CN102199003A - Porous membrane with two-dimensional ordered arrangement, and preparation method thereof - Google Patents

Porous membrane with two-dimensional ordered arrangement, and preparation method thereof Download PDF

Info

Publication number
CN102199003A
CN102199003A CN2010101373716A CN201010137371A CN102199003A CN 102199003 A CN102199003 A CN 102199003A CN 2010101373716 A CN2010101373716 A CN 2010101373716A CN 201010137371 A CN201010137371 A CN 201010137371A CN 102199003 A CN102199003 A CN 102199003A
Authority
CN
China
Prior art keywords
binary
substrate
preparation
solution
film
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN2010101373716A
Other languages
Chinese (zh)
Other versions
CN102199003B (en
Inventor
贾丽超
王洪强
蔡伟平
刘广强
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hefei Institutes of Physical Science of CAS
Original Assignee
Hefei Institutes of Physical Science of CAS
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hefei Institutes of Physical Science of CAS filed Critical Hefei Institutes of Physical Science of CAS
Priority to CN 201010137371 priority Critical patent/CN102199003B/en
Publication of CN102199003A publication Critical patent/CN102199003A/en
Application granted granted Critical
Publication of CN102199003B publication Critical patent/CN102199003B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Silicates, Zeolites, And Molecular Sieves (AREA)
  • Surface Treatment Of Glass (AREA)

Abstract

The invention discloses a porous membrane with a two-dimensional ordered arrangement, and a preparation method thereof. The porous membrane comprises a oxide with large spherical apertures and small spherical apertures, wherein a large spherical aperture size is in a range of 250nm to 5000nm and a small spherical aperture size is in a range of 50nm to 250nm, and a ratio of the large spherical aperture size to the small spherical aperture size is (5 to20) to 1. A thickness of the membrane is in a range of 250nm to 25000nm. In each layer of the membrane, the large spherical apertures are arranged according to an ordered hexagonal structure, and the small spherical apertures are arranged among the large spherical apertures and are communicated with the large apertures. The steps of the preparation method comprises immersing a two-dimensional ordered colloidal crystal template into a semiconductor oxide precursor solution with a concentration of from 0.05M to 0.2M, collecting two-dimensional ordered colloidal crystals by a substrate with a needed shape when the two-dimensional ordered colloidal crystals are separated from a previous substrate and float in the semiconductor oxide precursor solution, heating the substrate covered with the two-dimensional ordered colloidal crystal dipped with the semiconductor oxide precursor solution at a temperature of from 80 DEG C to 120 DEG C for 1 to 4 hours, repeating the above steps at least one time or not repeating the above steps, and annealing the resulting products at a temperature of from 300 DEG C to 4000 DEG C for 1 to 4 hours to obtain the porous membrane with a two-dimensional ordered arrangement. The porous membrane can be widely applied to the multiple fields of phonon diffraction grids, optical filters, interferometers, and chemical and biological sensors.

