CN104269452A - Perovskite solar battery made of silicon-based thin-film materials and manufacturing method thereof - Google Patents
Perovskite solar battery made of silicon-based thin-film materials and manufacturing method thereof Download PDFInfo
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- CN104269452A CN104269452A CN201410535451.5A CN201410535451A CN104269452A CN 104269452 A CN104269452 A CN 104269452A CN 201410535451 A CN201410535451 A CN 201410535451A CN 104269452 A CN104269452 A CN 104269452A
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- silica
- base film
- perovskite
- layer
- alloy
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- 239000000463 material Substances 0.000 title claims abstract description 50
- 239000010409 thin film Substances 0.000 title claims abstract description 12
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N silicon Chemical compound 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[Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 title abstract description 9
- 229910052710 silicon Inorganic materials 0.000 title abstract description 9
- 239000010703 silicon Substances 0.000 title abstract description 9
- 238000004519 manufacturing process Methods 0.000 title abstract description 6
- 239000011521 glass Substances 0.000 claims abstract description 52
- 230000027756 respiratory electron transport chain Effects 0.000 claims abstract description 30
- 229910052751 metal Inorganic materials 0.000 claims abstract description 17
- 239000002184 metal Substances 0.000 claims abstract description 17
- 239000010408 film Substances 0.000 claims description 52
- 230000005540 biological transmission Effects 0.000 claims description 28
- -1 silicon nitrogen Chemical compound 0.000 claims description 27
- 238000002360 preparation method Methods 0.000 claims description 21
- 238000005137 deposition process Methods 0.000 claims description 16
- 238000005229 chemical vapour deposition Methods 0.000 claims description 15
- 229910001199 N alloy Inorganic materials 0.000 claims description 12
- 229910000979 O alloy Inorganic materials 0.000 claims description 12
- 229910021483 silicon-carbon alloy Inorganic materials 0.000 claims description 12
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc monoxide Chemical compound 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[C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- OGIDPMRJRNCKJF-UHFFFAOYSA-N TiO Inorganic materials 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[Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 6
- 229960001296 Zinc Oxide Drugs 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 229910021424 microcrystalline silicon Inorganic materials 0.000 claims description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titan oxide Chemical compound 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O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 6
- 229910001929 titanium oxide Inorganic materials 0.000 claims description 6
- 235000014692 zinc oxide Nutrition 0.000 claims description 6
- 239000011787 zinc oxide Substances 0.000 claims description 6
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group 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[N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 5
- 238000001755 magnetron sputter deposition Methods 0.000 claims description 3
- 238000004528 spin coating Methods 0.000 claims description 3
- 239000011368 organic material Substances 0.000 abstract description 3
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- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminum Chemical compound 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[Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound 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- 239000000126 substance Substances 0.000 description 2
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound 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[Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- QNWMNMIVDYETIG-UHFFFAOYSA-N Gallium(II) selenide Chemical compound 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[Se]=[Ga] QNWMNMIVDYETIG-UHFFFAOYSA-N 0.000 description 1
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- OYPRJOBELJOOCE-UHFFFAOYSA-N calcium Chemical compound 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[Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000875 corresponding Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 150000002220 fluorenes Chemical class 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium Chemical compound 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- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium Chemical compound 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[Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
Classifications
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- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L31/00—Semiconductor devices sensitive to infra-red 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 infra-red 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
- H01L31/06—Semiconductor devices sensitive to infra-red 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 characterised by at least one potential-jump barrier or surface barrier
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- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L31/00—Semiconductor devices sensitive to infra-red 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
- H01L31/0248—Semiconductor devices sensitive to infra-red 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 characterised by their semiconductor bodies
- H01L31/0256—Semiconductor devices sensitive to infra-red 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 characterised by their semiconductor bodies characterised by the material
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- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L31/00—Semiconductor devices sensitive to infra-red 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
- H01L31/18—Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof
- H01L31/186—Particular post-treatment for the devices, e.g. annealing, impurity gettering, short-circuit elimination, recrystallisation
- H01L31/1864—Annealing
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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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- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Abstract
The invention provides a perovskite solar battery made of silicon-based thin-film materials and a manufacturing method of the perovskite solar battery. The perovskite solar battery made of the silicon-based thin-film materials structurally comprises conductive glass, an n-type electron transfer layer arranged on the conductive glass, a perovskite photosensitive layer arranged on the n-type electron transfer layer, a p-type hole transfer layer arranged on the perovskite photosensitive layer and a metal counter electrode arranged on the p-type hole transfer layer. The perovskite solar battery and the manufacturing method have the advantages that the p-type silicon-based thin-film materials low in cost and easy to combine are adopted as the hole transfer layer, expensive spiro-OMeTAD organic materials are replaced, and the long wave response and battery efficiency of the silicon solar battery are improved.
