, preferably acetone.

[0085] In step S4, when the silicon oxide powder coated with the amide solvent on the surface is compounded with the porous skeleton material containing the ketone solvent in the pores in sequence according to the level addition method, there is no particular restriction on the order of the levels.

[0086] For example, when multiple levels of silica powder include first-level silica powder, second-level silica powder and third-level silica powder, they can be compounded in order from small to large, that is, the first-level silica powder coated with an amide solvent on the surface, the second-level silica powder coated with an amide solvent on the surface, and the third-level silica powder coated with an amide solvent on the surface with a porous skeleton material containing a ketone solvent in the pores; or they can be compounded in order from large to small, that is, the third-level silica powder coated with an amide solvent on the surface, the second-level silica powder coated with an amide solvent on the surface, and the first-level silica powder coated with an amide solvent on the surface with a porous skeleton material containing a ketone solvent in the pores.

[0087] Of course, it can also be carried out in the following manner, for example, the first-level silica oxide powder whose surface is coated with an amide solvent, the third-level silica oxide powder whose surface is coated with an amide solvent, and the second-level silica oxide powder whose surface is coated with an amide solvent are sequentially compounded with a porous skeleton material containing a ketone solvent in the pores, or the third-level silica oxide powder whose surface is coated with an amide solvent, the first-level silica oxide powder whose surface is coated with an amide solvent, and the second-level silica oxide powder whose surface is coated with an amide solvent are sequentially compounded with a porous skeleton material containing a ketone solvent in the pores, or the second-level silica oxide powder whose surface is coated with an amide solvent, the first-level silica oxide powder whose surface is coated with an amide solvent, and the third-level silica oxide powder whose surface is coated with an amide solvent are sequentially compounded with a porous skeleton material containing a ketone solvent in the pores, etc.

[0088] Considering the filling amount of silicon dioxide powder in the porous skeleton material, in the present invention, it is preferred to compound the silicon dioxide powder coated with an amide solvent on the surface with the treated porous skeleton material in ascending order of level.

[0089] In one embodiment, the specific steps of compounding silicon dioxide powder coated with amide solvents with porous skeleton materials containing ketone solvents in the pores in order of grade are as follows: silicon dioxide powder coated with amide solvents with porous skeleton materials containing ketone solvents in the pores and solvent are mixed in order of grade to obtain a mixed solution, and then the mixed solution is washed and dried.

[0090] Specifically, when the multiple levels of silica powder are three levels of silica powder, namely, first-level silica powder, second-level silica powder and third-level silica powder, the first-level silica powder coated with an amide solvent on the surface is mixed with a porous skeleton material containing a ketone solvent in the pores and a solvent to obtain a first mixed solution; then the second-level silica powder coated with an amide solvent on the surface is added to the first mixed solution to mix, to obtain a second mixed solution; then the third-level silica powder coated with an amide solvent on the surface is added to the third mixed solution to mix, to obtain a third mixed solution; finally, the third mixed solution is washed and dried to obtain a composite.

[0091] It can be understood that in step S3, some ketone solvents will inevitably remain on the surface of the porous skeleton material containing ketone solvents in the pores obtained, resulting in the porous skeleton material containing ketone solvents in the pores being mixed with the silica powder coated with amide solvents on the surface, causing some silica powder to be adsorbed on the surface of the porous skeleton material. These silica powders will be completely removed after washing. Therefore, in step S4, the silica powder in the prepared composite only exists in the pores of the porous skeleton material.

[0092] In one embodiment, multiple centrifugal washing processes are used to remove silicon oxide powder with weak surface bonding strength of the porous skeleton material.

[0093] In one embodiment, the solvent may be water.

[0094] In one embodiment, the drying temperature is 70°C-90°C, preferably 80°C.

[0095] Optionally, the mass ratio of the porous skeleton material to the first-stage silicon oxide powder is 1:0.3-1:0.8, preferably 1:0.5-1:0.7.

[0096] Optionally, the mass ratio of the porous skeleton material to the second-stage silicon oxide powder is 1:0.05-1:0.3, preferably 1:0.1-1:0.2.

[0097] Optionally, the mass ratio of the porous skeleton material to the second-stage silicon oxide powder is 1:0.01-1:0.15, preferably 1:0.05-1:0.1.

