Lanthanide rare earth ytterbium-doped silver sulfide quantum dots, a preparing method thereof and applications of the quantum dots
A technology of lanthanide rare earths and silver sulfide, applied in chemical instruments and methods, zinc sulfide, luminescent materials, etc., can solve problems such as difficult to be widely used, and achieve the effect of simple preparation process, good biocompatibility, and uniform size
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0034] A preparation method for lanthanide rare earth ytterbium doped silver sulfide quantum dots, comprising the following steps:
[0035] 1) Preparation of the precursor silver diethylthiocarbamate: Dissolve 20mmol of sodium diethylthiocarbamate trihydrate and 20mmol of silver nitrate in 40ml of deionized water, stir magnetically under dark conditions, and react for 2 hours. , the reaction solution was centrifugally filtered to obtain the product, and the product was washed with water and absolute ethanol for 4 times, and then dried in an oven at 70°C to obtain the precursor silver diethylthiocarbamate.
[0036] 2) Preparation of near-infrared silver sulfide quantum dots: Dissolve 0.2 mmol of the precursor silver diethylthiocarbamate in 12 mL of dodecyl mercaptan, stir for 20 min, mix well to obtain a clear solution, and heat the clear solution under argon to carry out For the reaction, the reaction temperature is 220° C., and the reaction time is 2 hours. After the reaction...
Embodiment 2
[0042] A preparation method for lanthanide rare earth ytterbium doped silver sulfide quantum dots, comprising the following steps:
[0043] 1) Preparation of the precursor silver diethylthiocarbamate: Dissolve 25mmol of sodium diethylthiocarbamate trihydrate and 25mmol of silver nitrate in 50ml of deionized water, stir magnetically under dark conditions, and react for 3 hours. , the reaction solution was centrifuged to obtain the product, and the product was washed with water and absolute ethanol for 6 times, and then dried in an oven at 65°C to obtain the precursor silver diethylthiocarbamate.
[0044] 2) Preparation of near-infrared silver sulfide quantum dots: the precursor silver diethylthiocarbamate 0.4mmol was dissolved in 25mL of dodecanethiol, stirred for 10min, mixed evenly to obtain a clear solution, and the clear solution was heated under argon to carry out For the reaction, the reaction temperature is 200° C., and the reaction time is 2 hours. After the reaction is...
Embodiment 3
[0049] A preparation method for lanthanide rare earth ytterbium doped silver sulfide quantum dots, comprising the following steps:
[0050] 1) Preparation of the precursor silver diethylthiocarbamate: Dissolve 25mmol of sodium diethylthiocarbamate trihydrate and 25mmol of silver nitrate in 40ml of deionized water, stir magnetically under dark conditions, and react for 3 hours. , the reaction solution was centrifuged to obtain the product, washed with water and absolute ethanol for 5 times, and then dried in an oven at 60°C to obtain the precursor silver diethylthiocarbamate.
[0051] 2) Preparation of near-infrared silver sulfide quantum dots: Dissolve 0.2 mmol of silver diethylthiocarbamate precursor in 20 mL of dodecanethiol, stir for 10 min, mix well to obtain a clear solution, and heat the clear solution under argon to carry out For the reaction, the reaction temperature is 200° C., and the reaction time is 2 hours. After the reaction is completed, the near-infrared silver...
PUM
Property | Measurement | Unit |
---|---|---|
Particle size | 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