CN1547238A - Method for preparing CdSe quantum point - Google Patents
Method for preparing CdSe quantum point Download PDFInfo
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- CN1547238A CN1547238A CNA2003101114942A CN200310111494A CN1547238A CN 1547238 A CN1547238 A CN 1547238A CN A2003101114942 A CNA2003101114942 A CN A2003101114942A CN 200310111494 A CN200310111494 A CN 200310111494A CN 1547238 A CN1547238 A CN 1547238A
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Abstract
The invention discloses a method for producing CdSe quantum points. The invention uses the cadmium oxide and selenium as materials, produces the CdSe quantum points with variable particle size in condition of relative moderate environment. The method can avoid the problem that the tri-n-capryl phosphine (TOP) or tri-n-butyl group phosphine (TBP) are inflammable, explosive and expensive and that the toxin is strong. The operation is safe, convenient, the repeatability is good, it needn't the glove box, and the cost is low. The produce has excellent monodispersity, the particle size is controllable. The synthesized CdSe quantum points can be used as in label material light emission device, and laser field, or can be used in the biological detection and analysis further.
Description
Technical field
The present invention relates to the preparation method of CdSe quantum dot.
Background technology
Quantum dot be radius less than or approach the semiconductor nano crystal grain of exciton Bohr radius, because of having distinctive quantum size effect and skin effect, it is had broad application prospects at aspects such as luminescent material, light sensors.CdSe, II-VI type quantum dots such as CdS, has special and good visible region fluorescent emission character, its fluorescence intensity height, the bleaching speed low, fluorescence spectrum is narrow, highly sensitive, and excitation spectrum continuous distribution, the fluorescence spectra position can be regulated and control by the size that changes quantum dot, many II-VI type quantum dots, as CdS, CdSe, the emission spectrum of CdTe etc. is crossed over the visible range, can excite different quantum dots simultaneously at a certain wavelength, obtain the different visible emission spectrum of wide region, carry out multiplex fluorescence and detect.These characteristics make quantum dot can be used as the novel fluorescent marker of a class, have broad application prospects in biomolecule identification and in detecting.
Need pure, stable, monodispersed high-quality nanocrystal in the practical application, and this to be common sedimentation can not get, so the preparation of relevant quantum dot becomes hot research in recent years.CdO such as Peng, Cd (Ac)
2, CdCO
3Salt of weak acid and selenium powder Deng cadmium are made raw material, use TOPO, HDA, and stearic acid, TOP, TBP etc. have synthesized the II-VI type quantum dot of function admirable as solvent.Though can successfully synthesize II-VI type quantum dots such as CdSe in this way, because the quantum dot of preparation has adopted the inflammable reagent of the contour poison of TBP, TOP usually, generally to use glove box, harsh experiment condition has limited their application.
Summary of the invention
Problem to be solved by this invention provides a kind of preparation method of CdSe quantum dot, and this method materials safety is easy to get, and is cheap, and simple and safe operation does not need exacting terms.
Technical scheme provided by the invention is: a kind of preparation method of CdSe quantum dot, comprise the steps: that (a) joins selenium powder in the vaccenic acid, the content that makes selenium is 0.01~0.05mol/L, in the presence of argon gas, be heated to 200~220 ℃, be incubated after 10~30 minutes, be cooled to room temperature, remove insoluble matter, make the storing solution of selenium; (b) CdO and stearic acid are added in the vaccenic acid, make CdO and stearic content be respectively 0.01~0.05mol/L and 0.04~0.20mol/L, in the presence of argon gas, be heated to 130~200 ℃ and kept 10~30 minutes, reduce to room temperature then, make the storing solution of cadmium; (c) get the storing solution 1~10mL of selenium, join in 0.1~0.5g oxidation tri-n-octyl phosphine (TOPO) and the 0.3~2g cetylamine (HDA), in the presence of argon gas, stir and be heated to 260~290 ℃, the storing solution of 0.5~5mL cadmium is heated in the mixture of the storing solution that joins above-mentioned oxidation tri-n-octyl phosphine, cetylamine and selenium after 60 ℃~80 ℃, kept 10~300 seconds at 200~260 ℃, be cooled to 30-50 ℃ then, promptly make the CdSe quantum dot.Perhaps, get the storing solution 0.5~5mL of cadmium, join in 0.1~0.5g oxidation tri-n-octyl phosphine (TOPO) and the 0.3~2.0g cetylamine (HDA), in the presence of argon gas, stir and be heated to 260~290 ℃, storing solution with 1~10mL selenium is heated in the mixture of the storing solution that adds above-mentioned oxidation tri-n-octyl phosphine, cetylamine and selenium after 60 ℃~80 ℃ simultaneously, kept 10~300 seconds at 200~260 ℃, be cooled to 30-50 ℃ then, promptly make the CdSe quantum dot.
