Method for preparing high-voltage cathode material by body modification and regeneration of waste lithium cobaltate material

Abstract

The disclosure discloses a method for preparing a high-voltage cathode material by body modification and regeneration of a waste lithium cobaltate material. The waste lithium cobaltate cathode material is calcined, and then measured; a lithium source, a magnesium source, nano-scale TiO.sub.2 and the waste lithium cobaltate cathode material powder are mixed to obtain a mixture, placed in a ball milling tank containing absolute ethanol, and the resulting mixture is ball milled, and then dried to obtain a mixed powder; the mixed powder is calcined to obtain a magnesium-titanium co-doped regenerated lithium cobaltate cathode material; the magnesium-titanium co-doped regenerated lithium cobaltate cathode material is added into a mixed solution obtained by ultrasonically mixing absolute ethanol with the aluminum source, and then heated and stirred continually until the solvent evaporates to obtain a residue; the residue is calcined to obtain an aluminum-coated magnesium-titanium co-doped regenerated lithium cobaltate cathode material.

Claims

1. A method for preparing a high-voltage cathode material by body modification and regeneration of a waste lithium cobaltate material, including, (1) soaking a waste lithium cobaltate battery in a solution with a concentration of sodium chloride of 1 to 3 mol/L for 24 to 48 hours, disassembling and peeling off the waste lithium cobaltate battery to obtain a waste lithium cobaltate cathode sheet, soaking completely the waste lithium cobaltate cathode sheet in a solution with a concentration of sodium hydroxide of 1 to 3 mol/L, stirring and reacting for 5 to 15 hours, filtering and washing to obtain a waste lithium cobaltate cathode material, calcining the waste lithium cobaltate cathode material at a temperature of 500 to 700° C. for 2 to 5 hours, to obtain a waste lithium cobaltate cathode material powder; measuring the contents of Li and Co thereof; (2) mixing a lithium source, a magnesium source, nano-scale TiO.sub.2 and the waste lithium cobaltate cathode material powder to obtain a mixture, placing the mixture into a ball mill tank, adding absolute ethanol thereto, ball milling the mixture, and drying, to obtain a mixed powder; (3) calcining the mixed powder in an air atmosphere, to obtain a magnesium-titanium co-doped regenerated lithium cobaltate cathode material; (4) ultrasonically mixing absolute ethanol and an aluminum source for 30 minutes to obtain a mixed solution, adding the magnesium-titanium co-doped regenerated lithium cobaltate cathode material into the mixed solution, heating and stirring continually until the solvent in the mixed solution evaporates to obtain a residue; and (5) calcining the residue, to obtain an aluminum-coated magnesium-titanium co-doped regenerated lithium cobaltate cathode material.

2. The method for preparing a high-voltage cathode material by body modification and regeneration of a waste lithium cobaltate material according to claim 1, wherein in step (2), the lithium source is lithium carbonate or lithium hydroxide; the magnesium source is magnesium oxide or magnesium hydroxide.

3. The method for preparing a high-voltage cathode material by body modification and regeneration of a waste lithium cobaltate material according to claim 1, wherein in the mixture of step (2), a molar ratio of Co:Mg:Ti is in a range of (0.9-0.98):(0.01-0.05):(0.01-0.05), and a molar ratio of Li:M is in a range of (1.03-1.1):1, with the proviso that M=Mg+Ti+Co.

4. The method for preparing a high-voltage cathode material by body modification and regeneration of a waste lithium cobaltate material according to claim 1, wherein in step (2), the ball milling is performed in a mass ratio of ball-to-material of 5:1 to 15:1, and is performed at a ball milling rate of 100-300 r/min for 0.5-2 hours; absolute ethanol is added to reach ⅔ height of the ball mill tank.

5. The method for preparing a high-voltage cathode material by body modification and regeneration of a waste lithium cobaltate material according to claim 1, wherein in step (2), the drying is performed at a temperature of 90-150° C. for 10-20 hours.

