CN103680990A - Method for using alkaline liquor to clean substrate used for preparing dye-sensitized solar cell - Google Patents
Method for using alkaline liquor to clean substrate used for preparing dye-sensitized solar cell Download PDFInfo
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- CN103680990A CN103680990A CN201310746539.7A CN201310746539A CN103680990A CN 103680990 A CN103680990 A CN 103680990A CN 201310746539 A CN201310746539 A CN 201310746539A CN 103680990 A CN103680990 A CN 103680990A
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- substrate
- alkali lye
- dssc
- solar cell
- dye
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- 239000000758 substrate Substances 0.000 title claims abstract description 63
- 238000004140 cleaning Methods 0.000 title abstract description 40
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000008367 deionised water Substances 0.000 claims abstract description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 71
- 239000003513 alkali Substances 0.000 claims description 35
- 235000011121 sodium hydroxide Nutrition 0.000 claims description 34
- 238000002360 preparation method Methods 0.000 claims description 24
- 239000011521 glass Substances 0.000 claims description 18
- 239000002585 base Substances 0.000 claims description 12
- WMFOQBRAJBCJND-UHFFFAOYSA-M lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 claims description 9
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 9
- 238000004506 ultrasonic cleaning Methods 0.000 claims description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M NaHCO3 Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 3
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 claims description 3
- 229910001863 barium hydroxide Inorganic materials 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 239000001187 sodium carbonate Substances 0.000 claims description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 3
- 239000002699 waste material Substances 0.000 abstract description 10
- 239000003960 organic solvent Substances 0.000 abstract description 7
- 238000005406 washing Methods 0.000 abstract description 2
- 238000001035 drying Methods 0.000 abstract 1
- 239000000975 dye Substances 0.000 description 28
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 26
- 239000000243 solution Substances 0.000 description 19
- 235000010215 titanium dioxide Nutrition 0.000 description 13
- 239000002105 nanoparticle Substances 0.000 description 12
- 238000005245 sintering Methods 0.000 description 11
- 239000003792 electrolyte Substances 0.000 description 9
- 239000004408 titanium dioxide Substances 0.000 description 9
- 239000000084 colloidal system Substances 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- 229910010413 TiO 2 Inorganic materials 0.000 description 7
- 239000008151 electrolyte solution Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 238000007650 screen-printing Methods 0.000 description 6
- OGIDPMRJRNCKJF-UHFFFAOYSA-N TiO Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- RDFLLVCQYHQOBU-GPGGJFNDSA-O Cyanin Natural products O([C@H]1[C@H](O)[C@H](O)[C@H](O)[C@H](CO)O1)c1c(-c2cc(O)c(O)cc2)[o+]c2c(c(O[C@H]3[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O3)cc(O)c2)c1 RDFLLVCQYHQOBU-GPGGJFNDSA-O 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000005538 encapsulation Methods 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 238000011084 recovery Methods 0.000 description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 4
- 229910052719 titanium Inorganic materials 0.000 description 4
- 239000010936 titanium Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000007654 immersion Methods 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- VXUYXOFXAQZZMF-UHFFFAOYSA-N Titanium isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- WEVYAHXRMPXWCK-UHFFFAOYSA-N acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007772 electrode material Substances 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000005286 illumination Methods 0.000 description 2
- 150000007529 inorganic bases Chemical class 0.000 description 2
- 239000002159 nanocrystal Substances 0.000 description 2
- 238000009376 nuclear reprocessing Methods 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 230000000607 poisoning Effects 0.000 description 2
- 231100000572 poisoning Toxicity 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N precursor Substances N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- 125000001824 selenocyanato group Chemical group *[Se]C#N 0.000 description 2
- 230000001235 sensitizing Effects 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 238000003980 solgel method Methods 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N t-BuOH Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 239000005711 Benzoic acid Substances 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M CHEMBL593252 Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N Coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Natural products C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 1
- RKCAIXNGYQCCAL-UHFFFAOYSA-N Porphin Chemical compound N1C(C=C2N=C(C=C3NC(=C4)C=C3)C=C2)=CC=C1C=C1C=CC4=N1 RKCAIXNGYQCCAL-UHFFFAOYSA-N 0.000 description 1
- 208000008425 Protein Deficiency Diseases 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive Effects 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002322 conducting polymer Substances 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000010192 crystallographic characterization Methods 0.000 description 1
- 230000003247 decreasing Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000002803 fossil fuel Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 150000002475 indoles Chemical class 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-M laurate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 1
- 229940070765 laurate Drugs 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 231100000202 sensitizing Toxicity 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000001132 ultrasonic dispersion Methods 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
Images
Classifications
-
- 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
- Y02E10/542—Dye sensitized solar cells
Abstract
The invention relates to a method for using alkaline liquor to clean a substrate used for preparing a dye-sensitized solar cell. The method comprises the following steps: immersing the substrate into the alkaline liquor, and causing the alkaline liquor to submerge the top of the substrate for 8+-3mm; ultrasonically cleaning for 0-60 minutes at 0-50 DEG C, washing the substrate with deionized water, and drying the substrate. The method uses the inorganic alkaline liquor to replace an organic solvent to clean the substrate, and the dosage of the alkaline liquor is less, so that the cleaning cost can be reduced, and the harm for operators and environment is reduced. Waste liquor after cleaning can not be recycled to be directly drained into a drainage channel, and the problems of large amount of waste liquor and difficult recycle are solved.