Description
Technical field
The present invention relates to technical field of solar cells, refer to perovskite solar cell of a kind of silica-base film material and preparation method thereof especially.
Background technology
Current hull cell mainly with cadmium telluride (CdTe) and the Copper Indium Gallium Selenide sun (CIGS) battery for main representative, the small size battery conversion efficiency of current World Report reaches 19.6% and 19.8% respectively.But the cadmium element relating to expensive rare element tellurium, indium, gallium and human body and environment are had to huge pollution prepared in material by above hull cell, therefore the development of these hull cells in following terawatt (TW) level installation total amount level can be extremely restricted.
In the recent period, the great interest of photovoltaic cell circle has been attracted as the new calcium perovskite like structure thin film solar cell of dye-sensitized cell " upgrade version ".Within the four short years, efficiency of solar cell prepared by the plumbous iodine material of the organic and inorganic mixing methylamine based on perovskite structure is advanced by leaps and bounds.The element that material is earth's crust rich reserves prepared by this battery, and preparation method is simple, and full processing procedure low temperature, thus has boundless industrialization prospect.The plumbous halide light-sensitive material of this perovskite structure, there is typical semiconductor material characteristic and suitable energy gap, can reach more than 95% to the absorption efficiency being less than 800nm wavelength sunlight, and charge carrier have very high mobility and diffusion length, is particularly suitable for photovoltaic application.
But the efficient calcium titanium ore battery of existing efficiency more than 15% without exception all have employed spiral shell two fluorenes (spiro-OMeTAD) this organic compound as p-type hole transmission layer (HTM), its price is more than ten times (4000RMB/g) of gold, significantly limit the commercial application process of perovskite battery, seeking the more suitable cheap p-type hole transmission layer being easy to synthesize becomes the important actuating force promoting device development.Material as p-type hole transmission layer must form at the interface place with calcium titanium ore bed that typical hole is selected, the heterojunction of electron repelling, namely require that it has suitable band gap width, electron affinity and band edge position, and there is good photoconductivity and mobility.For meeting above-mentioned requirements, the nitrogen element that can adulterate suitable in p-type silica-base film material or carbon or oxygen element, thus the band structure significantly changing p-type silica-base film material.The present invention proposes to utilize p-type silica-base film material band gap adjustable, doping type is variable, sunlight is had to the excellent specific properties such as certain absorption, realize substituting spiro-OMeTAD organic material, and then greatly advance the combination of amorphous silicon industry and perovskite battery.
Summary of the invention
The object of the invention is to, perovskite solar battery structure of a kind of silica-base film material and preparation method thereof is provided, have with low cost, the p-type silica-base film material being easy to synthesize is as hole transmission layer, replace expensive spiro-OMeTAD organic material, improve the long-wave response of silicon solar cell and the advantage of battery efficiency.
For achieving the above object, the present invention proposes a kind of perovskite solar battery structure of silica-base film material, comprising:
One electro-conductive glass;
One N-shaped electron transfer layer, it is produced on electro-conductive glass;
One perovskite photosensitive layer, it is produced on N-shaped electron transfer layer;
One p-type hole transmission layer, it is produced on perovskite photosensitive layer;
One metal counter electrode, it is produced on p-type hole transmission layer.
The present invention also provides a kind of perovskite solar battery structure of silica-base film material, comprising:
One electro-conductive glass;
One p-type hole transmission layer, it is produced on electro-conductive glass;
One perovskite photosensitive layer, it is produced on p-type electron transfer layer;
One N-shaped electron transfer layer, it is produced on perovskite photosensitive layer;
One metal counter electrode, it is produced on N-shaped hole transmission layer.
