A high-nickel coated ternary positive electrode material pole piece and its preparation method and application

Abstract

The present invention discloses a coated high-nickel ternary positive electrode material pole piece, a preparation method, and an application thereof, and belongs to the field of lithium-ion battery positive electrode material preparation. The method for preparing the coated high-nickel ternary positive electrode material pole piece of the present invention comprises the following steps: (1) preparing an indium-doped high-nickel positive electrode material from a high-nickel ternary precursor; (2) preparing a high-nickel ternary positive electrode material pole piece using the indium-doped high-nickel positive electrode material as an active material; and (3) directly depositing indium oxide-tungsten oxide on the high-nickel ternary positive electrode material pole piece using a magnetron sputtering method to obtain the coated high-nickel ternary positive electrode material pole piece. The preparation process of the present invention is simple, and the surface In2O3, WO3, and internal doped indium ions are synergistically modified, significantly improving the material's cycle performance, rate performance, and safety performance in battery applications.

Description

Technical Field

[0001] The present invention relates to the field of preparation of lithium ion battery positive electrode materials, and in particular to a high-nickel coated ternary positive electrode material pole piece and a preparation method and application thereof. Background Art

[0002] Lithium-ion batteries, with their core advantages of high energy density, high power density, and high safety performance, are widely used in consumer electronics, power tools, power storage, aerospace and other fields. Among them, NCM ternary materials have extremely broad application prospects, ranging from small 3C product batteries to large electric vehicle power batteries and even future large-scale grid energy storage. Currently, NCM has become one of the key materials in the power battery field. In addition, compared with LCO, NCM has another unique advantage, namely the flexible and adjustable ratio of the ternary transition metals. The design of different transition metal ratios allows NCM to strike a balance between high energy density and high safety performance during the development stage.

[0003] NCM ternary materials have many advantages but also some disadvantages, such as: (1) Cation mixing. Excessive nickel content is the key to cation mixing, and a high degree of cation mixing will damage the electrochemical performance of high-nickel ternary positive electrode materials and reduce the first coulombic efficiency; (2) Microcracks. Long-term charge and discharge cycles are the main cause of microcracks. Long-term charge and discharge cycles will not only cause drastic changes in lattice parameters, causing the layered structure of the material to collapse, but also cause phase changes to produce various irregular volume changes, thereby leading to the generation of microcracks, destroying the integrity of the material, aggravating the side reactions between the material and the electrolyte, increasing its impedance, and reducing the battery's discharge capacity. Summary of the Invention

[0004] The purpose of the present invention is to provide a coated high-nickel ternary positive electrode material pole piece and its preparation method and application. The present invention obtains an indium-doped high-nickel positive electrode material by wet mixing and high-temperature solid-phase sintering, and then directly deposits indium oxide-tungsten oxide on the indium-doped high-nickel ternary positive electrode material pole piece by magnetron sputtering, thereby solving the problems of high-nickel ternary positive electrode material in the prior art in terms of gram capacity attenuation and poor cycle stability at higher current density.

[0005] The present invention first provides a method for preparing a high-nickel ternary positive electrode material coated electrode sheet, comprising the following steps:

[0006] (1) Preparation of indium-doped high-nickel cathode materials from high-nickel ternary precursors;

[0007] (2) preparing a high-nickel ternary positive electrode material electrode sheet using the indium-doped high-nickel positive electrode material as an active material;

[0008] (3) Indium oxide-tungsten oxide is directly deposited on the high-nickel ternary positive electrode material electrode piece by using a magnetron sputtering method to obtain the coated high-nickel ternary positive electrode material electrode piece.

[0009] The present invention uses indium-doped high-nickel positive electrode material to prepare the positive electrode material pole piece, and then uses magnetron sputtering to directly deposit indium oxide-tungsten oxide on the positive electrode material pole piece, which significantly improves the cycle performance, rate performance and safety performance of the positive electrode pole piece.