Description
Technical field
The present invention relates to a kind of cleaning method of the substrate for the preparation of DSSC, relate in particular to a kind of alkali lye and clean the method for the preparation of the substrate of DSSC.
Background technology
Instead the energy of fossil fuel, has utilized the solar cell of sunlight to receive publicity, and people have carried out various research to it.Solar cell is a kind of photoelectric conversion device that is electric energy by transform light energy, owing to usining sunlight as the energy, thus minimum on the impact of earth environment, can be popularized widely.
The research and development that converts solar energy in recent years luminous energy is very fast.Applied dye-sensitized solar cell (the Dye-Sensitized Solar Cell that the photoinduction electronics by dye sensitization moves, DSSC), instead the solar cell of future generation of silicon (Si) class solar cell etc. receives publicity in recent years, and is extensively studied.The advantage of DSSC (DSSC) is very outstanding: 1, make simply, cost is low; 2, the dye sensitizing agent using can be issued in very low light energy saturated, therefore can under various illumination conditions, use; 3, can in very wide temperature range, normally work; 4, transparent product be can make, door and window, roof and vehicle top are applied to.Therefore it becomes rapidly research emphasis and the focus of countries in the world, has obtained abundant achievement, has started the upsurge of various countries' research DSSC solar cell.
DSSC is as third generation solar cell, it is current most potential silicon solar cell cheap alternative, it is prepared into and has loose structure with cheap broad-band gap oxide semiconductor, the nano-crystal film of high-specific surface area, the semiconductive thin film of nanocrystalline structure is the core of work electrode, the feature of its porous and huge specific area have guaranteed the enough absorption of dye molecule, simultaneously, the dye molecule being adsorbed can make the migration of electronic high-effective with the interface forming between titanium dioxide nano-particle, and select suitable redox electrolytes matter, utilize dyestuff to capture sunlight.
On the light anode of dye-sensitized cell, light-sensitive coloring agent molecule absorption sunlight transits to excitation state, and the dyestuff in excitation state injects electronics so as to realizing separation of charge in the conduction band of conductor oxidate.The light anode porosity of dye-sensitized cell is higher, and absorbing dye is more, and the non equilibrium carrier density producing under illumination increases, and can make resistance decreasing, and cell photoelectric conversion efficiency improves.
But in the preparation method of existing dye-sensitized cell, exist and to use organic solvent cleaning base plate, serious to operating personnel, environmental hazard, cleaning cost is high, the phenomenons such as waste liquid yield is large, can not meet the requirement that industrialization is produced, and its related process also has to be further improved and optimizes.
Summary of the invention
The object of the invention is to overcome above-mentioned deficiency, a kind of cleaning method of the substrate for the preparation of DSSC is provided, to reduce cleaning cost, reduce the harm to operating personnel, environment, solve the difficult problem of the large recovery of waste liquid amount.
At this, the invention provides a kind of alkali lye and clean the method for the preparation of the substrate of DSSC, described method is that substrate is immersed in alkali lye, make alkali lye not have substrate top 8 ± 3mm, 0~50 ℃ of ultrasonic cleaning 0~60 minute, use afterwards deionized water rinsing substrate, and be dried.
The present invention replaces organic solvent to clean substrate with inorganic alkali lye, and alkali lye consumption is less, can reduce cleaning cost, and the harm of minimizing to operating personnel and environment, and the waste liquid after cleaning can not reclaim and directly enter drainage channel, solved the difficult problem of the large recovery of waste liquid amount.
Preferably, described substrate can comprise for carrying the substrate of light anode and/or for carrying the substrate to electrode.Include but not limited to comprise glass substrate and titanium-base.
Preferably, the alkali in described alkali lye can comprise at least one in sodium carbonate, sodium acid carbonate, lithium hydroxide, NaOH, potassium hydroxide and barium hydroxide.By using these cheap, to be difficult for generation murder by poisoning inorganic bases, can reduce cleaning cost, reduce the harm to operating personnel and environment, and be easy to reprocessing.