[0098] In the present invention, by controlling the amount of silica powder added to the porous skeleton material and each level, the silica powder can be better embedded in the pores of the porous skeleton material, thereby better recycling the silica powder and increasing the filling amount of silica powder in the porous skeleton material.

[0099] In step S5, the carbon coating method is selected from any one of gas phase coating, liquid phase coating or solid phase coating, preferably gas phase coating, which is conducive to obtaining a uniform carbon coating layer.

[0100] Specifically, in the gas phase coating method, the gas source is selected from at least one of acetylene, methane, ethane, propane, and ethylene; the gas source flow rate is 5L / min-20L / min; the carbon coating temperature is 800℃-1000℃, and the carbon coating time is 120min-300min.

[0101] Furthermore, after the carbon coating is completed, carbonization treatment is performed to obtain a silicon oxide composite negative electrode material, wherein the carbonization temperature is 800° C.-1000° C. and the carbonization time is 60 min-180 min.

[0102] In the present invention, by controlling the various process parameters in the vapor phase coating method, a uniform carbon coating layer can be obtained, which is conducive to building a more complete conductive network and improving the conductivity and structural stability of the silicon 2 oxide composite negative electrode material.

[0103] The present invention also provides a silicon oxide composite negative electrode material comprising a core and a carbon coating coated on the core. The core comprises a porous skeleton material, the pores of which are filled with multiple layers of silicon oxide particles, each layer having different particle sizes. This silicon oxide composite negative electrode material exhibits high initial efficiency and long-cycle stability, while also being low in production cost.

[0104] Optionally, the filling amount of the silicon monoxide particles is 65%-90% of the total mass of the core, preferably 80%-90%.

[0105] Optionally, the pore structure of the porous skeleton material gradually decreases from the outer surface of the porous skeleton material inward.

[0106] Optionally, a plurality of silicon oxide particle layers are sequentially filled into the pores of the porous skeleton material in order of particle size from small to large.

[0107] Optionally, the thickness of the carbon coating layer is 3nm-5nm. Such a configuration is conducive to forming a complete conductive network, while also being conducive to improving the structural stability of the silicon oxide composite negative electrode material, thereby improving the cycle stability of the silicon oxide composite negative electrode material.

[0108] In addition, the present invention also provides a negative electrode sheet prepared using the silicon monoxide composite negative electrode material as described above.

[0109] And, a secondary battery prepared using the negative electrode sheet as described above.

[0110] The following specific examples further illustrate the silicon 2 O composite negative electrode material, its preparation method, and its application. However, those skilled in the art will appreciate that the following examples are merely illustrative of the present invention and should not be construed as limiting the scope of the present invention. In the examples, where specific conditions are not specified, the experiments were performed under conventional conditions or those recommended by the manufacturer. Reagents or instruments used, where the manufacturer is not specified, are commercially available conventional products.

[0111] Example 1

[0112] Silica powder with a median particle size of 20nm-500nm is graded to obtain first-grade silica powder, second-grade silica powder and third-grade silica powder, wherein the median particle size of the first-grade silica powder is 20nm-50nm, the median particle size of the second-grade silica powder is 50nm-100nm, and the median particle size of the third-grade silica powder is 100nm-500nm.

[0113] 300 g of first-grade silicon oxide powder was placed in a DMF solution and stirred for 2 h, and then filtered to obtain the treated first-grade silicon oxide powder; 50 g of second-grade silicon oxide powder was placed in a DMF solution and stirred for 2 h, and then filtered to obtain the treated second-grade silicon oxide powder; 25 g of third-grade silicon oxide powder was placed in a DMF solution and stirred for 2 h, and then filtered to obtain the treated third-grade silicon oxide powder.

[0114] 1000g of dicyandiamide, 35g of ammonium bicarbonate and 500mL of deionized water were mixed and stirred for 5h, and dried by rotary evaporation to obtain an intermediate, which was then sintered at 500°C for 6h under argon conditions to obtain a porous carbon-nitrogen material. The porous carbon-nitrogen material was in the shape of a sheet, with a pore structure of wide outside and narrow inside, an average pore diameter of 300nm, and a specific surface area of ​​205m 2 / g, porosity is 55%; then 500g of the porous carbon nitride material is placed in an acetone solvent and stirred for 2h, and then centrifuged and washed three times with clean water to obtain the treated porous carbon nitride material.

