CN112745711A - Photovoltaic module with infrared absorption and hydrophobic coating and preparation method thereof - Google Patents
Photovoltaic module with infrared absorption and hydrophobic coating and preparation method thereof Download PDFInfo
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- CN112745711A CN112745711A CN202011600812.1A CN202011600812A CN112745711A CN 112745711 A CN112745711 A CN 112745711A CN 202011600812 A CN202011600812 A CN 202011600812A CN 112745711 A CN112745711 A CN 112745711A
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- 238000000576 coating method Methods 0.000 title claims abstract description 52
- 239000011248 coating agent Substances 0.000 title claims abstract description 51
- 230000002209 hydrophobic effect Effects 0.000 title claims abstract description 36
- 238000010521 absorption reaction Methods 0.000 title claims abstract description 16
- 238000002360 preparation method Methods 0.000 title claims abstract description 14
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims abstract description 17
- 229910000077 silane Inorganic materials 0.000 claims abstract description 17
- 238000010438 heat treatment Methods 0.000 claims abstract description 15
- 239000003960 organic solvent Substances 0.000 claims abstract description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 12
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims abstract description 9
- 230000002745 absorbent Effects 0.000 claims abstract description 9
- 239000002250 absorbent Substances 0.000 claims abstract description 9
- 239000000243 solution Substances 0.000 claims description 18
- 239000011259 mixed solution Substances 0.000 claims description 13
- ZNOKGRXACCSDPY-UHFFFAOYSA-N tungsten trioxide Chemical compound O=[W](=O)=O ZNOKGRXACCSDPY-UHFFFAOYSA-N 0.000 claims description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
- 239000011521 glass Substances 0.000 claims description 8
- 238000002156 mixing Methods 0.000 claims description 8
- 238000003756 stirring Methods 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 6
- 239000006096 absorbing agent Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims description 6
- 229910001887 tin oxide Inorganic materials 0.000 claims description 6
- 230000003301 hydrolyzing effect Effects 0.000 claims description 5
- 238000005507 spraying Methods 0.000 claims description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 4
- SCPWMSBAGXEGPW-UHFFFAOYSA-N dodecyl(trimethoxy)silane Chemical compound CCCCCCCCCCCC[Si](OC)(OC)OC SCPWMSBAGXEGPW-UHFFFAOYSA-N 0.000 claims description 4
- RSKGMYDENCAJEN-UHFFFAOYSA-N hexadecyl(trimethoxy)silane Chemical compound CCCCCCCCCCCCCCCC[Si](OC)(OC)OC RSKGMYDENCAJEN-UHFFFAOYSA-N 0.000 claims description 4
- MSRJTTSHWYDFIU-UHFFFAOYSA-N octyltriethoxysilane Chemical compound CCCCCCCC[Si](OCC)(OCC)OCC MSRJTTSHWYDFIU-UHFFFAOYSA-N 0.000 claims description 4
- BXDPLIQLAGJEFR-UHFFFAOYSA-N [Sb]=O.[Sn].[V].[W] Chemical compound [Sb]=O.[Sn].[V].[W] BXDPLIQLAGJEFR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052792 caesium Inorganic materials 0.000 claims description 3
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- PBYZMCDFOULPGH-UHFFFAOYSA-N tungstate Chemical compound [O-][W]([O-])(=O)=O PBYZMCDFOULPGH-UHFFFAOYSA-N 0.000 claims description 3
- KQAHMVLQCSALSX-UHFFFAOYSA-N decyl(trimethoxy)silane Chemical compound CCCCCCCCCC[Si](OC)(OC)OC KQAHMVLQCSALSX-UHFFFAOYSA-N 0.000 claims description 2
- 238000003618 dip coating Methods 0.000 claims description 2
- KKYDYRWEUFJLER-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,5,5,6,6,7,7,10,10,10-heptadecafluorodecyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)CCC(F)(F)F KKYDYRWEUFJLER-UHFFFAOYSA-N 0.000 claims 1
- 229910052782 aluminium Inorganic materials 0.000 claims 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 1
- 239000011247 coating layer Substances 0.000 claims 1
- 229910052738 indium Inorganic materials 0.000 claims 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims 1
- 238000002844 melting Methods 0.000 abstract description 19
- 230000008018 melting Effects 0.000 abstract description 18
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 238000005485 electric heating Methods 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- HAZUQFOASUBUNA-UHFFFAOYSA-N CCCCCCCCCCCCCCCCCCO[Si](OC)(OC)F Chemical compound CCCCCCCCCCCCCCCCCCO[Si](OC)(OC)F HAZUQFOASUBUNA-UHFFFAOYSA-N 0.000 description 1
