Preparation method of copper nano-clusters with adjustable and controllable fluorescent color
A copper nano-cluster and color technology, applied in the field of metal nano-cluster preparation, can solve the problems of few aggregation-induced preparation methods and uneven size of nano-cluster particles, and achieve the effects of low cost, simple preparation method and high stability
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Embodiment 1
[0027] Dissolve 30 mg of tetramethylammonium bromide and 68 mg of copper chloride dihydrate in 8 ml of deionized water, mix and stir at 750 rpm for 30 minutes at a temperature of 20°C. Weighed 3.8 mg of sodium borohydride and dissolved it in 2 ml of deionized water, and slowly added it dropwise to the above mixture, a solid was precipitated, and the reaction was continued for 4 hours with stirring. The above reaction solution was transferred to a 10ml centrifuge tube and centrifuged (12500g, 30 minutes) to obtain a precipitate. The precipitate was washed with water and centrifuged, specifically adding 10 ml of deionized water to resuspend the precipitate, and then centrifuged (12500 g, 30 minutes) to obtain the precipitate. Washing with water and centrifugation was repeated three times, and the precipitate was vacuum-dried to obtain a solid product of copper nanoclusters. analyzed by transmission electron microscopy (see figure 1 , figure 2 ) The solid product obtained is ...
Embodiment 2
[0029] 42 mg of tetraethylammonium bromide and 68 mg of copper chloride dihydrate were dissolved in 8 ml of deionized water, mixed and then stirred at a stirring speed of 750 rpm for 30 minutes at a temperature of 30°C. 17.6 mg of ascorbic acid was weighed and dissolved in 2 ml of deionized water, and slowly added dropwise to the above mixed solution, a solid was precipitated, and the stirring reaction was continued for 1 hour. The above reaction solution was transferred to a 10ml centrifuge tube and centrifuged (12500g, 20 minutes) to obtain a precipitate. The precipitate was washed with water and centrifuged, specifically adding 10 ml of deionized water to resuspend the precipitate, and then centrifuged (12500 g, 20 minutes) to obtain the precipitate. Washing with water and centrifugation was repeated three times, and the precipitate was vacuum-dried to obtain a solid product of copper nanoclusters. The solid product obtained by transmission electron microscopy analysis is ...
Embodiment 3
[0031] Dissolve 86 mg of tetrahexylammonium bromide and 85 mg of copper chloride dihydrate in 8 ml of deionized water, mix and stir at 750 rpm for 30 minutes at a temperature of 25°C. Weighed 7.6 mg of sodium borohydride and dissolved it in 2 ml of deionized water, and slowly added it dropwise to the above mixture, a solid was precipitated, and the reaction was continued for 3 hours with stirring. The above reaction solution was transferred to a 10ml centrifuge tube and centrifuged (12500g, 15 minutes) to obtain a precipitate. The precipitate was washed with water and centrifuged, specifically adding 10 ml of deionized water to resuspend the precipitate, and then centrifuged (12500 g, 15 minutes) to obtain the precipitate. Washing with water and centrifugation was repeated three times, and the precipitate was vacuum-dried to obtain a solid product of copper nanoclusters. The resulting solid copper nanoclusters were further analyzed by transmission electron microscopy.
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