[0115] The first-level silicon dioxide powder obtained above was mixed with the treated porous carbon nitrogen material obtained above and 500 mL of water, and stirred for 2 hours to obtain a first mixed solution; then the treated second-level silicon dioxide powder obtained above was added to the first mixed solution, and stirred for 6 hours to obtain a second mixed solution; then the treated third-level silicon dioxide powder obtained above was added to the second mixed solution, and stirred for 8 hours to obtain a third mixed solution; the third mixed solution obtained above was centrifuged and washed with water three times, and then placed in a vacuum drying oven for drying at 80°C to obtain a composite.

[0116] The above-obtained complex is carbon-coated by a gas phase coating method, wherein, in the gas phase coating method, the gas source is acetylene, the gas source flow rate is 10 L / min, the carbon coating time is 180 min, the carbon coating temperature is 900°C, and then the mixture is kept warm for 30 min to obtain a silicon oxide composite negative electrode material, wherein the filling amount of silicon oxide particles in the silicon oxide composite negative electrode material is 85%, and the thickness of the carbon coating layer is 4 nm.

[0117] Example 2

[0118] Silica powder with a median particle size of 20nm-500nm is graded to obtain first-grade silica powder, second-grade silica powder and third-grade silica powder, wherein the median particle size of the first-grade silica powder is 40nm-50nm, the median particle size of the second-grade silica powder is 80nm-100nm, and the median particle size of the third-grade silica powder is 200nm-300nm.

[0119] 350g of first-grade silicon oxide powder was placed in a DMF solution and stirred for 2h, and then filtered to obtain the treated first-grade silicon oxide powder; 100g of second-grade silicon oxide powder was placed in a DMF solution and stirred for 2h, and then filtered to obtain the treated second-grade silicon oxide powder; 50g of third-grade silicon oxide powder was placed in a DMF solution and stirred for 2h, and then filtered to obtain the treated third-grade silicon oxide powder.

[0120] 1000 g of dicyandiamide, 40 g of ammonium bicarbonate and 500 mL of deionized water were mixed and stirred for 5 h, and dried by rotary evaporation to obtain an intermediate. The intermediate was then sintered at 500 ° C for 6 h under argon conditions to obtain a porous carbon nitrogen material. The porous carbon nitrogen material was in the shape of a sheet, with a pore structure of wide outside and narrow inside, an average pore diameter of 450 nm, and a specific surface area of ​​190 m 2 / g, porosity is 50%; then 500g of the porous carbon nitride material is placed in an acetone solvent and stirred for 2h, and then centrifuged and washed three times with clean water to obtain the treated porous carbon nitride material.

[0121] The first-level silicon dioxide powder obtained above was mixed with the treated porous carbon nitrogen material obtained above and 500 mL of water, and stirred for 2 hours to obtain a first mixed solution; then the treated second-level silicon dioxide powder obtained above was added to the first mixed solution, and stirred for 6 hours to obtain a second mixed solution; then the treated third-level silicon dioxide powder obtained above was added to the second mixed solution, and stirred for 8 hours to obtain a third mixed solution; the third mixed solution obtained above was centrifuged and washed with water three times, and then placed in a vacuum drying oven for drying at 80°C to obtain a composite.

[0122] The above-obtained complex is carbon-coated by a gas phase coating method, wherein, in the gas phase coating method, the gas source is acetylene, the gas source flow rate is 15 L / min, the carbon coating time is 300 min, the carbon coating temperature is 1000°C, and then the mixture is kept warm for 180 min to obtain a silicon oxide composite negative electrode material, wherein the filling amount of silicon oxide particles in the silicon oxide composite negative electrode material is 90%, and the thickness of the carbon coating layer is 5 nm.

[0123] Example 3

[0124] Silica powder with a median particle size of 20nm-500nm is graded to obtain first-grade silica powder, second-grade silica powder and third-grade silica powder, wherein the median particle size of the first-grade silica powder is 20nm-30nm, the median particle size of the second-grade silica powder is 60nm-90nm, and the median particle size of the third-grade silica powder is 180nm-270nm.

[0125] 200 g of first-grade silicon oxide powder was placed in a DMF solution and stirred for 2 hours, and then filtered to obtain the treated first-grade silicon oxide powder; 30 g of second-grade silicon oxide powder was placed in a DMF solution and stirred for 2 hours, and then filtered to obtain the treated second-grade silicon oxide powder; 15 g of third-grade silicon oxide powder was placed in a DMF solution and stirred for 2 hours, and then filtered to obtain the treated third-grade silicon oxide powder.