[0010] In the above-mentioned method for preparing a coated high-nickel ternary positive electrode material electrode, step (1) adopts a wet mixing and high-temperature solid-phase sintering process to prepare an indium-doped high-nickel positive electrode material;

[0011] The high nickel ternary precursor is Ni x Co y Mn (1-x-y) (OH)2, wherein 0.75<x≤0.95, 0.05≤y≤0.2. Specifically, 0.80<x≤0.95, 0.05≤y≤0.15; more specifically, the high nickel ternary precursor is Ni 0.93 Co 0.05 Mn 0.02 (OH)2、Ni 0.90 Co 0.06 Mn 0.04 (OH)2 or Ni 0.83 Co 0.12 Mn 0.05 (OH)2.

[0012] In the above-mentioned preparation method of the coated high-nickel ternary positive electrode material electrode, step (1) specifically includes the following steps: dissolving a soluble indium salt and a high-nickel ternary precursor in a solvent, adding lithium hydroxide after wet mechanical grinding, continuing grinding and vacuum drying, and then sintering at a high temperature to obtain the indium-doped high-nickel positive electrode material.

[0013] In the above-mentioned method for preparing a coated high-nickel ternary positive electrode material electrode, the soluble indium salt is indium nitrate and / or indium sulfate;

[0014] The solvent is at least one of ethanol solution, anhydrous ethanol and acetone;

[0015] The molar ratio of the lithium hydroxide, the high nickel ternary precursor and the soluble indium salt is 1.02:1-a:a, wherein 0<a≤0.2; specifically, 0.01≤a≤0.03;

[0016] In an embodiment of the present invention, the molar ratio of the lithium hydroxide, the high nickel ternary precursor and the soluble indium salt is 1.02:0.99:0.01, 1.02:0.985:0.015 or 1.02:0.98:0.02.

[0017] The vacuum drying temperature is 80-120°C, specifically 90°C; the vacuum drying time is 10-14h, specifically 13h;

[0018] The high-temperature sintering is carried out in an oxygen atmosphere;

[0019] The high temperature sintering is firstly kept at 500-650°C for 3-8 hours, and then heated to 780-900°C and kept for 10-18 hours.

[0020] In the above-mentioned method for preparing the coated high-nickel ternary positive electrode material electrode sheet, step (2) specifically includes the following steps: mixing the indium-doped high-nickel positive electrode material, the conductive agent, the adhesive and the dispersant to prepare a slurry, then applying it on aluminum foil, drying, pressing and cutting to obtain the high-nickel ternary positive electrode material electrode sheet.

[0021] In the above-mentioned method for preparing a high-nickel ternary positive electrode material coated electrode sheet, the conductive agent is at least one of superconducting carbon, acetylene black, conductive carbon black, Ketjen black, carbon dots, carbon nanotubes, graphene and carbon nanofibers;

[0022] The adhesive is at least one of polyvinylidene fluoride, polytetrafluoroethylene, vinylidene fluoride-tetrafluoroethylene-propylene terpolymer, vinylidene fluoride-hexafluoropropylene-tetrafluoroethylene terpolymer, tetrafluoroethylene-hexafluoropropylene copolymer and fluorine-containing acrylate resin;

[0023] The dispersant is at least one of N-methyl-2-pyrrolidone, polycarboxylate (PO), polyvinylpyrrolidone (PVP) and carboxymethyl cellulose sodium salt (CMC);

[0024] Based on the total mass of the indium-doped high-nickel positive electrode material, the conductive agent and the binder, the mass percentage of the indium-doped high-nickel positive electrode material is 60%-95%, the mass percentage of the conductive agent is 3%-30%, and the mass percentage of the binder is 2%-25%.

[0025] Specifically, the mass percentage of the indium-doped high-nickel positive electrode material is 90%, the mass percentage of the conductive agent is 5%, and the mass percentage of the binder is 5%.

[0026] In the above-mentioned method for preparing a high-nickel coated ternary positive electrode material electrode sheet, in step (3), the magnetron sputtering adopts an In2O3-WO3 target; specifically, the mass percentage of In2O3 based on the total mass of the In2O3-WO3 target is 60%-90%; specifically, it can be 80%;

[0027] The magnetron sputtering has a power of 50-200 W, specifically 160 W, and a duration of 15-40 min, specifically 20 min.

