A kind of negative electrode material of lithium battery and preparation method thereof
A negative electrode material, lithium battery technology, applied in battery electrodes, lithium batteries, non-aqueous electrolyte batteries, etc., can solve the problems affecting the cycle performance and application of materials, loss of electrical contact of current collectors, and pulverization of electrode materials, etc. Inexpensive, maintains integrity, avoids chalking effects
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0023] A preparation method of a lithium battery negative electrode material, comprising the steps of:
[0024] Ⅰ Add 10g of ferric trichloride, 10g of tin tetrachloride, 10g of titanium tetrachloride, 1g of lanthanum chloride and 2g of sodium tetrafluoroborate into a beaker of 300g of ethylene glycol, stir for 1 hour, then slowly add 100g of sodium acetate , and after another 2 hours of vigorous stirring, the solution was transferred to a polyvinyl fluoride-lined hydrothermal reactor and reacted at 180 °C for 20 hours. After the reaction, the reactor was cooled to room temperature, the precipitate was separated by centrifugation, washed, and suction filtered, and finally the obtained sample was dried at 110°C for 18 hours, and the obtained product was porous Fe-Sn-La-O-B-F;
[0025] Ⅱ The porous Fe-Sn-La-O-B-F 12g prepared by step Ⅰ, trimethylvinylsilane 0.2g, 4,4,5,5-tetramethyl-2-(4-trifluorovinyloxy Base-phenyl)-[1,3,2]dioxaborane 0.3g, vinylcarbazole 0.5g, vinyl dimethyl...
Embodiment 2
[0030] A preparation method of a lithium battery negative electrode material, comprising the steps of:
[0031] Ⅰ Add 10g of ferric chloride, 10g of tin tetrachloride, 10g of titanium tetrachloride, 1g of lanthanum chloride and 2g of sodium tetrafluoroborate into a beaker of 350g of ethylene glycol, stir for 1.2 hours, then slowly add 100g of sodium acetate , and after another 2.3 hours of vigorous stirring, the solution was transferred to a polyvinyl fluoride-lined hydrothermal reactor and reacted at 185 °C for 22 hours. After the reaction, the reactor was cooled to room temperature, and the precipitate was separated by centrifugation, washed, and filtered with suction. Finally, the obtained sample was dried at 112°C for 19 hours, and the obtained product was porous Fe-Sn-La-O-B-F;
[0032] Ⅱ The porous Fe-Sn-La-O-B-F13g prepared by step I, 0.2g of trimethylvinylsilane, 4,4,5,5-tetramethyl-2-(4-trifluorovinyloxy Base-phenyl)-[1,3,2]dioxaborane 0.3g, vinylcarbazole 0.5g, viny...
Embodiment 3
[0037] A preparation method of a lithium battery negative electrode material, comprising the steps of:
[0038] Ⅰ Add 10g of ferric chloride, 10g of tin tetrachloride, 10g of titanium tetrachloride, 1g of lanthanum chloride and 2g of sodium tetrafluoroborate into a beaker of 400g of ethylene glycol, stir for 1.5 hours, then slowly add 100g of sodium acetate , and after another 2.5 hours of vigorous stirring, the solution was transferred to a polyvinyl fluoride-lined hydrothermal reactor and reacted at 190 °C for 23 hours. After the reaction, the reactor was cooled to room temperature, the precipitate was separated by centrifugation, washed, and suction filtered, and finally the obtained sample was dried at 115°C for 21 hours, and the obtained product was porous Fe-Sn-La-O-B-F;
[0039] Ⅱ The porous Fe-Sn-La-O-B-F 13.5g prepared by step Ⅰ, trimethylvinylsilane 0.2g, 4,4,5,5-tetramethyl-2-(4-trifluoroethylene 0.3g of oxy-phenyl)-[1,3,2]dioxaborane, 0.5g of vinyl carbazole, 0.5g o...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More