[0126] 1000g of dicyandiamide, 25g of ammonium bicarbonate and 500mL of deionized water were mixed and stirred for 5h, and dried by rotary evaporation to obtain an intermediate, which was then sintered at 500°C under argon for 6h to obtain a porous carbon-nitrogen material. The porous carbon-nitrogen material was in the shape of a sheet, with a pore structure of wide outside and narrow inside, an average pore diameter of 350nm, and a specific surface area of ​​210m 2 / g, porosity is 60%; then 500g of the porous carbon nitride material is placed in an acetone solvent and stirred for 2h, and then centrifuged and washed three times with clean water to obtain the treated porous carbon nitride material.

[0127] The first-level silicon dioxide powder obtained above was mixed with the treated porous carbon nitrogen material obtained above and 500 mL of water, and stirred for 2 hours to obtain a first mixed solution; then the treated second-level silicon dioxide powder obtained above was added to the first mixed solution, and stirred for 6 hours to obtain a second mixed solution; then the treated third-level silicon dioxide powder obtained above was added to the second mixed solution, and stirred for 8 hours to obtain a third mixed solution; the third mixed solution obtained above was centrifuged and washed with water three times, and then placed in a vacuum drying oven for drying at 80°C to obtain a composite.

[0128] The above-obtained complex is carbon-coated by a gas phase coating method, wherein, in the gas phase coating method, the gas source is acetylene, the gas source flow rate is 5 L / min, the carbon coating time is 120 min, the carbon coating temperature is 800°C, and then the mixture is kept warm for 60 min to obtain a silicon oxide composite negative electrode material, wherein the filling amount of silicon oxide particles in the silicon oxide composite negative electrode material is 89%, and the thickness of the carbon coating layer is 3 nm.

[0129] Example 4

[0130] Compared with Example 1, Example 4 differs only in that the amount of the first-stage silicon oxide powder used is 200 g, and the other conditions are the same, thereby obtaining a silicon oxide composite negative electrode material, wherein the filling amount of silicon oxide particles in the silicon oxide composite negative electrode material is 82%, and the thickness of the carbon coating layer is 3.8 nm.

[0131] Example 5

[0132] Compared with Example 1, Example 5 differs only in that the amount of the first-stage silicon oxide powder used is 400 g, and the other conditions are the same, thereby obtaining a silicon oxide composite negative electrode material, wherein the filling amount of silicon oxide particles in the silicon oxide composite negative electrode material is 88%, and the thickness of the carbon coating layer is 3.6 nm.

[0133] Example 6

[0134] Compared with Example 1, Example 6 differs only in that the amount of the second-stage silicon oxide powder used is 150 g, and the other conditions are the same, thereby obtaining a silicon oxide composite negative electrode material, wherein the filling amount of silicon oxide particles in the silicon oxide composite negative electrode material is 87%, and the thickness of the carbon coating layer is 4.1 nm.

[0135] Example 7

[0136] Compared with Example 1, Example 7 differs only in that the amount of the third-stage silicon dioxide powder used is 50 g, and the other conditions are the same, thereby obtaining a silicon dioxide composite negative electrode material, wherein the filling amount of silicon dioxide particles in the silicon dioxide composite negative electrode material is 81%, and the thickness of the carbon coating layer is 3.9 nm.

[0137] Example 8

[0138] Compared with Example 1, Example 8 differs only in that the median particle size of the first-level silicon oxide powder is 5nm-10nm, the median particle size of the second-level silicon oxide powder is 100nm-200nm, and the median particle size of the third-level silicon oxide powder is 400nm-500nm. The other conditions are the same, and a silicon oxide composite negative electrode material is obtained, wherein the filling amount of silicon oxide particles in the silicon oxide composite negative electrode material is 85%, and the thickness of the carbon coating layer is 3.9nm.

