Preparation method and application of cobalt tetrasulfide nickel and nickel-vanadium double-metal hydroxide composite material
A technology of cobalt tetrasulfide and hydroxide, applied in the manufacture of hybrid/electric double layer capacitors, hybrid capacitor electrodes, etc., can solve the problems of NiV-LDH ion transmission rate and electronic conductivity, poor conductivity of LDH, etc. , to achieve the effect of improving charging/discharging efficiency, low equipment requirements, and high specific capacitance
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specific Embodiment approach 1
[0040] Specific embodiment one: a kind of preparation method of dicobalt nickel tetrasulfide@nickel vanadium double metal hydroxide composite material is completed according to the following steps:
[0041] 1. Preparation of NiCo precursor:
[0042] ①. Dissolving cobalt nitrate hexahydrate, nickel nitrate hexahydrate and urea in deionized water, stirring evenly to obtain mixture I;
[0043]The mol ratio of cobalt nitrate hexahydrate, nickel nitrate hexahydrate and urea described in step 1. is (1~2):(1~2):6;
[0044] ②. Cut the large pieces of foamed nickel into small pieces of foamed nickel, collect the small pieces of foamed nickel, and obtain the raw material of foamed nickel;
[0045] The thickness of the small foam nickel described in step 1.2 is 1cm, and the surface area is 3cm 2 ~5cm 2 ;
[0046] ③. Transfer the mixture I and nickel foam raw materials to a polytetrafluoroethylene autoclave, then carry out hydrothermal reaction, and finally cool naturally to room temp...
specific Embodiment approach 2
[0066] Specific embodiment two: the difference between this embodiment and specific embodiment one is: the volume ratio of the amount of cobalt nitrate hexahydrate described in step one 1. to ionized water is (1mmol~2mmol): 80mL; step one 3. The temperature of the hydrothermal reaction described in is 80°C-120°C, and the time of the hydrothermal reaction is 5h-10h. Other steps are the same as in the first embodiment.
specific Embodiment approach 3
[0067] Embodiment 3: The difference between this embodiment and Embodiment 1 or 2 is that in Step 1 ④, first use deionized water to clean the reaction product I for 3 to 5 times, and then use absolute ethanol to clean the reaction product. I was washed 3 to 5 times, and finally the washed reaction product I was dried at a temperature of 70°C to 80°C and a drying time of 10h to 12h to obtain a NiCo precursor. Other steps are the same as those in Embodiment 1 or 2.
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