Description

Binary ordered porous thin-film and preparation method thereof
Technical field
The present invention relates to a kind of porous membrane and preparation method, especially a kind of binary ordered porous thin-film and preparation method thereof.
Background technology
The orderly hole of micro-nano structure film is because its numerous new good characteristics, can be widely used in fields such as phonon diffraction grid, optical filter, selective light resorber, interferometer, reflection coating, photocell, chemistry and biosensor, in addition, this class film also has important application prospects at aspects such as microelectronics, magnetics, catalysis and nanophotonics.Up to now, the orderly hole of the micro-nano structure film that people constitute for the hole that obtains two kinds of different diameters, done unremitting effort, as a kind of " multi-layer classification nanostructure ordered hole thin film type gas-sensitive sensor and preparation method thereof " of the applicant of disclosing among the disclosed Chinese invention patent Shen Qing Publication specification sheets CN 101435795A on May 20th, 2009.It is intended to provide, and a kind of universality is good, highly sensitive, response speed is fast, thin film type gas-sensitive sensor simple for production and its preparation method.Gas sensor comprises substrate, electrode and covers thereon air-sensitive film, wherein film by two-layer above, be that six sides closely arrange and the spherical poroid conductor oxidate that is interconnected constitutes, the aperture of spherical pore is 100~5000nm, hole size with one deck is identical, and the pore size ratio between different layers is 1.5~10: 1; The preparation method is, colloid monolayer crystal template immersion concentration with different sphere diameters is in the conductor oxidate precursor solution of 0.05~0.2M earlier, the colloid monolayer crystal for the treatment of different sphere diameters breaks away from after substrate swims in the surface of precursor solution, one of pick up in the colloid monolayer crystal with the substrate gradation that has electrode of desired shape, and place 80~120 ℃ to heat 1~4h down, be placed on 350~550 ℃ of annealing 1~4h down again, make the multi-layer classification nanostructure ordered hole thin film type gas-sensitive sensor.But, this thin film type gas-sensitive sensor and preparation method thereof all exists the shortcoming part, at first, though the film of gas sensor is made of the spherical pore of two kinds of different diameters, the spherical pore of right its different diameter but is distributed in the different levels, limit the field of its application and reduced its characteristic, make its spherical pore that can not be used for different diameter with thin film, and the practical requirement of minor diameter spherical pore between this layer major diameter spherical pore restricted between two kinds of different diameter spherical pores the performance because of the orderly pore membrane characteristic of the due micro-nano structure of contact again; Secondly, the preparation method can not make with containing two kinds of different diameter spherical pores on the thin film, and the film of minor diameter spherical pore between this layer major diameter spherical pore.
Summary of the invention
The technical problem to be solved in the present invention is for overcoming shortcoming part of the prior art, and the spherical pore that a kind of different diameter is provided is on thin film, and the binary ordered porous thin-film of minor diameter spherical pore between this layer major diameter spherical pore.
Another technical problem that the present invention will solve is for providing a kind of preparation method of binary ordered porous thin-film.
For solving technical problem of the present invention, the technical scheme that is adopted is: the binary ordered porous thin-film is made up of substrate and the film on it, particularly,
Described film is made of the spherical poroid oxide compound of two kinds of different diameters, and the size between described two kinds of spherical pore diameters is 5~20: 1, and wherein, the diameter of major diameter spherical pore is that the diameter of 250~5000nm, minor diameter spherical pore is 50~250nm;
Described every layer of major diameter spherical pore arranged by six side's ordered structures, and described minor diameter spherical pore and is interconnected between every layer of large and small diameter spherical pore between this layer major diameter spherical pore;
The thickness of described film is 250~25000nm, and described oxide compound is a conductor oxidate.
As the further improvement of binary ordered porous thin-film, described conductor oxidate is an indium trioxide, or tindioxide, or zinc oxide, or ferric oxide; Described substrate is a glass, or monocrystalline silicon piece, or pottery, or mica, or quartzy, and being shaped as of substrate is plane, or convex-shaped, or concave shape, or dome shape.
For solving another technical problem of the present invention, another technical scheme that is adopted is: the preparation method of binary ordered porous thin-film comprises that the colloidal spheres with two kinds of different diameters invests substrate surface formation major diameter colloidal spheres by six side's ordered structure monolayer alignment, the orderly colloidal crystal template of the binary of minor diameter colloidal spheres between the major diameter colloidal spheres, and particularly completing steps is as follows:
