KR20130065987A - Hierarchically structured titanium dioxide powder manufacturing method and quantum-dot-sensitized solar cell manufacturing method using the same - Google Patents
Hierarchically structured titanium dioxide powder manufacturing method and quantum-dot-sensitized solar cell manufacturing method using the same Download PDFInfo
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- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 title claims abstract description 423
- 239000004408 titanium dioxide Substances 0.000 title claims abstract description 211
- 239000000843 powder Substances 0.000 title claims abstract description 85
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 53
- 239000002096 quantum dot Substances 0.000 claims abstract description 57
- 238000000034 method Methods 0.000 claims abstract description 46
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 41
- 239000002105 nanoparticle Substances 0.000 claims abstract description 38
- 239000011148 porous material Substances 0.000 claims abstract description 31
- 238000006460 hydrolysis reaction Methods 0.000 claims abstract description 24
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims abstract description 22
- 239000002243 precursor Substances 0.000 claims abstract description 22
- 238000006243 chemical reaction Methods 0.000 claims abstract description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 19
- 238000000149 argon plasma sintering Methods 0.000 claims abstract description 12
- 229910021529 ammonia Inorganic materials 0.000 claims abstract description 11
- 230000031700 light absorption Effects 0.000 claims abstract description 8
- 230000007062 hydrolysis Effects 0.000 claims abstract description 6
- 238000003980 solgel method Methods 0.000 claims abstract description 6
- 239000000758 substrate Substances 0.000 claims description 19
- 238000001179 sorption measurement Methods 0.000 claims description 18
- JMXKSZRRTHPKDL-UHFFFAOYSA-N titanium ethoxide Chemical group [Ti+4].CC[O-].CC[O-].CC[O-].CC[O-] JMXKSZRRTHPKDL-UHFFFAOYSA-N 0.000 claims description 14
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 12
- 230000035484 reaction time Effects 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 10
- FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 claims description 6
- 238000001027 hydrothermal synthesis Methods 0.000 claims description 6
- 239000011780 sodium chloride Substances 0.000 claims description 6
- 238000007865 diluting Methods 0.000 claims description 5
- YBNMDCCMCLUHBL-UHFFFAOYSA-N (2,5-dioxopyrrolidin-1-yl) 4-pyren-1-ylbutanoate Chemical compound C=1C=C(C2=C34)C=CC3=CC=CC4=CC=C2C=1CCCC(=O)ON1C(=O)CCC1=O YBNMDCCMCLUHBL-UHFFFAOYSA-N 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- UHYPYGJEEGLRJD-UHFFFAOYSA-N cadmium(2+);selenium(2-) Chemical compound [Se-2].[Cd+2] UHYPYGJEEGLRJD-UHFFFAOYSA-N 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
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- 229910010413 TiO 2 Inorganic materials 0.000 description 9
- 239000002245 particle Substances 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 description 5
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 5
- 150000002500 ions Chemical class 0.000 description 5
- 229910044991 metal oxide Inorganic materials 0.000 description 3
- 150000004706 metal oxides Chemical class 0.000 description 3
- 239000011858 nanopowder Substances 0.000 description 3
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- 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
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- 238000007792 addition Methods 0.000 description 1
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- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 1
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- 150000001450 anions Chemical class 0.000 description 1
- XIEPJMXMMWZAAV-UHFFFAOYSA-N cadmium nitrate Inorganic materials [Cd+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XIEPJMXMMWZAAV-UHFFFAOYSA-N 0.000 description 1
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- NMHMNPHRMNGLLB-UHFFFAOYSA-N phloretic acid Chemical compound OC(=O)CCC1=CC=C(O)C=C1 NMHMNPHRMNGLLB-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
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- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G23/00—Compounds of titanium
- C01G23/04—Oxides; Hydroxides
- C01G23/047—Titanium dioxide
- C01G23/053—Producing by wet processes, e.g. hydrolysing titanium salts
-
- 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
- H01L31/0248—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 characterised by their semiconductor bodies
- H01L31/0256—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 characterised by their semiconductor bodies characterised by the material
- H01L31/0264—Inorganic materials
- H01L31/0296—Inorganic materials including, apart from doping material or other impurities, only AIIBVI compounds, e.g. CdS, ZnS, HgCdTe
-
- 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
- H01L31/0248—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 characterised by their semiconductor bodies
- H01L31/0352—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 characterised by their semiconductor bodies characterised by their shape or by the shapes, relative sizes or disposition of the semiconductor regions
- H01L31/035209—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 characterised by their semiconductor bodies characterised by their shape or by the shapes, relative sizes or disposition of the semiconductor regions comprising a quantum structures
- H01L31/035218—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 characterised by their semiconductor bodies characterised by their shape or by the shapes, relative sizes or disposition of the semiconductor regions comprising a quantum structures the quantum structure being quantum dots
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/16—Pore diameter
-
- 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
Abstract
The present invention relates to a method for producing a layered titanium dioxide powder or the like used in a photoelectrode of a quantum dot sensitive solar cell.