Preferably, the concentration of described alkali lye can be 0~15%.
Preferably, described being dried can be to dry up with air or nitrogen, can be also to dry in incubator.
The substrate that the method according to this invention is cleaned can be for the preparation of DSSC, the efficiency of prepared DSSC is suitable with the battery efficiency of the substrate mounting cleaning with organic solvent, can produce technical support is provided for the industrialization of DSSC.
Accompanying drawing explanation
Fig. 1 is the I-V curve of the DSSC prepared by the substrate that adopts the method for prior art and the method for example of the present invention to clean respectively.
Embodiment
Below in conjunction with accompanying drawing and following execution mode, further illustrate the present invention, should be understood that accompanying drawing and following execution mode are only for the present invention is described, and unrestricted the present invention.
The invention provides a kind of alkali lye and clean the method for the preparation of the substrate of DSSC: substrate is immersed in alkali lye, make alkali lye not have substrate top 8 ± 3mm, 0~50 ℃ of ultrasonic cleaning 0~60 minute, use afterwards deionized water rinsing substrate, and be dried, obtain clean substrate.
Wherein, substrate to be cleaned can be for the preparation of the substrate of light anode and/or for the preparation of the substrate to electrode.Such as can be electro-conductive glass for the preparation of light anode, for the preparation of to titanium-base of electrode etc.
Again, alkali lye can adopt industrial detergent, also can prepare alkali is soluble in water.The alkali adopting includes but not limited at least one in sodium carbonate, sodium acid carbonate, lithium hydroxide, NaOH, potassium hydroxide and barium hydroxide.The concentration of the alkali lye of preparing can be 0~15%.In present embodiment, use cheap, to be difficult for generation murder by poisoning inorganic base, can reduce cleaning cost, reduce the harm to operating personnel and environment, and be easy to reprocessing.Again, the consumption of alkali lye is less, as long as do not have substrate 8 ± 3mm, therefore can further reduce cleaning cost.
After substrate is rinsed well, can dry up with air or nitrogen, or dry in incubator.
The clean substrate of the method according to this invention can be for the preparation of DSSC.Preparation method for example can comprise the following steps.Should be understood that this preparation method is only for effect of the present invention is described, and unrestricted the present invention.
The preparation of light anode: silk screen printing TiO on clean electro-conductive glass
2colloid makes the light anode of DSSC and dries, and the light anode of oven dry is put into stove sintering.
The TiO adopting
2colloid can comprise TiO
2, solvent and binding agent, wherein, TiO
2content is 0~30%, and solvent is 0~20%, and binder content is 50~90%.
Further preferably, the TiO adopting
2colloid can by by titania nanoparticles and terpinol and cellulosic binder with (1~2): (0.2~0.5): the ratio of (5~9) is mixed, and obtain after magnetic agitation, high shear and ultrasonic dispersion.Cellulosic binder includes but not limited to ethyl cellulose.In one example, preparation TiO
2the titania nanoparticles adopting during colloid is anatase titanium dioxide nano particle, can adopt sol-gel process preparation.In one example, sol-gel process can be: by weight ratio, be (9~99): 1 titanium precursor body and the mixed solution of acetic acid are added drop-wise in deionized water, adding acid-conditioning solution pH value is 1~3,80 ℃~120 ℃ are reacted 6~24 hours, then be placed at 200 ℃~270 ℃ of reactors and be incubated 16~96 hours, collect, after washing, obtain 15~60 nano crystal anatase titanias.Wherein, the titanium precursor body adopting can be butyl titanate and/or tetraisopropyl titanate.Optional from sulfuric acid for the acid of regulator solution pH value, nitric acid, acetic acid, hydrochloric acid, benzoic acid, citric acid, laurate, and at least one in oxalic acid.Should understand and can be of a size of the above-mentioned little nano particle of 15~60nm titanium dioxide that is of a size of of the large nano particle replacement part of 200~500nm titanium dioxide, the mass ratio of the little nano particle of titanium dioxide and the large nano particle of titanium dioxide can be 1:(0~100).In one example, the mass ratio of the little nano particle of titanium dioxide and the large nano particle of titanium dioxide is 1:(0.1~0.4).In another example, the mass ratio of the little nano particle of titanium dioxide and the large nano particle of titanium dioxide can be (0.01~0.1): 1.
Oven dry can be of short duration oven dry on hot plate, for example, 0~300 ℃ of heating 0~20 minute.Sintering can be at 300~800 ℃ of sintering below 100 minutes.