Step 1, earlier the orderly colloidal crystal template of binary being immersed concentration is in the conductor oxidate precursor solution of 0.05~0.2M, after treating that the orderly colloidal crystal of binary breaks away from substrate and swims in the precursor solution, substrate with desired shape picks up the orderly colloidal crystal of binary, and make it be covered in substrate surface, again the substrate that is covered with the orderly colloidal crystal of binary that is soaked with precursor solution on it is placed 80~120 ℃ of heating 1~4h down;
Step 2, the number of times of repeating step 1 be more than 0 time after, be placed on 300~400 ℃ of down annealing 1~4h, make the binary ordered porous thin-film.
As the preparation method's of binary ordered porous thin-film further improvement, described conductor oxidate precursor solution is an indium nitrate solution, or tin tetrachloride solution, or zinc acetate solution, or iron nitrate solution; The number of times of described repeating step 1 is 1~4 time; Described temperature rise rate when being warming up to 300~400 ℃ is 3~10 ℃/min; Being shaped as of described substrate is plane, or convex-shaped, or concave shape, or dome shape, and substrate is a glass, or monocrystalline silicon piece, or pottery, or mica, or quartzy; It is that 10~30: 1 mixed is even according to volume ratio that the forming of the orderly colloidal crystal template of described binary earlier is mass percent solubility 1.5~10% major diameter polystyrene colloid ball solution and minor diameter polystyrene colloid ball solution, obtain mixed solution, spin coating is thrown away after mixed solution being dropped in the substrate again, is 24~28 ℃ seasoning afterwards through temperature; It is 4~10 μ L that described mixed solution drops to suprabasil volume, and the rotating speed when spin coating is thrown away is 300~1000r/s.
Beneficial effect with respect to prior art is, one, use scanning electron microscope and X-ray diffractometer to characterize respectively to the product that makes, by its result as can be known, the smooth surface of product, thickness is even, it is the film that places the spherical poroid oxide compound by two kinds of different diameters on the substrate to constitute, wherein, the thickness of film is 250~25000nm, size between two kinds of spherical pore diameters is 5~20: 1, the diameter of major diameter spherical pore is 250~5000nm, the diameter of minor diameter spherical pore is 50~250nm, every layer of major diameter spherical pore arranged by six side's ordered structures, the minor diameter spherical pore between this layer major diameter spherical pore, and every layer big, be interconnected between the minor diameter spherical pore.Oxide compound is a conductor oxidate, and it is an indium trioxide, or tindioxide, or zinc oxide, or ferric oxide.Substrate is a glass, or monocrystalline silicon piece, or pottery, or mica, or quartzy, and being shaped as of substrate is plane, or convex-shaped, or concave shape, or dome shape; They are two years old, the spherical pore of two kinds of different diameters of this employing is on thin film, and the binary ordered porous thin-film of minor diameter spherical pore between this layer major diameter spherical pore, not only have the rapid diffusion of macropore and the advantage of transmission, and the high-specific surface area and the advantage of high activity that also contain aperture simultaneously, the characteristic and the field that has enlarged its application of the orderly pore membrane of micro-nano structure have greatly been improved, except that having satisfied the practicality that only needs this kind structure requires, its performance is fully played; They are three years old, the preparation method has universality, as long as choose the orderly colloidal crystal template of the binary of suitable aperture and aperture ratio,, just can synthesize the large-area binary ordered porous thin-film of heterogeneity and film thickness by changing the concentration and the chemical ingredients of precursor solution.That is, not only can prepare inorganic semiconductor binary ordered porous thin-film, and can prepare organic binary ordered porous thin-film, greatly improve its value in actual applications; Its four, equipment used in the preparation process is few, inexpensive, technology is simple, cost is low, and is pollution-free, is suitable for large-scale industrial production.
Further embodiment as beneficial effect, the one, conductor oxidate is preferably indium trioxide or tindioxide or zinc oxide or ferric oxide, substrate is preferably glass or monocrystalline silicon piece or pottery or mica or quartz, the shape of substrate is preferably plane or convex-shaped or concave shape or dome shape, not only make raw-material source than horn of plenty, also satisfied the requirement of various use occasions product component and shape; The 2nd, the conductor oxidate precursor solution is preferably indium nitrate solution or tin tetrachloride solution or zinc acetate solution or iron nitrate solution, except that the shaping that is beneficial to conductor oxidate, also makes the easier enforcement of preparation technology and flexible; The 3rd, the number of times of repeating step 1 is preferably 1~4 time, has guaranteed that the thickness of product can satisfy actual application demand, is again stay-in-grade; The 4th, the temperature rise rate when being warming up to 300~400 ℃ is preferably 3~10 ℃/min, has guaranteed the quality and the quality of stability of product; The 5th, the formation of the orderly colloidal crystal template of binary is preferably and earlier mass percent solubility is 1.5~10% major diameter polystyrene colloid ball solution and minor diameter polystyrene colloid ball solution is that 10~30: 1 mixed is even according to volume ratio, obtain