Preparation method of multi-level structure carbon-coated zinc oxide quantum dot negative electrode material
A negative electrode material, zinc oxide technology, applied in the field of secondary battery material preparation, can solve the problems of low theoretical electrochemical capacity, unsatisfactory first discharge efficiency, poor cycle performance, etc., achieves simple and controllable process, and reduces volume expansion effect. , the effect of improving stability
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Embodiment 1
[0019] Weigh 10 g each of zinc chloride and 1,4-phthalic acid, put them into a polytetrafluoro reactor, add 50 g of deionized water, stir well, and adjust the pH value of the solution to 4 with 4 mol / L hydrochloric acid. After sealing the reaction kettle, keep it warm at 150°C for 12 hours, cool down to room temperature with the furnace, filter the reaction product, wash it 4 times with deionized water, and dry it. The dried product was placed in a tube furnace under N 2 Under the atmosphere, the temperature was raised at a rate of 3°C / min, heated at 600°C for 1 hour, and then cooled with the furnace to obtain a surface-coated zinc oxide material.
Embodiment 2
[0021] Weigh 15g of zinc carbonate and 12g of 1,3,5-benzenetricarboxylic acid, put them into a Teflon reaction kettle, add 60g of methanol, stir well, and adjust the pH value of the solution to 5 with 4mol / L hydrochloric acid. After sealing the reaction kettle, keep it warm at 100°C for 15 hours, cool down to room temperature with the furnace, filter the reaction product, wash it 4 times with deionized water, and dry it. The dried product was placed in a tube furnace under N 2 Under the atmosphere, the temperature was raised at a rate of 5°C / min, heated at 500°C for 2 hours, and then cooled with the furnace to obtain a surface-coated zinc oxide material.
Embodiment 3
[0023] Weigh 20 g of zinc sulfate and 18 g of 2,6-pyridinedicarboxylic acid, put them into a polytetrafluoroethylene reactor, add 45 g of ethanol, stir well, and adjust the pH value of the solution to 4 with 4 mol / L sulfuric acid. After sealing the reaction kettle, keep it warm at 120° C. for 10 h, cool down to room temperature with the furnace, filter the reaction product, wash it 4 times with deionized water, and dry it. The dried product was placed in a tube furnace under N 2 Under the atmosphere, the temperature was raised at a rate of 4°C / min, heated at 700°C for 1.5h, and then cooled with the furnace to obtain a surface-coated zinc oxide material.
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