Method for synthesizing copper indium diselenide quantum dot
A synthesis method and technology of quantum dots, applied in chemical instruments and methods, nanotechnology for materials and surface science, nanotechnology, etc., can solve problems such as being unsuitable for industrial production, unfavorable for industrial production, harsh reaction conditions, etc. The effect of stable structure, short process cycle and low cost
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2017-06-13
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Abstract
Description
technical field
[0001] The invention belongs to the field of photovoltaic materials, in particular to a copper indium selenide (CuInSe) 2 ) Synthetic method of quantum dots. Background technique
[0002] The lack of traditional energy and the pollution it brings make people pay attention to energy issues. Clean and renewable solar energy is the main energy source to solve human energy problems. Direct conversion of solar energy into electrical energy is one of the most direct and effective ways to utilize solar energy. Research in the traditional field of photovoltaics mainly focuses on silicon-based solar cells. With decades of development, crystalline silicon solar cells have the advantages of high photoelectric conversion efficiency and stability, but because they are based on the demand for a large number of silicon crystal materials, As a result, the cost is relatively high, and it cannot effectively compete with fossil energy, which has become a bottleneck restricti...
Examples
Embodiment 1
[0046] Weigh 0.1111mg (1.0mmol) of selenium dioxide and put it into a round bottom flask, add 3ml of oleylamine to it, put it in a constant temperature oil bath at 100°C for 6 minutes, and after cooling to room temperature, add 19.0mg (0.1mmol) of cuprous iodide to it , 58.4mg (0.2mmol) of indium acetate, the reaction vessel was placed in a 210°C constant temperature oil bath for 20 minutes, and then cooled to room temperature; the solution after the reaction was centrifuged, and the supernatant was discarded and washed with n-hexane. Centrifuge, discard the precipitate again, add ethanol to the supernatant to wash and centrifuge, repeat the washing and centrifugation several times until the supernatant after centrifugation is colorless and transparent, and take the final precipitate as the final product.
[0047] Product composition, structure and morphology characterization:
[0048] The final product is dissolved in dichloromethane, and after the dichloromethane volatilizes...
Embodiment 2
[0063] Weigh 0.1111mg (1.0mmol) of selenium dioxide and put it into a round bottom flask, add 3ml of oleylamine to it, put it in a constant temperature oil bath at 100°C for 6 minutes, and after cooling to room temperature, add 26.2mg (0.1mmol) of copper acetylacetonate, 82.4mg (0.2mmol) of indium acetylacetonate, the reaction vessel was placed in a 210°C constant temperature oil bath for 20 minutes, and then cooled to room temperature; the solution after the reaction was centrifuged, and the supernatant was discarded and washed with n-hexane. Centrifuge, discard the precipitate again, add ethanol to the supernatant to wash and centrifuge, repeat the washing and centrifugation several times until the supernatant after centrifugation is colorless and transparent, and take the final precipitate as the final product.
[0064] Product composition, structure and morphology characterization:
[0065] The final product is dissolved in dichloromethane, and after the dichloromethane vo...
Embodiment 3
[0073] Weigh 0.1111mg (1.0mmol) of selenium dioxide and put it into a round bottom flask, add 3ml of oleylamine to it, put it in a constant temperature oil bath at 100°C for 6 minutes, and after cooling to room temperature, add 19.0mg (0.1mmol) of cuprous iodide to it , 82.4mg (0.2mmol) indium acetylacetonate, put the reaction vessel in a constant temperature oil bath at 210°C for 20 minutes, then cool to room temperature; centrifuge the reacted solution, discard the precipitate and wash the supernatant with n-hexane And centrifugal separation, after discarding the precipitate again, add ethanol to the supernatant to wash and centrifuge, repeat the washing and centrifugation several times until the supernatant after centrifugation is colorless and transparent, take the final precipitate as the final product obtained .
[0074] The final product is dissolved in dichloromethane, and after the dichloromethane volatilizes, the product is subjected to XRD measurement, and the X-ray...