The present invention provides again a kind of preparation method of perovskite solar cell of silica-base film material, comprises the steps:
Step 1: get an electro-conductive glass;
Step 2: clean, dry up;
Step 3: depositing n-type electron transfer layer, perovskite photosensitive layer, p-type hole transmission layer and metal counter electrode successively on electro-conductive glass, complete preparation.
The present invention reoffers a kind of preparation method of perovskite solar cell of silica-base film material, comprises the steps:
Step 1: get an electro-conductive glass;
Step 2: clean, dry up;
Step 3: depositing p-type hole transmission layer, perovskite photosensitive layer, N-shaped electron transfer layer and metal counter electrode successively on electro-conductive glass, complete preparation.
The present invention has following beneficial effect:
1. utilize the present invention, the light activated charge carrier of long wave can be ensured at nearest silica-base film/perovskite heterojunction place separately, and add extra heterojunction electromotive force to device, significantly improve short circuit current and the open circuit voltage of device.
2. select layer material compared to other p-type holes, amorphous silicon band gap is adjustable, feature especially cheap and easy to manufacture, greatly can reduce the production cost of perovskite solar cell, accelerates the popularization of perovskite battery.
3. utilize the present invention, the full process vacuum depositing operation of battery can be realized, avoid solwution method and prepare p-type hole transmission layer technology, completely compatible with existing amorphous silicon battery production technology, be thus beneficial to large-scale production.
Accompanying drawing explanation
For further illustrating technology contents of the present invention, be described in detail as follows below in conjunction with embodiment and accompanying drawing, wherein:
Fig. 1 is perovskite/silicon-based thin-film lamination band structure schematic diagram;
Fig. 2 is the structural representation of the first embodiment of the present invention;
Fig. 3 is the structural representation of the second embodiment of the present invention;
Fig. 4 is the preparation flow figure of first embodiment of the invention;
Fig. 5 is the preparation flow figure of second embodiment of the invention.
Embodiment
Refer to shown in Fig. 1, the invention provides the operation principle of the perovskite solar cell of silica-base film material, be summarized as follows:
For the perovskite solar cell of NIP structure, be-3.93eV (relative to vacuum level) at the bottom of the conduction band of perovskite material, top of valence band is-5.43eV, and p-type noncrystal membrane is by alloy doping such as carbon, nitrogen, oxygen, conduction band limit and valence-band edge can be adjusted to higher than the corresponding band edge of perovskite I layer, the discrete band structure formed is as shown in Fig. 1 (a), and during unglazed photograph heat balance, band structure is as shown in Fig. 1 (b), and now Fermi level reaches unified.The heterostructure formed after connecting is applicable to hole and carries from perovskite I layer to P-type layer but electronics is stopped by conduction band, namely has obvious holoe carrier capacity gauge.In PIN structural, perovskite I layer can be with run-off the straight under both sides heterojunction Built-in field is through, and will speed up light induced electron and flow to N district, photohole flows to P district, produces significant photo-generated carrier field and helps collection effect.
Refer to shown in Fig. 2, the invention provides a kind of perovskite solar battery structure of silica-base film material, comprising:
One electro-conductive glass 1, the material of described electro-conductive glass 1 can be FTO glass, ito glass, AZO glass or IZO glass, and the square resistance of glass is 5-30 Ω/;
One N-shaped electron transfer layer 2, it is produced on electro-conductive glass 1, and described N-shaped electron transfer layer 2 is N-shaped zinc-oxide film, N-shaped thin film of titanium oxide or N-shaped silica-base film, and thickness is 5nm-50nm;
One perovskite photosensitive layer 3, it is produced on N-shaped electron transfer layer 2, and described perovskite photosensitive layer 3 is CH
3nH
3pbI
3or CH
3nH
3pbI
3-xcl
x, thickness is 50nm-2000nm;
One p-type hole transmission layer 4, it is produced on perovskite photosensitive layer 3, described p-type hole transmission layer 4 is p-type silica-base film, comprise silicon-base alloy film, as the one in microcrystal silicon carbon alloy, microcrystal silicon nitrogen alloy, microcrystal silicon oxygen alloy, non-crystal silicon carbon alloy, amorphous silicon nitrogen alloy or non-crystalline/micro-crystalline silicon oxygen alloy or its combination.Deposition process is plasma enhanced chemical vapor deposition, and thickness is at 10nm-100nm, and the atomic fraction of carbon containing is at 10%-30%, and nitrogenous atomic fraction is at 10%-30%, and oxygen containing atomic fraction is at 10%-30%;
One metal counter electrode 5, it is produced on p-type hole transmission layer 4, and described metal counter electrode 5 is one in gold, silver, copper or aluminium or its combination.
