Solid-state electrochemical cell
US-2024429457-A1 · Dec 26, 2024 · US
US10020488B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10020488-B2 |
| Application number | US-201314766874-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 20, 2013 |
| Priority date | Feb 13, 2013 |
| Publication date | Jul 10, 2018 |
| Grant date | Jul 10, 2018 |
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This disclosure synthesizes an anodic composite material Li(Li x Ni y Co z Mn w O 2+α ) of Li 2 MnO 3 series whose theoretical capacity is a level of about 460 mAh/g, and to produce an electrode of a high capacity using the synthesized anodic composite material. Also provided is a method for charging and discharging the electrode. Here, the method for producing an anodic composite material for a lithium secondary battery includes the steps of: mixing a nickel nitrate solution, a manganese nitrate solution, and a cobalt nitrate solution to produce a starting material solution; and mixing the starting material solution with a complexing agent so as to produce an anodic composite material Li(Li x Ni y Co z Mn w O 2+α ) of Li 2 MnO 3 series by means of coprecipitation.
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The invention claimed is: 1. A method of preparing an anode composite material for a lithium secondary battery, the method comprising: mixing an aqueous nickel nitrate solution, an aqueous manganese nitrate solution, and an aqueous cobalt nitrate solution to form a starting material solution; combining the starting material solution with a complexing agent under basic pH conditions maintained through addition of an aqueous NaOH solution to form an anode composite material precursor through a coprecipitation reaction, the anode composite material precursor comprising Li 2 MnO 3 in a mixture ratio of 21.3% to 29.2%; mixing the anode composite material precursor with LiOH·H 2 O to form a mixed powder; subjecting the mixed powder to a first sintering process to form a synthesized powder; and subjecting the synthesized powder to a second sintering process to form an anode composite material powder comprising Li(Li x Ni y Co z Mn w O 2+α ), wherein x is 0.2 to 0.5, y is 0.1 to 0.2, z is 0.1 to 0.2, and w is 0.5 to 0.7. 2. The method of claim 1 , wherein the anode composite material powder comprises Li 1.5 (Ni 0.17 Mn 0.66 Co 0.17 )O 2 . 3. The method of claim 1 , wherein subjecting the mixed powder to a first sintering process comprises heating the mixed powder at a temperature of 500° C. 4. The method of claim 1 , wherein subjecting the synthesized powder to a second sintering process comprises heating the synthesized powder at a temperature of 650° C. to 1000° C. 5. The method of claim 1 , wherein the Li(Li x Ni y Co z Mn w O 2+α ) of the anode composite material powder exhibits two super lattice peaks at a temperature greater than or equal to 800° C. 6. The method of claim 1 , wherein mixing an aqueous nickel nitrate solution, an aqueous manganese nitrate solution, and an aqueous cobalt nitrate solution comprises mixing Ni(NO 3 ) 2 ·H 2 O, Mn(NO 3 ) 2 ·H 2 O and Co(NO 3 ) 2 ·H 2 O at a molar ratio of 1:4:1. 7. The method of claim 1 , wherein combining the starting material solution with a complexing agent comprises combining the starting material solution with 0.8 mole ammonia water. 8. The method of claim 1 , further comprising selecting the aqueous NaOH solution to comprise a 1 M aqueous NaOH solution prepared by dissolving NaOH powder in water. 9. The method of claim 1 , wherein mixing the anode composite material precursor with LiOH·H 2 O comprises adding 103% by weight (wt %) of the LiOH·H 2 O to the anode composite material precursor. 10. The method of claim 1 , wherein combining the starting material solution with a complexing agent under basic pH conditions maintained through addition of an aqueous NaOH solution comprises maintaining a pH of 11 through the addition of the aqueous NaOH solution. 11. The method of claim 1 , wherein combining the starting material solution with a complexing agent under basic pH conditions maintained through addition of an aqueous NaOH solution comprises: titrating the starting material solution at a rate of about 4 milliliters per minute; titrating the complexing agent at a rate of about 4 milliliters per minute; and titrating the aqueous NaOH solution to maintain basic pH during the coprecipitation reaction. 