CN105399061B - A kind of preparation method of one-dimensional tin selenide monocrystal nanowire - Google Patents
A kind of preparation method of one-dimensional tin selenide monocrystal nanowire Download PDFInfo
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- 239000002070 nanowire Substances 0.000 title claims abstract description 37
- 238000002360 preparation method Methods 0.000 title claims abstract description 17
- MFIWAIVSOUGHLI-UHFFFAOYSA-N selenium;tin Chemical compound [Sn]=[Se] MFIWAIVSOUGHLI-UHFFFAOYSA-N 0.000 title claims abstract description 11
- 239000000463 material Substances 0.000 claims abstract description 34
- 238000000034 method Methods 0.000 claims abstract description 17
- 239000003054 catalyst Substances 0.000 claims abstract description 11
- 230000001681 protective effect Effects 0.000 claims abstract description 10
- 239000000843 powder Substances 0.000 claims abstract description 9
- 239000000758 substrate Substances 0.000 claims abstract description 6
- 238000010438 heat treatment Methods 0.000 claims abstract description 5
- 239000007789 gas Substances 0.000 claims description 24
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 16
- 239000002245 particle Substances 0.000 claims description 11
- 239000010453 quartz Substances 0.000 claims description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 229910052786 argon Inorganic materials 0.000 claims description 8
- 239000000084 colloidal system Substances 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000010431 corundum Substances 0.000 claims description 2
- 229910052593 corundum Inorganic materials 0.000 claims description 2
- 229910021419 crystalline silicon Inorganic materials 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 239000010445 mica Substances 0.000 claims 1
- 229910052618 mica group Inorganic materials 0.000 claims 1
- 238000012423 maintenance Methods 0.000 abstract 1
- KBPGBEFNGHFRQN-UHFFFAOYSA-N bis(selanylidene)tin Chemical compound [Se]=[Sn]=[Se] KBPGBEFNGHFRQN-UHFFFAOYSA-N 0.000 description 41
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 12
- 239000003708 ampul Substances 0.000 description 8
- 238000002441 X-ray diffraction Methods 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- 239000002105 nanoparticle Substances 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- 229910052573 porcelain Inorganic materials 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000003863 metallic catalyst Substances 0.000 description 3
- 239000002086 nanomaterial Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 229910052711 selenium Inorganic materials 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229910052718 tin Inorganic materials 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 229910005900 GeTe Inorganic materials 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 239000007790 solid phase Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 239000011232 storage material Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910018731 Sn—Au Inorganic materials 0.000 description 1
- DPRMFUAMSRXGDE-UHFFFAOYSA-N ac1o530g Chemical compound NCCN.NCCN DPRMFUAMSRXGDE-UHFFFAOYSA-N 0.000 description 1
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- 238000004458 analytical method Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
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- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001786 chalcogen compounds Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000009415 formwork Methods 0.000 description 1
- 239000008246 gaseous mixture Substances 0.000 description 1
- 238000001093 holography Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000001027 hydrothermal synthesis Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
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- 239000002127 nanobelt Substances 0.000 description 1
- 239000006250 one-dimensional material Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229910021426 porous silicon Inorganic materials 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000010532 solid phase synthesis reaction Methods 0.000 description 1
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- 230000005619 thermoelectricity Effects 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
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- Crystals, And After-Treatments Of Crystals (AREA)
Abstract
The invention discloses a kind of preparation method of one-dimensional tin selenide monocrystal nanowire; SnSe powder is placed in high-temperature resistant container; and put it into high temperature resistant boiler tube; boiler tube is put into vacuum tube furnace; base material with catalyst is placed in the boiler tube, closed boiler tube, makes to be in anaerobic vacuum state inside the boiler tube; protective gas is passed through afterwards, and adjusts intraductal pressure to 10 50 Torr;Open heater, the central high temperature area of the vacuum tube furnace is heated to 550 650 DEG C, mobile boiler tube pipe, the high-temperature resistant container in the placement source is located at central high temperature area, the substrate with catalyst and be located at low-temperature region, stopping heating obtaining one-dimensional inorganic nanometer wire structural material after the completion of maintenance said temperature treats nanowire growth.The method of SnSe nano wires prepared by the method is simple, practical, and product component is single, and the length of obtained SnSe nano wires, diameter are easily controlled, and yield is high.
