Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Preparation method of ZnSe-to-Cu quantum point

A quantum dot and content technology, which is applied in the field of ZnSe:Cu quantum dot preparation, can solve the problems of dangerous operation, high price, harsh conditions, etc., and achieve the effect of simple and safe operation and reduced preparation cost

Inactive Publication Date: 2009-12-09
UNIV OF JINAN
View PDF0 Cites 27 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

D.J.Norris et al. (Nano Lett.2001,1,1:3-7.) based on the synthesis of ZnSe quantum dots by Margaret A et al. (J.Phys.Chem.B.1998,102,19:3655-3657. ), using dimethyl manganese as a dopant to obtain ZnSe:Mn quantum dots with good monodispersity and high fluorescence performance; however, TOP is not stable as a raw material, the price is high, and the reaction needs to be performed in a high temperature environment under strict conditions
In 2007, Peng et al. proposed to use a green synthesis method to synthesize ZnSe:Mn quantum dots with high quantum yield and color controllable by nucleation and doping (J.AM.CHEM.SOC.2007, 129, 3339-3347.) ; But the synthesis temperature is still around 300°C, the operation is dangerous

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation method of ZnSe-to-Cu quantum point
  • Preparation method of ZnSe-to-Cu quantum point
  • Preparation method of ZnSe-to-Cu quantum point

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] (1) Preparation of Se precursor

[0024] Under the protection of nitrogen, 0.007g of Se powder and 0.01g of sodium borohydride were dissolved in 3ml of distilled water, and heated appropriately to completely dissolve them to obtain a Se precursor solution.

[0025] (2) Preparation of Zn and Cu mixed solution

[0026] Dissolve 0.15g of zinc acetate and 0.0003g of copper acetate in 25ml of distilled water, add 54μl of thioglycolic acid, stir evenly with a magnetic force, and adjust the pH to 8.5 with 1mol / L NaOH to prepare a mixed solution of Zn and Cu.

[0027] (3) Synthesis of ZnSe:Cu quantum dots

[0028] Rapidly inject the Se precursor solution into the mixed solution of Zn and Cu, reflux the oil bath (90° C.), react for 1 hour, and cool to room temperature to obtain the ZnSe:Cu quantum dot aqueous solution. At room temperature, it can be directly used for spectral testing.

[0029] (4) Add 30ml of isopropanol to the ZnSe obtained above: Cu quantum dot aqueous solu...

Embodiment 2

[0031] (1) Preparation of Se precursor

[0032] Under the protection of inert gas argon, 0.006g of Se powder and 0.009g of sodium borohydride were dissolved in 2ml of distilled water, and heated appropriately to completely dissolve them to prepare a Se precursor solution.

[0033] (2) Preparation of Zn and Cu mixed solution

[0034] Dissolve 0.12g of zinc acetate and 0.0002g of copper acetate in 20ml of distilled water, add 48μl of thioglycolic acid, stir evenly with a magnetic force, and adjust the pH to 10.5 with 1mol / L NaOH to prepare a mixed solution of Zn and Cu.

[0035] (3) Synthesis of ZnSe:Cu quantum dots

[0036] Rapidly inject the Se precursor solution into the Zn precursor solution, reflux in an oil bath (100° C.), react for 1 hour, and cool to room temperature to obtain a ZnSe:Cu quantum dot aqueous solution. At room temperature, it can be directly used for spectral testing.

[0037] (4) Add 25ml of isopropanol to the ZnSe obtained above: Cu quantum dot aqueous...

Embodiment 3

[0039] (1) Preparation of Se precursor

[0040] Under the protection of inert gas nitrogen or argon, 0.01g of Se powder and 0.014g of sodium borohydride were dissolved in 3ml of distilled water, and heated appropriately to completely dissolve them to obtain a Se precursor solution.

[0041] (2) Preparation of Zn precursor

[0042] Dissolve 0.13g of zinc acetate and 0.0001g of copper acetate in 20ml of distilled water, add 50μl of mercaptoacetic acid, stir evenly with a magnetic force, adjust the pH to 9.0 with 1mol / L NaOH, and prepare a mixed solution of Zn and Cu.

[0043] (3) Synthesis of ZnSe:Cu quantum dots

[0044] Rapidly inject the Se precursor solution into the Zn precursor solution, reflux in an oil bath (100° C.), react for 2 hours, and cool to room temperature to obtain ZnSe quantum dot aqueous solutions with different reaction times. At room temperature, it can be directly used for spectral testing.

[0045] (4) Add 25ml of isopropanol to the ZnSe obtained above...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention belongs to the technical field of the preparation method of a nano material, in particular to a preparation method of a ZnSe-to-Cu quantum point. The preparation method comprises the following steps that: (1), under the protection of inert gases, Se powder and sodium borohydride are dissolved in distilled water, the amount of substance of the sodium borohydride is equal to or greater than that of the Se powder, the mixture is heated to be completely dissolved, and a Se solution with the Se content of 0.01 to 0.75mol / L is manufactured; (2), zinc acetate and copper acetate are dissolved in the distilled water, the mole number of copper ions does not exceed 15% of that of zinc ions, thioglycollic acid is added into the mixture, the pH is regulated to 8 to 13, and a Zn solution with the Zn content of 0.01 to 0.1mol / L is manufactured; and (3), the manufactured Se solution is injected into the manufactured Zn solution, the mixture reacts for 1 to 5 hours in oil bath at 90 to 150 DEG C and is cooled to room temperature, ZnSe-to-Cu quantum point water solution is obtained, then isopropanol is added into the ZnSe-to-Cu quantum point water solution, and a ZnSe-to-Cu quantum point is obtained by centrifugation and separation. The invention has the beneficial effects that cheap raw materials are adopted to substitute an expensive and dangerous organic metal precursor, which is green and environment-friendly, and the preparation cost is reduced; and the water solution is used as a reaction solvent, thus the reaction temperature is reduced and the operation is simple and safe.

Description

technical field [0001] The invention relates to a preparation method of a nano-luminescent material, in particular to a preparation method of ZnSe:Cu quantum dots. Background technique [0002] Since Ni et al. reported on CdSe quantum dots in Science in 1998, the application of II-VI quantum dots as fluorescent probes in the field of life medicine has greatly attracted the attention of scholars at home and abroad. At present, Cd-containing quantum dots (CdSe, CdTe, CdS, etc.) are the most used, but they cannot be widely used due to their biological toxicity; chalcogenides (ZnS, ZnSe, etc.) have become a research hotspot due to their low toxicity. , but its pure compound has the disadvantages of low luminous efficiency and poor stability, which requires scholars to modify it to improve luminous efficiency. At present, the common method is doping transition metal ions, which can not only overcome the problem of biological toxicity, but also have excellent luminescent properti...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C09K11/88
Inventor 刘福田李姗姗王群陈秀秀姜庆辉王冬至杨萍
Owner UNIV OF JINAN
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products