mixed solution, spin coating is thrown away after mixed solution being dropped in the substrate again, be 24~28 ℃ seasoning afterwards through temperature, guaranteed that the orderly colloidal crystal template of binary that obtains is that to place the suprabasil thickness that is made of the polystyrene colloid ball of two kinds of different diameters be the colloidal crystal of 250~5000nm, size between two kinds of colloidal spheres diameters is 5~20: 1, wherein, the spherical diameter of major diameter colloidal spheres is 250~5000nm, the spherical diameter of minor diameter colloidal spheres is 50~250nm, and how diameter difference and blending ratio between no matter large or small diameter colloidal spheres change, all by six side's ordered structure monolayer alignment, the minor diameter colloidal spheres is all between the major diameter colloidal spheres for major diameter colloidal spheres in the colloidal crystal; The 6th, mixed solution drops to suprabasil volume and is preferably 4~10 μ L, is beneficial to the formation of template, and the rotating speed when spin coating is thrown away is preferably 300~1000r/s, is convenient to mixed solution is thrown away equably.
Description of drawings
Below in conjunction with accompanying drawing optimal way of the present invention is described in further detail.
Fig. 1 is one of result who respectively orderly colloidal crystal template of binary that obtains and the product use scanning electron microscope (SEM) that makes is characterized.Wherein, Figure 1A is for being that the polystyrene colloid ball of 1000nm and 200nm invests major diameter colloidal spheres that plane the forms SEM photo by six side's ordered structure monolayer alignment, the binary orderly colloidal crystal template of minor diameter colloidal spheres between the major diameter colloidal spheres with diameter, and the upper left corner of photo is its SEM photo that has amplified; Figure 1B is for being template with the orderly colloidal crystal template of the binary shown in Figure 1A, tin tetrachloride solution is the conductor oxidate precursor solution, plane ceramic plate is the 1000nm major diameter spherical pore periodic arrangement that substrate makes, and 200nm minor diameter spherical pore is centered around the product between its ball crack---the SEM photo of binary ordered porous thin-film.
Fig. 2 is to being that the orderly colloidal crystal template of binary that the polystyrene colloid ball of 2000nm and 200nm is made is a template with the diameter, and indium nitrate solution is precursor solution, the result that the product that plane quartz makes for substrate uses scanning electron microscope to characterize.
Fig. 3 is the result who uses X-ray diffraction (XRD) instrument to characterize to Figure 1B and product shown in Figure 2 respectively.Wherein, Fig. 3 A is the XRD spectra of product shown in Figure 1B, and Fig. 3 B is the XRD spectra of product shown in Figure 2; By the position of each diffraction peak in these two XRD spectra and relative intensity as can be known, product is made of tindioxide shown in the pairing Figure 1B of Fig. 3 A, and the pairing product shown in Figure 2 of Fig. 3 B is made of indium trioxide.
Embodiment
At first buy or make with ordinary method from market:
Mass percent solubility is 1.5~10% major diameter polystyrene colloid ball solution and minor diameter polystyrene colloid ball solution; Wherein, the colloidal spheres diameter of major diameter polystyrene colloid ball solution is that the colloidal spheres diameter of 250~5000nm, minor diameter polystyrene colloid ball solution is 50~250nm.On this basis, earlier mass percent solubility being 1.5~10% major diameter polystyrene colloid ball solution and minor diameter polystyrene colloid ball solution is that 10~30: 1 mixed is even according to volume ratio, obtain mixed solution, spin coating is thrown away after mixed solution being dropped in the substrate again, wherein, it is 4~10 μ L that mixed solution drops to suprabasil volume, rotating speed when spin coating is thrown away is 300~1000r/s, be 24~28 ℃ seasoning afterwards through temperature, obtain as or be similar to the colloidal spheres shown in Figure 1A and invest substrate surface and form 250~5000nm major diameter colloidal spheres by six side's ordered structure monolayer alignment with two kinds of different diameters, the binary orderly colloidal crystal template of 50~250nm minor diameter colloidal spheres between 250~5000nm major diameter colloidal spheres.
Indium nitrate solution, tin tetrachloride solution, zinc acetate solution and iron nitrate solution as the conductor oxidate precursor solution.
As glass, monocrystalline silicon piece, pottery, mica and the quartz of substrate, wherein, being shaped as of substrate is plane, or convex-shaped, or concave shape, or dome shape.
Then,
Embodiment 1
The concrete steps of preparation are:
Step 1, the orderly colloidal crystal template immersion of the binary concentration that earlier the colloidal spheres diameter on it is respectively 1000nm and 200nm is in the conductor oxidate precursor solution of 0.05M, after treating that the orderly colloidal crystal of binary breaks away from substrate and swims in the precursor solution, substrate with desired shape picks up the orderly colloidal crystal of binary, and makes it be covered in substrate surface; Wherein, the conductor oxidate precursor solution is a tin tetrachloride solution, and substrate is plane pottery.Again the substrate that is covered with the orderly colloidal crystal of binary that is soaked with precursor solution on it is placed 80 ℃ of heating 4h down.
