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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Embodiment 1
[0029] (1) Cut 12mm thick commercial nickel foam into small pieces with a length of 4cm and a width of 2.5cm, ultrasonically clean them with 1.0mol / L dilute hydrochloric acid, absolute ethanol and deionized water to remove surface impurities, and vacuum dry them 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 respectively dissolved in deionized water according to the molar concentration of 1.25mol / L, 0.25mol / L, and 0.5mol / L, and stirred for 2h.
[0031] (3) Transfer the mixed solution stirred in step (2) to a polytetrafluoroethylene lining, and immerse the foamed nickel obtained in step (1) into the mixed solution, and react in a hydrothermal kettle at 120° C. for 8 hours, Then cooled to room temperature, washed and dried to obtain a foam nickel (Co(OH)F / NF) composite precursor modified by Co(OH)F nanobrush.
[0032](4) Nitriding the composite precursor obtained in step (3) in an ammonia atmosp...
Embodiment 2
[0034] (1) Cut 12mm thick commercial nickel foam into small pieces with a length of 4cm and a width of 2.5cm, ultrasonically clean them with 1.0mol / L dilute hydrochloric acid, absolute ethanol and deionized water to remove surface impurities, and vacuum dry them 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 respectively dissolved in deionized water according to the molar concentration ratio of 1.75mol / L, 0.25mol / L, and 0.5mol / L, and stirred for 3h.
[0036] (3) Transfer the mixed solution stirred in step (2) to a polytetrafluoroethylene lining, and immerse the foamed nickel obtained in step (1) into the mixed solution, and react in a hydrothermal kettle at 90° C. for 10 h, Then cooled to room temperature, washed and dried to obtain Ni(OH)F nanobrush-modified foam nickel (Ni(OH)F / NF) composite precursor.
[0037] (4) Nitriding the composite precursor obtained in step (3) in an ammonia atmosphe...
Embodiment 3
[0039] (1) Cut 12mm thick commercial nickel foam into small pieces with a length of 4cm and a width of 2.5cm, ultrasonically clean them with 1.0mol / L dilute hydrochloric acid, absolute ethanol and deionized water to remove surface impurities, and vacuum dry them 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 respectively dissolved in deionized water according to the molar concentration ratio 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 a polytetrafluoroethylene lining, and immerse the foamed nickel obtained in (1) into the mixed solution, react in a hydrothermal kettle at 180°C for 5h, and then Cool to room temperature, wash and dry to obtain Fe(OH)F nanobrush-modified foam nickel (Fe(OH)F / NF) composite precursor.
[0042] (4) Nitriding the composite precursor obtained in step (3) in an ammonia atmosphere, ...
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