[0028] In the above-mentioned method for preparing the coated high-nickel ternary positive electrode material electrode piece, step (3) includes the following steps: fixing the high-nickel ternary positive electrode material electrode piece on the sample stage, and setting the target-substrate distance to 3-7 cm; before sputtering, the vacuum degree of the cavity is pumped to 4×10 -4 -6×10 -4 Pa, the electrode is heated at a constant temperature to remove residual moisture and other organic matter on the electrode; the rotation rate of the electrode is set to 5-15 r / min; argon is used as the sputtering gas, the gas flow rate is 20-40 sccm, and the sputtering pressure is 0.8-1.5 Pa; after ignition, the sputtering power is 150-180 W, and the In2O3-WO3 target surface is pre-sputtered for 15-45 min to remove impurities attached to the target surface; then sputtering is performed, and the time for In2O3-WO3 to coat the high nickel ternary electrode is set to 15-35 min to obtain the coated high nickel ternary positive electrode material electrode.

[0029] The constant temperature heating temperature is 90-120° C., specifically 110° C.; the constant temperature heating time is 0.3-0.7 h, specifically 0.5 h.

[0030] The present invention also provides a high-nickel coated ternary positive electrode material electrode prepared by the above preparation method.

[0031] Finally, the application of the above-mentioned coated high-nickel ternary positive electrode material electrode in the preparation of lithium-ion batteries also falls within the scope of protection of the present invention.

[0032] The present invention has the following beneficial effects:

[0033] (1) The present invention adopts indium doping. The radius of indium ions is slightly larger than that of lithium ions, which effectively reduces the mixing of lithium and nickel cations and improves the order of the layered structure. At the same time, indium ions enter the lithium layer, which increases the unit cell volume and the c / a value of the lattice, widens the lithium ion transmission channel, and improves the rate performance of the material. Under high voltage, the indium ions doped in the bulk lattice lithium site bond to the adjacent transition metal layer through O-In-O, which can suppress the repulsion between oxygen layers and play a "pillar effect", reducing the irreversible phase change of the material and improving the stability.

[0034] (2) In2O3 and WO3 form a smooth coating on the surface of the electrode. The coating presents a continuous network structure composed of nanoparticles, which reduces the structural changes of the electrode during the charge and discharge cycle, inhibits HF corrosion of the electrode, and improves its room temperature cycle performance and rate performance;

[0035] (3) The synergistic modification of surface In2O3, WO3 and internal doped indium ions significantly improves the cycle performance, rate performance and safety performance of the material in battery applications;

[0036] (4) The overall coating of the electrode sheet provided by the present invention is a new coating method that can provide good protection on the electrode surface, thereby improving the electrochemical properties of the positive electrode active material and will not hinder the transport of lithium ions or electrons inside the electrode;

[0037] (5) The preparation process of the present invention is simple and the electrical performance is significantly improved. DETAILED DESCRIPTION

[0038] The present invention will be further described in detail below in conjunction with specific embodiments. The examples given are only for illustrating the present invention, not for limiting the scope of the present invention.

[0039] The experimental methods in the following examples are conventional methods unless otherwise specified.

[0040] The quantitative tests in the following examples were all repeated three times, and the results were averaged.

[0041] Unless otherwise specified, the materials and reagents used in the following examples can be obtained from commercial sources.

[0042] In the following examples and comparative examples, the electrochemical performance testing method is as follows:

[0043] CR2032 batteries were fabricated in an argon-filled glove box using the ternary cathode material prepared in the examples and comparative examples as the positive electrode, a lithium metal sheet as the negative electrode, a polypropylene microporous membrane as the separator, and a 1 mol / L LiPF6 electrolyte (the solvent was a mixture of EC, DEC, and DMC in a 1:1:1 volume ratio). Constant current charge and discharge tests were conducted at room temperature at various rates, with charge and discharge cutoff voltages ranging from 2.8V to 4.35V.