Step 2 after the number of times of repeating step 1 is 0 time, is placed on 300 ℃ of annealing 4h down; Temperature rise rate when wherein, being warming up to 300 ℃ is 3 ℃/min.Make shown in Figure 1B, and the binary ordered porous thin-film shown in the curve among Fig. 3 A.
Embodiment 2
The concrete steps of preparation are:
Step 1, the orderly colloidal crystal template immersion of the binary concentration that earlier the colloidal spheres diameter on it is respectively 2000nm and 200nm is in the conductor oxidate precursor solution of 0.08M, after treating that the orderly colloidal crystal of binary breaks away from substrate and swims in the precursor solution, substrate with desired shape picks up the orderly colloidal crystal of binary, and makes it be covered in substrate surface; Wherein, the conductor oxidate precursor solution is an indium nitrate solution, and substrate is plane quartz.Again the substrate that is covered with the orderly colloidal crystal of binary that is soaked with precursor solution on it is placed 90 ℃ of heating 3h down.
Step 2 after the number of times of repeating step 1 is 1 time, is placed on 330 ℃ of annealing 3h down; Temperature rise rate when wherein, being warming up to 330 ℃ is 5 ℃/min.Make as shown in Figure 2, and the binary ordered porous thin-film shown in the curve among Fig. 3 B.
Embodiment 3
The concrete steps of preparation are:
Step 1, the orderly colloidal crystal template immersion of the binary concentration that earlier the colloidal spheres diameter on it is respectively 1000nm and 200nm is in the conductor oxidate precursor solution of 0.1M, after treating that the orderly colloidal crystal of binary breaks away from substrate and swims in the precursor solution, substrate with desired shape picks up the orderly colloidal crystal of binary, and makes it be covered in substrate surface; Wherein, the conductor oxidate precursor solution is a tin tetrachloride solution, and substrate is plane pottery.Again the substrate that is covered with the orderly colloidal crystal of binary that is soaked with precursor solution on it is placed 100 ℃ of heating 2h down.
Step 2 after the number of times of repeating step 1 is 2 times, is placed on 350 ℃ of annealing 2h down; Temperature rise rate when wherein, being warming up to 350 ℃ is 7 ℃/min.Make shown in Figure 1B, and the binary ordered porous thin-film shown in the curve among Fig. 3 A.
Embodiment 4
The concrete steps of preparation are:
Step 1, the orderly colloidal crystal template immersion of the binary concentration that earlier the colloidal spheres diameter on it is respectively 2000nm and 200nm is in the conductor oxidate precursor solution of 0.015M, after treating that the orderly colloidal crystal of binary breaks away from substrate and swims in the precursor solution, substrate with desired shape picks up the orderly colloidal crystal of binary, and makes it be covered in substrate surface; Wherein, the conductor oxidate precursor solution is an indium nitrate solution, and substrate is plane quartz.Again the substrate that is covered with the orderly colloidal crystal of binary that is soaked with precursor solution on it is placed 110 ℃ of heating 1.5h down.
Step 2 after the number of times of repeating step 1 is 3 times, is placed on 380 ℃ of annealing 1.5h down; Temperature rise rate when wherein, being warming up to 380 ℃ is 8.5 ℃/min.Make as shown in Figure 2, and the binary ordered porous thin-film shown in the curve among Fig. 3 B.
Embodiment 5
The concrete steps of preparation are:
Step 1, the orderly colloidal crystal template immersion of the binary concentration that earlier the colloidal spheres diameter on it is respectively 1000nm and 200nm is in the conductor oxidate precursor solution of 0.2M, after treating that the orderly colloidal crystal of binary breaks away from substrate and swims in the precursor solution, substrate with desired shape picks up the orderly colloidal crystal of binary, and makes it be covered in substrate surface; Wherein, the conductor oxidate precursor solution is a tin tetrachloride solution, and substrate is plane pottery.Again the substrate that is covered with the orderly colloidal crystal of binary that is soaked with precursor solution on it is placed 120 ℃ of heating 1h down.
Step 2 after the number of times of repeating step 1 is 4 times, is placed on 400 ℃ of annealing 1h down; Temperature rise rate when wherein, being warming up to 400 ℃ is 10 ℃/min.Make shown in Figure 1B, and the binary ordered porous thin-film shown in the curve among Fig. 3 A.
Select for use the colloidal spheres diameter on it to be respectively the orderly colloidal crystal template of binary that the arbitrary diameter among 250~5000nm and the 50~250nm forms again respectively, and select indium nitrate solution or tin tetrachloride solution or zinc acetate solution or iron nitrate solution for use as the conductor oxidate precursor solution, glass or monocrystalline silicon piece or pottery or mica or quartz as substrate, wherein, substrate be shaped as plane or convex-shaped or concave shape or dome shape, repeat the foregoing description 1~5, made equally as or be similar to Figure 1B or shown in Figure 2, and as or be similar to the binary ordered porous thin-film shown in the curve among Fig. 3 A or Fig. 3 B.
Obviously, those skilled in the art can carry out various changes and modification to binary ordered porous thin-film of the present invention and preparation method thereof and not break away from the spirit and scope of the present invention.Like this, if of the present invention these are revised and modification belongs within the scope of claim of the present invention and equivalent technologies thereof, then the present invention also is intended to comprise these changes and modification interior.

