Modified nickel cobalt manganese ternary composite electrode material coated on oxide surface and preparation method thereof
A composite electrode and surface coating technology, applied in active material electrodes, positive electrodes, battery electrodes, etc., can solve the problems of reducing surface impedance, fast capacity decay, poor stability of nickel-cobalt-manganese ternary electrode materials, etc. Impedance, low cost, effect of enhancing cycle stability
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Embodiment 1
[0030] Weigh 3.3g of lithium acetate, 5.31g of nickel acetate, 1.77g of cobalt acetate, and 1.73g of manganese acetate in a ball mill jar, add 100ml of absolute ethanol, and then add 0.0486g of niobium oxide and 0.0486g of zirconium oxide into the above solution. The above solution was fully dispersed and ball milled for 4 hours to obtain a uniformly dispersed solution, and the above solution was dried in an oven at 100° C. to obtain a dry oxide-coated nickel-cobalt-manganese composite electrode material precursor. Put this precursor in a box furnace, calcinate at 900°C for 24 hours, and the heating rate is 3°C / min, and prepare niobium oxide and zirconium oxide coatings, with an oxide coating with a mass percentage of about 2%. Nickel-cobalt-manganese composite electrode material. The composite electrode material was assembled into a button battery for charge and discharge tests, and compared with the uncoated nickel-cobalt-manganese electrode material. According to the test,...
Embodiment 2
[0032] Weigh 3.3g of lithium acetate, 5.3g of nickel acetate, 1.77g of cobalt acetate, and 1.73g of manganese acetate in a ball mill jar, add 100ml of absolute ethanol, and then add 0.097g of niobium oxide and 0.097g of zirconium oxide into the above solution. The above solution was fully dispersed and ball milled for 4 hours to obtain a uniformly dispersed solution, and the above solution was dried in an oven at 100° C. to obtain a dry oxide-coated nickel-cobalt-manganese composite electrode material precursor. The precursor was placed in a box furnace and calcined at 900°C for 24 hours with a heating rate of 3°C / min to prepare an oxide coating with a mass percentage of niobium oxide and zirconium oxide coatings of about 4%. Nickel-cobalt-manganese composite electrode material. The composite electrode material was assembled into a button battery for charge and discharge tests, and compared with the uncoated nickel-cobalt-manganese electrode material. After testing, the nicke...
Embodiment 3
[0034] Weigh 3.3g of lithium acetate, 5.31g of nickel acetate, 1.77g of cobalt acetate, and 1.73g of manganese acetate in a ball mill jar, add 100ml of absolute ethanol, and then add 0.146g of niobium oxide and 0.146g of zirconium oxide into the above solution. The above solution was fully dispersed and ball milled for 4 hours to obtain a uniformly dispersed solution, and the above solution was dried in an oven at 100° C. to obtain a dry oxide-coated nickel-cobalt-manganese composite electrode material precursor. The precursor was placed in a box furnace, calcined at 900°C for 24 hours, and the heating rate was 3°C / min, and an oxide coating with a mass percentage of niobium oxide and zirconium oxide coating layers of about 6% was prepared. Nickel-cobalt-manganese composite electrode material. The composite electrode material was assembled into a button battery for charge and discharge tests, and compared with the uncoated nickel-cobalt-manganese electrode material. According ...
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