The method for preparing a layered titanium dioxide powder according to the present invention comprises mixing the first solution with a first solution containing a titanium dioxide precursor and a second solution for supplying water molecules required for hydrolysis of the titanium dioxide precursor. Titanium dioxide nanoparticles are produced from the titanium dioxide precursor through a hydrolysis reaction between the second solutions, and the titanium dioxide nanoparticles are aggregated into aggregated titanium dioxide aggregates using a sol-gel method to form amorphous titanium dioxide powder. The amorphous titanium dioxide powder forming step of forming and the amorphous titanium dioxide powder are immersed in a solution containing water, ethanol and ammonia for a predetermined temperature and time to hydrothermally react between the titanium dioxide nanoparticles constituting the titanium dioxide aggregate. The meso pore forming step of forming meso pores .
According to the present invention, the size of the titanium dioxide aggregate formed by the aggregation of the titanium dioxide nanoparticles can be easily adjusted, and both functions of light scattering and light absorption can be performed at the same time. In addition, there is an effect that a quantum dot-sensitized solar cell having improved photoelectric conversion efficiency is provided by applying a layered titanium dioxide powder to the photoelectrode.
Description
The present invention is a technology for a solar cell that converts solar energy into electrical energy, and more particularly, utilizing TiO 2 nanoparticles of a size-controlled layer structure as a photoelectrode of a quantum dot-sensitive solar cell to improve efficiency. The present invention relates to a quantum dot sensitized solar cell, a manufacturing method thereof, and the like.
Solar cells are devices that convert solar energy into electrical energy. Since the quantum dot-sensitized solar cell was devised in 1991 by Michel Gratzel of the Swiss National Institute of Advanced Technology (EPFL), research has been actively conducted in this area. Such quantum dot-sensitized solar cells can be manufactured at a lower cost than PN-type semiconductor solar cells, but are attracting attention as one of the next generation solar cells due to their high photoelectric energy conversion efficiency.
A quantum dot-sensitized solar cell absorbs light to form quantum dot molecules, which form electron-hole pairs, photoelectrodes of metal oxide semiconductors that serve as electron transport paths, and reduce oxidized quantum dots. that to the electronic exchange to be the electrolyte is a photoelectric chemical cell consisting of (I - - / I 3 of the liquid system).
In quantum dot-sensitized solar cells, the main material of the photoelectrode is TiO 2 nanoparticles on anatase. TiO 2 nanoparticle photoelectrodes with a size of 10-30 nm can adsorb a sufficient amount of quantum dot molecules due to their large specific surface area (> 50 m 2 / g), and light absorption occurs in proportion to the adsorbed quantum dots. Will be able to produce.
However, increasing the thickness of the light absorbing layer TiO 2 nanoparticle photoelectrode to increase the quantum dot adsorption increases the resistance, the efficiency is reduced above the limit thickness. In order to solve this problem, a light scattering layer composed of micro or hundreds of nm metal oxide particles may be additionally introduced onto the light absorbing layer to reflect light transmitted through the light absorbing layer to increase efficiency. However, the metal oxide particles used as the light scattering layer have a disadvantage in that they do not efficiently adsorb quantum dots due to a very low specific surface area.
An object of the present invention is to provide a layered titanium dioxide powder and a method of manufacturing the same which can perform both functions of light scattering and light absorption at the same time.
In addition, the present invention provides a method for producing a layered titanium dioxide powder that can easily control the size of the titanium dioxide aggregate formed by the agglomeration of titanium dioxide nanoparticles and the layered titanium dioxide powder produced by the method It is a task.
The present invention also provides a quantum dot-sensitized solar cell having improved photoelectric conversion efficiency.
