CN1557717A - Method for preparing zinc oxide nanometer material with orientation arrangement nano-towers - Google Patents
Method for preparing zinc oxide nanometer material with orientation arrangement nano-towers Download PDFInfo
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- CN1557717A CN1557717A CNA2004100159866A CN200410015986A CN1557717A CN 1557717 A CN1557717 A CN 1557717A CN A2004100159866 A CNA2004100159866 A CN A2004100159866A CN 200410015986 A CN200410015986 A CN 200410015986A CN 1557717 A CN1557717 A CN 1557717A
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Abstract
The preparation process of nano tower oriented nano zinc oxide material includes dissolving zinc salt, ammonia water, thiourea and ammonium salt in certain proportion in deionized water to prepare film growing reaction solution; and soaking processed substrate inside the reaction solution, heating to 94-97 deg.c to reaction for 45-60 min to obtain compact nano tower oriented nano zinc oxide material. The said process of the present invention is simple, low in cost and short in production period, and the prepared nano zinc oxide material consists of oriented nano tower of average diameter of 600 nm and length of 6 micron.
Description
Technical field
The present invention relates to a kind of preparation method of nano zinc oxide material, relate in particular to a kind of preparation method of nano zinc oxide material of nano tower oriented nano, adopt the chemical solution growth method to prepare the nano zinc oxide material of nano tower oriented nano.
Background technology
Nano material's structure and pattern have very big influence to the performance and the application of nano material, and the nano crystal material of preparing ad hoc structure and pattern has important meaning for the frontier of developing the nano material function.One-dimensional nano structure material is owing to having the bigger length-to-diameter ratio person of having good application prospects.In these nano materials, zinc oxide owing to have good light, electricity, magnetic property at the uv-absorbing material, photocatalyst material is widely used on functional nano material such as varistor, electrode materials, solar cell and the device, thereby enjoys attention.In the numerous one dimension pattern of nano zinc oxide material (nanometer rod, nano wire, nano belt, nanofiber, nanotube), also there is not the report of tower shape nano structure of zinc oxide material at present.And the research of nano zinc oxide material at present has two weak points, and one is that the preparation method requires height, and the preparation method of the one-dimensional zinc oxide nanometer material of having reported at present mainly contains two kinds of vapor phase process and solvent-thermal methods.And these two kinds of methods need extreme exacting terms such as high temperature, high pressure or high vacuum, and these conditions have brought very adverse influence for the cost and the efficient of material preparation, thereby need to be improved or replace.The another one weak point is that the one-dimensional zinc oxide nanometer material of preparing at present mainly is Powdered random dispersion, and the application for nano-device also has certain distance like this.And the monodimension nanometer material of tower shape is aligned on the semiconductor material and will the application of nano-device be had great significance according to certain mode.
Summary of the invention
The objective of the invention is at the deficiencies in the prior art, provide a kind of simple to operate, the preparation method of the nano zinc oxide material of the nano tower oriented nano that temperature of reaction is low, cost is low, production efficiency is high.
For realizing such purpose, in the technical scheme of the present invention, adopt chemical solution method to prepare the nano zinc oxide material of nano tower oriented nano.The substrate of handling is immersed in zinc salt, ammoniacal liquor, thiocarbamide and the ammonium salt mixing solutions for preparing, treat to be warming up to 94～97 ℃ after the solution clarification, react the nano zinc oxide material that the tower shape aligns that has that can obtain densification in 45～60 minutes.The nano zinc oxide material of the nano tower oriented nano of preparation is made up of aligning of Vita shape nanocrystal, and the mean diameter of nanometer tower is 600nm, length 6 μ m.Preparation method of the present invention comprises following concrete steps:
1. the preparation of chemically grown reaction solution: zinc salt, ammoniacal liquor, thiocarbamide and ammonium salt are dissolved in deionized water by a certain percentage, are prepared into the film growth reaction solution.Contain zinc salt 0.01mol, mass ratio in every 100ml reaction solution and be 25% ammoniacal liquor 5ml, thiocarbamide 0.01mol and ammonium salt 0.002mol.