[0044] DSC test: 1) Fully charge the prepared CR2032 battery and let it stand; 2) Disassemble the half-cell and scrape the powder off the positive electrode; 3) Spread the powder evenly on the bottom of the crucible and add electrolyte for DSC testing. Test parameters: Temperature range: room temperature to 400°C; Heating rate: 10°C / min; Atmosphere: Compressed air.

[0045] Example 1

[0046] (1) According to the molar ratio of LiOH·H2O, precursor, and In(NO3)3·9H2O of 1.02:0.99:0.01, In(NO3)3·9H2O and commercial precursor Ni 0.93 Co 0.05Mn 0.02 (OH)2 was dissolved in anhydrous ethanol, and after wet mechanical grinding, LiOH·H2O was added and mechanical grinding was continued. The mixture was vacuum dried at 90°C for 13 hours, placed in a tube furnace, and calcined at high temperature under an oxygen atmosphere. The mixture was pre-sintered at 500°C for 5 hours, then heated to 850°C for 14 hours, and cooled to obtain an indium-doped high-nickel cathode material.

[0047] (2) The indium-doped high-nickel positive electrode material prepared in step (1) is used as the active material, SP (conductive carbon black) is used as the conductive agent, PVDF (polyvinylidene fluoride) is used as the binder, and N-methyl-2-pyrrolidone (NMP) is used as the dispersant. The slurry is prepared according to the mass ratio of active material: SP: PVDF = 90:5:5, and the slurry is applied on aluminum foil for drying, pressing, and cutting to obtain a high-nickel ternary positive electrode material electrode.

[0048] (3) The target material used was a commercial In2O3-WO3 target (Jiangxi Kete New Materials Co., Ltd., target material specifications: In2O3 (80%)-WO3 (20%) wt%, purity 99.95%, diameter 50 mm * thickness 3 mm). The high nickel ternary positive electrode material electrode prepared in step (2) was mounted on the substrate clamp, sent into the cavity and fixed on the sample stage, and the target-substrate distance was set to 5 cm; before the sputtering experiment, the vacuum degree of the cavity was pumped to 5×10 -4 Pa, the electrode was heated at a constant temperature of 110°C for 0.5 h to remove residual moisture and other organic matter on the electrode, and the rotation rate of the electrode was set to 10 r / min to ensure the uniformity of the film formation; argon (purity: 99.999%) was used as the sputtering gas, the gas flow rate was 30 sccm, and the sputtering pressure was 1 Pa; after ignition, the sputtering power was 160 W, and the In2O3-WO3 target surface was pre-sputtered for 30 min to remove impurities attached to the target surface; then sputtering was carried out, and the time for In2O3-WO3 coating the high nickel ternary electrode was set to 20 min to obtain a coated high nickel ternary positive electrode material electrode.

[0049] Example 2

[0050] The preparation method is the same as that of Example 1, except that the molar ratio of LiOH·H2O, precursor and In(NO3)3·9H2O in step (1) is changed to 1.02:0.985:0.015 to obtain a coated high-nickel ternary positive electrode material electrode.

[0051] Example 3

[0052] The preparation method is the same as that of Example 1, except that the molar ratio of LiOH·H2O, precursor and In(NO3)3·9H2O in step (1) is changed to 1.02:0.98:0.02 to obtain a coated high-nickel ternary positive electrode material electrode.

[0053] Example 4

[0054] The precursor used in Example 1 was replaced by Ni 0.90 Co 0.06 Mn 0.04 (OH)2, and other synthesis conditions are the same as those in Example 1 to obtain a coated high-nickel ternary positive electrode material electrode.

[0055] Example 5

[0056] The precursor used in Example 1 was replaced by Ni 0.83 Co 0.12 Mn 0.05 (OH)2, and other synthesis conditions are the same as those in Example 1 to obtain a coated high-nickel ternary positive electrode material electrode.