In addition, the present invention aggregates titanium dioxide nanoparticles to form titanium dioxide aggregates, and broadly forms mesopores between the titanium dioxide nanoparticles constituting the titanium dioxide aggregate, thereby forming ions for forming quantum dots through the mesopores. It is a technical problem to increase the photoelectric conversion efficiency of a solar cell by allowing them to be easily diffused and greatly increasing the surface area for quantum dot adsorption.
In addition, the present invention is to make it possible to simultaneously implement the photocurrent production according to the quantum dot adsorption and the light scattering effect according to the reflection characteristics by the pores, to significantly improve the photoelectric conversion efficiency of the quantum dot-sensitized solar cell as a technical problem.
In order to solve this problem, the method for preparing a layered titanium dioxide powder according to the present invention is a state in which a first solution containing a titanium dioxide precursor is mixed with a second solution for supplying water molecules required for hydrolysis of the titanium dioxide precursor. Titanium dioxide nanoparticles are generated from the titanium dioxide precursor through a hydrolysis reaction between the first solution and the second solution at, and the titanium dioxide nanoparticles are aggregated into titanium dioxide aggregates having a spherical shape using a sol-gel method. Forming an amorphous titanium dioxide powder by immersing the amorphous titanium dioxide powder in a solution containing water, ethanol, and ammonia for a predetermined temperature and time and hydrothermally reacting to form the titanium dioxide aggregate. Form mesopores between titanium nanoparticles Comprising the mesopores forming step is configured.
In the method for preparing a layered titanium dioxide powder according to the present invention, the titanium dioxide precursor is titanium tetraethoxide, and the first solution is the titanium tetraethoxide and hexadecylamine in ethanol. The dilute solution is characterized in that the second solution is a solution of dilute sodium chloride solution in ethanol.
In the method for producing a hierarchical structure of titanium dioxide powder according to the present invention, controlling the size of the titanium dioxide aggregate constituting the amorphous titanium dioxide powder by controlling the amount of water molecules supplied by adjusting the concentration of the second solution. It features.
In the method for producing a hierarchical structure of titanium dioxide powder according to the present invention, the size of the titanium dioxide aggregate is greatly controlled by lowering the concentration of the second solution to increase the hydrolysis reaction time.
In the method for producing a hierarchical structure of titanium dioxide powder according to the present invention, the size of the titanium dioxide aggregate is reduced by increasing the concentration of the second solution to reduce the hydrolysis reaction time.
In the method for producing a hierarchical structure of titanium dioxide powder according to the present invention, in the meso pore forming step, the size of the meso pores is controlled by controlling the amount of the ammonia.
The hierarchical titanium dioxide powder according to the present invention is characterized in that it is prepared by the method for producing a hierarchical titanium dioxide powder according to the present invention.
In the method of manufacturing a quantum dot-sensitized solar cell according to the present invention, a porous titanium dioxide electrode layer forming step of forming a porous titanium dioxide electrode layer made of a layered titanium dioxide powder on a transparent conductive substrate, and heat-treating the transparent conductive substrate on which the porous titanium dioxide electrode layer is formed And a quantum dot adsorption step of adsorbing a material for forming a quantum dot on the porous titanium dioxide electrode layer, wherein the hierarchical titanium dioxide powder comprises a first solution containing a titanium dioxide precursor and the titanium dioxide precursor. Titanium dioxide nanoparticles are generated from the titanium dioxide precursor through a hydrolysis reaction between the first solution and the second solution in a state in which a second solution for supplying water molecules required for hydrolysis is mixed, and the titanium dioxide nanoparticles Using the sol-gel method Aqueous titanium dioxide powder forming step of agglomeration with aggregated titanium dioxide aggregates to form amorphous titanium dioxide powder and hydrothermal reaction by immersing the amorphous titanium dioxide powder in a solution containing water, ethanol and ammonia for a predetermined temperature and time It is characterized in that it was prepared through the meso pore forming step of forming meso pores between the titanium dioxide nanoparticles constituting the titanium dioxide aggregate.
In the method of manufacturing a quantum dot-sensitized solar cell according to the present invention, the titanium dioxide precursor is titanium tetraethoxide, and the first solution is the titanium tetraethoxide and hexadecylamine in ethanol. The dilute solution is characterized in that the second solution is a solution of dilute sodium chloride solution in ethanol.