Above-mentioned gained CdSe quantum dot is joined in the n-hexane, centrifugal, after discarding lower sediment, in solution, add acetone, leave standstill and make the product precipitation, centrifugal, obtain the CdSe precipitation of flow-like, it is dissolved in the n-hexane, centrifugal once more, remove the hyperfluorescence clear solution that post precipitation obtains the CdSe quantum dot.
The present invention is directed to the major defect of quantum dot preparation method in the prior art, replace TOP or TBP to prepare the storing solution of selenium, under gentle, safe relatively condition, prepared the CdSe quantum dot of different-grain diameter, narrow size distribution with vaccenic acid (ODE).Adopt the present invention, materials safety is easy to get, and is cheap, and simple and safe operation does not need harsh experiment condition, makes laboratory mass preparation and even suitability for industrialized production become possibility.Transmission electron microscope, uv-visible absorption spectra, method characterization results such as fluorescence spectrum prove, product homogeneous and good monodispersity, good stability are arranged.Can be used for fields such as light emitting devices and Laser Devices, be used for the biological substance analysis after further modifying.
Description of drawings
Fig. 1 is the TEM image of 2.5nmCdSe quantum dot of the present invention;
Fig. 2 is the TEM image of 3.9nmCdSe quantum dot;
Fig. 3 is the TEM image of 7.0nmCdSe quantum dot;
Fig. 4 is 2.5nmCdSe quantum dot absorption spectrum and fluorescence emission spectrum; Wherein curve (a) is an absorption spectrum, and curve (b) is a fluorescence emission spectrum;
Fig. 5 is 3.9nmCdSe quantum dot absorption spectrum and fluorescence emission spectrum; Wherein curve (c) is an absorption spectrum, and curve (d) is a fluorescence emission spectrum;
Fig. 6 is 7.0nmCdSe quantum dot absorption spectrum and fluorescence emission spectrum; Wherein curve (e) is an absorption spectrum; Curve (f) is a fluorescence emission spectrum;
Embodiment
Embodiment one:
1. take by weighing selenium powder 0.079g, put into the flask that 20mL vaccenic acid (ODE) is housed, adopt the Schlenk technology, charge into Ar gas after vacuumizing with vacuum pump, six times so that be full of Ar gas in the reaction vessel so repeatedly, be heated to 200~220 ℃ then, be incubated 20 minutes, be cooled to room temperature, if any a small amount of insoluble matter, it is discarded, make the storing solution of 0.05mol/L selenium.
2. take by weighing 0.0512gCdO, 0.456g stearic acid and 10mL ODE and put into three mouthfuls of Schlenk reaction vessels, adopt the Schlenk technology, charge into Ar gas after vacuumizing with vacuum pump, six times so that be full of Ar gas in the reaction vessel so repeatedly, then be heated to 150 ℃ and be incubated about 20min, CdO is fully dissolved; Reduce to room temperature preservation then.Make the storing solution of Cd.The Cd storing solution need be heated to 60~80 ℃ before using.
3. get the storing solution 4mL of 0.05mol/L selenium, add 0.25g oxidation tri-n-octyl phosphine (TOPO) and 0.75g cetylamine (HDA), after adopting the described Schlenk technology degassing of step 1, stir, be heated to 290 ℃, the storing solution 0.5mL with Cd injects reaction vessel rapidly simultaneously, is incubated 10~300 seconds according to the size of required quantum dot about 260 ℃, remove heater rapidly and make product be cooled to 30-50 ℃, promptly make the CdSe quantum dot.Keep to obtain the 2.5nmCdSe quantum dot in 10 seconds; Keep to obtain the 7.0nmCdSe quantum dot in 5 minutes.Fig. 1 and Fig. 3 are respectively the TEM image of 2.5nm of the present invention and 7.0nmCdSe quantum dot, the CdSe quantum point grain diameter distribution uniform of being synthesized as can be seen from Figure.Along with the prolongation in reaction time, particle diameter can increase gradually.Fig. 4 is 2.5nmCdSe quantum dot absorption spectrum and fluorescence emission spectrum, and wherein curve (a) is an absorption spectrum, and curve (b) is a fluorescence emission spectrum; Fig. 6 is 7.0nmCdSe quantum dot absorption spectrum and fluorescence emission spectrum; Wherein curve (e) is an absorption spectrum, and curve (f) is a fluorescence emission spectrum.The synthetic CdSe quantum dot of other method of the feature of these figure and bibliographical information is consistent, shows that synthetic is the CdSe quantum dot really.
4. add n-hexane in the product in step 3, centrifugal, after discarding lower sediment, in solution, add acetone, leave standstill and product was precipitated in 10 minutes, centrifugal, the CdSe precipitation of removing behind the solution flow-like is dissolved in the n-hexane, centrifugal once more, the product that the removal post precipitation obtains is the clear solution of hyperfluorescence, and its color changes with the size of CdSe particle diameter.
