Positive electrode active material and preparation method thereof, positive electrode and lithium ion battery
A technology of positive electrode active materials and ternary materials, which is applied in the field of preparation of positive electrode active materials, and can solve problems such as high energy consumption, high cost, and cumbersome process
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[0050] The embodiment of the present application provides a method for preparing a positive electrode active material, comprising the following steps:
[0051] Step S1: providing nickel salt, cobalt salt, manganese salt, lithium salt, strong lye, and coated co-dopants;
[0052] Step S2: mixing the nickel salt, cobalt salt, manganese salt, and strong lye to obtain a mixed solution;
[0053] Step S3: Under an inert atmosphere, heat the mixed solution to obtain a nickel-cobalt-manganese precursor, the structural formula of the nickel-cobalt-manganese precursor is Ni x co y mn z (OH) 2 , wherein, x+y+z=1, 0.33<x<1, 0<y<0.33, 0<z<0.33;
[0054] Step S4: mixing the nickel-cobalt-manganese precursor, the lithium salt, and the coated co-dopant to obtain a mixture;
[0055] Step S5: Sintering the mixture under an oxygen atmosphere to obtain a positive electrode active material, the positive electrode active material includes a nickel-cobalt-manganese ternary material and a coating...
Embodiment 1
[0107] Provides Ni(NO 3 ) 2 ·6H 2 O, Co(NO 3 ) 2 ·6H 2 O, Mn(NO 3 ) 2 ·6H 2 O, water, wherein the molar ratio of Ni:Co:Mn is 8:1:1;
[0108] Ni(NO 3 ) 2 ·6H 2 O, Co(NO 3 ) 2 ·6H 2 O, Mn(NO 3 ) 2 ·6H 2 O is added to water to obtain a mixed solution, and the sum of the ion concentrations of the mixed solution is 2mol / L;
[0109] Provide the sodium hydroxide solution that concentration is 4mol / L and the ammonia solution that concentration is 4mol / L;
[0110] Pour the mixed solution, sodium hydroxide solution, and ammonia solution into the reactor simultaneously at the speed of 30ml / min, 10ml / min, and 8ml / min, respectively, to obtain a mixed solution with a pH value of 11.2;
[0111] Heating the mixed solution to 50°C, feeding nitrogen gas into the reactor, and continuously stirring the mixed solution at a speed of 300r / min, and filtering to obtain nickel-cobalt-manganese precursor precipitation;
[0112] After washing the precipitation of the nickel-cobalt-mang...
Embodiment 2
[0125] The difference from Example 1 includes: in the mixture, the mass percentage content of the sodium monofluorophosphate is 1wt.%.
[0126] Other steps are the same as in Embodiment 1 and will not be repeated.
[0127] see image 3 , the XRD diffraction peaks of the positive electrode active material in Example 2 are sharp, indicating that the positive electrode active material in Example 2 has high crystallinity and no impurity phase.
[0128] see Figure 4 , the positive electrode active material in the second embodiment has a coating layer.
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Abstract
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