In the method of manufacturing a quantum dot-sensitized solar cell according to the present invention, controlling the size of the titanium dioxide aggregate constituting the amorphous titanium dioxide powder by controlling the amount of water molecules supplied by adjusting the concentration of the second solution. It features.
In the method of manufacturing a quantum dot-sensitized solar cell according to the present invention, the size of the titanium dioxide aggregate is largely controlled by lowering the concentration of the second solution to increase the hydrolysis reaction time.
In the method of manufacturing a quantum dot-sensitized solar cell according to the present invention, the size of the titanium dioxide aggregate is controlled to be small by increasing the concentration of the second solution to reduce the hydrolysis reaction time.
In the method of manufacturing a quantum dot-sensitized solar cell according to the present invention, in the meso pore forming step, the size of the meso pores is controlled by adjusting the amount of the ammonia.
In the method of manufacturing a quantum dot-sensitive solar cell according to the present invention, the porous titanium dioxide electrode layer has a thickness of 10 μm or more and 20 μm or less.
In the method of manufacturing a quantum dot-sensitized solar cell according to the present invention, the porous titanium dioxide electrode layer is characterized in that it performs the function of light absorption and light scattering.
In the method of manufacturing a quantum dot-sensitized solar cell according to the present invention, the material for forming the quantum dot is adsorbed on the porous titanium dioxide electrode layer by using a continuous iononic layer adsorption and reaction (SILAR) in the quantum dot adsorption step. It is characterized by.
In the method of manufacturing a quantum dot-sensitive solar cell according to the present invention, the material for forming a quantum dot is characterized in that it comprises one or more selected from the group consisting of CdS, CdSe, PbS, Ag 2 S and PbSe.
The quantum dot sensitized solar cell according to the present invention is characterized in that it is manufactured by the method for manufacturing a quantum dot sensitized solar cell according to the present invention.
According to the present invention, there is provided an effect of providing a layered titanium dioxide powder and a method of manufacturing the same, which can simultaneously perform two functions of light scattering and light absorption.
In addition, there is provided an effect of providing a layered titanium dioxide powder and a method of manufacturing the same that can easily control the size of the titanium dioxide aggregate formed by the aggregation of titanium dioxide nanoparticles.
In addition, there is an effect that a quantum dot sensitive solar cell with improved photoelectric conversion efficiency is provided.
In addition, by agglomerating the titanium dioxide nanoparticles to form titanium dioxide aggregates, and by forming a wide meso pores between the titanium dioxide nanoparticles constituting the titanium dioxide aggregate, ions for forming quantum dots through the meso pores easily Since it can be diffused and the surface area for quantum dot adsorption is greatly increased, the photoelectric conversion efficiency of the solar cell is improved.
In addition, it is possible to simultaneously implement the light scattering effect according to the photocurrent production and the reflection characteristics by the pores by the quantum dot adsorption, there is an effect that the photoelectric conversion efficiency of the quantum dot-sensitized solar cell is greatly improved.
1 is a view showing a method for manufacturing a layered titanium dioxide powder according to an embodiment of the present invention.
2 is a photograph of a hierarchical titanium dioxide powder prepared according to an embodiment of the present invention, a quantum dot deposited titanium dioxide powder, a conventional commercial titanium dioxide powder, a commercial titanium dioxide powder deposited quantum dots.
3 is a view conceptually showing the titanium dioxide aggregate constituting the hierarchical titanium dioxide powder prepared by the hierarchical structure of titanium dioxide powder according to an embodiment of the present invention.
4 is a process flowchart illustrating a method of manufacturing a quantum dot-sensitized solar cell according to an embodiment of the present invention.
5 to 19 are process cross-sectional views illustrating a method of manufacturing a quantum dot-sensitized solar cell according to an embodiment of the present invention.
10 is a graph showing a photocurrent-photovoltage characteristic curve of a quantum dot-sensitized solar cell manufactured according to an embodiment of the present invention compared with the conventional case.
Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings.
1 is a view showing a method for manufacturing a layered titanium dioxide powder according to an embodiment of the present invention.
Referring to FIG. 1, the method for preparing a hierarchical titanium dioxide powder according to an embodiment of the present invention includes an amorphous titanium dioxide powder forming step S10 and a meso pore forming step S20.