- 235000014245 Ceanothus cuneatus Nutrition 0.000 description 1
- 240000008069 Ceanothus cuneatus Species 0.000 description 1
- 235000014233 Ceanothus velutinus Nutrition 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000010408 sweeping Methods 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/32—Radiation-absorbing paints
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/042—PV modules or arrays of single PV cells
- H01L31/048—Encapsulation of modules
- H01L31/0481—Encapsulation of modules characterised by the composition of the encapsulation material
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2231—Oxides; Hydroxides of metals of tin
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
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- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2258—Oxides; Hydroxides of metals of tungsten
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- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K3/2279—Oxides; Hydroxides of metals of antimony
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
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Abstract
The invention provides a photovoltaic component with an infrared absorption and hydrophobic coating and a preparation method thereof, wherein the surface of the photovoltaic component is sprayed or dipped with an infrared absorption and hydrophobic coating solution, and the infrared absorption and hydrophobic coating solution comprises the following components in parts by weight: 2-10 parts of long-chain silane; 1-3 parts of tetraethyl silicate; 30-60 parts of organic solvent; 20-50 parts of water; 0.5 to 5 portions of infrared absorbent. The photovoltaic module provided by the invention has the advantages that the accumulated snow is difficult to deposit and is convenient to clean due to the existence of the hydrophobic coating, meanwhile, the coating has the functions of infrared absorption and heating, the infrared in the air can be absorbed, the surface temperature of the module is increased, a small amount of accumulated snow can be quickly melted, the automatic snow melting of the photovoltaic module is realized, and the automatic snow melting of the surface of the photovoltaic module can be realized without providing extra energy.
Description
Technical Field
The invention belongs to the technical field of functional modified coatings, and particularly relates to a photovoltaic module with an infrared absorption and hydrophobic coating and a preparation method thereof.
Background
In winter, severe ice and snow weather often occurs in severe cold regions. In general, the low-temperature weather causes the ice and snow on the surface of the photovoltaic module to melt for a longer time, and the photovoltaic power generation efficiency is influenced. Moreover, the partially melted snow can also cause hot spot effect on the photovoltaic module, which affects the service life of the photovoltaic module and may even cause fire. Therefore, in severe cold areas where ice and snow easily occur, snow on the surface of the photovoltaic module needs to be removed manually to maintain the operation of the photovoltaic power station.
In the prior art, a specially-made snow removing device is adopted for cleaning and removing snow or an electric heating mode is adopted for heating and melting snow removal. For example, chinese patent CN204231282U discloses an automatic snow removing device for a roof photovoltaic power station, which first uses a heating film on a photovoltaic module to melt snow, so as to avoid the influence of icing on a snow brush, and uses a snow sweeping brush to sweep snow on the basis of melting snow on the heating film.
Chinese patent CN109904254A discloses a snow-melting dual-glass photovoltaic module, which is an electric heating wire connected with a module lead through a junction box controller on the high-transparency glass on the back side of the battery piece, wherein the junction box controller controls the electric heating wire to heat the dual-glass photovoltaic module to eliminate snow melting.
The mode that adopts in above technique all needs to use extra energy to remove the snow, or uses the brush cleaner, or uses the heater strip heating, and these modes all need consume extra energy.
