Method for improving cycle performance of lithium nickel manganese oxide lithium ion cathode material
A lithium nickel manganese oxide and positive electrode material technology, applied in the field of lithium ion battery positive electrode materials, can solve the problems of inapplicability to large-scale industrial production, difficulty in controlling the operation of the coating process, and difficulty in industrial production of the solution method, achieving easy operation, The effect of good material consistency and improved cycle performance
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Embodiment 1
[0026] Weigh 371.86g of lithium carbonate, 382.12g of nickel oxide, and 1322.12g of manganese dioxide, add 2.1L of absolute ethanol, mix in a stirring mill for 4h and stir evenly, dry in a blast drying oven at 80°C and place in a muffle furnace for 600 Sintering at ℃ for 6h to obtain lithium nickel manganese oxide precursor;
[0027] Weigh 1500g of lithium nickel manganese oxide precursor, weigh 62.4g of lithium carbonate, 64.6g of ammonium metavanadate, and 50g of dispersant PEG4000 according to the lithium vanadate content of 5%wt, add 1.6L of absolute ethanol and mix in a stirring mill for 4h , the precursor was dried in a blast drying oven at 80°C and then sintered in a muffle furnace at 900°C for 12h to obtain a lithium vanadate-coated lithium nickel manganese oxide lithium ion cathode material.
Embodiment 2
[0029] Weigh 371.86g of lithium carbonate, 382.12g of nickel oxide, and 1322.12g of manganese dioxide, add 2.1L of absolute ethanol, mix in a stirring mill for 4h and stir evenly, dry in a blast drying oven at 80°C and place in a muffle furnace for 500 ℃ sintering for 8h to obtain lithium nickel manganese oxide precursor;
[0030] Weigh 1500g of finished lithium nickel manganese oxide, weigh 62.4g of lithium carbonate, 64.6g of ammonium metavanadate, and 50g of dispersant PEG4000 according to the lithium vanadate content of 5%wt, add 1.6L of absolute ethanol and mix in a 10L stirring mill for 4h, The precursor was dried in a blast drying oven at 80°C, and then sintered in a muffle furnace at 900°C for 12 hours to obtain lithium vanadate-coated lithium nickel manganate lithium ion cathode material.
Embodiment 3
[0032] Weigh 371.86g of lithium carbonate, 382.12g of nickel oxide, and 1322.12g of manganese dioxide, add 2.1L of absolute ethanol, mix in a stirring mill for 4h and stir evenly, dry in a blast drying oven at 80°C and place in a muffle furnace for 600 Sintering at ℃ for 6h to obtain lithium nickel manganese oxide precursor;
[0033] Weigh 1500g of finished lithium nickel manganese oxide, weigh 24.5g of lithium carbonate, 25.9g of ammonium metavanadate, and 50g of dispersant PEG4000 according to the lithium vanadate content of 2%wt, add 1.6L of absolute ethanol and mix in a stirring mill for 4h, the precursor The body was dried in a blast drying oven at 80°C, and then sintered in a muffle furnace at 900°C for 12 hours to obtain a lithium vanadate-coated lithium nickel manganese oxide lithium ion positive electrode material.
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