<Amorphous titanium dioxide powder forming step (S10)>
In the amorphous titanium dioxide powder forming step (S10), a process of generating an amorphous titanium dioxide powder from a titanium dioxide precursor is performed. The resulting amorphous titanium dioxide powder is composed of titanium dioxide aggregates in which titanium dioxide nanoparticles are aggregated.
Hereinafter, the titanium dioxide precursor is titanium tetraethoxide, the first solution is a solution obtained by diluting titanium tetraethoxide and hexadecylamine in ethanol, and the second solution is an aqueous sodium chloride solution. For example, in the case of a solution diluted in ethanol, the amorphous titanium dioxide powder forming step will be described in more detail as follows.
First, in step S12, a first solution of 3.42 g of titanium tetraethoxide and 1.33 g of hexadecylamine diluted in 100 ml of ethanol is supplied with water molecules for hydrolysis of the titanium tetraethoxide. In order to mix a second solution, that is, a sodium chloride solution (sodium chlroride) in dilute ethanol at a concentration of 0.2 M, a second solution is mixed. As will be described later, the size of the titanium dioxide aggregate produced is adjusted according to the concentration of the second solution.
Next, in step S14, a process of generating titanium dioxide nanoparticles from titanium tetraethoxide, which is a titanium dioxide precursor, is performed through a hydrolysis reaction between the first solution and the second solution.
Next, in step S16, the titanium dioxide nanoparticles produced from the titanium tetraethoxide by the hydrolysis reaction are aggregated into aggregates of titanium dioxide having a spherical shape using the sol-gel method to form amorphous titanium dioxide powder. The process of generating is performed.
On the other hand, the size of the titanium dioxide aggregate constituting the amorphous titanium dioxide powder can be adjusted by adjusting the amount of water molecules supplied to the hydrolysis reaction supplied by adjusting the concentration of the second solution in step S12.
As an example, when the concentration of the second solution is lowered, the amount of water molecules to be supplied increases, and accordingly, the hydrolysis reaction time is lengthened, thereby increasing the number of aggregated titanium dioxide nanopowders and greatly controlling the size of the titanium dioxide aggregate. do.
As another example, when the concentration of the second solution is increased, the amount of water molecules to be supplied is reduced, and accordingly, the hydrolysis reaction time is shortened, so that the number of aggregated titanium dioxide nanopowders is reduced and the size of the titanium dioxide aggregate is controlled to be small. .
<Mesopore forming step (S20)>
In the meso pore forming step (S20), a process of forming meso pores (mesopores) between the titanium dioxide nanoparticles constituting the titanium dioxide aggregate by hydrothermally reacting the amorphous titanium dioxide powder composed of the titanium dioxide aggregate is performed.
If this is described with a specific example as follows.
As described above, titanium dioxide aggregates having a spherical shape controlled by sol-gel are subjected to hydrothermal reaction in an environment in which 4 ml of ammonia is added to a solution of water and ethanol 1: 2. At this time, the temperature of the hydrothermal reaction can be set to 160 ℃, the reaction time to 16 hours.
Through this hydrothermal reaction, fine mesopores are formed between the titanium dioxide nanoparticles constituting the titanium dioxide aggregate, and after the end of the hydrothermal reaction, the titanium dioxide aggregates constituting the amorphous titanium dioxide powder have a network of mesopores therein. It will have a hierarchical structure with
On the other hand, in the meso pore forming step, the size of the meso pores can be adjusted by adjusting the amount of ammonia added.
Residual impurities may be removed from the prepared layered titanium dioxide powder by performing a washing process using anhydrous ethanol.
Figure 2 (a) is a photograph of a hierarchical titanium dioxide powder prepared according to an embodiment of the present invention, Figure 2 (c) is a photograph of a conventional commercial titanium dioxide powder, Figure 3 1 is a view conceptually showing one titanium dioxide aggregate constituting the layered titanium dioxide powder prepared according to an embodiment of the present invention.
In FIG. 3, T1 is a case where the size of the titanium dioxide aggregate is 1554 nm, T2 is 757 nm, and T3 is 587 nm.
As can be seen through (a) and 3 of FIG. 2, the aggregated titanium dioxide constituting the prepared layered titanium dioxide nano powder has a size of about 587-1554nm, the inside of the titanium dioxide of about 10nm size It has a structure in which nanoparticles are aggregated and aggregated. In contrast, referring to FIG. 2C, it can be seen that the porosity is very low in the conventional commercial titanium dioxide powder.