Disclosure of Invention
Aiming at the defects, the invention provides the photovoltaic module with the infrared absorption and hydrophobic coating and the preparation method thereof, the accumulated snow is difficult to deposit and is convenient to clean due to the existence of the hydrophobic coating, and meanwhile, the coating has the functions of infrared absorption and heating, can absorb the infrared rays in the air, so that the surface temperature of the module is raised, a small amount of accumulated snow can be quickly melted, the automatic snow melting of the photovoltaic module is realized, and the automatic snow melting of the surface of the photovoltaic module can be realized without providing extra energy.
The invention provides the following technical scheme: an infrared absorbing and hydrophobic coating photovoltaic module, the surface of the photovoltaic module is sprayed or dipped with infrared absorbing and hydrophobic coating solution, and the infrared absorbing and hydrophobic coating solution comprises the following components by weight:
2-10 parts of long-chain silane;
1-3 parts of tetraethyl silicate;
30-60 parts of organic solvent;
20-50 parts of water;
0.5 to 5 portions of infrared absorbent.
Further, the long-chain silane is a silane having 8 or more carbon atoms.
Further, the long-chain silane is one or more of hexadecyl trimethoxy silane, dodecyl trimethoxy silane, n-octyl triethoxy silane, n-decyl trimethoxy silane or heptadecyl fluoro trimethoxy silane.
Further, the organic solvent is one or more of ethanol, isopropanol, butanol, acetone and ethyl acetate.
Further, the infrared absorbent is one or more of nano tungsten trioxide, nano aluminum-doped tin oxide, nano tungsten vanadium tin antimony oxide, nano indium-doped tin oxide and nano cesium tungstate. The nano aluminum-doped tin oxide is called nano ATO for short, the nano tungsten-vanadium-tin-antimony oxide is called nano GTO for short, and the nano indium-doped tin oxide is called nano ITO for short.
The invention also provides a preparation method of the photovoltaic module with the infrared absorption and hydrophobic coating, which comprises the following steps:
1) mixing the organic solvent with the weight part of 1-50 parts of water to form a water-organic solvent mixed solution;
2) dissolving the long-chain silane with the weight component in the water-organic solvent mixed solution obtained in the step 1), adjusting the pH value to 4-5, heating to 45 ℃, hydrolyzing for 10-15 h, adding the tetraethyl silicate with the weight component, continuously reacting for 12-24 h, adding the infrared absorbent with the weight component, and uniformly stirring to obtain the infrared absorbing and hydrophobic coating solution;
3) coating the infrared-absorbing and hydrophobic coating solution obtained in the step 2) on the surfaces of the glass and the frame of the photovoltaic module in a spraying or dip-coating manner;
4) and drying under a heating condition to obtain the photovoltaic module with the cured infrared absorption and hydrophobic coating.
Further, the heating temperature of the step 4) is 120-150 ℃.
Further, the drying time of the step 4) is 5 min-10 min.
Further, the adding ratio of the organic solvent to the water in the step 1) is 3: 1.
Further, the thickness of the cured coating of the photovoltaic module obtained in the step 4) is 1-5 μm.
The invention has the beneficial effects that:
1. the photovoltaic module provided by the invention can conveniently realize the automatic snow melting function without consuming extra energy, is convenient to construct compared with the prior art, and can melt and clear snow without consuming electric energy.
2. The coating solution of the photovoltaic module provided by the invention adopts the long-chain alkyl with a specific chain length (the number of carbon atoms is more than or equal to 8) in the preparation process, and the long-chain alkyl is hydrolyzed and condensed with tetraethyl silicate to prepare the coating solution, so that a coating with a thickness of 1-5um and a hydrophobic effect can be formed on the surface of the photovoltaic module, and the hydrophobic coating can make accumulated snow difficult to deposit and is convenient to clean.
