Boron-phosphorus co-doped porous silicon negative electrode material and preparation method thereof
A negative electrode material and co-doping technology, applied in the direction of chemical instruments and methods, nanotechnology for materials and surface science, silicon oxide, etc., can solve the problem of ensuring uniform dispersion of different components in composite materials and reducing porous silicon Electrochemical performance, increasing the difficulty of preparation and other issues, to improve the comprehensive electrochemical performance, good practical prospects, and solve the effect of volume expansion
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Embodiment 1
[0029] Take boric acid, phosphoric acid and ethyl orthosilicate according to the mass ratio of the elements boron, phosphorus and silicon in the compound as 5:25:100, dissolve them in 10 times the volume of ethanol, stir evenly for 10 minutes, and then add 0.06 with a relative total volume of 0.4 mol / L hydrochloric acid solution was uniformly stirred at 60°C for 3 hours and then cooled to room temperature to obtain solution A; then ammonia water, deionized water, and absolute ethanol were uniformly mixed at a volume ratio of 1:2:3 to obtain solution B; Quickly pour solution A into solution B at a ratio of 1:1, stir at room temperature for 3 hours, let stand for 12 hours, and finally wash the obtained precipitate repeatedly with ethanol and water, separate and dry the obtained powder in an air atmosphere at 550°C After calcination for 2 hours, the silicon dioxide precursor can be obtained.
[0030] Take 1g of the above-mentioned silica precursor, grind it with 1g of magnesium p...
Embodiment 2
[0035] According to the mass ratio of the elements boron, phosphorus and silicon in the compound is 2.5:12.5:100, take boric acid, phosphoric acid and ethyl orthosilicate, dissolve them in 10 times the volume of ethanol, stir evenly for 10 minutes, and then add 0.06 with a relative total volume of 0.8 mol / L hydrochloric acid solution was uniformly stirred at 60°C for 3 hours and then cooled to room temperature to obtain solution A; then ammonia water, deionized water, and absolute ethanol were uniformly mixed at a volume ratio of 1:1:1 to obtain solution B; Quickly pour solution A into solution B at a ratio of 1:1, stir at room temperature for 3 hours, let stand for 12 hours, and finally wash the obtained precipitate repeatedly with ethanol and water, separate and dry the obtained powder in an air atmosphere at 400°C Calcined for 6 hours, the silicon dioxide precursor can be obtained.
[0036] Take 1g of the above-mentioned silica precursor, grind it with 1g of magnesium powde...
Embodiment 3
[0041] Take sodium borate, ammonium dihydrogen phosphate and sodium silicate according to the mass ratio of boron, phosphorus and silicon in the compound as 5:25:100, dissolve them in 10 times the volume of ethanol, stir evenly for 10 minutes, and then add the relative total volume of 0.8 The 0.1mol / L hydrochloric acid solution was uniformly stirred at 60°C for 3 hours and then cooled to room temperature to obtain solution A; then ammonia water, deionized water, and absolute ethanol were uniformly mixed at a volume ratio of 1:5:5 to obtain solution B; The volume ratio is 1:1, quickly pour solution A into solution B, stir at room temperature for 3 hours, and let it stand for 12 hours. Finally, the obtained precipitate is repeatedly washed with ethanol and water, and the powder obtained after separation and drying is air-conditioned at 700°C. The silicon dioxide precursor can be obtained by calcining in the atmosphere for 1 h.
[0042] Take 1g of the above-mentioned silica precu...
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