6. The method for preparing a high-voltage cathode material by body modification and regeneration of a waste lithium cobaltate material according to claim 1, wherein in step (3), the calcining is performed at a temperature of 800-1100° C. for 10-20 hours.

7. The method for preparing a high-voltage cathode material by body modification and regeneration of a waste lithium cobaltate material according to claim 1, wherein in step (4), the aluminum source is aluminium isopropoxide or aluminum tri-sec-butoxide; a mass-volume ratio of the aluminum source to absolute ethanol is in a range of (0.08-4) g:1000 mL.

8. The method for preparing a high-voltage cathode material by body modification and regeneration of a waste lithium cobaltate material according to claim 1, wherein in step (4), a mass-volume ratio of the magnesium-titanium co-doped regenerated lithium cobaltate cathode material to the mixed solution is in a range of (0.02-0.04) g:1 mL.

9. The method for preparing a high-voltage cathode material by body modification and regeneration of a waste lithium cobaltate material according to claim 1, wherein in step (4), the heating and stirring are performed at a temperature of 40-70° C.

10. The method for preparing a high-voltage cathode material by body modification and regeneration of a waste lithium cobaltate material according to claim 1, wherein in step (5), the calcining is performed at a temperature of 600-900° C. for 2-6 hours.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 shows a process flow diagram of Example 1 of the present disclosure;

(2) FIG. 2 shows an XRD (Diffraction of X-rays) diagram of the waste lithium cobaltate cathode material and the prepared regenerated lithium cobaltate cathode material in Example 1 of the present disclosure;

(3) FIG. 3 shows an EDS (Energy Dispersive Spectroscopy) diagram of the magnesium-titanium co-doped regenerated lithium cobaltate cathode material as prepared in Example 2 of the present disclosure;

(4) FIG. 4 shows a 1C cycle performance curve of the waste lithium cobaltate cathode material and the prepared regenerated lithium cobaltate cathode material in Example 3 of the present disclosure.

DETAILED DESCRIPTION OF THE EMBODIMENTS

(5) The present disclosure will be further described below in conjunction with embodiments and drawings.

Example 1

(6) A method for preparing a high-voltage cathode material by body modification and regeneration of a waste lithium cobaltate material, as shown in FIG. 1, specifically including the following steps:

(7) (1) a waste lithium cobaltate battery was completely soaked in a solution with a concentration of sodium chloride of 2 mol/L for 36 hours, then the waste lithium cobaltate battery was manually disassembled and peeled off to obtain a waste lithium cobaltate cathode sheet, then the waste lithium cobaltate cathode sheet was completely soaked in a solution with a concentration of sodium hydroxide of 1.5 mol/L, and stirred and reacted for 10 hours, the resulting mixture was filtered, and the filter cake was washed to obtain a waste lithium cobaltate cathode material; the waste lithium cobaltate cathode material was placed in a muffle furnace and calcined at 650° C. for 3 hours under an air atmosphere to obtain a waste lithium cobaltate cathode material powder; the contents of Li and Co in the obtained waste lithium cobaltate cathode material powder were measured;

(8) (2) lithium carbonate, magnesium oxide and nano-scale TiO.sub.2 provided according to the contents of Li and Co and the waste lithium cobaltate cathode material powder were mixed to obtain a mixture, wherein in the mixture, a molar ratio of Li:M (M=Mg+Ti+Co) was 1.03:1, and a molar ratio of Co:Mg:Ti was 0.98:0.01:0.01; the mixture was placed into a ball mill tank, absolute ethanol as a dispersing agent was added to reach ⅔ height of the ball mill tank, and the resulting mixture was subjected to a ball milling, wherein the ball milling was performed in a mass ratio of ball-to-material of 5:1, and at a ball milling rate of 200 r/min for 1 hour. After the ball milling was completed, the mixture was dried in a blast drying oven at 100° C. for 15 hours to obtain a mixed powder;

(9) (3) the mixed powder was placed in a muffle furnace and calcined at a temperature of 800° C. for 20 hours in an air atmosphere, to obtain a magnesium-titanium co-doped regenerated lithium cobaltate cathode material;

