Preparation method of spherical N-doped C-coated metal oxide negative electrode material with multi-stage structure
A negative electrode material and oxide technology, which is applied in the field of preparation of spherical N-doped C-coated metal oxide negative electrode materials, can solve the problems of material loss of activity, poor NiO cycle performance, poor conductivity, etc. Uniform, wide potential window reversible capacity, good dispersion effect
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Embodiment 1
[0024] Dissolve 0.15g of polyvinylidene fluoride and 0.2g of guanidine hydrochloride in 2.85g of N-methylpyrrolidone, stir and mix, dry and calcinate, grind and pass through a fine sieve to obtain N-doped C powder. Dissolve sodium molybdate, nickel nitrate, ammonium fluoride and urea in a mixed solution of ethanol and water with a volume ratio of 1:3, stir for 1 hour, then transfer to a reaction kettle for 12 hours at 120°C, cool to room temperature, and filter , washed 4 times with a mixed solution of deionized water and ethanol, and dried at 60°C to obtain a precursor; then N-doped C powder was mixed with the precursor, ball milled, and put into a tube furnace in a nitrogen-argon gas mixture ( NiO / NiMoO 4 @N-C material. Will take 500mg of NiO / NiMoO obtained 4 @C material was put into 50mL distilled water, and ultrasonically dispersed for 2h, then 10mg sodium dodecylbenzenesulfonate was added as a surfactant, and stirred for 12h. Add 0.035mL pyrrole and 0.5mL1mol / L hydroch...
Embodiment 2
[0026]Dissolve 0.15g of polyvinylidene fluoride and 0.2g of guanidine hydrochloride in 2.85g of N-methylpyrrolidone, stir and mix, dry and calcinate, grind and pass through a fine sieve to obtain N-doped C powder. Dissolve sodium molybdate, nickel nitrate, ammonium fluoride and urea in a mixed solution of ethanol and water with a volume ratio of 1:3, stir for 1 hour, then transfer to a reaction kettle for 12 hours at 100°C, cool to room temperature, and filter , washed 4 times with a mixed solution of deionized water and ethanol, and dried at 60°C to obtain a precursor; then N-doped C powder was mixed with the precursor, ball milled, and put into a tube furnace in a nitrogen-argon gas mixture ( NiO / NiMoO 4 @N-C material. Will take 500mg of NiO / NiMoO obtained 4 The @N-C material was put into 50mL distilled water and ultrasonically dispersed for 2h, then 10mg sodium dodecylbenzenesulfonate was added as a surfactant, and stirred for 12h. Add 0.035mL pyrrole and 0.5mL1mol / L hyd...
Embodiment 3
[0028] Dissolve 0.15g of polyvinylidene fluoride and 0.2g of guanidine hydrochloride in 2.85g of N-methylpyrrolidone, stir and mix, dry and calcinate, grind and pass through a fine sieve to obtain N-doped C powder. Dissolve sodium molybdate, nickel nitrate, ammonium fluoride and urea in a mixed solution of ethanol and water with a volume ratio of 1:3, stir for 1 hour, then transfer to a reaction kettle for 8 hours at 160°C, cool to room temperature, and filter , washed 4 times with a mixed solution of deionized water and ethanol, and dried at 60°C to obtain a precursor; then N-doped C powder was mixed with the precursor, ball milled, and put into a tube furnace in a nitrogen-argon gas mixture ( NiO / NiMoO 4 @N-C material. Will take 500mg of NiO / NiMoO obtained 4 The @N-C material was put into 50mL of distilled water and ultrasonically dispersed for 2h, then 10mg of sodium dodecylbenzenesulfonate was added as a surfactant, and stirred for 12h. Add 0.035mL pyrrole and 0.5mL1mol...
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