3. According to the photovoltaic module coating solution provided by the invention, infrared absorbers such as nano tungsten trioxide, nano ATO, nano GTO, nano ITO and nano cesium tungstate are added, the hydrophobic effect cannot be damaged due to the addition of the infrared absorbers, more heat energy can be provided by absorbing infrared rays, so that the infrared absorbers have snow melting capability, and the hydrophobic and infrared absorbing double-function coating is formed by combining the infrared absorbers and the infrared absorbers, so that the photovoltaic module can automatically melt snow.
Detailed description of the preferred embodiments
The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
Example 1
The invention provides a photovoltaic module with an infrared absorption and hydrophobic coating, which comprises the following steps:
1) preparation of the Mixed solution
Mixing water and isopropanol according to a weight ratio of 1: 3, mixing to obtain a mixed solution for later use.
2) Preparation of coating solution
Taking 90g of the mixed solution prepared in the step 1), adding long-chain silane n-octyltriethoxysilane, stirring until the long-chain silane n-octyltriethoxysilane is completely dissolved, adding a proper amount of hydrochloric acid to adjust the pH to 4, heating to 45 ℃, hydrolyzing for 10h, adding 2g of tetraethyl silicate, continuing to react for 24h, adding 3g of infrared absorbent nano ATO, and uniformly stirring for later use.
3) Photovoltaic module with snow melting function prepared by coating
And (3) uniformly spraying the coating solution prepared in the step 2) on the surfaces of the photovoltaic module glass and the frame, and drying at 120 ℃ for 5min to obtain a photovoltaic module with a snow melting function, wherein the thickness of the coating is 2 microns.
Example 2
The invention provides a photovoltaic module with an infrared absorption and hydrophobic coating, which comprises the following steps:
1) preparation of the Mixed solution
Mixing water and ethanol according to a weight ratio of 1: 3, mixing to obtain a mixed solution for later use.
2) Preparation of coating solution
Taking 90g of the mixed solution prepared in the step 1), adding long-chain silane dodecyl trimethoxy silane, stirring until the long-chain silane dodecyl trimethoxy silane is completely dissolved, adding a proper amount of hydrochloric acid to adjust the pH value to 4.5, heating to 45 ℃, hydrolyzing for 12.5h, adding 2g of tetraethyl silicate, continuing to react for 12h, adding 3g of infrared absorbent nano tungsten trioxide, and uniformly stirring for later use.
3) Photovoltaic module with snow melting function prepared by coating
And (3) uniformly spraying the coating solution prepared in the step 2) on the surfaces of the photovoltaic module glass and the frame, and drying at 135 ℃ for 10min to obtain the photovoltaic module with the snow melting function, wherein the thickness of the coating is 1 um.
Example 3
1) Preparation of the Mixed solution
Mixing water and ethyl acetate according to a weight ratio of 1: 3, mixing to obtain a mixed solution for later use.
2) Preparation of coating solution
Taking 90g of the mixed solution prepared in the step 1), adding long-chain silane hexadecyl trimethoxy silane, stirring until the long-chain silane hexadecyl trimethoxy silane is completely dissolved, adding a proper amount of hydrochloric acid to adjust the pH value to be 5, heating to 45 ℃, hydrolyzing for 15h, adding 2g of tetraethyl silicate, continuing to react for 18h, adding 3g of infrared absorbent nano tungsten trioxide, and uniformly stirring for later use.
3) Photovoltaic module with snow melting function prepared by coating
And (3) uniformly spraying the coating solution prepared in the step 2) on the surfaces of the photovoltaic module glass and the frame, and drying at 120 ℃ for 8min to obtain a photovoltaic module with a snow melting function, wherein the thickness of the coating is 5 microns.
Test example
The power of the photovoltaic module is tested by adopting a 3500SLP module IV power tester (the photovoltaic module adopts the same materials except the coating), the water contact angle and the separation angle are tested by adopting a DR-1000 contact angle tester, and the surface temperature of the module is tested by adopting a Fluke62 infrared thermometer. The environment temperature in the snowy day was-13.7 ℃. The results are shown in Table 1.
