Lithium secondary battery lithium-rich cathode composite and preparation method thereof
A lithium secondary battery, composite material technology, applied in battery electrodes, circuits, electrical components, etc., can solve problems such as poor cycle performance
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[0041] The invention provides a method for preparing a lithium-rich cathode composite material for a lithium secondary battery, comprising the following steps:
[0042] Precipitating a reaction solution containing nickel salt, cobalt salt, manganese salt, sodium carbonate and a chelating agent to obtain a precursor;
[0043] Pre-calcining the precursor to obtain a pre-calcining precursor;
[0044] Calcining the mixture comprising the pre-calcined precursor and the lithium salt for the first time to obtain a matrix material;
[0045] The matrix material and the tungsten salt are mixed and calcined for the second time to obtain a lithium-rich cathode composite material.
[0046] In the invention, the reaction solution containing nickel salt, cobalt salt, manganese salt, sodium carbonate and chelating agent is subjected to precipitation reaction to obtain the precursor. In the present invention, the nickel salt is preferably one, two or three of nickel carbonate, nickel sulfate...
Embodiment 1
[0074] Add ammonia water dropwise to the mixed solution of 0.5 mol / L nickel nitrate, 0.5 mol / L cobalt carbonate and 2 mol / L manganese sulfate until the concentration of ammonia water is 0.2 mol / L. Then, add sodium carbonate until the concentration of sodium carbonate is 0.5mol / L. Precipitate at 60°C for 12 hours to obtain a pale yellow solution. After standing for 6 hours, wash with distilled water, filter, and dry the filtered solid at 60°C for 24 hours to obtain the precursor Mn 0.54 Ni 0.13 co 0.13 (CO 3 ) 0.8 .
[0075] The precursor was pre-calcined at 300° C. for 4 hours to obtain a pre-calcined precursor. A mixture of 1 part by mass of the pre-calcined precursor and 0.8 parts by mass of lithium carbonate was ball milled at a speed of 200 r / min for 8 hours, and the mixture obtained by ball milling was calcined at 800 °C for 12 hours in an air atmosphere, and then cooled to room temperature to obtain a matrix material LMSS.
[0076] Dissolve 1 part by mass of LMSS...
Embodiment 2
[0083] to 0.5mol / L NiSO 4 .6H 2 O, 0.5mol / L CoSO 4 .7H 2 O, 2mol / L MnSO 4 .H 2 Aqueous ammonia was added dropwise to the mixed solution of O to a concentration of 0.5mol / L. Then, add sodium carbonate until the concentration of sodium carbonate is 0.2mol / L. The precipitation reaction was carried out at 80° C. for 10 hours to obtain a pale yellow solution. After standing for 6 hours, wash with distilled water, filter, and dry the filtered solid at 60°C for 24 hours to obtain the precursor Mn 0.54 Ni 0.13 co 0.13 (CO 3 ) 0.8 .
[0084] The precursor was pre-calcined at 450° C. for 8 hours to obtain a pre-calcined precursor. A mixture of 1 mass part of pre-calcined precursor and 0.8 mass part of lithium carbonate was ball milled at a speed of 250r / min for 8 hours, and the mixture obtained by ball milling was calcined at 900°C for 10h in an air atmosphere, and then cooled to room temperature to obtain a matrix material LMSS.
[0085] Dissolve 1 part by mass of LMSS an...
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