Refer to shown in Fig. 3, the present invention provides a kind of perovskite solar battery structure of silica-base film material in addition, comprising:
One electro-conductive glass 1, the material of described electro-conductive glass 1 can be FTO glass, ito glass, AZO glass or IZO glass, and the square resistance of glass is 5-30 Ω/;
One p-type hole transmission layer 4, it is produced on electro-conductive glass 1, described p-type hole transmission layer 4 is p-type silica-base film, comprise silicon-base alloy film, as the one in microcrystal silicon carbon alloy, microcrystal silicon nitrogen alloy, microcrystal silicon oxygen alloy, non-crystal silicon carbon alloy, amorphous silicon nitrogen alloy or non-crystalline/micro-crystalline silicon oxygen alloy or its combination.Deposition process is plasma enhanced chemical vapor deposition, and thickness is at 10nm-100nm, and the atomic fraction of carbon containing is at 10%-30%, and nitrogenous atomic fraction is at 10%-30%, and oxygen containing atomic fraction is at 10%-30%;
One perovskite photosensitive layer 3, it is produced on p-type electron transfer layer 4, and described perovskite photosensitive layer 3 is CH
3nH
3pbI
3or CH
3nH
3pbI
3-xcl
x, thickness is 50nm-2000nm;
One N-shaped electron transfer layer 2, it is produced on perovskite photosensitive layer 3, and described N-shaped electron transfer layer 2 is N-shaped zinc-oxide film, N-shaped thin film of titanium oxide or N-shaped silica-base film, and thickness is 5nm-50nm;
One metal counter electrode 5, it is produced on N-shaped electron transfer layer 2, and described metal counter electrode 5 is one in gold, silver, copper or aluminium or its combination.
Refer to Fig. 4, in conjunction with consulting Fig. 2, a kind of perovskite solar cell preparation method of silica-base film material, comprises the steps:
Step 1: get an electro-conductive glass 1.The material of described electro-conductive glass 1 can be FTO glass, ito glass, AZO glass or IZO glass, and the square resistance of glass is 5-30 Ω/, plays support and the electric action of follow-up film plating layer.
Step 2: clean, dry up.After the cleaning of ultrasonic wave organic solvent, dry up with nitrogen.Carry out local corrosion on the electrically conductive or cover, when avoiding follow-up plated film, upper/lower electrode forms short circuit.