[0139] Example 9

[0140] Compared with Example 1, Example 9 differs only in that the third-level silicon dioxide powder obtained above is mixed with the treated porous carbon-nitrogen material obtained above and 500 mL of water, and stirred for 2 hours to obtain a first mixed solution; then the treated second-level silicon dioxide powder obtained above is added to the first mixed solution, and stirred for 6 hours to obtain a second mixed solution; then the treated first-level silicon dioxide powder obtained above is added to the second mixed solution, and stirred for 8 hours to obtain a third mixed solution; the third mixed solution obtained above is centrifuged and washed three times, and then placed in a vacuum drying oven for drying at 80°C to obtain a composite, and the other conditions are the same to obtain a silicon dioxide composite negative electrode material, wherein, in the silicon dioxide composite negative electrode material, the filling amount of silicon dioxide particles is 65%, and the thickness of the carbon coating layer is 4.1 nm.

[0141] Example 10

[0142] Compared with Example 1, Example 10 differs only in that the first-level silicon dioxide powder obtained above is mixed with the treated porous carbon-nitrogen material obtained above and 500 mL of water, and stirred for 2 hours to obtain a first mixed solution; then the treated third-level silicon dioxide powder obtained above is added to the first mixed solution, and stirred for 6 hours to obtain a second mixed solution; then the treated second-level silicon dioxide powder obtained above is added to the second mixed solution, and stirred for 8 hours to obtain a third mixed solution; the third mixed solution obtained above is centrifuged and washed three times, and then placed in a vacuum drying oven for drying at 80°C to obtain a composite, and the other conditions are the same to obtain a silicon dioxide composite negative electrode material, wherein, in the silicon dioxide composite negative electrode material, the filling amount of silicon dioxide particles is 75%, and the thickness of the carbon coating layer is 3.7 nm.

[0143] Example 11

[0144] The only difference between Example 11 and Example 1 is that commercial porous carbon (average pore size of about 50 nm, specific surface area of ​​1500 m 2 / g, porosity 60%) instead of the porous carbon nitrogen material, and the other conditions are the same to obtain a silicon oxide composite negative electrode material, wherein the filling amount of silicon oxide particles in the silicon oxide composite negative electrode material is 65%, and the thickness of the carbon coating layer is 4.2nm.

[0145] Example 12

[0146] The only difference between Example 12 and Example 1 is that porous carbon nanosheets are used instead of porous carbon nitrogen materials, wherein the porous carbon nanosheets are in the shape of sheets, the pore structure is circular, the average pore diameter is about 100nm, and the specific surface area is 175m 2 / g, a porosity of 40%, and other conditions being the same to obtain a silicon oxide composite negative electrode material, wherein the filling amount of silicon oxide particles in the silicon oxide composite negative electrode material is 70%, and the thickness of the carbon coating layer is 5nm.

[0147] Example 13

[0148] Compared with Example 1, Example 13 differs only in that acetamide is used instead of DMF solution and cyclohexanone is used instead of acetone solvent. The other conditions are the same to obtain a silicon oxide composite negative electrode material, wherein the filling amount of silicon oxide particles in the silicon oxide composite negative electrode material is 84%, and the thickness of the carbon coating layer is 4 nm.

[0149] Comparative Example 1

[0150] The only difference between Comparative Example 1 and Example 1 is that the step of grading the 20nm-500nm silicon dioxide powder is not included. That is, 375g of 20nm-500nm silicon dioxide powder is directly placed in DMF solution and stirred for 2h, and then filtered to obtain the treated silicon dioxide powder.

[0151] The treated silicon oxide powder obtained above is evenly mixed with the treated porous carbon nitrogen material obtained above and 500 mL of water to obtain a mixed solution; the mixed solution obtained above is centrifuged and washed three times with water, and then placed in a vacuum drying oven and dried at 80°C to obtain a composite. The other conditions are the same to obtain a silicon oxide composite negative electrode material, wherein the filling amount of silicon oxide particles in the silicon oxide composite negative electrode material is 50%, and the thickness of the carbon coating layer is 3.7 nm.

[0152] Comparative Example 2

[0153] Comparative Example 2 is different from Example 1 only in that it does not contain the steps of placing the first-level silicon oxide powder, the second-level silicon oxide powder and the third-level silicon oxide powder in DMF solution and stirring for 2 hours, and then filtering. That is, 300g of the first-level silicon oxide powder is directly mixed with the treated porous carbon-nitrogen material obtained above and 500mL of water, and stirred for 2 hours to obtain a first mixed solution; then 50g of the second-level silicon oxide powder is added to the first mixed solution, and stirred for 6 hours to obtain a second mixed solution; then 25g of the third-level silicon oxide powder is added to the second mixed solution, and stirred for 8 hours to obtain a third mixed solution; the third mixed solution obtained above is centrifuged and washed three times, and then placed in a vacuum drying oven for drying at 80°C to obtain a composite. The other conditions are the same to obtain a silicon oxide composite negative electrode material, wherein the filling amount of silicon oxide particles in the silicon oxide composite negative electrode material is 63%, and the thickness of the carbon coating layer is 4.1nm.

