Multi-mode luminescent carbon dots as well as preparation method and application thereof
A multi-mode, carbon dot technology, applied in luminescent materials, chemical instruments and methods, fluorescence/phosphorescence, etc., can solve the problems of limited application, limited carbon dot concentration, reduced information encryption and anti-counterfeiting security, etc., to improve Preparation efficiency, wide application value, and good safety performance
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[0043] In one aspect of the present invention, there is also provided a method for preparing multi-mode luminescent carbon dots, comprising the following steps:
[0044] S10, mixing silk protein, alkali and water at a mass ratio of 1:(0.1-10):(10-500) to form a mixed solution;
[0045] S20, placing the mixed solution in a microwave reactor for microwave reaction, the microwave power is 100W-1000W, and the reaction time is 0.5min-10min; and
[0046] S30, purifying and drying the product after the microwave reaction.
[0047] The preparation method of multi-mode luminescent carbon dots provided by the embodiment of the present invention, on the one hand, uses microwaves to induce rapid oscillation of polar molecules in the reaction system, such as water, polar amino acid groups, etc., to generate a large amount of heat, thereby raising the temperature. At the same time, under the action of microwaves, the polar amino acid groups in the molecular chain of silk protein can be qui...
Embodiment 1
[0061] 1. Weigh 0.1g of sericin and 0.1g of sodium hydroxide respectively and place them in a beaker, then add 10mL of water, stir well, and ultrasonically obtain a clear solution.
[0062] 2. Place the beaker containing the clear solution in a microwave oven and react with a microwave power of 800W for 2.5 minutes to obtain a yellow solid.
[0063] 3. Take out the beaker, let it cool naturally, add 10mL of deionized water into it, stir, and neutralize it with 0.1mol / L hydrochloric acid until neutral, then centrifuge at 10000r / min for 10min, and take the supernatant.
[0064] 4. The supernatant was frozen by liquid nitrogen, and then freeze-dried in a freeze dryer at -50°C for 24 hours to obtain carbon dot powder.
Embodiment 2
[0066] 1. Weigh 0.1g of silk fibroin and 0.1g of sodium hydroxide into a beaker, then add 10mL of water, stir well, and ultrasonically obtain a clear solution.
[0067] 2. Place the beaker containing the clear solution in a microwave oven and react with a microwave power of 800W for 2.5 minutes to obtain a yellow solid.
[0068] 3. Take out the beaker, let it cool naturally, add 10mL of deionized water into it, stir, and neutralize it with 0.1mol / L hydrochloric acid until neutral, then centrifuge at 10000r / min for 10min, and take the supernatant.
[0069] 4. The supernatant was frozen by liquid nitrogen, and then freeze-dried in a freeze dryer at -50°C for 24 hours to obtain carbon dot powder.
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