Description
Technical field
The present invention relates to a kind of preparation method of one-dimensional tin selenide monocrystal nanowire, belong to semiconductor phase-change storage material skill
Art field.
Background technology
Stannic selenide (SnSe) is a kind of important group IV-VI semiconductor, belongs to typical laminated metal chalcogen compound
(LMCs), the indirect band gap of its body phase material is 0.90eV, and direct band gap is 1.30eV, can absorb the exhausted big portion of solar spectrum
Point, with superior electricity, optical property, while also having, thermal property is excellent, earth resource is abundant, environment-friendly, change
Property stabilization and the low feature of cost are learned, in infrared electro instrument, memory switching switch, thermoelectric-cooled material, optical filter, optics
Deposited in terms of recording materials, solar cell material, super-ionic material, sensor and laser material, the solid-phase media of hologram
In huge application value.
In terms of the research of early stage is concentrated mainly on the thermoelectric property research of SnSe crystalline materials.In recent years, as phase transformation is deposited
The rise of investigation of materials upsurge is stored up, SnSe materials are due to average with the phase-change storage material-GeTe identicals of current main flow
Valence electron number, approximate energy gap (GeTe:0.73-0.95eV, SnSe:0.95eV), and room temperature heat endurance is good, crystallization
Speed is big, and the advantages of crystallization time is short is very suitable for the lifting of data holding ability, gradually causes the concern of people.But with
Going deep into for research, people gradually have found, it is single that the phase change memory device of SnSe crystal series has an energy gap, continues resistance to
By poor in terms of property, the problem of can only maintaining less in terms of individual erasable circulation.And compare, low-dimension nano material has huge
Big specific surface area and the contribution of enhanced surface conductance.The anisotropic geometry feature of its one-dimensional material and the two of exciton
Dimension limitation, makes that the transmission of its carrier is limited in two dimensional surface, density of electronic states is greatly improved, and electrical conductivity is accordingly reduced, from
And the electricity completely different with body material, optically and thermally machinery, property are shown, therefore show the nano particle than zero dimension
More superior property.
But, from the point of view of the preparation and progress with regard to current low-dimensional SnSe nano materials, however it remains yield is small, easily by oxygen
Change, containing the problems such as impurity is more, electrical properties are unstable, such as:2003, Qian etc. with hydro-thermal method it is tentative be prepared for selenizing
Stannum nanowire (Chem.Lett., 2003,32,426), but its obtained stannic selenide nanowire diameter reaches 50nm, product amount
It is extremely few, and pattern is difficult to control to, simultaneously containing very many impurity (pattern and tin oxide of such as non-nano line);2006
Year, Zhao etc. using Woelm Alumina and porous silicon be template prepare SnSe nano wires (Angew.Chem.Int.Ed., 2006,
45,311), but its obtained selenizing stannum nanowire is polycrystalline, and the reaction time is up to 36 hours, obtains before pure products more
Cumbersome operation is needed to remove alumina formwork;2011, the molten liquid-liquid phase-solid phase method of the utilization such as Liu (Solution-
Liquid-Solid, SLS) by the use of Bi nano particles as catalyst, SnSe nano wires are prepared for, but XRD test results are shown
The SnSe prepared using this method crystal orientation is not single (Angew.Chem.Int.Ed., 2011,50,12050);2014,
Butt etc. is by the use of Sn and Se simple substance as raw material using chemical vapor deposition (Chemical Vapor Deposition, CVD) side
Method prepares SnSe nano wires, but prepare in product still containing many nanometer plates or lance type nanobelt (CrystEngComm,
2014,16,3470).So the system of high-quality one-dimensional SnSe monocrystal nanowires that are thinner, can accurately controlling Sn, Se ratio
Standby is still at present urgent problem to be solved.
The content of the invention
The purpose of the present invention is just to provide for a kind of preparation method of one-dimensional tin selenide monocrystal nanowire, using solution-air-
Gu the high-quality one-dimensional SnSe nano wires of growth mechanism.The method has that preparation method is simple, easily controllable, stable components uniform,
The advantages of nanowire diameter is homogeneous adjustable, the SnSe nano wires prepared with the method also have more preferable electric property.
