Method for preparing nano-scale lithium ion battery anode material
A technology for lithium ion batteries and positive electrode materials, which is applied in battery electrodes, circuits, electrical components, etc., can solve the problems of mechanical mixing uniformity, uneven particle size distribution, large reaction time and energy consumption, and achieves excellent processing performance. The effect of high tap density and reactant activity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0016] Example 1: Lithium nitrate, nickel nitrate, cobalt nitrate, and manganese nitrate were respectively dissolved in deionized water to form a homogeneous solution, wherein the molar ratio of Li:Ni:Co:Mn was 1:0.3:0.4:0.3, and the above solutions were mixed After fully stirring, add 2 times the total amount of all metal ion substances to the above mixed solution of urea solution as a precipitant, then move it into a water bath and heat at a constant temperature of 95°C. After full reaction, LiNi is obtained. 0.3 Co 0.4 Mn 0.3 O 2 The precursor precipitated, filtered and washed with deionized water 3 times the volume of the precipitate for 3 times, and the suspension was spray-dried. The inlet temperature was set to 180°C, and the resulting dried precursor was sintered at 850°C in air Get it in 10 hours figure 1 The spherical aggregate structure α-NaFeO with the primary particle size shown in the nanometer order 2 Type LiNi 0.3 Co 0.4 Mn 0.3 O 2 Cathode material.
Embodiment 2
[0017] Example 2: Lithium nitrate, nickel acetate, cobalt oxalate, and manganese nitrate were respectively dissolved in deionized water to form a homogeneous solution, where the molar ratio of Li:Ni:Co:Mn was 1:0.2:0.6:0.2, and the above solutions were mixed After fully stirring, add 3 times the total amount of all metal ion substances to the above mixed solution as a precipitant urea solution, then move it into a water bath and heat at a constant temperature of 90°C. After full reaction, LiNi is obtained. 0.2 Co 0.6 Mn 0.2 O 2 The precursor precipitates. After filtration, it is washed twice with deionized water 5 times the volume of the precipitate, and the suspension is spray-dried. The inlet temperature is set to 165°C. The resulting dried precursor is sintered at 900°C in the air Within 6 hours, a spherical aggregate structure α-NaFeO with a particle size of nanometers can be obtained 2 Type LiNi 0.3 Co 0.4 Mn 0.3 O 2 Cathode material.
Embodiment 3
[0018] Example 3: Lithium nitrate, nickel sulfate, cobalt oxalate, and manganese nitrate were respectively dissolved in deionized water to form a homogeneous solution, where the molar ratio of Li:Ni:Co:Mn was 1:0.4:0.2:0.4, and the above solutions were mixed After fully stirring, add 3 times the total amount of all metal ion substances to the above mixed solution as a precipitant urea solution, then move it into a water bath and heat at a constant temperature of 85°C. After full reaction, LiNi is obtained. 0.4 Co 0.2 Mn 0.4 O 2 The precursor precipitates, filtered and washed with deionized water twice the volume of the precipitate for 5 times, and the suspension is spray-dried. The inlet temperature is set to 165°C. The resulting dried precursor is sintered in the air at 750°C Within 15 hours, a spherical aggregate structure α-NaFeO with a particle size of nanometers can be obtained 2 Type LiNi 0.4 Co 0.2 Mn 0.4 O 2 Cathode material.
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 