Method of manufacturing cathode active material
A technology of positive active material and manufacturing method, which is applied in the direction of active material electrode, electrode manufacturing, positive electrode, etc., and can solve the problems of battery fire and scrapping
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Embodiment 1
[0114] First, nickel sulfate, cobalt sulfate and sodium aluminate were dissolved in water and stirred well, while sodium hydroxide solution was added to obtain a nickel-cobalt-aluminum composite coprecipitation with a molar ratio of Ni:Co:Al=77:20:3 hydroxide. Next, a precursor having a molar ratio of Li:(Ni+Co+Al)=105:100 was obtained by rinsing and drying the coprecipitated hydroxide with water and adding lithium hydroxide hydrate. The precursor was calcined at a temperature of 700° C. for 10 hours in an oxygen atmosphere, cooled to room temperature, and then pulverized, so as to be able to obtain a compound having a composition of Li 11.03 Ni 0.77 Co 0.20 Al 0.03 O 2 Composite oxide particles of lithium nickelate as the main component. In addition, the average particle diameter of the obtained composite oxide particles was measured by a laser light scattering method, and the obtained diameter value was 13 μm.
[0115] 100 parts by weight of the composite oxide particl...
Embodiment 2
[0117] Different from Example 1, the positive active material was prepared by using 0.34 parts by weight of ammonium pentaborate ((NH 4 ) 2 ·5B 2 O 3 ·8H 2 O) instead of 0.83 parts by weight of ammonium sulfate ((NH 4 ) 2 SO 4 ) obtained. Other conditions were set to be the same as those of Example 1.
Embodiment 3
[0119] Different from Example 1, the positive active material was prepared by using 0.83 parts by weight of ammonium sulfate ((NH 4 ) 2 SO 4 ) and 0.17 parts by weight of ammonium pentaborate ((NH 4 ) 2 ·5B 2 O 3 ·8H 2 O) mixture instead of 0.83 parts by weight of ammonium sulfate ((NH 4 ) 2 SO 4 ) obtained. Other conditions were set to be the same as those of Example 1.
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