The said zinc salt of the present invention is a zinc nitrate hexahydrate; Ammonium salt is an ammonium chloride.
2. the pre-treatment of substrate: at first substrate was immersed in the vitriol oil of ebullient 98% 5～10 hours, was immersed in then in the acetone ultrasonic 30～60 minutes, next use a large amount of deionized water rinsings, at last substrate is dried in vacuum drying oven, stand-by.
The said substrate of the present invention is sheet glass or quartz substrate.
3. the nano zinc oxide material of nano tower oriented nano is synthetic: before reaction, at first substrate is soaked in the above-mentioned chemically grown reaction soln for preparing; Reaction system is warming up to 94～97 ℃ again, temperature rise rate 10～20 degree/minute, reacted 45～60 minutes down at 94～97 ℃.Reaction finishes the back cools off fast with frozen water, substrate is put in deionized water for ultrasonic 1～2 minute then, uses a large amount of deionized water rinsings, through repeatedly drying the nano zinc oxide material that can obtain nano tower oriented nano naturally after the washing.
Excellent results of the present invention is:
1. owing to adopted the buffered soln of ammoniacal liquor and ammonium salt as reaction solution, make in the process of zinc-oxide nano tower crystal growth reaction soln pH value keep stable to a certain extent, this even growth of arranging for the nanometer tower provides good growth sublimity, thereby the zinc-oxide nano tower good uniformity of preparation.
2. because the chemical solution method temperature of reaction that the present invention adopts is low, have only 94～97 ℃, reaction times is short, only need 45～60 minutes, reaction raw materials is cheap, only need zinc salt, thiocarbamide, ammoniacal liquor and ammonium salt commonly used, thereby the inventive method is simple to operate, cost is low, efficient height, the nano zinc oxide material of the nano tower oriented nano of preparation are that the hexagonal nano tower of 6 microns of 600 nanometers, length aligns and forms by mean diameter.
Description of drawings
Fig. 1 is the x-ray diffraction pattern of the nano zinc oxide material of the embodiment of the invention 1 resulting nano tower oriented nano.
Fig. 2 is the EDS figure of the nano zinc oxide material of the embodiment of the invention 1 resulting nano tower oriented nano.
Fig. 3 is the electron scanning micrograph of the nano zinc oxide material of the embodiment of the invention 1 resulting nano tower oriented nano.
Embodiment
The following examples are to further specify of the present invention, rather than limit the scope of the invention.
Embodiment 1
1. in the ptfe plastic bottle of a 100mL, 0.01mol zinc nitrate, 0.01mol thiocarbamide, 0.002mol ammonium chloride are dissolved in the 95mL deionized water, be stirred to the ammoniacal liquor that adds 5ml 25% after whole dissolvings, continue when adding to stir, just be prepared into the reaction solution of zinc-oxide film growth after the solution clarification.
2. quartz plate that will the wide 20mm of long 50mm is immersed in the ebullient vitriol oil, and soak and immerse again in the acetone soln after 10 hours, ultrasonic 30 minutes, use a large amount of deionized water rinsings again, it is dry to put into vacuum drying oven at last.
3. will be immersed in according in the reaction solution that is 1. disposed according to the quartz substrate that 2. step is handled, then reaction flask be placed oil bath pan, according to 10 the degree/minute speed temperature of reaction is risen to 95 ℃, kept 45 minutes.Then quartz substrate is immersed in the frozen water territory and cools off.After the cooling quartz substrate is immersed in deionized water for ultrasonic 2 minutes, uses a large amount of deionized water rinsings again.To dry under the quartz substrate room temperature at last, promptly obtain the nano zinc oxide material of nano tower oriented nano.