Step 3: depositing n-type electron transfer layer 2, perovskite photosensitive layer 3, p-type hole transmission layer 4 and metal counter electrode 5 successively on electro-conductive glass 1, complete preparation.Described N-shaped electron transfer layer 2 is zinc oxide or thin film of titanium oxide, and thickness is 5nm-50nm, and deposition process is magnetron sputtering method, also can be N-shaped silica-base film, comprise N-shaped microcrystal silicon or the N-shaped amorphous silicon of hydrogen dilution or non-hydrogen dilution, thickness is 5-50nm, and deposition process is chemical vapour deposition technique.Can corrode to define source region figure to glass conductive layer with acid solution before depositing n-type electron transfer layer 2, and can clean with oxygen or nitrogen plasma effects on surface.Described perovskite photosensitive layer 3 is CH
3nH
3pbI
3or CH
3nH
3pbI
3-xcl
xdeposition process is organic and inorganic double source coevaporation method or spin-coating method, thickness is 50nm-2000nm, through annealing steps after deposition, form stable perovskite photosensitive layer, annealing way comprises hot plate annealing, baking oven annealing, furnace anneal or sintering furnace annealing, and annealing temperature is 70-200 DEG C, and the time is 10min-100min.Described p-type hole transmission layer 4 is p-type silicon-base alloy film, comprises the one in microcrystal silicon carbon alloy, microcrystal silicon nitrogen alloy, microcrystal silicon oxygen alloy, non-crystal silicon carbon alloy, amorphous silicon nitrogen alloy or non-crystalline/micro-crystalline silicon oxygen alloy or its combination.Deposition process is chemical vapour deposition (CVD), comprise plasma activated chemical vapour deposition, hot-wire chemical gas-phase deposition, photoinduction chemical vapour deposition (CVD), thickness is at 10nm-100nm, the atomic fraction of carbon containing is at 10%-30%, nitrogenous atomic fraction is at 10%-30%, and oxygen containing atomic fraction is at 10%-30%.Described metal counter electrode 5 is one in gold, silver, copper or aluminium or its combination, and deposition process comprises electron beam evaporation or resistance heat evaporation.
Refer to Fig. 5, in conjunction with consulting Fig. 3, the perovskite solar cell preparation method of another silica-base film material, comprises the steps:
Step 1: get an electro-conductive glass 1.The material of described electro-conductive glass 1 can be FTO glass, ito glass, AZO glass or IZO glass, and the square resistance of glass is 5-30 Ω/, plays support and the electric action of follow-up film plating layer.
Step 2: clean, dry up.After the cleaning of ultrasonic wave organic solvent, dry up with nitrogen.Carry out local corrosion on the electrically conductive or cover, when avoiding follow-up plated film, upper/lower electrode forms short circuit.
Step 3: depositing p-type hole transmission layer 4, perovskite photosensitive layer 3, N-shaped electron transfer layer 2 and metal counter electrode 5 successively on electro-conductive glass 1, complete preparation.Described p-type hole transmission layer 4 is p-type silicon-base alloy film, comprises the one in microcrystal silicon carbon alloy, microcrystal silicon nitrogen alloy, microcrystal silicon oxygen alloy, non-crystal silicon carbon alloy, amorphous silicon nitrogen alloy or non-crystalline/micro-crystalline silicon oxygen alloy or its combination.Deposition process is chemical vapour deposition (CVD), comprise plasma activated chemical vapour deposition, hot-wire chemical gas-phase deposition, photoinduction chemical vapour deposition (CVD), thickness is at 10nm-100nm, the atomic fraction of carbon containing is at 10%-30%, nitrogenous atomic fraction is at 10%-30%, and oxygen containing atomic fraction is at 10%-30%.Described perovskite photosensitive layer 3 is CH
3nH
3pbI
3or CH
3nH
3pbI
3-xcl
xdeposition process is organic and inorganic double source coevaporation method or spin-coating method, thickness is 50nm-2000nm, through annealing steps after deposition, form stable perovskite photosensitive layer, annealing way comprises hot plate annealing, baking oven annealing, furnace anneal or sintering furnace annealing, and annealing temperature is 70-200 DEG C, and the time is 10min-100min.Described N-shaped electron transfer layer 2 is zinc oxide or thin film of titanium oxide, and thickness is 5nm-50nm, and deposition process is magnetron sputtering method, also can be N-shaped silica-base film, comprise N-shaped microcrystal silicon or the N-shaped amorphous silicon of hydrogen dilution or non-hydrogen dilution, thickness is 5-50nm, and deposition process is chemical vapour deposition technique.Can corrode to define source region figure to glass conductive layer with acid solution before depositing n-type electron transfer layer 2, and can clean with oxygen or nitrogen plasma effects on surface.Described metal counter electrode 5 is one in gold, silver, copper or aluminium or its combination, and deposition process comprises electron beam evaporation or resistance heat evaporation.
Above-described specific embodiment, has carried out further detailed description to object of the present invention, technical scheme and beneficial effect, and institute it should be understood that and the foregoing is only specific embodiments of the invention, does not limit the present invention.Within the spirit and principles in the present invention all, any amendment made, equivalent replacement, improvement etc., all should be included within protection scope of the present invention.