To achieve the above object, the present invention takes following technical scheme:The present invention is gas-liquid-solid using catalyst auxiliary
(Vapor-liquid-solid) growing technology, including processing step are as follows:
A kind of preparation method of one-dimensional tin selenide monocrystal nanowire, is comprised the following steps that:
(1) SnSe powder is placed in high-temperature resistant container (preferably porcelain boat), then the high-temperature resistant container that SnSe powder will be filled
It is put into high temperature resistant boiler tube, high temperature resistant boiler tube is put into vacuum tube furnace, SnSe powder is located at vacuum tube furnace fire door
Position, the base material with catalyst is placed in the high temperature resistant boiler tube, the closed high temperature resistant boiler tube, makes the vacuum
Anaerobic vacuum state is in inside tube furnace, protective gas is passed through afterwards, and adjust the high temperature resistant boiler tube pressure to 10-
50Torr;
(2) heater is opened, the central high temperature area of the vacuum tube furnace is heated to 550-650 DEG C, mobile resistance to height
Warm boiler tube, makes the high-temperature resistant container be located at central high temperature area, the substrate with catalyst and is located at low-temperature region, maintain above-mentioned temperature
Degree is treated to stop heating after the completion of nanowire growth, obtains one-dimensional tin selenide monocrystal nanowire.
High temperature resistant furnace tube material is corundum or quartz in the step (1).
Catalyst is the Au nano-colloid particles that particle diameter is 10-60nm in the step (1).
Base material is the resistance to backing material for being higher than 500 DEG C in the step (1), and the base material is single crystalline Si or cloud
It is female.
Make in the step (1) specific as follows in the method for anaerobic vacuum state in the furnace chamber of the vacuum tube furnace:Profit
It is not higher than after 50mTorr, is passed through into pipe in protective gas to the furnace chamber with pressure in mechanical pumpijg gas to the furnace chamber
Pressure be not less than 1Torr, then be evacuated body to intraductal pressure not higher than 50mTorr, so repeatedly 2-4 (preferably 3) secondary anaerobic is true
Dummy status.
Protective gas in the step (1) is that nitrogen, argon gas or volume ratio are 90:The mixing of 10 argon gas and hydrogen,
Gas flow is 50-1000sccm.
The nanowire growth time in the step (2) is 60-300min.
In the step (2) 550-650 DEG C is heated to 70 DEG C/min of speed.
One-dimensional tin selenide monocrystal nanowire prepared by above-mentioned method.
Nano wire made from the above method is preparing phase-change storage material, infrared electro instrument, memory switching switch, thermoelectricity
Coolant, optical filter, optical writing material, solar cell material, super-ionic material, sensor and laser material, holography
Application in the solid-phase media of figure.
The low-temperature space of vacuum tube furnace in the step (2) is specially temperature range at 450-610 DEG C.
One-dimensional inorganic nanometer wire structural material in the step (2) is the SnSe nanometers along direction of growth uniform diameter
Line.
Beneficial effect:
The invention provides a kind of method using the one-dimensional SnSe nano-materials of gas-liquid-solid growth mechanism.This method profit
With pure SnSe as source, by being thermally formed gaseous state and incorporating the Sn-Au of formation nanoscale in Au nano particles in bases
Alloy solution drop, with the gradually increase of Sn contents in the nano-liquid droplet, solution progressivelyes reach supersaturation.Continue evaporation source material
Material, then can be such that solid-state Sn is gradually separated out from drop, and generate SnSe with the Se reactions in atmosphere, form the one-dimensional of uniform diameter
SnSe nano wires.Therefore the one-dimensional SnSe nano thread structures of uniform diameter are prepared by the size control of catalyst, and by adjusting
Reaction condition is controlled, such as growth time, evaporating temperature, growth pressure, gas flow rate realize the company of one-dimensional SnSe nanowire lengths
Continuous change.
Compared with current one-dimensional SnSe nano thread structures material, the present invention has:
(1) preparation method is simple, equipment is cheap, it is easily controllable, toxic organic compound when preparing source material can be reduced, such as:Two
Glycol (diethylene glycol), the contact of ethylenediamine (ethylenediamine) etc. and is used.