The layered titanium dioxide powder composed of titanium dioxide aggregates having meso pores formed therein may be used as a means for improving the photoelectric conversion efficiency of a quantum dot-sensitized solar cell described below.
4 is a process flowchart illustrating a method of manufacturing a quantum dot sensitive solar cell according to an embodiment of the present invention, and FIGS. 5 to 9 are process cross-sectional views thereof.
4 to 9, the quantum dot-sensitive solar cell manufacturing method according to an embodiment of the present invention is a porous titanium dioxide electrode layer forming step (S100), firing step (S200), quantum dot adsorption step (S300) and bonding / It is configured to include an electrolyte filling step (S400).
First, referring to FIGS. 4 and 5, in step S100, a process of forming the porous titanium
For example, the porous titanium
The porous titanium
Next, referring to FIG. 4 and FIG. 6, in step S200, a process of heat treating and baking the lower transparent
For example, after forming the porous titanium
Next, referring to FIGS. 4 and 7, in step S300, a process of adsorbing the quantum dots absorbing light in the visible light region to the porous titanium
For example, in the quantum dot adsorption step, the quantum dot forming material may be adsorbed onto the porous titanium
In this embodiment, cadmium sulfide (CdS), which is commonly used, was used. CdS quantum dot deposition was performed using a successive Ionic Layer Adsorption and Reaction (SILAR). The continuous ion layer adsorption reaction is a method of forming quantum dots on the surface of an oxide layer by alternately dipping a substrate in a cation and an anion solution. We by diluting the cadmium nitrate of 0.1 M in ethanol was prepared by Cd 2 + S 2 solution by diluting a 0.1 M of sodium sulfide in methanol to prepare a solution. Wash with ethanol and methanol to remove the remaining ions in the middle. This process was carried out a total of 12 times.
Figure 2 (b) is a photograph of a layered titanium dioxide powder deposited quantum dots according to the present embodiment, Figure 2 (d) is a photograph of a commercial titanium dioxide powder deposited quantum dots. As can be seen through this, according to the present embodiment, the quantum dots are smoothly diffused through the mesopores to be uniformly deposited on the surface of the layered titanium dioxide powder.
Next, referring to FIGS. 4, 8, and 9, a bonding and electrolyte filling process is performed.
That is, in step S400, a process of bonding the lower transparent
A porous titanium
Specific examples of such a bonding and electrolyte filling method will be described.
First, the microcavity of about 0.75 mm is formed on the
The
The electrolyte is filled in the space between the two electrodes through the micropores formed in the counter cathode electrode (40). At this time, after the electrolyte is filled to dissolve the thermosetting surlyn to block the fine pores. Through this process, the electrolyte can be prevented from being volatilized and lost.
Hereinafter, the results of comparative experiments with the characteristics of the quantum dot-sensitized solar cell manufactured according to an embodiment of the present invention will be described.
The photocurrent-photovoltage curve and the photoelectric conversion efficiency of the quantum dot-sensitized solar cell according to this embodiment were measured using a solar simulator (Oriel 300 W Xe lamp and Keithley 2400) of 1 Sun (100 mW / cm 2 ) AM1.5. The results are summarized in FIG. 10 and Table 1 below. Here, the efficiency characteristics regarding the battery T20 using a commercially available nanoparticle photoelectrode alone and the battery MS including the hierarchical TiO 2 particles according to the present embodiment are compared.
While the battery T20 having a photoelectrode structure generally exhibits an efficiency of 1.2%, a high efficiency of 1.9% can be obtained in a battery composed of hierarchical TiO 2 particles according to the present embodiment. In conclusion, the hierarchical TiO 2 particles according to the present embodiment are optical electrode materials in which light scattering characteristics due to higher reflectances and photocurrent production effects due to higher specific surface area of nanoparticles are simultaneously realized than commercial nanoparticles. Therefore, the quantum dot-sensitized solar cell manufactured using the hierarchical TiO 2 particles according to the present embodiment as the photoelectrode can achieve the improvement of the photoelectric conversion efficiency.
As described in detail above, according to the present invention, there is an effect of providing a layered titanium dioxide powder and a method of manufacturing the same, which can simultaneously perform two functions of light scattering and light absorption.
In addition, there is provided an effect of providing a layered titanium dioxide powder and a method of manufacturing the same that can easily control the size of the titanium dioxide aggregate formed by the aggregation of titanium dioxide nanoparticles.