(10) (4) aluminum isopropoxide and absolute ethanol were ultrasonically mixed for 30 minutes with a mass-volume ratio of 4 g:1000 mL to obtain a mixed solution; the magnesium-titanium co-doped regenerated lithium cobaltate cathode material was added into the mixed solution with a mass-volume ratio of 0.04 g:1 mL, and the resulting mixture was heated and stirred at a temperature of 40° C. until the solvent in the mixed solution evaporates to obtain a residue; and

(11) (5) the residue was calcined in a muffle furnace under an air atmosphere at a temperature of 750° C. for 5 hours, to obtain an aluminum-coated magnesium-titanium co-doped regenerated lithium cobaltate cathode material.

(12) FIG. 2 shows the XRD diagram of the waste lithium cobaltate cathode material and the prepared regenerated lithium cobaltate material in Example 1. As can be seen from FIG. 2, the waste lithium cobaltate cathode material and the regenerated lithium cobaltate cathode material both belong to the R-3m space group, have a layered hexagonal structure, while the regenerated lithium cobaltate cathode material does not contain Co.sub.3O.sub.4 impurity phase, shows good crystallinity, and has effectively repaired crystal structures.

Example 2

(13) A method for preparing a high-voltage cathode material by body modification and regeneration of a waste lithium cobaltate material, specifically including the following steps:

(14) (1) a waste lithium cobaltate battery was completely soaked in a solution with a concentration of sodium chloride of 1 mol/L for 48 hours, then the waste lithium cobaltate battery was manually disassembled and peeled off to obtain a waste lithium cobaltate cathode sheet, then the waste lithium cobaltate cathode sheet was completely soaked in a solution with a concentration of sodium hydroxide of 3 mol/L, and stirred and reacted for 5 hours, the resulting mixture was filtered, and the filter cake was washed to obtain a waste lithium cobaltate cathode material; the waste lithium cobaltate cathode material was placed in a muffle furnace and calcined at 500° C. for 5 hours under an air atmosphere to obtain a waste lithium cobaltate cathode material powder; the contents of Li and Co in the obtained waste lithium cobaltate cathode material powder were measured;

(15) (2) lithium hydroxide powder, magnesium hydroxide powder and nano-scale TiO.sub.2 provided according to the contents of Li and Co and the waste lithium cobaltate cathode material powder were mixed to obtain a mixture, wherein in the mixture, a molar ratio of Li:M (M=Mg+Ti+Co) was 1.08:1, and a molar ratio of Co:Mg:Ti was 0.94:0.04:0.02; the mixture was placed into a ball mill tank, absolute ethanol as a dispersing agent was added to reach ⅔ height of the ball mill tank, and the resulting mixture was subjected to a ball milling, wherein the ball milling is performed in a mass ratio of ball-to-material of 10:1, and at a ball milling rate of 100 r/min for 2 hours. After the ball milling is completed, the mixture was dried in a blast drying oven at 90° C. for 20 hours to obtain a mixed powder;

(16) (3) the mixed powder was placed in a muffle furnace and calcined at a temperature of 1000° C. for 12 hours in an air atmosphere, to obtain a magnesium-titanium co-doped regenerated lithium cobaltate cathode material;

(17) (4) aluminum tri-sec-butoxide and absolute ethanol were ultrasonically mixed for 30 minutes with a mass-volume ratio of 0.08 g:1000 mL to obtain a mixed solution; the magnesium-titanium co-doped regenerated lithium cobaltate cathode material was added into the mixed solution with a mass-volume ratio of 0.02 g:1 mL, and the resulting mixture was heated and stirred at a temperature of 70° C. until the solvent in the mixed solution evaporates to obtain a residue; and

(18) (5) the residue was calcined in a muffle furnace under an air atmosphere at a temperature of 600° C. for 6 hours, to obtain an aluminum-coated magnesium-titanium co-doped regenerated lithium cobaltate cathode material.

