Positive electrode material for lithium ion cell, its preparing method and lithium ion cell
A technology for lithium ion batteries and cathode materials, which is applied in the field of cathode materials for lithium ion batteries, can solve the problems of poor homogeneity of target products, no commercial value, small particles, etc., and achieves improved high temperature cycle stability, simple and easy implementation process, Reduces the effect of oxidative decomposition reactions
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Embodiment 1
[0028] Example 1 Functional Polymerization Modified LiMn 2 o 4 Preparation of polymers used in electrode sheets
[0029] The mass ratio of monomer acrylonitrile (AN): monomer N-vinylpyrrolidone (NVP) is respectively 7: 2, 5: 4, 6: 3, 8: 7 and 8: 5. 1%, 3%, 5%, and 5% of the total mass of the monomers were added into the initiator AIBN, a certain amount of secondary deionized water was added, and nitrogen gas was passed through for half an hour to remove oxygen in the reaction system. Heating and constant temperature to 65°C, the reaction was terminated after 6 hours of reaction, the prepared polymer was suction filtered, and dried in a vacuum drying oven to obtain a polymer containing functional groups capable of complexing with Mn ions.
Embodiment 2
[0031] The preparation method of the polymer of this embodiment is the same as that of Example 1, and the difference is that acrylamide (AM) monomer is added, and the mass ratio of the reaction raw materials is AN: AM: NVP=5: 4: 2, 6 : 4: 1 and 7: 3: 1, the prepared polymers are all white powdery solids.
Embodiment 3
[0033] In this embodiment, the polymer used to modify the lithium manganate functional material is obtained by copolymerizing the monomer acrylamide (AM) and the monomer cis-2-butenoic anhydride (MAH) in the oil phase, and the mass ratio of the reaction raw materials is The ratio is: AM:MAH=1.3:1.0, and the product is a white solid.
[0034] The preparation method of the functional material polymer used for modifying the lithium manganate electrode is as follows: add 10 parts of cis-2-butenoic anhydride and 30 parts of butanone into the reaction vessel, stir and dissolve, the speed is 100 rpm, and nitrogen gas is introduced into the reaction vessel. Drive oxygen for 1 hour; heat and keep the temperature at 60°C; then add 5 parts of initiator azobisisobutyronitrile; add 13 parts of acrylamide and 50 parts of methyl ethyl ketone in a constant pressure dropping funnel, and add dropwise for 4 hours; react 8 hours are over. A polymer of the above composition was prepared.
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