(2) nano wire using the metal simple-substance of uniform particle diameter nano particle as catalyst preparation have diameter it is homogeneous, can
The advantages of tune.
(3) also ensure that product proportioning is stable, products collection efficiency is high, impurity is few, chemical property is stable as source with SnSe
The features such as.
(4) SnSe nano wire uniform components prepared by the inventive method.
Brief description of the drawings
Fig. 1 is SEM (SEM) figure of the product of embodiment 1;
Fig. 2 is X-ray diffraction (XRD) figure of the product of embodiment 1;
Fig. 3 is X-ray diffraction transmission electron microscope (TEM) figure of the product of embodiment 1.
Embodiment
The preferred embodiments of the present invention are illustrated below in conjunction with accompanying drawing, it will be appreciated that preferred reality described herein
Apply example and be only limitted to the interpretation present invention, be not intended to limit the present invention.Unless otherwise specified, it is conventional method;The examination
Agent and material can be obtained from open commercial sources unless otherwise instructed.
SnSe powder used in following embodiments, is Tin Selenide, CAS:1315-06-5, Fw:197.65,
Density:6.18g/mL.
Embodiment 1
Take a certain amount of SnSe blocks to be put into porcelain alms bowl to pulverize, take out be placed in porcelain boat afterwards, porcelain boat is put in stone
Ying Guanzhong, and be positioned over the fire door position of vacuum tube furnace, carry the top of air-flow;Particle diameter is molten for 20nm Au nano-colloids
Drop is in Si<100>A period of time is stood in substrate, afterwards Si substrates are dried up using drying nitrogen, is placed on and carries air-flow
Lower section, the position apart from SnSe sources 9-14cm, closed quartz tube;Intraductal pressure not higher than 50mTorr is pumped to using mechanical pump
Afterwards, the pressure being passed through into pipe in argon gas to the pipe that flow is 100sccm is not less than 1Torr, then is evacuated in body to furnace chamber
Pressure is not higher than 50mTorr, and it is anaerobic vacuum state that so repeatedly 3 times, which make in furnace chamber, is passed through argon gas again afterwards and keeps stream
Measure as 70sccm, while it is 10torr to adjust intraductal pressure;With 70 DEG C/min speed heating furnace body center temperature to 600
℃;After mobile quartz ampoule after temperature stabilization, SnSe sources powder is set to be located exactly at body of heater center heating zone.Maintain above-mentioned 120 points of state
Clock;Bell is opened afterwards, quartz ampoule is naturally cooled to room temperature;Adjustment is passed through the flow of argon gas in quartz ampoule, makes intraductal pressure
For an atmospheric pressure, quartz ampoule is opened, the one-dimensional SnSe nano thread structures of uniform diameter are obtained in Si substrates.
Sample is taken out from quartz ampoule, observed under a scanning electron microscope, (as shown in Figure 1) is that 2-5 can be observed
The long SnSe nano thread structures of micron;Through X-ray diffraction measurements determination:Using the above method growth SnSe nano wires, directly
Footpath about 20nm (accompanying drawing 3) crystalline quality preferably (accompanying drawing 2), does not contain other impurities.Tested (EDS) point through electron spectrum simultaneously
Analysis, gained nano wire Sn, Se proportioning is Sn:Se=1:1.
Embodiment 2
According to the method growth of one-dimensional SnSe nano thread structure materials of embodiment 1.Difference is:Institute in the present embodiment
Metallic catalyst is the Au nano-colloid particles that particle diameter is 60nm, and non-oxidizable protective gas used is argon hydrogen gaseous mixture
(volume ratio is 90 to body:10), growth pressure used is 50torr, is passed through gas flow for 1000sccm, growth temperature is 610
DEG C, 120min is maintained at this temperature.
Sample is taken out from quartz ampoule, you can obtain corresponding SnSe nano wires.
