A kind of carbon quantum dot and its preparation method and application
A carbon quantum dot and carbon cloth technology, applied in the field of carbon quantum dot preparation, can solve the problems of inability to prepare hetero-element modification and passivation, difficulty in separation and purification of carbon quantum dots, unfavorable industrialized mass production, etc., so as to reduce the preparation cost and yield. The effect of improving and improving productivity
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Embodiment 1
[0090] This embodiment provides a method for preparing nitrogen-doped carbon quantum dots, wherein the method includes:
[0091] 1) Weigh 25.5 mg of nitrogen-doped porous carbon, mix 4.5 μL of PTFE binder, add it into a mortar, add 2 mL of ethanol, grind until a uniformly dispersed dispersion slurry is formed, and then directly coat it on a 2cm×2cm On carbon cloth, dry at 80°C for 12h to obtain electrodes;
[0092] 2) The electrode obtained in step 1) is used as the anode, the graphite rod is used as the counter electrode, and the sodium hydroxide ethanol aqueous solution (which is prepared by 30mgNaOH, 35mL ethanol and 8ml deionized water, wherein, the deionized water at 24 ° C is prepared. The resistivity is 18.25MΩ / cm) as the electrolyte, the DC power supply is turned on, the voltage is adjusted to 5V, and after electrolysis for 36h, the electrolyte containing nitrogen-doped carbon quantum dots is obtained;
[0093] 3) Use a 0.22 μm microporous membrane to filter to remove...
Embodiment 2
[0096] This embodiment provides a method for preparing iron-nitrogen-doped carbon quantum dots, wherein the method differs from Embodiment 1 only in that the carbon material used is iron-nitrogen-doped porous carbon (instead of nitrogen-doped porous carbon), and other All are the same as the preparation method of Example 1.
[0097] Wherein, the preparation method of the iron-nitrogen-doped porous carbon is: adding 0.5 mmol of FeCl 3 ·6H 2 O, 1.5mmol of 1,10-phenanthroline and 1g of MgO template agent were dissolved in 100mL of ethanol and stirred for 12h, and the ethanol solvent was removed by rotary evaporation to obtain solid powder; / min) black solid powder obtained by calcination in argon atmosphere for 2 hours; the obtained black solid powder was dispersed in 100 mL of dilute hydrochloric acid with a concentration of 1 mol / L, stirred at 80 °C for 2 hours to remove unstable iron particles generated on the surface, and then dried for 6 hours An iron-nitrogen-doped porous...
Embodiment 3
[0099] This embodiment provides a method for preparing carbon quantum dots, wherein the method differs from Embodiment 1 only in that the carbon material used is undoped porous carbon (instead of nitrogen-doped porous carbon), and the others are the same as those of Embodiment 1. The preparation method is the same.
[0100] Wherein, the preparation method of the undoped porous carbon is as follows: dissolving 1.5 mmol of triphenylmethane and 1 g of MgO template agent in 100 mL of ethanol, stirring for 12 h, and removing the ethanol solvent by rotary evaporation to obtain solid powder; Black solid powder obtained by calcining in argon atmosphere at 800°C (heating rate of 10°C / min) for 2h; disperse the obtained black solid powder in 100mL of dilute hydrochloric acid with a concentration of 1mol / L, and stir at room temperature for 30min to remove the MgO template agent , and then dried for 6 h to obtain undoped porous carbon.
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