[0154] Comparative Example 3

[0155] Compared with Example 1, Comparative Example 3 differs only in that it does not contain the step of placing 500 g of porous carbon-nitrogen material in an acetone solvent and stirring for 2 hours, and then centrifugally washing it three times with clean water to obtain the treated porous carbon-nitrogen material. That is, the first-level silicon dioxide powder obtained above is directly mixed with 500 g of porous carbon-nitrogen material and 500 mL of water, and stirred for 2 hours to obtain a first mixed solution. The other conditions are the same to obtain a silicon dioxide composite negative electrode material, wherein the filling amount of silicon dioxide particles in the silicon dioxide composite negative electrode material is 60%, and the thickness of the carbon coating layer is 3.9 nm.

[0156] Comparative Example 4

[0157] Comparative Example 4 is compared with Example 1, except that the treated first-level silicon oxide powder, the treated second-level silicon oxide powder, the treated third-level silicon oxide powder, the treated porous carbon-nitrogen material and 500 mL of water are mixed and stirred for 2 hours to obtain a mixed solution; the mixed solution obtained above is centrifuged and washed three times, and then placed in a vacuum drying oven for drying at 80°C to obtain a composite. The other conditions are the same to obtain a silicon oxide composite negative electrode material, wherein the filling amount of silicon oxide particles in the silicon oxide composite negative electrode material is 52%, and the thickness of the carbon coating layer is 3.8 nm.

[0158] Comparative Example 5

[0159] Comparative Example 5 is compared with Example 1, except that 1000 g of dicyandiamide and 500 mL of deionized water are mixed and stirred for 5 h, and then dried by rotary evaporation to obtain an intermediate, and then the intermediate is sintered at 500 ° C under argon conditions for 6 h to obtain a carbon-nitrogen material; then 500 g of the carbon-nitrogen material is placed in an acetone solvent and stirred for 2 h, and then centrifuged and washed three times with clean water to obtain the treated carbon-nitrogen material.

[0160] The first-level silicon dioxide powder obtained above was mixed with the treated carbon-nitrogen material obtained above and 500 mL of water, and stirred for 2 hours to obtain a first mixed solution. The other conditions were the same to obtain a silicon dioxide composite negative electrode material, wherein the filling amount of silicon dioxide particles in the silicon dioxide composite negative electrode material was 5%, and the thickness of the carbon coating layer was 4.0 nm.

[0161] Comparative Example 6

[0162] Compared with Example 1, Comparative Example 6 differs only in that it does not contain the step of carbon-coating the above-obtained composite by the vapor phase coating method, and the other conditions are the same to obtain a silicon oxide composite negative electrode material (i.e., a composite), wherein the filling amount of silicon oxide particles in the silicon oxide composite negative electrode material is 86%, and the thickness of the carbon coating layer is 10 nm.

[0163] Performance testing:

[0164] The electrochemical cycle performance of the silicon 2 Oxide composite negative electrode materials prepared in Examples 1-13 and Comparative Examples 1-6 was tested using the following method. The test results are shown in Table 1.

[0165] Among them, the silicon oxide composite negative electrode materials prepared in Examples 1-13 and Comparative Examples 1-6 were used as negative electrode materials to prepare button batteries, and the specific steps were as follows: the silicon oxide composite negative electrode material, conductive agent SP, dispersant CMC, and binder AONE obtained above were mixed in a mass ratio of 70:15:5:10, and water was used as a solvent to prepare a negative electrode slurry; the negative electrode slurry was coated on a copper foil, and a lithium sheet was used as a counter electrode and a Celgard 2400 microporous polypropylene film was used as a separator to prepare a button battery.