Embodiment two:
1. take by weighing selenium powder 0.079g, put into the flask that 20mL vaccenic acid (ODE) is housed, adopt the Schlenk technology, charge into Ar gas after vacuumizing with vacuum pump, six times so that be full of Ar gas in the reaction vessel so repeatedly, be heated to 200 ℃ then, be incubated after 20 minutes, be cooled to room temperature, if any a small amount of insoluble matter, it is discarded, make the storing solution of 0.05mol/L selenium.
2. take by weighing 0.0512gCdO, 0.456g stearic acid and 10mL ODE and put into three mouthfuls of Schlenk reaction vessels, adopt the Schlenk technology, charge into Ar gas after vacuumizing with vacuum pump, six times so that be full of Ar gas in the reaction vessel so repeatedly, then be heated to 150 ℃ and be incubated about 20min, CdO is fully dissolved, reduce to room temperature preservation then, make the cadmium storing solution.The Cd storing solution need be heated to 60~80 ℃ before using.
3. get the storing solution 0.5mL of 0.04mol/L Cd, add 0.25g oxidation tri-n-octyl phosphine (TOPO) and 0.75g cetylamine (HDA), after adopting the described Schlenk technology degassing of step 1, stir, be heated to 290 ℃, the storing solution 4mL of 0.05mol/L selenium is injected reaction vessel rapidly, about 260 ℃, be incubated and held 10 seconds, remove heater rapidly and make product be cooled to 30-50 ℃, promptly make the 3.9nmCdSe quantum dot.Fig. 2 is the TEM image of 3.9nmCdSe quantum dot; Fig. 5 is 3.9nmCdSe quantum dot absorption spectrum and fluorescence emission spectrum, and wherein curve (c) is an absorption spectrum, and curve (d) is a fluorescence emission spectrum.These features all feature with the synthetic CdSe quantum dot of other method of bibliographical information are consistent.Its rule also with people such as Peng report (Qu L.and Peng X., J.Am.Chem.Soc., 2002,124:2049-2055.) similar.
4. in the product of present embodiment 3, add n-hexane, centrifugal, discard post precipitation, in solution, add acetone, leave standstill and made product precipitation, centrifugation in 10 minutes, the CdSe precipitation of flow-like is dissolved in the hexane, and centrifugal once more, the product that the removal post precipitation obtains is the clear solution of hyperfluorescence.
Adopt the present invention to prepare quantum dot, have the following advantages: 1. adopting low toxicity, stable, cheap reagent ODE to replace toxicity height, inflammable and explosive, reagent TBP or TOP that cost is high, is a kind of green chemical synthesis method of real meaning; 2. product homogeneous and good monodispersity, adjustable grain are arranged; 3. such quantum dot can be used for fields such as light emitting devices and Laser Devices, can be used for the biological substance analysis after the modification.
Claims (4)
1.CdSe the preparation method of quantum dot comprises the steps: that (a) adds selenium powder in the vaccenic acid, the content that makes selenium is 0.01~0.05mol/L, in the presence of argon gas, be heated to 200~220 ℃, be incubated after 10~30 minutes, be cooled to room temperature, remove insoluble matter, make the storing solution of selenium; (b) CdO and stearic acid are added in the vaccenic acid, make CdO and stearic content be respectively 0.01~0.05mol/L and 0.04~0.20mol/L, in the presence of argon gas, be heated to 130~200 ℃ and kept 10~30 minutes, reduce to room temperature then, make the storing solution of cadmium; (c) get the storing solution 1~10mL of selenium, join in 0.1~0.5g oxidation tri-n-octyl phosphine and the 0.3~2.0g cetylamine, stirring and be heated to 260~290 ℃ in the presence of argon gas simultaneously; The storing solution of 0.5~5mL cadmium is heated in the mixture of the storing solution that joins above-mentioned oxidation tri-n-octyl phosphine, cetylamine and selenium after 60 ℃~80 ℃, kept 10~300 seconds, be cooled to 30-50 ℃ then, promptly make the CdSe quantum dot at 200~260 ℃.
2. according to the preparation method of claim 1, it is characterized in that: will make the CdSe quantum dot and join in the n-hexane, centrifugal, after discarding lower sediment, in solution, add acetone, leave standstill and make the product precipitation, centrifugal, the CdSe precipitation of removing behind the solution flow-like is dissolved in the n-hexane, and is centrifugal once more, removes the hyperfluorescence clear solution that precipitation obtains containing the CdSe quantum dot.