12. A method of manufacturing an electrode of a lithium secondary battery, the method comprising: mixing an aqueous nickel nitrate solution, an aqueous manganese nitrate solution, and an aqueous cobalt nitrate solution to form a starting material solution; combining the starting material solution with a complexing agent under basic pH conditions maintained through addition of an aqueous NaOH solution to form an anode composite material precursor through a coprecipitation reaction, the anode composite material precursor comprising Li 2 MnO 3 in a mixture ratio of 21.3% to 29.2%; mixing the anode composite material precursor with LiOH·H 2 O to form a mixed powder; subjecting the mixed powder to a first sintering process to form a synthesized powder; and subjecting the synthesized powder to a second sintering process to form an anode composite material powder comprising Li(Li x Ni y Co z Mn w O 2+α ), wherein x is 0.2 to 0.5, y is 0.1 to 0.2, z is 0.1 to 0.2, and w is 0.5 to 0.7; mixing the anode composite material powder with a conductive agent and a binder to form a slurry; applying the slurry to a foil structure to form a slurry film; drying the slurry film to form a dried slurry film; pressing the dried slurry film to form a pressed slurry film; punching the pressed slurry film to form an anode; and forming a cell using the anode. 13. The method of claim 12 , wherein forming a cell using the anode comprises forming a coin cell or three-electrode cell. 14. The method of claim 13 , wherein forming a cell comprises forming the coin cell, the coin cell comprising the anode, a cathode of lithium metal, a PE separator as a separator membrane, and an electrolyte obtained by dissolving 1 mole of LiPF 6 in a mixture of ethylene carbonate and dimethyl carbonate at a volume ratio of 1:1. 15. The method of claim 13 , wherein forming a cell comprises forming the three-electrode cell, the three-electrode cell comprising the anode, an auxiliary electrode of lithium metal, a reference electrode of lithium metal, a PE separator as a separator membrane, and an electrolyte obtained by dissolving 1 mole of LiPF 6 in a mixture solvent of ethylene carbonate and dimethyl carbonate at a volume ratio of 1:1. 16. The method of claim 12 , wherein mixing the anode composite material powder with a conductive agent and a binder comprises mixing the anode composite material powder, the conductive agent, and the binder at a weight percentage (wt %) ratio of 80:10:10. 17. The method of claim 12 , wherein applying the slurry to a foil comprises applying the slurry to aluminum foil to a thickness of 100 μm to 110 μm. 18. The method of claim 17 , wherein pressing the dried slurry film comprises forming the pressed slurry film to exhibit a thickness of 60 μm to 70 μm on the aluminum foil. 19. A method of charging and discharging a lithium secondary battery which repeats charging and discharging of a cell with a constant current and a constant voltage in a range of 2.0 to 4.6 V, the cell comprising an anode formed by the process comprising: mixing an aqueous nickel nitrate solution, an aqueous manganese nitrate solution, and an aqueous cobalt nitrate solution to form a starting material solution; combining the starting material solution with a complexing agent under basic pH conditions maintained through addition of an aqueous NaOH solution to form an anode composite material precursor through a coprecipitation reaction, the anode composite material precursor comprising Li 2 MnO 3 in a mixture ratio of 21.3% to 29.2%; mixing the anode composite material precursor with LiOH·H 2 O to form a mixed powder; subjecting the mixed powder to a first sintering process to form a synthesized powder; and subjecting the synthesized powder to a second sintering process to form an anode composite material powder comprising Li(Li x Ni y Co z Mn w O 2+α ), wherein x is 0.2 to 0.5, y is 0.1 to 0.2, z is 0.1 to 0.2, and w is 0.5 to 0.7. 20. The method of claim 19 , wherein oxidation and reduction behavior of lithium as an anode material of the cell is identified using a three-electrode cell at a scan rate of 0.05 mV/S in a charge and discharge voltage range of 2.0 to 4.9 V by a potential sweep method.
Polyolefins · CPC title
involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis · CPC title
Cross-Sectional Technologies · mapped topic
Electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx · CPC title
of electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx · CPC title
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