[0166] The button battery obtained above was tested on the Blue Electric Battery Test System CT2001A equipment. At 25°C, the charge and discharge cycle characteristics of the button battery were detected using the Blue Electric test cabinet, specifically as follows: first discharge to 0.005V at 0.1C, then discharge to 0.001V at 0.08C, discharge to 0.001V at 0.05C, discharge to 0.001V at 0.02C, and let stand for 10 minutes; then charge to 1.5V at 0.1C, let stand for 10 minutes, record the charge and discharge capacity after the first cycle, and calculate the first coulombic efficiency; cycle 100 times in the above manner, record the charge and discharge capacity after 100 times, and calculate the capacity retention rate after 100 cycles.

[0167] Table 1

[0168]

[0169] From the data of Example 1 and Examples 4-5 in Table 1, it can be seen that changing the input amount of the first-stage silicon oxide powder, for example, reducing the input amount can increase the cycle but the capacity is significantly reduced. When the usage amount of the first-stage silicon oxide powder is increased, the silicon oxide powder will be suspended on the surface of the porous carbon nitrogen material, affecting the cycle retention rate.

[0170] From the data of Example 1 and Examples 6-7 in Table 1, it can be seen that an increase in the input amount of the second-stage silicon oxide powder and the third-stage silicon oxide powder will lead to excessive loading of the porous carbon-nitrogen material, causing the battery to expand significantly in volume during the cycle, resulting in a sharp decrease in the cycle stability of the battery.

[0171] From the data of Example 1 and Example 8 in Table 1, it can be seen that selecting appropriate median particle size of the first-stage silicon oxide powder, the median particle size of the second-stage silicon oxide powder, and the median particle size of the third-stage silicon oxide powder is beneficial to increasing the filling amount of silicon oxide powder in the porous carbon-nitrogen material, thereby improving the cycle performance and first efficiency of the battery.

[0172] From the data of Example 1 and Example 9 in Table 1, it can be seen that since Example 9 did not compound the treated first-level silicon oxide powder, the treated second-level silicon oxide powder and the treated third-level silicon oxide powder with the treated porous skeleton material in sequence according to the particle size from small to large, the amount of silicon oxide powder embedded in the pores of the porous skeleton material is small, which is not conducive to the cycle and resistance of the battery.

[0173] From the data of Example 1 and Example 11 in Table 1, it can be seen that the use of a porous carbon-nitrogen material with a pore structure that is wide on the outside and narrow on the inside is beneficial to increasing the amount of silicon oxide powder embedded in the pores of the porous skeleton material, while improving the cycle stability of the battery.

[0174] From the data of Example 1 and Examples 12-13 in Table 1, it can be seen that compounding the silicon dioxide powder coated with an amide solvent on the surface with the treated porous skeleton material in order from small to large level is beneficial to increasing the amount of silicon dioxide powder embedded in the pores of the porous skeleton material and improving the cycle stability of the battery.

[0175] In addition, compared with Example 1, since the silicon oxide powder in Comparative Example 1 was not graded, the amount of silicon oxide embedded in the pores was reduced, and most of it was directly compounded on the surface of the porous carbon-nitrogen material, which was not conducive to the cycle and resistance of the battery.

[0176] Compared with Example 1, in Comparative Example 2, since the first-stage silicon oxide powder, the second-stage silicon oxide powder and the third-stage silicon oxide powder were not treated with DMF solution, and in Comparative Example 3, the porous carbon nitrogen material was not treated with acetone solution, silicon oxide could not be accurately embedded in the pores of the porous carbon nitrogen material, resulting in a reduction in the amount of silicon oxide in the pores. Most of the silicon oxide is directly compounded on the surface of the porous carbon nitrogen material, which is not conducive to the cycle and resistance of the battery.

[0177] Compared with Example 1, in Comparative Example 4, since the first-level silicon oxide powder, the second-level silicon oxide powder and the third-level silicon oxide powder are directly mixed with the porous carbon nitrogen material, the amount of silicon oxide embedded in the pores is reduced, and most of it is directly compounded on the surface of the porous carbon nitrogen material, which is not conducive to the cycle and resistance of the battery.

[0178] Compared with Example 1, in Comparative Example 5, due to the use of non-porous carbon nitrogen material as a carrier and composite with silicon oxide, part of the silicon oxide is wrapped and part is exposed. In the later gas phase coating process, silicon oxide will agglomerate, resulting in a significant decrease in battery efficiency in the later stage of the cycle.

[0179] Compared with Example 1, since no carbon layer coating is performed in Comparative Example 6, silicon monoxide is directly exposed to the electrolyte, resulting in volume expansion during the cycle, decreased cycle life, and poor conductivity.