Embodiment 3
According to the method growth of one-dimensional SnSe nano thread structure materials of embodiment 1.Difference is:Institute in the present embodiment
Metallic catalyst is the Au nano-colloid particles that particle diameter is 10nm, and non-oxidizable protective gas used is nitrogen, used
Growth pressure be 10torr, be passed through gas flow for 50sccm, growth temperature is 650 DEG C, and 60min is maintained at this temperature.
Sample is taken out from quartz ampoule, you can obtain corresponding SnSe nano wires.
Embodiment 4
According to the method growth of one-dimensional SnSe nano thread structure materials of embodiment 1.Difference is:Institute in the present embodiment
Metallic catalyst is the Au nano-colloid particles that particle diameter is 60nm, and non-oxidizable protective gas used is nitrogen, used
Growth pressure be 50torr, be passed through gas flow for 700sccm, growth temperature is 550 DEG C, is maintained at this temperature
300min。
Sample is taken out from quartz ampoule, you can obtain corresponding SnSe nano wires.
Although above-mentioned the embodiment of the present invention is described with reference to accompanying drawing, not to present invention protection model
The limitation enclosed, one of ordinary skill in the art should be understood that on the basis of technical scheme those skilled in the art are not
Need to pay various modifications or deform still within protection scope of the present invention that creative work can make.
Claims (7)
1. a kind of preparation method of one-dimensional tin selenide monocrystal nanowire, it is characterized in that, comprise the following steps that:
(1) SnSe powder is placed in high-temperature resistant container, then the high-temperature resistant container for filling SnSe powder is put into high temperature resistant boiler tube
It is interior, high temperature resistant boiler tube is put into vacuum tube furnace, SnSe powder is located at the position of vacuum tube furnace fire door, will have particle diameter
Base material for 10-60nm Au nano-colloid beaded catalysts is placed in the high temperature resistant boiler tube, the closed high temperature resistant
Boiler tube, makes the electron tubes type furnace interior be in anaerobic vacuum state, protective gas is passed through afterwards, and adjust the high temperature resistant stove
Pipe pressure is to 10-50Torr;
(2) heater is opened, the central high temperature area of the vacuum tube furnace is heated to 550-650 DEG C, mobile high temperature resistant stove
Pipe, makes the high-temperature resistant container be located at central high temperature area, the substrate with catalyst and is located at low-temperature region, maintain said temperature to treat
Stop heating after the completion of nanowire growth, obtain one-dimensional tin selenide monocrystal nanowire.
2. preparation method as claimed in claim 1, it is characterized in that, in the step (1) high temperature resistant furnace tube material be corundum or
Quartz.
3. preparation method as claimed in claim 1, it is characterized in that, base material is higher than 500 DEG C to be resistance in the step (1)
Backing material.
4. preparation method as claimed in claim 3, it is characterized in that, the base material is single crystalline Si or mica.
5. preparation method as claimed in claim 1, it is characterized in that, make the furnace chamber of the vacuum tube furnace in the step (1)
The interior method in anaerobic vacuum state is specific as follows:50mTorr is not higher than using pressure in mechanical pumpijg gas to the furnace chamber
Afterwards, the pressure being passed through into pipe in protective gas to the furnace chamber is not less than 1Torr, then is evacuated body to intraductal pressure and is not higher than
50mTorr, it is anaerobic vacuum state that so repeatedly 2-4 times, which makes furnace chamber interior,.
6. preparation method as claimed in claim 1, it is characterized in that, the protective gas in the step (1) is nitrogen, argon gas or
Volume ratio is 90:The mixing of 10 argon gas and hydrogen, gas flow is 50-1000sccm.
7. preparation method as claimed in claim 1, it is characterized in that, it is heated in the step (2) with 70 DEG C/min of speed
550-650 DEG C, the nanowire growth time is 60-300min.
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CN109972202B (en) * | 2019-04-29 | 2020-10-20 | 国家纳米科学中心 | Preparation method of tungsten trioxide single crystal nanowire |
CN110937582B (en) * | 2019-12-10 | 2021-10-19 | 山东师范大学 | Zinc selenide nanowire and application thereof as surface enhanced Raman scattering substrate |
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CN103482589B (en) * | 2013-09-29 | 2015-09-16 | 国家纳米科学中心 | A kind of one dimension Tin diselenide nano-array, its preparation method and application |
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