Claims (10)

1. a binary ordered porous thin-film is made up of substrate and the film on it, it is characterized in that:
Described film is made of the spherical poroid oxide compound of two kinds of different diameters, and the size between described two kinds of spherical pore diameters is 5~20: 1, and wherein, the diameter of major diameter spherical pore is that the diameter of 250~5000nm, minor diameter spherical pore is 50~250nm;
Described every layer of major diameter spherical pore arranged by six side's ordered structures, and described minor diameter spherical pore and is interconnected between every layer of large and small diameter spherical pore between this layer major diameter spherical pore;
The thickness of described film is 250~25000nm, and described oxide compound is a conductor oxidate.
2. binary ordered porous thin-film according to claim 1 is characterized in that conductor oxidate is an indium trioxide, or tindioxide, or zinc oxide, or ferric oxide.
3. binary ordered porous thin-film according to claim 1 is characterized in that substrate is a glass, or monocrystalline silicon piece, or pottery, or mica, or quartzy, and being shaped as of substrate is plane, or convex-shaped, or concave shape, or dome shape.
4. the preparation method of the described binary ordered porous thin-film of claim 1, comprise that the colloidal spheres with two kinds of different diameters invests substrate surface formation major diameter colloidal spheres by six side's ordered structure monolayer alignment, the orderly colloidal crystal template of the binary of minor diameter colloidal spheres between the major diameter colloidal spheres, is characterized in that completing steps is as follows:
Step 1, earlier the orderly colloidal crystal template of binary being immersed concentration is in the conductor oxidate precursor solution of 0.05~0.2M, after treating that the orderly colloidal crystal of binary breaks away from substrate and swims in the precursor solution, substrate with desired shape picks up the orderly colloidal crystal of binary, and make it be covered in substrate surface, again the substrate that is covered with the orderly colloidal crystal of binary that is soaked with precursor solution on it is placed 80~120 ℃ of heating 1~4h down;
Step 2, the number of times of repeating step 1 be more than 0 time after, be placed on 300~400 ℃ of down annealing 1~4h, make the binary ordered porous thin-film.
5. the preparation method of binary ordered porous thin-film according to claim 4 is characterized in that the conductor oxidate precursor solution is an indium nitrate solution, or tin tetrachloride solution, or zinc acetate solution, or iron nitrate solution.
6. the preparation method of binary ordered porous thin-film according to claim 4, the number of times that it is characterized in that repeating step 1 is 1~4 time.
7. the preparation method of binary ordered porous thin-film according to claim 4, the temperature rise rate when it is characterized in that being warming up to 300~400 ℃ is 3~10 ℃/min.
8. the preparation method of binary ordered porous thin-film according to claim 4 is characterized in that being shaped as of substrate is plane, or convex-shaped, or concave shape, or dome shape, and substrate is a glass, or monocrystalline silicon piece, or pottery, or mica, or quartzy.
9. the preparation method of binary ordered porous thin-film according to claim 4, it is characterized in that it is that 10~30: 1 mixed is even according to volume ratio that forming of the orderly colloidal crystal template of binary earlier is mass percent solubility 1.5~10% major diameter polystyrene colloid ball solution and minor diameter polystyrene colloid ball solution, obtain mixed solution, spin coating is thrown away after mixed solution being dropped in the substrate again, is 24~28 ℃ seasoning afterwards through temperature.
10. the preparation method of binary ordered porous thin-film according to claim 9 is characterized in that it is 4~10 μ L that mixed solution is dropped to suprabasil volume, and the rotating speed when spin coating is thrown away is 300~1000r/s.
CN 201010137371 2010-03-23 2010-03-23 Porous membrane with two-dimensional ordered arrangement, and preparation method thereof Expired - Fee Related CN102199003B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 201010137371 CN102199003B (en) 2010-03-23 2010-03-23 Porous membrane with two-dimensional ordered arrangement, and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 201010137371 CN102199003B (en) 2010-03-23 2010-03-23 Porous membrane with two-dimensional ordered arrangement, and preparation method thereof

