Method for preparing titanium substrate/titanium spherical composite lithium-ion battery negative electrode material by one-step method
A technology for ion batteries and negative electrode materials, which can be applied to battery electrodes, circuits, electrical components, etc., and can solve problems such as potential safety hazards
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Embodiment 1
[0020] (1) Dissolve 0.5 parts by mass of cetylamine in 100 parts by volume of analytical ethanol, stir at room temperature for 30 minutes, add 1 volume part of concentrated ammonia water, add 2 volume parts of isopropyl titanate under vigorous stirring, and add 50 volume parts of distilled water (Containing 0.03 parts by mass of LiOH·H 2 O) The reaction solution was moved to a 200ml reactor, and reacted for 12h at 100°C.
[0021] (2) After the kettle was cooled to room temperature, a white precipitate was obtained by centrifugation and washing. Dry the white samples.
[0022] (3) The dried samples were calcined at 500°C for 2h.
Embodiment 2
[0024] (1) Dissolve 1 part by mass of cetylamine in 100 parts by volume of analytical ethanol, stir for 30 minutes at room temperature, add 1.2 parts by volume of concentrated ammonia water, add 2.5 parts by volume of isopropyl titanate under vigorous stirring, and add 50 parts by volume of distilled water (Containing 0.03 parts by mass of LiOH·H 2 O) the reaction solution was moved to a 200ml reactor, and reacted at 120 degrees for 48h.
[0025] (2) After the kettle was cooled to room temperature, a white precipitate was obtained by centrifugation and washing. Dry the white samples.
[0026] (3) The dried samples were calcined at 600°C for 2h.
Embodiment 3
[0028] (1) Dissolve 1.5 parts by mass of cetylamine in 100 parts by volume of analytical ethanol, stir for 30 minutes at room temperature, add 1.2 parts by volume of concentrated ammonia water, add 2 parts by volume of isopropyl titanate under vigorous stirring, and add 50 parts by volume of distilled water (Containing 0.13 parts by mass of LiOH·H 2 O) the reaction solution was moved to a 200ml reactor, and reacted for 24h at 200°C.
[0029] (2) After the kettle was cooled to room temperature, a white precipitate was obtained by centrifugation and washing. Dry the white samples.
[0030] (3) Calcinate the dried sample at 500-800 degrees for 2 hours.
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