Preparation method of three-dimensional conductive skeleton/metal nitride composite lithium metal negative electrode current collector
A metal anode and nitride technology, which is applied in the field of preparation of three-dimensional conductive framework/metal nitride composite lithium metal anode current collector, can solve problems such as poor practicability, and achieve the effects of good practicability, long cycle life and growth inhibition.
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[0028] Example 1:
[0029] (1) Cut 12mm thick commercial nickel foam into small pieces with a length of 4cm and a width of 2.5cm, followed by ultrasonic cleaning with 1.0mol / L dilute hydrochloric acid, absolute ethanol and deionized water to remove surface impurities, and vacuum drying for later use.
[0030] (2) Cobalt nitrate hexahydrate (CoNO 3 6H 2 O), ammonium fluoride (NH 4 F) and urea (CON 2 H 4 ) were dissolved in deionized water according to the molar concentration of 1.25mol / L, 0.25mol / L and 0.5mol / L respectively, and stirred for 2h.
[0031] (3) Transfer the mixed solution after stirring in step (2) to the polytetrafluoroethylene lining, and immerse the nickel foam obtained in step (1) into the mixed solution, and react at 120° C. for 8h in a hydrothermal kettle, Then cooled to room temperature, washed and dried to obtain a precursor of nickel foam (Co(OH)F / NF) composite modified by Co(OH)F nanobrush.
[0032](4) The composite precursor obtained in the step (...
Example Embodiment
[0033] Example 2:
[0034] (1) Cut 12mm thick commercial nickel foam into small pieces with a length of 4cm and a width of 2.5cm, followed by ultrasonic cleaning with 1.0mol / L dilute hydrochloric acid, absolute ethanol and deionized water to remove surface impurities, and vacuum drying for later use.
[0035] (2) Nickel nitrate hexahydrate (NiNO 3 6H 2 O), ammonium fluoride (NH 4 F) and urea (CON 2 H 4 ) were dissolved in deionized water according to the molar concentration ratios of 1.75mol / L, 0.25mol / L and 0.5mol / L respectively, and stirred for 3h.
[0036] (3) Transfer the mixed solution after stirring in step (2) to the polytetrafluoroethylene lining, and immerse the nickel foam obtained in step (1) into the mixed solution, and react in a hydrothermal kettle at 90° C. for 10 hours, Then cooled to room temperature, washed and dried to obtain a nickel foam (Ni(OH)F / NF) composite precursor modified by Ni(OH)F nanobrushes.
[0037] (4) Nitriding the composite precursor ...
Example Embodiment
[0038] Example 3:
[0039] (1) Cut 12mm thick commercial nickel foam into small pieces with a length of 4cm and a width of 2.5cm, followed by ultrasonic cleaning with 1.0mol / L dilute hydrochloric acid, absolute ethanol and deionized water to remove surface impurities, and vacuum drying for later use.
[0040] (2) Ferric chloride hexahydrate (FeCl 3 6H 2 O), ammonium fluoride (NH 4 F) and urea (CON 2 H 4 ) were dissolved in deionized water according to the molar concentration ratios of 2.5mol / L, 0.5mol / L and 1mol / L, and magnetically stirred for 4h.
[0041] (3) Transfer the mixed solution stirred in step (2) to the polytetrafluoroethylene lining, and immerse the nickel foam obtained in (1) into the mixed solution, react in a hydrothermal kettle at 180° C. for 5 h, and then Cooled to room temperature, washed and dried to obtain Fe(OH)F nanobrush modified nickel foam (Fe(OH)F / NF) composite precursor.
[0042] (4) The composite precursor obtained in the step (3) is subjecte...
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