In addition, there is an effect that a quantum dot sensitive solar cell with improved photoelectric conversion efficiency is provided.
In addition, by agglomerating the titanium dioxide nanoparticles to form titanium dioxide aggregates, and by forming a wide meso pores between the titanium dioxide nanoparticles constituting the titanium dioxide aggregate, ions for forming quantum dots through the meso pores easily Since it can be diffused and the surface area for quantum dot adsorption is greatly increased, the photoelectric conversion efficiency of the solar cell is improved.
In addition, it is possible to simultaneously implement the light scattering effect according to the photocurrent production and the reflection characteristics by the pores by the quantum dot adsorption, there is an effect that the photoelectric conversion efficiency of the quantum dot-sensitized solar cell is greatly improved.
Although the preferred embodiments of the present invention have been disclosed for illustrative purposes, those skilled in the art will appreciate that various modifications, additions and substitutions are possible, without departing from the scope and spirit of the invention as disclosed in the accompanying claims. In addition, it is obvious that any person skilled in the art may make various modifications and imitations without departing from the scope of the technical idea of the present invention.
10: lower transparent conductive substrate
20: porous titanium dioxide electrode layer
30: upper transparent conductive substrate
40: relative reduction electrode
50: electrolyte layer
S10: forming porous titanium dioxide powder
S20: meso pore forming step
Claims (20)
The dioxide is obtained through a hydrolysis reaction between the first solution and the second solution in a state in which a first solution containing a titanium dioxide precursor is mixed with a second solution for supplying water molecules required for hydrolysis of the titanium dioxide precursor. An amorphous titanium dioxide powder forming step of producing titanium dioxide nanoparticles from a titanium precursor and agglomerating the titanium dioxide nanoparticles into aggregates of titanium dioxide having a spherical shape using a sol-gel method to form amorphous titanium dioxide powder; And
Meso pore forming step of forming meso pores between the titanium dioxide nanoparticles constituting the titanium dioxide aggregate by immersing the amorphous titanium dioxide powder in a solution containing water and ammonia for a predetermined temperature and time for hydrothermal reaction; The method of manufacturing a layered titanium dioxide powder.
The titanium dioxide precursor is titanium tetraethoxide,
The first solution is a solution obtained by diluting the titanium tetraethoxide and hexadecylamine in ethanol,
The second solution is a method of producing a layered titanium dioxide powder, characterized in that the solution of dilute sodium chloride solution in ethanol.
And controlling the size of the titanium dioxide aggregate constituting the amorphous titanium dioxide powder by controlling the amount of water molecules supplied by adjusting the concentration of the second solution.
The method of claim 1, wherein the size of the titanium dioxide aggregate is largely controlled by lowering the concentration of the second solution to increase the hydrolysis reaction time.
The method of manufacturing a layered titanium dioxide powder, characterized in that to reduce the size of the titanium dioxide aggregate by increasing the concentration of the second solution to reduce the hydrolysis reaction time.
The method of claim 1, wherein the solution in which the amorphous titanium dioxide powder is immersed in the meso pore forming step further comprises ethanol.
In the meso pore forming step
Method for producing a layered titanium dioxide powder, characterized in that for controlling the size of the mesopores by adjusting the amount of the ammonia.
A porous titanium dioxide electrode layer forming step of forming a porous titanium dioxide electrode layer made of a layered titanium dioxide powder on a transparent conductive substrate;
A firing step of heating and baking the transparent conductive substrate on which the porous titanium dioxide electrode layer is formed;
And a quantum dot adsorption step of adsorbing a material for forming a quantum dot on the porous titanium dioxide electrode layer,
The hierarchical titanium dioxide powder is
The dioxide is obtained through a hydrolysis reaction between the first solution and the second solution in a state in which a first solution containing a titanium dioxide precursor is mixed with a second solution for supplying water molecules required for hydrolysis of the titanium dioxide precursor. An amorphous titanium dioxide powder forming step of forming titanium dioxide nanoparticles from a titanium precursor and agglomerating the titanium dioxide nanoparticles into aggregates of titanium dioxide having a spherical shape using a sol-gel method to form amorphous titanium dioxide powder, and the amorphous titanium dioxide powder It is prepared through a meso pore forming step of forming a meso pore between the titanium dioxide nanoparticles constituting the titanium dioxide aggregate by immersing the powder in a solution containing water and ammonia for a predetermined temperature and time. Quantum dot-sensitized solar cell manufacturing method .