[0057] Comparative Example 1 (Unmodified High Nickel Ternary Cathode Material Pole)

[0058] (1) According to the molar ratio of LiOH·H2O and precursor of 1.02:1, the commercial precursor Ni 0.83 Co 0.12 Mn 0.05 (OH)2 was dissolved in anhydrous ethanol, and after wet mechanical grinding, LiOH·H2O was added and mechanical grinding was continued. The mixture was vacuum dried at 90°C for 13 hours, placed in a tube furnace, and calcined at high temperature under an oxygen atmosphere. The mixture was pre-sintered at 500°C for 5 hours, then heated to 850°C for 14 hours, and cooled to obtain an undoped high-nickel positive electrode material.

[0059] (2) The undoped high nickel cathode material of step (1) is used as the active material, SP is used as the conductive agent, PVDF is used as the binder, and N-methyl-2-pyrrolidone (NMP) is used as the dispersant. The slurry is prepared in a mass ratio of undoped high nickel cathode material: SP: PVDF = 90:5:5, and the slurry is applied on aluminum foil for drying, pressing, and cutting to obtain an undoped high nickel ternary cathode material electrode.

[0060] Comparative Example 2 (Indium-doped high-nickel ternary positive electrode material electrode)

[0061] Without step (3) of Example 1, other synthesis conditions are the same as those of Example 1, and an indium-doped high-nickel ternary positive electrode material electrode is obtained.

[0062] Comparative Example 3 (coated undoped high-nickel ternary positive electrode material electrode)

[0063] Except for weighing LiOH·H2O and precursor at a molar ratio of 1.02:1 in step (1), other synthesis conditions are the same as those in Example 1, and a coated undoped high-nickel ternary positive electrode material electrode is obtained.

[0064] Table 1 Summary of electrical properties of button cells prepared from positive electrode material sheets prepared in Examples and Comparative Examples

[0065]

[0066] Table 1 is a summary of the electrical properties of button cells prepared from the positive electrode material sheets prepared in the Examples and Comparative Examples. As can be seen from Table 1, the positive electrode material sheets prepared in Examples 1-3 not only have an advantage in initial discharge specific capacity compared to the unmodified high-nickel ternary positive electrode material sheet of Comparative Example 1 and the indium-doped high-nickel ternary positive electrode material sheet of Comparative Example 2, but also have good capacity retention after 100 cycles. When the molar ratio of the precursor to In(NO3)3·9H2O is 0.985:0.015, the electrochemical performance of the high-nickel ternary positive electrode sheet is significantly improved, thus indicating that Example 2 is the best example, indicating that the coated high-nickel ternary positive electrode sheet provided by the present invention has better electrochemical performance.

[0067] Table 2 Summary of electrical properties of button cells prepared from the positive electrode material sheets prepared in Example 2 and Comparative Example 1

[0068]

[0069] Table 2 shows the DSC performance of button batteries prepared from the positive electrode material pole pieces prepared in Comparative Example 1 and Example 2 of the present invention. The button voltage range is 2.8-4.35V. The peak decomposition temperature of Example 2 is 208.45°C, and the peak decomposition temperature of Comparative Example 1 is 200.93°C, which is increased by 7.52°C, and the safety performance is improved.

Claims

1. A method for preparing a high-nickel ternary positive electrode material coated electrode, characterized in that: The steps include: (1) Preparation of indium-doped high-nickel cathode material from high-nickel ternary precursor; (2) preparing a high-nickel ternary positive electrode material electrode sheet using the indium-doped high-nickel positive electrode material as an active material; (3) Indium oxide-tungsten oxide is directly deposited on the high-nickel ternary positive electrode material electrode piece by using a magnetron sputtering method to obtain the coated high-nickel ternary positive electrode material electrode piece.

2. The method for preparing a high-nickel ternary positive electrode material coated electrode sheet according to claim 1, characterized in that: Step (1) preparing an indium-doped high-nickel cathode material by wet mixing and high-temperature solid-phase sintering process; The high nickel ternary precursor is Ni x Co y Mn (1-x-y) (OH)2, where 0.75<x≤0.95, 0.05≤y≤0.

