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High-quantum-yield eigenstate-fluorescence-adjustable carbon dot and preparing method and application thereof

An eigenstate, high-quantum technology, applied in luminescent materials, chemical instruments and methods, electrical components, etc., can solve problems such as low performance of light-emitting diode devices, limited effective carrier injection, and changes in fluorescence emission peaks, etc., to achieve The effect of high yield, high crystallinity and simple method

Active Publication Date: 2017-04-19
BEIJING NORMAL UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The carbon dots currently reported in the literature often have poor crystallinity, and the surface often contains a large number of defects, which in turn will generate a large number of defect state energy levels, so that the fluorescence of carbon dots is often dominated by the surface defect states, showing that the fluorescence emission peak position varies with the excitation wavelength. Fluorescent properties of defect states that change
For the application of optoelectronic devices such as electroluminescent diodes, the defect state fluorescence of carbon dots greatly limits the effective injection of carriers, making the performance of light-emitting diodes very low, which greatly limits its application in the field of electroluminescent diodes. Applications
[0004] At present, although the excitation-independent intrinsic state fluorescent carbon dots can be prepared using aniline as a precursor, its quantum yield is relatively low (20%).
Using a simple method to prepare carbon dots with high quantum yield and tunable intrinsic state fluorescence whose fluorescence emission peak does not change with the excitation wavelength is still a big challenge

Method used

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  • High-quantum-yield eigenstate-fluorescence-adjustable carbon dot and preparing method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0044] Example 1. Preparation of intrinsic blue carbon dots with a quantum yield of 75%

[0045] Weigh 0.01 g each of 2,3-diaminonaphthalene and citric acid solids with a mass ratio of 1:1, and dissolve them in 10 ml of ethanol under ultrasonic stirring. 0.1ml of concentrated sulfuric acid was added to the reaction system as a reaction catalyst. Transfer the above solution to a 25ml polytetrafluoroethylene lined stainless steel autoclave, and tighten the lid. Solvothermally react at 140℃ for 4 hours, then let the reaction kettle cool to room temperature naturally to obtain a light yellow carbon dot ethanol solution, then neutralize to neutral with 20ml 0.01 mole per liter sodium hydroxide aqueous solution, then filter Take the filtrate and place it in a dialysis bag (1000Da) and dialyze it in deionized water for two days, changing the deionized water every three hours. After the dialysis, the solution in the dialysis bag is collected and freeze-dried to obtain the carbon dot so...

Embodiment 2

[0049] Example 2. Preparation of intrinsic green carbon dots with a quantum yield of 73%

[0050] The specific steps are the same as in Example 1, except that the precursor 2,3-diaminonaphthalene and citric acid solid are 0.1 and 0.01 g, respectively, the mass ratio is 10:1, the reaction temperature is 180° C., and the solvothermal reaction time is 9 hours. The resulting dilute ethanol solution of carbon dots emits bright green fluorescence under a portable ultraviolet lamp (365nm), and the green carbon dots exhibit excitation-independent intrinsic state fluorescence characteristics ( Picture 10 ), the emission peak is at 513nm. Green carbon dots have high crystallinity, with an average particle size of 2.41nm ( Picture 11 ). The measured absolute fluorescence quantum yield is as high as 73%.

Embodiment 3

[0051] Example 3. Preparation of intrinsic state yellow carbon dots with a quantum yield of 58%

[0052] The specific steps are the same as in Example 1. The difference is that the precursors are 1,5-diaminonaphthalene and citric acid, the masses are 0.04 and 0.01g, respectively, the mass ratio is 4:1, and the volume-to-mass ratio of ethanol to carbon source precursor is mL / The mg is 1:5, the reaction temperature is 200°C, and the solvothermal reaction time is 9 hours. The resulting dilute ethanol solution of carbon dots emits bright yellow fluorescence under a portable ultraviolet lamp (365nm), and the yellow carbon dots exhibit excitation-independent intrinsic state fluorescence characteristics ( Picture 12 ), the emission peak is at 535nm. Yellow carbon dots have high crystallinity, with an average particle size of 3.78nm ( Figure 13 ). The measured absolute fluorescence quantum yield is as high as 58%.

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Abstract

The invention relates to the field of fluorescence carbon nanomaterials, in particular to a high-quantum-yield eigenstate-fluorescence-adjustable carbon dot and a preparing method and application thereof. Diaminonaphthalene or a hydroxyl, carboxyl, methyl, ethyl, N,N-dimethyl and N,N-diethyl substituted ramification of the diaminonaphthalene and citric acid serve as carbon source precursors, an eigenstate fluorescence carbon dot solution can be obtained through a solvothermal method. The prepared eigenstate fluorescence carbon dot has the beneficial effects of being high in crystallization, high in surface passivation degree, even in nitrogen doping, even in size distribution and the like, and has the wide application prospect.

Description

Technical field [0001] The invention relates to the field of fluorescent carbon nanomaterials, and in particular to carbon dots with high quantum yield and adjustable intrinsic state fluorescence, and a preparation method and application thereof. Background technique [0002] Carbon Dots (CDs), as a new type of carbon nanomaterials with a size of less than 10nm, exhibit low toxicity, good biocompatibility, chemical inertness, stable fluorescence properties, and better surface modification capabilities. Devices, biomedicine, and sensors have broad application prospects. At present, the methods for preparing carbon dots are mainly divided into two categories: top-down and bottom-up. The top-down method generally uses bulk carbon materials as carbon sources, such as graphite, carbon fiber, carbon nanotubes, carbon black, coal, etc., to obtain carbon dots by means of violent oxidation and stripping. The bottom-up method is mainly based on small organic molecules or polymers as carb...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C09K11/65H01L33/50
CPCC09K11/65H01L33/502
Inventor 范楼珍袁方龙杨世和
Owner BEIJING NORMAL UNIVERSITY
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