Claims (10)
1. a perovskite solar battery structure for silica-base film material, comprising:
One electro-conductive glass;
One N-shaped electron transfer layer, it is produced on electro-conductive glass;
One perovskite photosensitive layer, it is produced on N-shaped electron transfer layer;
One p-type hole transmission layer, it is produced on perovskite photosensitive layer;
One metal counter electrode, it is produced on p-type hole transmission layer.
2. a perovskite solar battery structure for silica-base film material, comprising:
One electro-conductive glass;
One p-type hole transmission layer, it is produced on electro-conductive glass;
One perovskite photosensitive layer, it is produced on p-type electron transfer layer;
One N-shaped electron transfer layer, it is produced on perovskite photosensitive layer;
One metal counter electrode, it is produced on N-shaped hole transmission layer.
3. the perovskite solar battery structure of silica-base film material according to claim 1 and 2, the material of wherein said N-shaped electron transfer layer is N-shaped zinc-oxide film, N-shaped thin film of titanium oxide or N-shaped silica-base film, and thickness is 5nm-50nm.
4. the perovskite solar battery structure of silica-base film material according to claim 1 and 2, the material of wherein said perovskite photosensitive layer is CH
3nH
3pbI
3or CH
3nH
3pbI
3-xcl
x, thickness is 50nm-2000nm.
5. the perovskite solar battery structure of silica-base film material according to claim 1 and 2, the material of wherein said p-type hole transmission layer is p-type silica-base film, this p-type silica-base film comprises silicon-base alloy film, and the material of this p-type silica-base film is one in microcrystal silicon carbon alloy, microcrystal silicon nitrogen alloy, microcrystal silicon oxygen alloy, non-crystal silicon carbon alloy, amorphous silicon nitrogen alloy or non-crystalline/micro-crystalline silicon oxygen alloy or its combination; The thickness of this p-type silica-base film is 10nm-100nm.
6. a preparation method for the perovskite solar cell of silica-base film material, comprises the steps:
Step 1: get an electro-conductive glass;
Step 2: clean, dry up;
Step 3: depositing n-type electron transfer layer, perovskite photosensitive layer, p-type hole transmission layer and metal counter electrode successively on electro-conductive glass, complete preparation.
7. a preparation method for the perovskite solar cell of silica-base film material, comprises the steps:
Step 1: get an electro-conductive glass;
Step 2: clean, dry up;
Step 3: depositing p-type hole transmission layer, perovskite photosensitive layer, N-shaped electron transfer layer and metal counter electrode successively on electro-conductive glass, complete preparation.
8. the preparation method of the perovskite solar cell of the silica-base film material according to claim 6 or 7, the material of wherein said N-shaped electron transfer layer is zinc oxide or thin film of titanium oxide, thickness is 5nm-50nm, deposition process is magnetron sputtering method, or the material of N-shaped electron transfer layer is N-shaped silica-base film, thickness is 5-50nm, and deposition process is chemical vapour deposition technique.
9. the preparation method of the perovskite solar cell of the silica-base film material according to claim 6 or 7, the material of wherein said perovskite photosensitive layer is CH
3nH
3pbI
3or CH
3nH
3pbI
3-xcl
x, thickness is 50nm-2000nm, and deposition process is organic and inorganic double source coevaporation method or spin-coating method.
10. the preparation method of the perovskite solar cell of the silica-base film material according to claim 6 or 7, the material of wherein said p-type hole transmission layer is p-type silicon-base alloy film, comprise one in microcrystal silicon carbon alloy, microcrystal silicon nitrogen alloy, microcrystal silicon oxygen alloy, non-crystal silicon carbon alloy, amorphous silicon nitrogen alloy or non-crystalline/micro-crystalline silicon oxygen alloy or and combination, deposition process is chemical vapour deposition (CVD), deposit thickness is 10nm-100nm, the atomic fraction of carbon containing is at 10%-30%, nitrogenous atomic fraction is at 10%-30%, and oxygen containing atomic fraction is at 10%-30%.
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