Publications (2)

Publication Number Publication Date
CN102199003A true CN102199003A (en) 2011-09-28
CN102199003B CN102199003B (en) 2013-04-03

Family

ID=44660031

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 201010137371 Expired - Fee Related CN102199003B (en) 2010-03-23 2010-03-23 Porous membrane with two-dimensional ordered arrangement, and preparation method thereof

Country Status (1)

Country Link
CN (1) CN102199003B (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103288359A (en) * 2013-04-03 2013-09-11 中国科学院合肥物质科学研究院 Preparation method for oxide micro/nano-structured ordered porous array through oxygen-plasma irradiation
CN103739007A (en) * 2013-12-30 2014-04-23 扬州大学 Preparation of porous tin dioxide nano structure with controllable size by employing template method
CN105016296A (en) * 2015-06-11 2015-11-04 吉林大学 Three-dimensionally ordered macro-porous structured thin film and electric sensor for detecting diabetes and lung cancer markers
CN106082363A (en) * 2016-05-26 2016-11-09 中国科学院合肥物质科学研究院 Iron-doped Nickel Oxide composite hollow ball array films and preparation method thereof
CN107445477A (en) * 2016-05-23 2017-12-08 陈玉彬 Energy-saving glass and manufacturing method thereof
CN108963080A (en) * 2018-07-07 2018-12-07 河南大学 A kind of preparation method of porous organic semiconductor thin-film
CN112340787A (en) * 2020-11-09 2021-02-09 东北大学秦皇岛分校 Single-phase spinel type high-entropy oxide, preparation method and application
CN115072765A (en) * 2022-06-22 2022-09-20 通化师范学院 Method for preparing hexagonal prism-shaped zinc oxide

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5858462A (en) * 1995-08-14 1999-01-12 Central Glass Company, Limited Porous metal-oxide thin film and method of forming same on glass substrate
JP2002201045A (en) * 2000-12-27 2002-07-16 Toto Ltd Hydrophilic thin film

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5858462A (en) * 1995-08-14 1999-01-12 Central Glass Company, Limited Porous metal-oxide thin film and method of forming same on glass substrate
JP2002201045A (en) * 2000-12-27 2002-07-16 Toto Ltd Hydrophilic thin film

