Composite structure quantum dot, preparation method and use thereof
A composite structure, quantum dot technology, applied in chemical instruments and methods, luminescent materials, nanotechnology, etc., can solve the problems of the half-peak width of III-V quantum dots, reduce the use value, etc., and achieve simple operation and short process. Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0085] The preparation method of the composite structure quantum dot provided in this embodiment is as follows:
[0086] (1) To SiO with uniform particle size distribution 2 Add 0.34mmol InCl to core 1 3 , 2.2 mmol ZnI 2 and 5ml oleylamine, heated to 140°C and vacuumed for 1h, heated to 200°C under argon atmosphere, and added 2.4mmol (DMA) dropwise using a syringe pump 3 The mixture of P and 1ml oleylamine was reacted for 20min to obtain the intermediate product.
[0087] (2) Heating the intermediate product in step (1) to 300° C., adding 1 ml of selenium precursor dropwise, reacting for 5 minutes, adding 0.65 ml of zinc precursor dropwise, and reacting for 10 minutes to obtain the composite structure quantum dots.
[0088] Among them, the SiO 2 The preparation method of core 1 is as follows: using silicon tetrachloride as raw material, silicon tetrachloride gas is used to hydrolyze silicon tetrachloride gas under high temperature of hydrogen and oxygen flow to obtain smok...
Embodiment 2
[0096] The preparation method of the composite structure quantum dot provided in this embodiment is as follows:
[0097] (1) To SiO with uniform particle size distribution 2 Add 0.34mmol InCl to core 1 3 , 2.2 mmol ZnI 2 and 5ml oleylamine, heated to 140°C and vacuumed for 1h, heated to 200°C under argon atmosphere, and added 2.4mmol (DMA) dropwise using a syringe pump 3 The mixture of P and 1ml oleylamine was reacted for 20min to obtain the intermediate product.
[0098] (2) Heating the intermediate product in step (1) to 300° C., adding 0.28 mmol dodecanethiol dropwise, reacting for 5 minutes, adding 0.65 ml zinc precursor dropwise, and reacting for 10 minutes to obtain the composite structure quantum dots.
[0099] Among them, the SiO 2 The preparation method of core 1 is as follows: using silicon tetrachloride as raw material, silicon tetrachloride gas is used to hydrolyze silicon tetrachloride gas under high temperature of hydrogen and oxygen flow to obtain smoky sili...
Embodiment 3
[0105] The preparation method of the composite structure quantum dot provided in this embodiment is as follows:
[0106] (1) Add 0.3mmol InCl to polystyrene core 1 with uniform particle size distribution 3 , 2 mmol ZnI 2 and 4.5ml of oleylamine, heated to 120°C and evacuated for 0.75h, heated to 180°C under argon atmosphere, and added 2mmol (DMA) dropwise using a syringe pump 3 The mixture of P and 1ml oleylamine was reacted for 25min to obtain the intermediate product.
[0107] (2) Heating the intermediate product in step (1) to 280° C., adding 0.28 mmol dodecanethiol dropwise, reacting for 4 minutes, adding 0.65 ml zinc precursor dropwise, and reacting for 8 minutes to obtain the composite structure quantum dots.
[0108] The preparation method of the zinc precursor is as follows: add 6mmol ZnO, 18mmol oleic acid, and 14ml paraffin oil into a three-necked flask, and heat it to 300°C under an argon atmosphere, and the obtained colorless and transparent liquid is the zinc pr...
PUM
Property | Measurement | Unit |
---|---|---|
thickness | aaaaa | aaaaa |
thickness | aaaaa | aaaaa |
diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com