Preparation to electrode: apply electrode material on clean titanium-base.
To electrode material, can be wherein the different materials such as graphite, platinum or conducting polymer.In one example, thus silk screen printing carbon pastes oven dry on clean titanium-base, sintering make electrode.Oven dry can be of short duration oven dry on hot plate, for example, 0~300 ℃ of heating 0~20 minute.Sintering can be at 300~800 ℃ of sintering below 100 minutes.
After sintering, cooling good light anode, puts into dye solution and soaks.Immersion finishes rear taking-up light anode, with 2~100mL absolute ethyl alcohol, washes away dye solution, dry 0.5~10 minute.
The dye solution adopting for example can comprise dyestuff, solvent and coadsorbent.In one example, dyestuff molar percentage: 0.1mmol/L~5mol/L; Solvent volume is than 1:100~100:1; Coadsorbent molar percentage: 0.001mmol/L~3mol/L.The dyestuff that wherein adopted can be N3, N719, black dye, Z907, K8, K19, N945, Z910, K73, K51, Z955, cyanine, cumarin, porphyrin, indoles, perylene flower cyanines and half one or more that spend in cyanines.The solvent adopting can be acetonitrile, the tert-butyl alcohol, dimethyl formamide and/or dimethyl sulfoxide (DMSO).The coadsorbent adopting can be DPA.
The assembling of DSSC
Have the light anode of dye solution to immerse in electrolyte solution 2~20 minutes immersion, after taking out with electrode is encapsulated to form DSSC.Or immersion is had to the light anode of dye solution with together with electrode assembling, between them, inject electrolyte solution, form DSSC.
Wherein, electrolyte solution can be comprised of three parts: organic solvent, redox duplet and additive.Organic solvent can be nitrile or carbonates.Redox duplet can be I
3-/ I
-, SCN
-/ (SCN)
2, SeCN
-/ (SeCN).
The performance characterization of DSSC
The photoelectric properties of DSSC for example can be tested under the standard sources of AM1.5, known after tested, and the photoelectric conversion efficiency of prepared DSSC is more than 7%.
Fig. 1 illustrates the I-V curve of the DSSC of being prepared by the substrate that adopts the method for prior art and the method for example of the present invention to clean respectively, the photoelectric properties of the DSSC that the photoelectric properties of as seen from the figure, using the prepared DSSC of the substrate that cleans by method of the present invention are prepared with using the substrate that cleans by organic solvent are suitable.
Good effect of the present invention is: the DSSC of using the substrate that cleans by the inventive method to prepare, (1) reduces and cleans cost.(2) reduce to operating personnel the harm to environment.(3) solve the difficult problem of the large recovery of waste liquid amount, waste liquid can enter drainage channel.(4) for the industrialization of DSSC, produce technical support is provided.
Further exemplify embodiment below to describe the present invention in detail.Should understand equally; following examples are only used to further illustrate the present invention; can not be interpreted as limiting the scope of the invention, some nonessential improvement that those skilled in the art's foregoing according to the present invention is made and adjustment all belong to protection scope of the present invention.The technological parameter that following example is concrete etc. is only also an example in OK range, and those skilled in the art can be done in suitable scope and be selected by explanation herein, and do not really want to be defined in the below concrete numerical value of example.
Embodiment 1
Take 400 grams of alkali lye, pour in 7600 grams of deionized waters, stir.
Embodiment 2
1 raw material
Dyestuff Z991:3.9g, DMSO1000ml, TiO
2colloid 500g, electrolyte 50ml, electro-conductive glass (FTO), DPA;
2 preparation methods
Glass substrate alkali lye cleans, and titanium-base organic solution is cleaned
The alkali lye preparing is poured in the container that fills glass substrate, alkali lye did not have substrate top 8 ± 3mm, and deionized water rinsing substrate is used in ultrasonic cleaning afterwards, finally with compressed air, dries up.Clean electro-conductive glass is placed in automatic screen printing machine, with the homemade TiO2 jel print in laboratory, makes dye-sensitized solar cell anode, is placed on of short duration oven dry on hot plate.The light anode of oven dry is put into stove sintering.Cooling good light anode, puts into dye solution and soaks.After taking out, with 2-100ml absolute ethyl alcohol, wash away dye solution, dry 0.5-10 minute, injects electrolyte with note electrolytic solution device, takes out encapsulation;
The efficiency of obtained battery is 7.05%, 7.08%, 7.21%.
