Method for preparing composite of grapheme with different oxidation degrees and manganese dioxide
A technology of manganese dioxide and oxidation degree, which is applied in capacitors, circuits, electrolytic capacitors, etc., can solve the problems that the application of graphene and nano-manganese dioxide composite electrodes has not been found, and achieve obvious supercapacitive performance, low energy consumption, and simple operation Effect
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Embodiment 1
[0023] Step 1: Pour 120mL of concentrated sulfuric acid with a mass fraction of 98% into a beaker containing 3g of raw graphite, and stir for 15min under ice bath conditions; slowly add 15gKMnO to the mixture 4 And keep the temperature not higher than 4°C. After the addition, stir in an ice bath for 2 hours; move the mixture to a 35°C water bath and continue stirring for 1 hour, then raise the temperature to 60°C and keep it for 30 minutes. Slowly add 250mL of deionized water to the mixture to control The dropping speed keeps the temperature of the system at 60±3°C; take it out after stirring for 15 minutes after adding, stir at room temperature and quickly add 500mL deionized water and 30mLH 2 o 2 , the reaction was terminated after stirring for 15 min, and a golden yellow suspension was obtained. The sulfate ions were removed by centrifugal washing with 10% dilute hydrochloric acid, dried at 60 °C for 24 h, and ground to obtain GO powder.
[0024] Step 2: Take 0.1 g of GO ...
Embodiment 2
[0027] Step 1: Prepare graphite oxide as in Step 1 in Example 1.
[0028] Step 2: Take 0.1 g of GO powder prepared in Step 1 and add it to 100 mL of deionized water, sonicate for 2 hours to obtain a uniformly dispersed 1 mg / mL graphite oxide solution, transfer the solution to a round bottom flask, add 100 μL of hydrazine hydrate, shake well, and put Reflux in a water bath furnace at 80°C, control the reduction time for 30 minutes, take it out, filter it with suction, wash it, and then ultrasonically disperse it in deionized water to obtain a uniform suspension, and obtain graphene oxide with a large specific surface area by freeze-drying.
[0029] Step 3: weigh the prepared graphene oxide powder 0.066g and MnCl 2 4H 2 O (0.27g) was mixed in 50mL isopropanol and sonicated for 2h, the dispersed mixed solution was placed in a water bath at 80°C and stirred, and 5mL dissolved in 0.15g KMnO was quickly poured into it. 4 deionized water, reflux for 30min, take out suction filtrati...
Embodiment 3
[0031] Step 1: Prepare graphite oxide as in Example 1.
[0032] Step 2: Take 0.1 g of GO powder prepared in Step 1 and add it to 100 mL of deionized water, sonicate for 2 hours to obtain a uniformly dispersed 1 mg / mL graphite oxide solution, transfer the solution to a round bottom flask, add 100 μL of hydrazine hydrate, shake well, and put Reflux in a water-bath furnace at 80°C, control the reduction time for 1 hour, take it out, filter it with suction, wash it, and then ultrasonically disperse it in deionized water to obtain a uniform suspension, and obtain graphene oxide with a large specific surface area by freeze-drying.
[0033] Step 3: weigh 0.066g of graphene oxide powder prepared in step 2 and MnCl 2 4H 2 O (0.27g) was mixed in 50mL isopropanol and sonicated for 2h, the dispersed mixed solution was placed in a water bath at 80°C and stirred, and 5mL dissolved in 0.15g KMnO was quickly poured into it. 4 deionized water, reflux for 30min, take out suction filtration, w...
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