X-ray diffraction spectrogram such as Fig. 1 that resulting zinc-oxide nano tower is arranged.Prepared as seen from Figure 1 material is pure zinc oxide, does not have other impurity, and crystalline form is a hexagonal crystal shape.For further proof degree of purity of production, the element EDS that product has been carried out scanning electron microscope analyzes, and Fig. 2 is the EDS figure of product, and as seen from the figure, product has only zinc and two kinds of elements of oxygen, does not have the impurity of element such as other sulphur.Electron scanning micrograph such as Fig. 3, wherein a figure is the positive Electronic Speculum picture of prepared nano material, and b figure is the amplification picture of a figure, and c figure is the side photo of nanometer tower.Prepared as seen from Figure 3 zinc oxide material is made up of the nanometer tower of hexagonal prism shape, and the diameter of zinc-oxide nano tower is about 600 nanometers, about 6 microns of length, and length-to-diameter ratio is about 12.
Embodiment 2
1. in the ptfe plastic bottle of a 100mL, 0.01mol zinc nitrate, 0.01mol thiocarbamide, 0.002mol ammonium chloride are dissolved in the 95mL deionized water, be stirred to the ammoniacal liquor that adds 5ml 25% after whole dissolvings, continue when adding to stir, just be prepared into the reaction solution of zinc-oxide film growth after the solution clarification.
2. sheet glass that will the wide 20mm of long 50mm is immersed in the ebullient vitriol oil, and soak and immerse again in the acetone soln after 10 hours, ultrasonic 60 minutes, use a large amount of deionized water rinsings again, it is dry to put into vacuum drying oven at last.
3. will be immersed in according in the reaction solution that is 1. disposed according to the glass substrate that 2. step is handled, then reaction flask be placed oil bath pan, according to 20 the degree/minute speed temperature of reaction is risen to 97 ℃, kept 60 minutes.Then glass substrate is immersed in the frozen water territory and cools off.After the cooling glass substrate is immersed in deionized water for ultrasonic 1 minute, uses a large amount of deionized water rinsings again.To dry under the glass substrate room temperature at last, promptly obtain the nano zinc oxide material of nano tower oriented nano.
Embodiment 3
1. in the ptfe plastic bottle of a 100mL, 0.01mol zinc nitrate, 0.01mol thiocarbamide, 0.002mol ammonium chloride are dissolved in the 95mL deionized water, be stirred to the ammoniacal liquor that adds 5ml 25% after whole dissolvings, continue when adding to stir, just be prepared into the reaction solution of the nano zinc oxide material growth of nano tower oriented nano after the solution clarification.
2. quartz plate that will the wide 20mm of long 50mm is immersed in the ebullient vitriol oil, and soak and immerse again in the acetone soln after 8 hours, ultrasonic 45 minutes, use a large amount of deionized water rinsings again, it is dry to put into vacuum drying oven at last.
3. will be immersed in according in the reaction solution that is 1. disposed according to the quartz substrate that 2. step is handled, then reaction flask be placed oil bath pan, according to 15 the degree/minute speed temperature of reaction is risen to 94 ℃, kept 45 minutes.Then quartz substrate is immersed in the frozen water territory and cools off.After the cooling quartz substrate is immersed in deionized water for ultrasonic 1 minute, uses a large amount of deionized water rinsings again.To dry under the quartz substrate room temperature at last, promptly obtain the nano zinc oxide material of nano tower oriented nano.