Embodiment 3
1 raw material
Dyestuff Z991:3.9g, DMSO1000ml, TiO
2colloid 500g, electrolyte 50ml, electro-conductive glass (FTO), DPA;
2 preparation methods
Titanium-base alkali lye cleans, and glass substrate organic solution is cleaned
The alkali lye preparing is poured in the container that fills titanium-base, alkali lye did not have substrate top 8 ± 3mm, and deionized water rinsing substrate is used in ultrasonic cleaning afterwards, finally with compressed air, dries up.Clean titanium-base is placed in automatic screen printing machine, with the homemade carbon pastes printing in laboratory, makes DSSC to electrode, is placed on of short duration oven dry on hot plate.By what dry, electrode is put into stove sintering.Light anode is put into dye solution and is soaked.After taking out, with 2-100ml absolute ethyl alcohol, wash away dye solution, dry 0.5-10 minute, injects electrolyte with note electrolytic solution device, takes out encapsulation;
The efficiency of obtained battery is 7.07%, 7.13%, 7.06%.
Embodiment 4
1 raw material
Dyestuff Z991:3.9g, DMSO1000ml, TiO
2colloid 500g, electrolyte 50ml, electro-conductive glass (FTO), DPA;
2 preparation methods
Glass substrate alkali lye cleans, and titanium-base aqueous slkali cleans the alkali lye preparing is poured in the container that fills glass (titanium) substrate, and alkali lye did not have substrate top 8 ± 3mm, and deionized water rinsing substrate is used in ultrasonic cleaning afterwards, finally with compressed air, dries up.Clean glass substrate is placed in automatic screen printing machine, with the homemade TiO in laboratory
2slurry printing makes dye-sensitized solar cell anode, is placed on of short duration oven dry on hot plate.The light anode of oven dry is put into stove sintering.Cooled smooth anode is put into dye solution and is soaked.After taking out, with 2-100ml absolute ethyl alcohol, wash away dye solution, dry 0.5-10 minute, injects electrolyte with note electrolytic solution device, takes out encapsulation;
The efficiency of obtained battery is 7.05%, 7.05%, 7.08%.
Comparative example 1
1 raw material
Dyestuff Z991:3.9g, DMSO1000ml, TiO
2colloid 500g, electrolyte 50ml, electro-conductive glass (FTO), DPA;
2 preparation methods
Glass substrate organic solution is cleaned, and titanium-base organic solution is cleaned
Acetone is poured in the container that fills glass (titanium) substrate, alkali lye did not have substrate top 8 ± 3mm, and ultrasonic cleaning, dries up with compressed air afterwards.Clean glass substrate is placed in automatic screen printing machine, with the homemade TiO in laboratory
2slurry printing makes dye-sensitized solar cell anode, is placed on of short duration oven dry on hot plate.The light anode of oven dry is put into stove sintering.Cooled smooth anode is put into dye solution and is soaked.After taking out, with 2-100ml absolute ethyl alcohol, wash away dye solution, dry 0.5-10 minute, injects electrolyte with note electrolytic solution device, takes out encapsulation;
The efficiency of obtained battery is 7.05%, 7.05%, 7.12%.
In above embodiment 2~4 and comparative example 1, the photoelectric properties result of prepared battery is referring to table 1 and Fig. 1;
The various cleaning way cell photoelectric of table 1 conversion efficiency
From table 1 and Fig. 1, the photoelectric efficiency of the prepared battery of embodiment 2~4 and comparative example 1 prepared battery is suitable.
Industrial applicability: the present invention can reduce base-plate cleaning cost, the harm of minimizing to operating personnel and environment, solve the difficult problem of the large recovery of waste liquid amount, waste liquid can enter drainage channel, can produce technical support is provided for the industrialization of DSSC.
Claims (6)
1. alkali lye cleans the method for the preparation of the substrate of DSSC, it is characterized in that, substrate is immersed in alkali lye, make alkali lye not have substrate top 8 ± 3mm, 0~50 ℃ of ultrasonic cleaning 0~60 minute, use afterwards deionized water rinsing substrate, and be dried.
2. method according to claim 1, is characterized in that, described substrate comprises for carrying the substrate of light anode and/or for carrying the substrate to electrode.
3. method according to claim 2, is characterized in that, described substrate comprises glass substrate and titanium-base.
4. according to the method in any one of claims 1 to 3, it is characterized in that, the alkali in described alkali lye comprises at least one in sodium carbonate, sodium acid carbonate, lithium hydroxide, NaOH, potassium hydroxide and barium hydroxide.
5. according to the method described in any one in claim 1 to 4, it is characterized in that, the concentration of described alkali lye is 0~15%.
6. according to the method described in any one in claim 1 to 5, it is characterized in that, described being dried is to dry up with air or nitrogen, or dries in incubator.
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