TABLE 1
Through the test results, the power of the photovoltaic module with the automatic snow melting function is not obviously reduced compared with the power of the photovoltaic module without the coating. However, the water contact angle of the surface of the photovoltaic module with the automatic snow melting function is obviously increased, the departure angle is obviously reduced, and the temperature of the module is improved. This means that in rainy or snowy weather, snow on the surface of the component can be melted and can roll away from the surface of the component quickly, thereby realizing automatic snow melting. We can also see from the comparative data of the snow thickness on the surface of the assembly, which lasts 10h in snow, that the snow thickness of the three examples of the patent is significantly lower than that of the comparative example.
While the invention has been described with reference to a preferred embodiment, various modifications may be made and equivalents may be substituted for elements thereof without departing from the scope of the invention. In particular, the technical features mentioned in the embodiments can be combined in any way as long as there is no structural conflict. It is intended that the invention not be limited to the particular embodiments disclosed, but that the invention will include all embodiments falling within the scope of the appended claims.
Claims (10)
1. An infrared absorbing and hydrophobic coating photovoltaic module, the surface of the photovoltaic module is sprayed or dipped with infrared absorbing and hydrophobic coating solution, and the infrared absorbing and hydrophobic coating solution comprises the following components by weight:
2-10 parts of long-chain silane;
1-3 parts of tetraethyl silicate;
30-60 parts of organic solvent;
20-50 parts of water;
0.5 to 5 portions of infrared absorbent.
2. The infrared-absorptive and hydrophobic-coated photovoltaic module of claim 1, wherein the long-chain silane is a silane having 8 or more carbon atoms.
3. The infrared absorbing and hydrophobic coated photovoltaic module of claim 1, wherein said long chain silane is one or more of hexadecyl trimethoxysilane, dodecyl trimethoxysilane, n-octyl triethoxysilane, n-decyl trimethoxysilane, or heptadecafluorodecyl trimethoxysilane.
4. The infrared-absorptive and hydrophobic-coated photovoltaic module of claim 1, wherein the organic solvent is one or more of ethanol, isopropanol, butanol, acetone, and ethyl acetate.
5. The infrared absorbing and hydrophobic coated photovoltaic module of claim 1, wherein said infrared absorbing agent is one or more of nano tungsten trioxide, nano aluminum doped tin oxide ATO, nano tungsten vanadium tin antimony oxide GTO, nano indium doped tin oxide ITO, nano cesium tungstate.
6. Method for the preparation of an infrared-absorbing and hydrophobic-coated photovoltaic module according to any of claims 1 to 5, characterized in that it comprises the following steps:
1) mixing the organic solvent with the weight part of 1-50 parts of water to form a water-organic solvent mixed solution;
2) dissolving the long-chain silane with the weight component in the water-organic solvent mixed solution obtained in the step 1), adjusting the pH value to 4-5, heating to 45 ℃, hydrolyzing for 10-15 h, adding the tetraethyl silicate with the weight component, continuously reacting for 12-24 h, adding the infrared absorbent with the weight component, and uniformly stirring to obtain the infrared absorbing and hydrophobic coating solution;
3) coating the infrared-absorbing and hydrophobic coating solution obtained in the step 2) on the surfaces of the glass and the frame of the photovoltaic module in a spraying or dip-coating manner;
4) and drying under a heating condition to obtain the photovoltaic module with the cured infrared absorption and hydrophobic coating.
7. The method for preparing an infrared-absorptive and hydrophobic-coated photovoltaic module according to claim 6, wherein the heating temperature in step 4) is 120 ℃ to 150 ℃.
8. The method for preparing the photovoltaic module with the infrared absorption and hydrophobic coating layer according to claim 6, wherein the drying time of the step 4) is 5-10 min.
9. The method of claim 6, wherein the organic solvent is added to the water in a ratio of 3:1 in step 1).
10. The method for preparing a photovoltaic module with infrared absorption and hydrophobic coating according to claim 5, wherein the thickness of the cured coating of the photovoltaic module obtained in step 4) is 1 μm to 5 μm.
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