[0180] The technical features of the above-mentioned embodiments can be combined arbitrarily. In order to make the description concise, not all possible combinations of the technical features in the above-mentioned embodiments are described. However, as long as there is no contradiction in the combination of these technical features, they should be considered to be within the scope of this specification.

[0181] The above-described embodiments merely illustrate several implementations of the present invention, and while their descriptions are relatively specific and detailed, they should not be construed as limiting the scope of the patent. It should be noted that a person skilled in the art would be able to make numerous variations and improvements without departing from the spirit of the present invention, all of which fall within the scope of protection of the present invention. Therefore, the scope of protection of the patent for this invention shall be determined by the appended claims.

Claims

1. A method for preparing a silicon oxide composite negative electrode material, characterized in that: The following steps are involved: The silicon oxide powder is graded according to particle size to obtain multiple levels of silicon oxide powder, wherein the median particle size of the silicon oxide powder is 20 nm to 500 nm, and the median particle size ratio of silicon oxide powders of adjacent levels in the multiple levels of silicon oxide powder is 1:1.5 to 1:3, and among the multiple levels of silicon oxide powder, the larger the level, the larger the median particle size of the silicon oxide powder; Each level of silicon oxide powder is treated with an amide solvent to obtain silicon oxide powder with the surface coated with the amide solvent; Treating the porous skeleton material with a ketone solvent to obtain a porous skeleton material containing the ketone solvent in the pores, wherein the pore structure of the porous skeleton material gradually decreases from the outer surface of the porous skeleton material inward; The silicon oxide powder coated with an amide solvent on the surface is compounded with a porous skeleton material containing a ketone solvent in the pores in order from small to large to obtain a composite; The composite is carbon-coated to obtain a silicon 2 oxide composite negative electrode material.

2. The method for preparing the silicon 2 Oxide composite negative electrode material according to claim 1, wherein: In the step of classifying the silicon oxide powder to obtain silicon oxide powder of multiple grades, the silicon oxide powder is silicon oxide fine powder produced during the air flow milling process.

3. The method for preparing the silicon 2 Oxide composite negative electrode material according to claim 2, wherein: The multiple levels of silicon oxide powder include first-level silicon oxide powder, second-level silicon oxide powder and third-level silicon oxide powder, and meet at least one of the following conditions: (1) The median particle size of the first-stage silicon oxide powder is 20 nm to 50 nm; (2) The median particle size of the second-stage silicon oxide powder is 50nm-100nm; (3) The median particle size of the third-grade silicon oxide powder is 100 nm to 500 nm; (4) The mass ratio of the porous skeleton material to the first-stage silicon oxide powder is 1:0.5-1:0.7; (5) The mass ratio of the porous skeleton material to the second-stage silicon oxide powder is 1:0.1-1:0.2; (6) The mass ratio of the porous skeleton material to the third-level silicon oxide powder is 1:0.05-1:0.

1.

4. The method for preparing a silicon 2 Oxide composite negative electrode material according to claim 1, wherein: In the step of treating the porous skeleton material with a ketone solvent, at least one of the following conditions is met: (1) The average pore size of the porous skeleton material is 10 nm to 500 nm; (2) The specific surface area of ​​the porous skeleton material is 190m 2 / g-210m 2 / g; (3) The porosity of the porous skeleton material is 50%-60%; (4) The porous skeleton material is selected from porous carbon-nitrogen materials.

5. A silicon oxide composite negative electrode material prepared by the method for preparing a silicon oxide composite negative electrode material according to any one of claims 1 to 4, characterized in that: The silicon monoxide composite negative electrode material includes a core and a carbon coating layer coated on the surface of the core, the core includes a porous skeleton material, the pores of the porous skeleton material are filled with multiple silicon monoxide particle layers, and the particle size level of the silicon monoxide particles in each silicon monoxide particle layer is different.

6. The silicon 2 Oxide composite negative electrode material according to claim 5, characterized in that: The silicon oxide composite negative electrode material meets at least one of the following conditions: (1) The filling amount of the silicon oxide particles is 65%-90% of the total mass of the core; (2) The thickness of the carbon coating layer is 3nm-5nm.

7. A negative electrode sheet prepared using the silicon 2 Oxide composite negative electrode material according to claim 5 or 6.

8. A secondary battery prepared using the negative electrode sheet according to claim 7.

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