Lithium ion battery positive electrode material, preparation method and lithium ion battery
A technology for lithium ion batteries and cathode materials, which is applied in the fields of lithium ion battery materials, cathode materials for lithium ion batteries, and preparation, can solve the problems of uncontrollable coating thickness, low electronic conductivity, gel, etc., and achieves the electrochemical performance of the battery. Lifting, high ionic conductivity, effect of simplifying the pulping process
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[0051] Embodiments of the present disclosure also provide a method for preparing a positive electrode material for a lithium-ion battery, the method comprising:
[0052] Prepare the main body of the positive electrode material of the lithium ion battery;
[0053] Covering the outer surface of the main body of the positive electrode material of the lithium ion battery with a Si-O layer;
[0054] coating the outer surface of the Si-O layer with a conductive polymer layer;
[0055] A conductive carbon material layer is coated on the outer surface of the conductive polymer layer.
[0056] By adopting the above preparation method, the outer surface of the main body can be coated with a Si—O layer, a conductive polymer layer and a conductive carbon material layer in sequence.
[0057] Described preparation method specifically comprises:
[0058] S101. Preparing a nickel-cobalt-manganese hydroxide precursor, mixing the nickel-cobalt-manganese hydroxide precursor with a lithium sou...
Embodiment 1
[0077] S101, according to Ni element, Co element, Mn element molar ratio is 8:1:1 NiSO 4 ·6H 2 O, CoSO 4 ·7H 2 O and MnSO 4 ·6H 2 O is dissolved in deionized water to form a 1.5mol / L mixed metal ion solution; under a nitrogen atmosphere, the mixed metal ion solution, ammonia water and NaOH solution are mixed to obtain a mixed solution, and the mixed solution is stirred for 24 hours and then co-precipitated to get spherical Ni 0.8 co 0.1 mn 0.1 (OH) 2 powder, the spherical Ni 0.8 co 0.1 mn 0.1 (OH) 2 After the powder was filtered, it was washed several times with deionized water at 60 °C, and then vacuum-dried at 120 °C for 12 h to obtain Ni 0.8 co 0.1 mn 0.1 (OH) 2 Precursor; the Ni 0.8 co 0.1 mn 0.1 (OH) 2 The precursor and lithium hydroxide monohydrate are uniformly mixed according to the molar ratio of Li element to M element Li / M=1.05, pre-calcined at 200°C-1200°C, and then calcined in an oxygen atmosphere of 600°C-2000°C to produce Lithium-nickel-cobal...
Embodiment 2
[0082] S101, according to Ni element, Co element, Mn element molar ratio is 8:1:1 NiSO 4 ·6H 2 O, CoSO 4 ·7H 2 O and MnSO 4 ·6H 2 O is dissolved in deionized water to form a 1.5mol / L mixed metal ion solution; under a nitrogen atmosphere, the mixed metal ion solution, ammonia water and NaOH solution are mixed to obtain a mixed solution, and the mixed solution is stirred for 20 hours and then co-precipitated to get spherical Ni 0.8 co 0.1 mn 0.1 (OH) 2 powder, the spherical Ni 0.8 co 0.1 mn 0.1 (OH) 2 After the powder was filtered, it was washed several times with deionized water at 50 °C, and then vacuum-dried at 150 °C for 10 h to obtain Ni 0.8 co 0.1 mn 0.1 (OH) 2 Precursor; the Ni 0.8 co 0.1 mn 0.1 (OH) 2 The precursor and lithium hydroxide monohydrate are uniformly mixed according to the molar ratio of Li element to M element Li / M=1, pre-calcined at 200°C-1200°C, and then calcined in an oxygen atmosphere of 600°C-2000°C to produce Lithium-nickel-cobalt-m...
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