2.

3. The method for preparing a high-nickel ternary positive electrode material coated electrode sheet according to claim 2, characterized in that: Step (1) specifically includes the following steps: dissolving a soluble indium salt and a high-nickel ternary precursor in a solvent, adding lithium hydroxide after wet mechanical grinding, continuing grinding and vacuum drying, and then sintering at a high temperature to obtain the indium-doped high-nickel positive electrode material.

4. The method for preparing a high-nickel ternary positive electrode material coated electrode sheet according to claim 3, characterized in that: The soluble indium salt is indium nitrate and / or indium sulfate; The solvent is at least one of ethanol solution, anhydrous ethanol and acetone; The molar ratio of the lithium hydroxide, the high nickel ternary precursor and the soluble indium salt is 1.02:1-a:a, wherein 0<a≤0.2; The vacuum drying temperature is 80-120°C; the vacuum drying time is 10-14 hours; The high-temperature sintering is carried out in an oxygen atmosphere; The high temperature sintering is firstly kept at 500-650°C for 3-8 hours, and then heated to 780-900°C and kept for 10-18 hours.

5. The method for preparing a high-nickel ternary positive electrode material coated electrode sheet according to claim 1, characterized in that: Step (2) specifically includes the following steps: mixing the indium-doped high-nickel positive electrode material, conductive agent, adhesive and dispersant to prepare a slurry, then applying it on aluminum foil, drying, pressing and cutting to obtain the high-nickel ternary positive electrode material electrode.

6. The method for preparing a high-nickel ternary positive electrode material coated electrode sheet according to claim 5, characterized in that: The conductive agent is at least one of superconducting carbon, acetylene black, conductive carbon black, Ketjen black, carbon dots, carbon nanotubes, graphene and carbon nanofibers; The adhesive is at least one of polyvinylidene fluoride, polytetrafluoroethylene, vinylidene fluoride-tetrafluoroethylene-propylene terpolymer, vinylidene fluoride-hexafluoropropylene-tetrafluoroethylene terpolymer, tetrafluoroethylene-hexafluoropropylene copolymer and fluorine-containing acrylate resin; The dispersant is at least one of N-methyl-2-pyrrolidone, polycarboxylate, polyvinylpyrrolidone and sodium carboxymethyl cellulose; Based on the total mass of the indium-doped high-nickel positive electrode material, the conductive agent and the adhesive, the mass percentage of the indium-doped high-nickel positive electrode material is 60%-95%, the mass percentage of the conductive agent is 3%-30%, and the mass percentage of the adhesive is 2%-25%.

7. The method for preparing a high-nickel ternary positive electrode material coated electrode sheet according to claim 1, characterized in that: In step (3), the magnetron sputtering uses an In2O3-WO3 target; The power of the magnetron sputtering is 50-200W, and the time is 15-40 minutes.

8. The method for preparing a high-nickel ternary positive electrode material coated electrode sheet according to claim 7, characterized in that: Step (3) includes the following steps: fixing the high nickel ternary cathode material electrode on the sample table, and setting the target-substrate distance to 3-7 cm; before sputtering, pumping the vacuum degree of the cavity to 4×10 -4 -6×10 -4 Pa, the electrode is heated at a constant temperature to remove residual moisture and other organic matter on the electrode; the rotation rate of the electrode is set to 5-15r / min; argon is used as the sputtering gas, the gas flow rate is 20-40sccm, and the sputtering pressure is 0.8-1.5Pa; after ignition, the sputtering power is 150-180W, and the In2O3-WO3 target surface is pre-sputtered for 15-45min; then sputtering is performed, and the time for In2O3-WO3 to coat the high nickel ternary electrode is set to 15-35min to obtain the coated high nickel ternary positive electrode material electrode.

9. A high-nickel coated ternary positive electrode material electrode prepared by the preparation method according to any one of claims 1 to 8.

10. Use of the coated high-nickel ternary positive electrode material electrode according to claim 9 in the preparation of lithium-ion batteries.

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