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103288359A (en) * 2013-04-03 2013-09-11 中国科学院合肥物质科学研究院 Preparation method for oxide micro/nano-structured ordered porous array through oxygen-plasma irradiation
CN103739007A (en) * 2013-12-30 2014-04-23 扬州大学 Preparation of porous tin dioxide nano structure with controllable size by employing template method
CN103739007B (en) * 2013-12-30 2016-01-20 扬州大学 The porous SnO 2 nanostructure that template synthesis size is controlled
CN105016296A (en) * 2015-06-11 2015-11-04 吉林大学 Three-dimensionally ordered macro-porous structured thin film and electric sensor for detecting diabetes and lung cancer markers
CN107445477A (en) * 2016-05-23 2017-12-08 陈玉彬 Energy-saving glass and manufacturing method thereof
CN107445477B (en) * 2016-05-23 2019-12-03 陈玉彬 Method for manufacturing energy-saving glass
CN106082363A (en) * 2016-05-26 2016-11-09 中国科学院合肥物质科学研究院 Iron-doped Nickel Oxide composite hollow ball array films and preparation method thereof
CN106082363B (en) * 2016-05-26 2017-09-19 中国科学院合肥物质科学研究院 Iron-doped Nickel Oxide composite hollow ball array films and preparation method thereof
CN108963080A (en) * 2018-07-07 2018-12-07 河南大学 A kind of preparation method of porous organic semiconductor thin-film
CN112340787A (en) * 2020-11-09 2021-02-09 东北大学秦皇岛分校 Single-phase spinel type high-entropy oxide, preparation method and application
CN115072765A (en) * 2022-06-22 2022-09-20 通化师范学院 Method for preparing hexagonal prism-shaped zinc oxide
CN115072765B (en) * 2022-06-22 2023-06-23 通化师范学院 Method for preparing hexagonal prism-shaped zinc oxide

Also Published As

Publication number Publication date
CN102199003B (en) 2013-04-03

Similar Documents

Publication Publication Date Title
CN102199003B (en) Porous membrane with two-dimensional ordered arrangement, and preparation method thereof
Cho et al. Gas sensing properties of p-type hollow NiO hemispheres prepared by polymeric colloidal templating method
Shaban et al. Nanostructured ZnO thin films for self-cleaning applications
Pan et al. Block copolymer-templated synthesis of highly organized mesoporous TiO2-based films and their photoelectrochemical applications
US8753526B2 (en) Porous thin film having holes and a production method therefor
Yao et al. Synthesis, self-assembly, disassembly, and reassembly of two types of Cu2O nanocrystals unifaceted with {001} or {110} planes
Li et al. Polystyrene sphere-assisted one-dimensional nanostructure arrays: synthesis and applications
Wang et al. A sol–gel dip/spin coating method to prepare titanium oxide films
Xi et al. TiO2 thin films prepared via adsorptive self-assembly for self-cleaning applications
Gao et al. Novel near infrared reflective pigments based on hollow glass microsphere/BiOCl1-xIx composites: Optical property and superhydrophobicity
CN100422730C (en) Nano-structural ordered porous thin-film type gas sensor and method for preparing same
Apeh et al. Properties of nanostructured ZnO thin films synthesized using a modified aqueous chemical growth method
CN101435795A (en) Thin film type gas-sensitive sensor of multi-layer classification nanostructure ordered hole and preparing method thereof
Hung et al. A vertically integrated ZnO-based hydrogen sensor with hierarchical bi-layered inverse opals
Zhang et al. Effects of seed layers on controlling of the morphology of ZnO nanostructures and superhydrophobicity of ZnO nanostructure/stearic acid composite films
Su et al. A substrate-independent fabrication of hollow sphere arrays via template-assisted hydrothermal approach and their application in gas sensing
Miki et al. Preparation of nanoporous TiO2 film with large surface area using aqueous sol with trehalose
JP5630746B2 (en) Manganese oxide nanowire-covered structure and method for producing the same
CN103232172B (en) Big area prepares the method for nano titania hollow ball order thin film
Hu et al. Fabrication of Zn (OH) 2/ZnO Nanosheet‐ZnO Nanoarray Hybrid Structured Films by a Dissolution–Recrystallization Route
KR20110126966A (en) Hydrophobic sheet and preparation method thereof
CN102851736A (en) Surface ordered pore array zinc oxide nano-film and preparation method thereof
Miki et al. Preparation of thick TiO 2 film with large surface area using aqueous sol with poly (ethylene glycol)
CN106958006A (en) Multicomponent alloy not close arranges the preparation method of spherical nanoparticle array
Qu et al. Effects of the co-addition of Zn2+ and sodium dodecylbenzenesulfonate on photocatalytic activity and wetting performance of anatase TiO2 nanoparticle films

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20130403

Termination date: 20140323