US20090320914A1 - Dye-sensitized solar cell and method of fabricating the same - Google Patents
Dye-sensitized solar cell and method of fabricating the same Download PDFInfo
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- US20090320914A1 US20090320914A1 US12/118,557 US11855708A US2009320914A1 US 20090320914 A1 US20090320914 A1 US 20090320914A1 US 11855708 A US11855708 A US 11855708A US 2009320914 A1 US2009320914 A1 US 2009320914A1
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- 239000004065 semiconductor Substances 0.000 claims abstract description 56
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- 238000000034 method Methods 0.000 claims description 20
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- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 17
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 13
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- 229910052731 fluorine Inorganic materials 0.000 claims description 6
- 239000011737 fluorine Substances 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 6
- 239000011787 zinc oxide Substances 0.000 claims description 6
- 229910052787 antimony Inorganic materials 0.000 claims description 5
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- 229920001940 conductive polymer Polymers 0.000 claims description 5
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Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/20—Light-sensitive devices
- H01G9/2027—Light-sensitive devices comprising an oxide semiconductor electrode
- H01G9/2031—Light-sensitive devices comprising an oxide semiconductor electrode comprising titanium oxide, e.g. TiO2
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F10/00—Individual photovoltaic cells, e.g. solar cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/20—Light-sensitive devices
- H01G9/209—Light trapping arrangements
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F71/00—Manufacture or treatment of devices covered by this subclass
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F77/00—Constructional details of devices covered by this subclass
- H10F77/20—Electrodes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/20—Light-sensitive devices
- H01G9/2059—Light-sensitive devices comprising an organic dye as the active light absorbing material, e.g. adsorbed on an electrode or dissolved in solution
-
- 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
-
- 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
Definitions
- the present invention disclosed herein relates to a dye-sensitized solar cell and a method of fabricating the same, and more particularly, to a dye-sensitized solar cell including an electrode structure having a conductor with pores regularly formed, which is fabricated by the use of a template, and a method of fabricating the dye-sensitized solar cell.
- the present invention has been derived from research undertaken as a part of IT R & D program of the Ministry of Information and Communication and Institution of Information Technology Association (MIC/IITA) [2006-S-006-02], Components/Module technology for ubiquitous terminals.
- MIC/IITA Information Technology Association
- a dye-sensitized solar cell includes a dye molecule capable of receiving incident light with a visible wavelength to form electron-hole pairs, a semiconductor oxide capable of receiving excited electrons, and an electrolyte reacting with the electrons after working and returning to the solar cell, which significantly differs from a compound solar cell or a wafer type silicon solar cell using p-n junction.
- a dye-sensitized solar cell which has been well known hitherto, was published by Michael Gratzel et al. (refer to U.S. Pat. No. 4,927,721).
- a photoelectrochemical solar cell published by Michael Gratzel et al. includes a photosensitive dye molecule capable of absorbing a visible light to generate electron-hole pairs, an electrode structure which is a semiconductor oxide formed of nanoparticle titanium oxide (TiO 2 ) with dye molecules adsorbed, an opposite electrode coated with platinum (Pt) or carbon (C), and an electrolyte filled between the semiconductor oxide and the opposite electrode. Because such the photoelectrochemical solar cell can be fabricated with low fabrication cost per electrical power in comparison with the wafer type silicon solar cell that utilizes a p-n junction, so the photoelectrochemical solar cell is being in the limelight recently.
- FIG. 1 is a partial sectional view illustrating a flow of electrons created by sunlight in a conventional dye-sensitized solar cell.
- dye molecules excited by light emitted from the sun eject electrons (e-) into a conduction band of a semiconductor oxide layer 20 formed of nanoparticle titanium oxide.
- the electrons ejected into the conduction band pass through the nanoparticle titanium oxide and arrive at a conductive substrate 10 formed of a glass coated with fluorine doped SnO 2 (FTO).
- FTO fluorine doped SnO 2
- the electrons are transferred to an external circuit (not shown).
- the electrons, which come back after performing an electrical work in the external circuit are injected into the semiconductor oxide layer 20 formed of nanoparticle semiconductor oxide through an opposite electrode (not shown), e.g., platinum or carbon electrode, by means of the electron transfer function of an oxidation/reduction electrolyte 30 .
- the electrons reduce the dye molecule 24 deficient in electrons. In this manner, the conventional dye-sensitized solar cell is operated.
- a moving passage through which the electrons injected from the dye molecules to the semiconductor oxide layer move to the conductive substrate is also made of the nanoparticle titanium oxide. Accordingly, the electron encounters a strong electrical resistance while the electron moves to a 3-dimensional structured semiconductor oxide layer, leading to a decrease in short-circuit current density (Jsc).
- Jsc short-circuit current density
- Example of a conventional method of minimizing the decrease of the photovoltaic energy conversion efficiency occurring in the semiconductor oxide, e.g., the titanium oxide, is as followings.
- the semiconductor oxide formed of the titanium oxide is used as the electrode structure, and coated with a semiconductor oxide material having high band gap energy, for example, niobium oxide (Nb 2 O 5 ) to form an energy barrier between the semiconductor oxide layer and the electrolyte, thus preventing the recombination.
- the photovoltaic energy conversion efficiency was somewhat enhanced.
- the titanium oxide is basically used as a material for the electrode structure, there is a limitation in electron movement. Therefore, an increase in the photovoltaic energy conversion efficiency was limited. Adsorptive properties of the dye molecule on the niobium oxide are poorer than that of the dye molecule on the titanium oxide.
- the electrode structure made of nanowire-, nanorod- and nanotube-shaped semiconductor oxide exhibits poorer photovoltaic energy conversion efficiency compared to the case of using the nanoparticle semiconductor oxide as the electrode structure. Possibly, this is ascribed to the fact that the electrode structure made of the nanowire-, nanorod- and nanotube-shaped semiconductor oxide has a smaller surface area than the nanoparticle semiconductor oxide.
