Method for reducing content of residual alkali on surface of positive electrode material and application thereof
A cathode material, surface residue technology, applied in chemical instruments and methods, battery electrodes, nickel compounds, etc., can solve the problems of lithium-ion battery gas production, shortened cycle shelf life, and potential safety hazards, and achieves improved electrochemical performance. performance, improving the capacity fade problem, solving the effect of the hazard
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Embodiment 1
[0057] Weigh 1mol of Ni 0.835 co 0.1074 mn 0.0575 (OH) 2 and 1.02mol of LiOH·H 2 O was placed in a mortar, thoroughly ground and mixed evenly, then placed in a box-type atmosphere furnace at 740°C and oxygen atmosphere for high-temperature sintering for 10 hours, and the material was taken out for ultra-centrifugal grinding and sieving to obtain the positive electrode matrix material; weigh 1mol positive electrode matrix material, 0.01mol Mn(CH 3 COO) 2 , 0.02mol LiOH·H 2 O, placed in a mortar for thorough grinding and mixing, and then placed in a box-type atmosphere furnace for high-temperature sintering at 700°C and oxygen atmosphere for 6h to obtain the final desired positive electrode material.
Embodiment 2
[0059] Weigh 1mol of Ni 0.835 co 0.1074 mn 0.0575 (OH) 2 and 1.02mol of LiOH·H 2 O was placed in a mortar, thoroughly ground and mixed evenly, then placed in a box-type atmosphere furnace at 740°C and oxygen atmosphere for high-temperature sintering for 10 hours, and the material was taken out for ultra-centrifugal grinding and sieving to obtain the positive electrode matrix material; weigh 1mol positive electrode matrix material, 0.03mol Mn(CH 3 COO) 2 , 0.06mol LiOH·H 2 O, placed in a mortar for thorough grinding and mixing, and then placed in a box-type atmosphere furnace for high-temperature sintering at 700°C and oxygen atmosphere for 6h to obtain the final desired positive electrode material.
Embodiment 3
[0061] Weigh 1mol of Ni 0.835 co 0.1074 mn 0.0575 (OH) 2 and 1.02mol of LiOH·H 2 O was placed in a mortar, thoroughly ground and mixed evenly, and then placed in a box-type atmosphere furnace at 740 ° C and oxygen atmosphere for high-temperature sintering for 10 h, and the material was taken out for ultra-centrifugal grinding and sieving; weighed 1 mol of positive electrode material, 0.03 mol Mn(CH 3 COO) 2 , 0.0598molLiOH·H 2 O, placed in a mortar for thorough grinding and mixing, and then placed in a box-type atmosphere furnace for high-temperature sintering at 700°C and oxygen atmosphere for 6h to obtain the final desired positive electrode material.
[0062] Under the same conditions, the positive electrode materials obtained in Examples 1-3 and Comparative Examples 1-2 were evaluated respectively
[0063] 1. The positive electrode materials obtained in Examples 1-3 and Comparative Examples 1-2 are tested for surface residual alkali content
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