Nickel-based active material precursor, method of preparing same, nickel-based active material, and lithium secondary battery
A lithium secondary battery and active material technology, applied in the direction of secondary batteries, lithium batteries, active material electrodes, etc., can solve the problems of lithium secondary battery deterioration, long-term life, low charging/discharging efficiency, increased resistance, etc.
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[0032] According to one embodiment, a nickel-based active material precursor for a lithium secondary battery includes a secondary particle comprising a plurality of granular structures, wherein each granular structure includes a porous core portion and a shell portion, wherein the The shell portion includes primary particles radially arranged on the porous core portion, and wherein the secondary particles have a plurality of radial centers.
[0033] refer to figure 1 , a nickel-based active material precursor for a lithium secondary battery includes secondary particles 200 including a plurality of granular structures 100 . refer to Figure 2A and 2B , the granular structures 100 each include a porous core portion 10 and a shell portion 20 including primary particles 30 radially arranged on the porous core portion 10 . refer to figure 1 , 2A and 2B, the secondary particle 200 includes the granular structures 100, and the granular structures 100 each have a radial center. ...
preparation Embodiment 1
[0103] Preparation Example 1: Preparation of nickel-based active material precursor (6:2:2): three-step method
[0104] Synthesis of nickel-based active material precursors (Ni 0.6 co 0.2 mn 0.2 (OH) 2 ). In the following preparation process, nickel sulfate (NiSO 4 ·6H 2 O), cobalt sulfate (CoSO 4 ·7H 2 O) and manganese sulfate (MnSO 4 ·H 2 O) Dissolved in distilled water as a solvent at a molar ratio of 6:2:2 to prepare a mixed solution. In addition, in order to form complex compounds, sodium hydroxide (NaOH) and ammonia water (NH 4 OH).
[0105] Step 1: 5.0L / hour feed rate, 1.5kW / m 3 stirring power, NH 4 OH 0.35M, 10.5 to 11.0 pH
[0106] Aqueous ammonia was added to a reactor equipped with a stirrer at a concentration of 0.35 mol / L (M). Maintaining 1.5kW / m 3 While the stirring power and the reaction temperature of 50 ℃, add the metal raw material (the mixed solution of nickel sulfate, cobalt sulfate and manganese sulfate) of 2mol / L (M) with the feed r...
preparation Embodiment 2
[0111] Preparation Example 2: Preparation of Nickel-Based Active Material Precursor (7:1.5:1.5)
[0112] A mixed solution was prepared in the same manner as in Preparation Example 1, except that nickel sulfate (NiSO 4 ·6H 2 O), cobalt sulfate (CoSO 4 ·7H 2 O) and manganese sulfate (MnSO 4 ·H 2 O) As the metal raw material, the molar ratio of 7:1.5:1.5 is mixed instead of 6:2:2, and the nickel-based active material precursor (Ni 0.7 co 0.15 mn 0.15 (OH) 2 ).
[0113] Step 1: 5.0L / hour feed rate, 3.0kW / m 3 stirring power, NH 4 OH 0.35M, 11.0 to 11.5 pH
[0114] Aqueous ammonia was added to a reactor equipped with a stirrer at a concentration of 0.35 mol / L (M). Maintaining 3.0kW / m 3While the stirring power and the reaction temperature of 50 ℃, add the metal raw material (the mixed solution of nickel sulfate, cobalt sulfate and manganese sulfate) of 2mol / L (M) with the feed rate of 5.0L / hour and 0.53L / hour respectively And 0.35mol / L (M) ammonia water. Subse...
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