(19) FIG. 3 shows the EDS diagram of the magnesium-titanium co-doped regenerated lithium cobaltate cathode material prepared in Example 2. As can be seen from FIG. 3, cobalt, magnesium and titanium are evenly distributed in the cathode material obtained after ball milling and calcining of waste lithium cobaltate cathode material powder.

Example 3

(20) A method for preparing a high-voltage cathode material by body modification and regeneration of a waste lithium cobaltate material, specifically including the following steps:

(21) (1) a waste lithium cobaltate battery was completely soaked in a solution with a concentration of sodium chloride of 3 mol/L for 24 hours, then the waste lithium cobaltate battery was manually disassembled and peeled off to obtain a waste lithium cobaltate cathode sheet, then the waste lithium cobaltate cathode sheet was completely soaked in a solution with a concentration of sodium hydroxide of 1 mol/L, and stirred and reacted for 15 hours, the resulting mixture was filtered, and the filter cake was washed to obtain a waste lithium cobaltate cathode material; the waste lithium cobaltate cathode material was placed in a muffle furnace and calcined at 700° C. for 2 hours under an air atmosphere to obtain a waste lithium cobaltate cathode material powder; the contents of Li and Co in the obtained waste lithium cobaltate cathode material powder were measured;

(22) (2) lithium carbonate, magnesium oxide and nano-scale TiO.sub.2 provided according to the contents of Li and Co and the waste lithium cobaltate cathode material powder were mixed to obtain a mixture, wherein in the mixture, a molar ratio of Li:M (M=Mg+Ti+Co) was 1.1:1, and a molar ratio of Co:Mg:Ti was 0.9:0.05:0.05; the mixture was placed into a ball mill tank, absolute ethanol as a dispersing agent was added to reach ⅔ height of the ball mill tank, and the resulting mixture was subjected to a ball milling, wherein the ball milling is performed in a mass ratio of ball-to-material of 15:1, and at a ball milling rate of 300 r/min for 0.5 hours. After the ball milling is completed, the mixture was dried in a blast drying oven at 150° C. for 10 hours to obtain a mixed powder;

(23) (3) the mixed powder was placed in a muffle furnace and calcined at a temperature of 1100° C. for 10 hours in an air atmosphere, to obtain a magnesium-titanium co-doped regenerated lithium cobaltate cathode material;

(24) (4) aluminum isopropoxide and absolute ethanol were ultrasonically mixed for 30 minutes with a mass-volume ratio of 0.5 g:1000 mL to obtain a mixed solution; the magnesium-titanium co-doped regenerated lithium cobaltate cathode material was added into the mixed solution with a mass-volume ratio of 0.025 g:1 mL, and the resulting mixture was heated and stirred at a temperature of 60° C. until the solvent in the mixed solution evaporates to obtain a residue; and

(25) (5) the residue was calcined in a muffle furnace under an air atmosphere at a temperature of 900° C. for 2 hours, to obtain an aluminum-coated magnesium-titanium co-doped regenerated lithium cobaltate cathode material.

(26) As shown in FIG. 4, the electrochemical performance of the waste lithium cobaltate cathode material and the regenerated lithium cobaltate cathode material in the half-cell (3-4.5V) were evaluated. The specific discharge capacity of the waste lithium cobaltate cathode material and the regenerated lithium cobaltate cathode material in the first cycle at 1C (1C=150 mAh.Math.g.sup.−1) is 142.2 mAh.Math.g.sup.−1 and 179.62 mAh.Math.g.sup.−1 respectively; after 30 cycles, the capacity retention rate of the regenerated lithium cobaltate cathode material is 98.69%, while that of the waste lithium cobaltate cathode material is 96.2%.

(27) The present application describes the process method of the disclosure by the above-mentioned examples, but is not limited to the above-mentioned process steps. Those skilled in the art should understand that the equivalent replacement of the raw materials selected, the addition of auxiliary components, and the choice of the specific manners in the present disclosure all fall within the scope of protection and disclosure of the present disclosure.