The titanium dioxide precursor is titanium tetraethoxide,
The first solution is a solution obtained by diluting the titanium tetraethoxide and hexadecylamine in ethanol,
The second solution is a quantum dot-sensitized solar cell manufacturing method, characterized in that the solution of diluted sodium chloride in ethanol.
And controlling the size of the titanium dioxide aggregate constituting the amorphous titanium dioxide powder by adjusting the amount of water molecules supplied by adjusting the concentration of the second solution.
The method of manufacturing a quantum dot-sensitized solar cell, characterized in that the size of the titanium dioxide aggregate is greatly controlled by lowering the concentration of the second solution to increase the hydrolysis reaction time.
The method of manufacturing a quantum dot-sensitized solar cell, characterized in that to reduce the size of the titanium dioxide aggregate by increasing the concentration of the second solution to reduce the hydrolysis reaction time.
The method of claim 1, wherein the solution in which the amorphous titanium dioxide powder is immersed in the meso pore forming step further comprises ethanol.
In the meso pore forming step
And controlling the size of the mesopores by adjusting the amount of the ammonia.
The thickness of the porous titanium dioxide electrode layer is characterized in that the quantum dot sensitized solar cell, characterized in that 10㎛ 20㎛ or less.
The porous titanium dioxide electrode layer is characterized in that to perform the function of light absorption and light scattering, quantum dot sensitive solar cell manufacturing method.
The quantum dot sensitized solar cell manufacturing method, characterized in that in the quantum dot adsorption step (Successive Ionic Layer Adsorption and Reaction, SILAR) to adsorb the material for forming the quantum dot to the porous titanium dioxide electrode layer.
The quantum dot forming material is characterized in that it comprises at least one selected from the group consisting of CdS, CdSe, PbS, Ag 2 S and PbSe, quantum dot sensitized solar cell manufacturing method.
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CN106830069A (en) * | 2017-02-15 | 2017-06-13 | 齐鲁工业大学 | A kind of flower-shaped mesoporous TiO 2 hierarchy and preparation method thereof |
WO2019112121A1 (en) * | 2017-12-05 | 2019-06-13 | 한국에너지기술연구원 | Method for producing photoresponsive automatic color change precursor and photoresponsive automatic color change element, and photoresponsive automatic color change element produced thereby |
KR20200010915A (en) * | 2018-07-23 | 2020-01-31 | 재단법인대구경북과학기술원 | Quantumdot solar cell including adsorbant |
US10984959B1 (en) * | 2020-04-13 | 2021-04-20 | United Arab Emirates University | Quantum dot-sensitized solar cell and method of making the same |
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KR100836710B1 (en) | 2007-07-12 | 2008-06-10 | 한국에너지기술연구원 | Method for preparing nano particle powder of titanium dioxide for dye-sensitized solar cell by sol-gel combustion hybrid method |
KR20090080205A (en) * | 2008-01-21 | 2009-07-24 | 조선대학교산학협력단 | Syntesis of titanium dioxide by aging and peptization methods for photo-electrode of dye-sensitized solar cells |
KR100937799B1 (en) * | 2008-04-01 | 2010-01-20 | 재단법인서울대학교산학협력재단 | Double layer titanium dioxide electrode for dye-sensitized solar cell, Method of preparing the same and Dye-sensitized solar cell prepared by using the same |
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Publication number | Priority date | Publication date | Assignee | Title |
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CN106830069A (en) * | 2017-02-15 | 2017-06-13 | 齐鲁工业大学 | A kind of flower-shaped mesoporous TiO 2 hierarchy and preparation method thereof |
WO2019112121A1 (en) * | 2017-12-05 | 2019-06-13 | 한국에너지기술연구원 | Method for producing photoresponsive automatic color change precursor and photoresponsive automatic color change element, and photoresponsive automatic color change element produced thereby |
KR20200010915A (en) * | 2018-07-23 | 2020-01-31 | 재단법인대구경북과학기술원 | Quantumdot solar cell including adsorbant |
US10984959B1 (en) * | 2020-04-13 | 2021-04-20 | United Arab Emirates University | Quantum dot-sensitized solar cell and method of making the same |
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