3.CdSe the preparation method of quantum dot comprises the steps: that (a) adds selenium powder in the vaccenic acid, the content that makes selenium is 0.01~0.05mol/L, and in the presence of argon gas, be heated to 200~220 ℃, and be incubated after 10~30 minutes, be cooled to room temperature, remove insoluble matter, make the storing solution of selenium; (b) CdO and stearic acid are added in the vaccenic acid, make CdO and stearic content be respectively 0.01~0.05mol/L and 0.04~0.2mol/L, and in the presence of argon gas, be heated to 130~200 ℃, be incubated 10~30 minutes, reduce to room temperature then, make the storing solution of cadmium; (c) get the storing solution 0.5~5mL of cadmium, join in 0.1~0.5g oxidation tri-n-octyl phosphine and the 0.3~2.0g cetylamine, and in the presence of argon gas, stir and be heated to 260~290 ℃, storing solution with 1~10mL selenium is heated in the mixture of the storing solution that joins above-mentioned oxidation tri-n-octyl phosphine, cetylamine and selenium after 60 ℃~80 ℃ simultaneously, kept 10~300 seconds at 200~260 ℃, be cooled to 30-50 ℃ then, promptly make the CdSe quantum dot.
4. according to the preparation method of claim 3, it is characterized in that: will make the CdSe quantum dot and add n-hexane, centrifugal, after discarding lower sediment, in solution, add acetone, leave standstill and make the product precipitation, centrifugal, the CdSe precipitation of removing behind the solution flow-like is dissolved in the hexane, and is centrifugal once more, removes the clear solution of the hyperfluorescence that contains the CdSe quantum dot that post precipitation obtains.
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1328351C (en) * | 2005-09-23 | 2007-07-25 | 上海大学 | Method for preparing II-VI family fluorescent mark semiconductor quantum point MX |
CN100352886C (en) * | 2005-12-28 | 2007-12-05 | 武汉大学 | Method for preparing CdSe quantum |
CN100413938C (en) * | 2006-07-07 | 2008-08-27 | 中国科学技术大学 | Au/CdSe heterostructure quantum point and its preparation method |
CN100503774C (en) * | 2005-10-21 | 2009-06-24 | 中国科学院上海应用物理研究所 | Cadmium sulfide bare quantum spot and preparation process |
CN101181978B (en) * | 2007-11-15 | 2010-06-02 | 合肥工业大学 | Method for synthesizing cadmium selenide or zinc selenide quantum-dot by selenium dioxide |
CN101332979B (en) * | 2008-08-01 | 2010-06-02 | 湖南大学 | Method for preparing CdSe and ZnSe quantum dot nanometer granules |
CN101186825B (en) * | 2007-11-15 | 2011-03-30 | 合肥工业大学 | Selenium precursor fluid and method for preparing cadmium selenide or zinc selenide quantum dots by using the same |
CN101290319B (en) * | 2007-04-16 | 2013-05-08 | 北京出入境检验检疫局检验检疫技术中心 | H5N1 type highly pathogenic avian influenza nanometer quantum point detection method |
CN104910918A (en) * | 2015-04-30 | 2015-09-16 | 中国科学院半导体研究所 | Core-shell quantum dot material and preparation method thereof |
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2003
- 2003-12-02 CN CN 200310111494 patent/CN1260771C/en not_active Expired - Fee Related
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1328351C (en) * | 2005-09-23 | 2007-07-25 | 上海大学 | Method for preparing II-VI family fluorescent mark semiconductor quantum point MX |
CN100503774C (en) * | 2005-10-21 | 2009-06-24 | 中国科学院上海应用物理研究所 | Cadmium sulfide bare quantum spot and preparation process |
CN100352886C (en) * | 2005-12-28 | 2007-12-05 | 武汉大学 | Method for preparing CdSe quantum |
CN100413938C (en) * | 2006-07-07 | 2008-08-27 | 中国科学技术大学 | Au/CdSe heterostructure quantum point and its preparation method |
CN101290319B (en) * | 2007-04-16 | 2013-05-08 | 北京出入境检验检疫局检验检疫技术中心 | H5N1 type highly pathogenic avian influenza nanometer quantum point detection method |
CN101181978B (en) * | 2007-11-15 | 2010-06-02 | 合肥工业大学 | Method for synthesizing cadmium selenide or zinc selenide quantum-dot by selenium dioxide |
CN101186825B (en) * | 2007-11-15 | 2011-03-30 | 合肥工业大学 | Selenium precursor fluid and method for preparing cadmium selenide or zinc selenide quantum dots by using the same |
CN101332979B (en) * | 2008-08-01 | 2010-06-02 | 湖南大学 | Method for preparing CdSe and ZnSe quantum dot nanometer granules |
CN104910918A (en) * | 2015-04-30 | 2015-09-16 | 中国科学院半导体研究所 | Core-shell quantum dot material and preparation method thereof |
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