Method for preparing lithium silicate coated lithium ion battery ternary layered anode material
A ternary layered, ion battery technology, applied in the direction of battery electrodes, electrical components, circuits, etc., to achieve the effects of high production efficiency, large output, and easy access to raw materials
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[0015] The preparation method of lithium silicate-coated lithium-ion battery ternary layered cathode material proposed by the present invention comprises the following steps:
[0016] (1) Preparation of oxalate precursor:
[0017] According to the molar ratio NiSO 4 、CoSO 4 , MnSO 4 Dissolve in 50ml of water so that the molar concentration of metal Ni ions, metal Co ions and metal Mn ions is 2mol / L to obtain a mixed solution of metal ions, and then configure NaC with a molar concentration of 2mol / L 2 o 4 Solution 50mL, under magnetic stirring, NaC 2 o 4 The solution was added to the mixed solution of metal ions to produce a precipitate. After stirring for 2 hours, it was centrifuged, and the precipitate was washed twice with deionized water and absolute ethanol respectively, and the precipitate was dried in an oven at 70°C for 12 hours to obtain the Salt precursor, the molecular formula of the oxalate precursor is: Ni 0.333 co 0.333 mn 0.333 C 2 o 4 2H 2 O;
[001...
Embodiment 1
[0024] (1) According to the molar ratio, NiSO 4 、CoSO 4 , MnSO 4 Dissolve in 50ml of water so that the molar concentrations of metal Ni ions, metal Co ions and metal Mn ions are all 2 mol / L to obtain a mixed solution of metal ions. Then configure 2mol / L NaC 2 o 4 Solution 50mL, under magnetic stirring, NaC 2 o 4 The solution was added to the mixed solution of metal ions, and a large amount of precipitation was produced immediately. After stirring for 2 hours, it was centrifuged, washed twice with deionized water and absolute ethanol, and dried in a 70-degree oven for 12 hours to obtain the oxalate precursor. body;
[0025] (2) SiO 2 Synthesis of coated oxalate precursor: Weigh 1.2 mmol of the above-obtained oxalate precursor and disperse it in 13 ml of absolute ethanol, stir and ultrasonically disperse. According to the molar ratio of Si:(Ni+Co+Mn)=3:100, Si(OC 2 h 5 ) 4Anhydrous ethanol solution, stir to disperse evenly. Then the mixed solution was transferred to ...
Embodiment 2
[0029] (1) Preparation of oxalate precursor: mix NiSO 4 、CoSO 4 , MnSO 4 Dissolve in 50ml of water so that the molar concentrations of metal Ni ions, metal Co ions and metal Mn ions are all 2 mol / L to obtain a mixed solution of metal ions. Then configure 2mol / L NaC 2 o 4 Solution 50mL, under magnetic stirring, NaC 2 o 4 The solution was added to the mixed solution of metal ions, and a large amount of precipitation was produced immediately. After stirring for 2 hours, it was centrifuged, washed twice with deionized water and absolute ethanol, and dried in a 70-degree oven for 12 hours to obtain the oxalate precursor. body;
[0030] (2) SiO 2 Synthesis of coated oxalate precursor: Weigh 1.2 mmol of the above-obtained oxalate precursor and disperse it in 13 ml of absolute ethanol, stir and ultrasonically disperse. According to the molar ratio of Si:(Ni+Co+Mn)=3:100, Si(OC 2 h 5 ) 4 Anhydrous ethanol solution, stir to disperse evenly. Then the mixed solution was transf...
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