Claims (3)
1. the preparation method of the nano zinc oxide material of a nano tower oriented nano is characterized in that comprising the steps:
1) preparation of chemically grown reaction solution: zinc salt, ammoniacal liquor, thiocarbamide and ammonium salt are dissolved in deionized water, be prepared into the film growth reaction solution, contain zinc salt 0.01mol, mass ratio in every 100ml reaction solution and be 25% ammoniacal liquor 5ml, thiocarbamide 0.01mol and ammonium salt 0.002mol;
2) pre-treatment of substrate: substrate was immersed in the vitriol oil of ebullient 98% 5～10 hours, was immersed in then in the acetone ultrasonic 30～60 minutes, dry with being placed in the vacuum drying oven behind the deionized water rinsing again, stand-by;
What 3) the zinc-oxide nano tower was arranged is synthetic: substrate is soaked in the chemically grown reaction soln for preparing, reaction system is warming up to 94～97 ℃ again, temperature rise rate 10～20 degree/minute, reacted 45～60 minutes down at 94～97 ℃, reaction finishes the back cools off fast, substrate is put in deionized water for ultrasonic 1～2 minute then, repeatedly washing the back with deionized water dries naturally, can obtain the nano zinc oxide material that the nanometer tower is arranged, the mean diameter of nanometer tower is 600nm, length 6 μ m.
2, the preparation method of the nano zinc oxide material of nano tower oriented nano as claimed in claim 1 is characterized in that described zinc salt is a zinc nitrate hexahydrate, and described ammonium salt is an ammonium chloride.
3, the preparation method of the nano zinc oxide material of nano tower oriented nano as claimed in claim 1 is characterized in that described substrate is sheet glass or quartz substrate.
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| CN 200410015986 CN1234610C (en) | 2004-01-19 | 2004-01-19 | Method for preparing zinc oxide nanometer material with orientation arrangement nano-towers |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100383049C (en) * | 2005-11-02 | 2008-04-23 | 东南大学 | Method of growing nano-rod shaped zinc oxide by hydrothermal decomposition |
| CN100396615C (en) * | 2006-06-30 | 2008-06-25 | 华东师范大学 | Process for preparing nano ZnO |
| CN100582012C (en) * | 2006-09-26 | 2010-01-20 | 中国科学院上海硅酸盐研究所 | Nano porous zinc oxide thin film with high C-axis orientation and preparation method thereof |
| CN101481134B (en) * | 2008-01-11 | 2010-12-08 | 南京理工大学 | Process for preparing zinc oxide nano film |
| CN102832120A (en) * | 2012-09-07 | 2012-12-19 | 天津大学 | Method for applying prestress on nanometer device surface |
| CN104003434A (en) * | 2014-06-16 | 2014-08-27 | 安徽师范大学 | Three-dimensional self-assembling zinc oxide nanometer heterogeneous material and preparing method and application thereof |
| CN112098390A (en) * | 2020-09-16 | 2020-12-18 | 燕山大学 | Surface enhanced Raman scattering substrate and preparation method thereof |
-
2004
- 2004-01-19 CN CN 200410015986 patent/CN1234610C/en not_active Expired - Fee Related
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100383049C (en) * | 2005-11-02 | 2008-04-23 | 东南大学 | Method of growing nano-rod shaped zinc oxide by hydrothermal decomposition |
| CN100396615C (en) * | 2006-06-30 | 2008-06-25 | 华东师范大学 | Process for preparing nano ZnO |
| CN100582012C (en) * | 2006-09-26 | 2010-01-20 | 中国科学院上海硅酸盐研究所 | Nano porous zinc oxide thin film with high C-axis orientation and preparation method thereof |
| CN101481134B (en) * | 2008-01-11 | 2010-12-08 | 南京理工大学 | Process for preparing zinc oxide nano film |
| CN102832120A (en) * | 2012-09-07 | 2012-12-19 | 天津大学 | Method for applying prestress on nanometer device surface |
| CN104003434A (en) * | 2014-06-16 | 2014-08-27 | 安徽师范大学 | Three-dimensional self-assembling zinc oxide nanometer heterogeneous material and preparing method and application thereof |
| CN112098390A (en) * | 2020-09-16 | 2020-12-18 | 燕山大学 | Surface enhanced Raman scattering substrate and preparation method thereof |
| CN112098390B (en) * | 2020-09-16 | 2021-12-14 | 燕山大学 | Surface enhanced Raman scattering substrate and preparation method thereof |
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| CN1234610C (en) | 2006-01-04 |
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