- the present invention provides a dye-sensitized solar cell capable of maximizing photovoltaic energy conversion efficiency.
- the present invention also provides a method of fabricating a dye-sensitized solar cell capable of maximizing photovoltaic energy conversion efficiency.
- Embodiments of the present invention provide dye-sensitized solar cells including: an electrode structure including a conductive layer including pores which are regularly arranged; a semiconductor oxide layer disposed on a surface of the conductive layer; and a dye layer disposed on a surface of the semiconductor oxide layer.
- the conductive layer includes at least one selected from the group consisting of tin oxide, indium doped tin oxide, antimony doped tin oxide, fluorine doped tin oxide, metal, conductive polymer and a nano carbon material.
- the semiconductor oxide layer includes at least one selected from the group consisting of zinc oxide, tin oxide and titanium oxide.
- the dye-sensitized solar cells further include: a bottom electrode structure disposed one side of the electrode structure, and contacting the electrode structure; a top electrode structure disposed on the other side of the electrode structure; and an electrolyte layer interposed between the electrode structure and the top electrode structure, and filling the pores.
- the dye-sensitized solar cells further include a catalyst layer interposed between the electrode structure and the electrolyte layer.
- the catalyst layer includes platinum or carbon.
- the electrolyte has one state of liquid, solid and gel.
- methods of fabricating a dye-sensitized solar cell include: forming an electrode structure including: preparing a template having pores that are regularly arranged; forming a conductive layer on a surface of the template; forming a semiconductor oxide layer on a surface of the conductive layer; and forming a dye layer on a surface of the semiconductor oxide layer.
- the methods further include removing the template.
- the template is formed of at least one material selected from the group consisting of polystyrene, poly methyl methacrylate (PMMA) and block co-polymer.
- PMMA poly methyl methacrylate
- the template is burn out and removed during a thermal treatment of forming the electrode structure.
- the template is formed of alumina. In this case, the template is removed after formation of the electrode structure.
- the conductive layer is formed of at least one selected from the group consisting of tin oxide, indium doped tin oxide, antimony doped tin oxide, fluorine doped tin oxide, metal, conductive polymer and a nano carbon material.
- the forming of the semiconductor oxide layer is performed using at least one method selected from the group consisting of a deep coating method, an electrophoretic method, and an electroplating method.
- the forming of the semiconductor oxide layer includes anodizing or thermally oxidizing a metal or a metal precursor.
- the semiconductor oxide layer includes at least one selected from the group consisting of zinc oxide, tin oxide and titanium oxide.
- a dye-sensitized solar cell includes an electrode structure having pores regularly arranged, thus making it possible to minimize the recombination due to oxidation/reduction reaction occurring at a boundary between the electrode structure and an electrolyte. Furthermore, it is possible to minimize a moving passage of an electron in the electrode structure. Consequently, the dye-sensitized solar cell can maximize its photovoltaic energy conversion efficiency.
- FIG. 1 is a partial sectional view illustrating a flow of electrons created by sunlight in a conventional dye-sensitized solar cell
- FIG. 2 is a plan view illustrating an electrode structure of a dye-sensitized solar cell and a method of fabricating the same according to an embodiment of the present invention
- FIG. 3 is a sectional view illustrating a dye-sensitized solar cell and a method of fabricating the same according to an embodiment of the present invention.
- FIG. 4 is a partial sectional view illustrating a flow of electrons created by sunlight in the dye-sensitized solar cell according to the embodiment of the present invention.
- FIG. 2 is a plan view illustrating an electrode structure of a dye-sensitized solar cell and a method of fabricating the same according to an embodiment of the present invention.
- the electrode structure of the dye-sensitized solar cell may include a conductive layer 120 , a semiconductor oxide layer 122 and a dye layer 124 .
- the conductive layer 120 may have pores that are regularly arranged.
- the conductive layer 120 may be formed by coating a surface of a template (not shown) having pores regularly arranged with a transparent and conductive material.
- the conductive material contained in the conductive layer 120 may include at least one material selected from the group consisting of tin oxide (SnO 2 ), indium doped tin oxide (ITO), antimony doped tin oxide (ATO), fluorine doped tin oxide (FTO), metal, conductive polymer and a nano carbon material.
- the conductive layer 120 may be formed of tin oxide.
- the template used to form the conductive layer 120 having pores regularly arranged may have a shape that allows a surface area of the electrode structure to be maximized, for example, a honeycomb, nanowire, nanorod, or nanotube shape.
- the template may include at least one material selected from the group consisting of polystyrene, poly methyl methacrylate (PMMA), block co-polymer and alumina.
- the semiconductor oxide layer 122 may be formed on a surface of the conductive layer 120 .
- the semiconductor oxide layer 122 may be formed using one method selected from the group consisting of a deep coating method, an electrophoretic method, and an electroplating method.
- the semiconductor oxide layer 122 may be formed by anodizing or thermally oxidizing a metal or a metal precursor.
- the semiconductor oxide layer 122 may include at least one selected from the group consisting of zinc oxide, tin oxide and titanium oxide.
- the semiconductor oxide layer 122 may include titanium oxide.
- the dye layer 124 may be formed on a surface of the semiconductor oxide layer 122 .
- the dye layer 124 may be formed by adsorbing dye molecules on the semiconductor oxide layer 122 . Accordingly, it is possible to form the electrode structure having pores regularly arranged.
- the template may be burn out and removed during a thermal treatment process of forming the electrode structure.
- the template may be removed after the formation of the electrode structure. This is because the inorganic-based template is not sintered during the thermal process of forming the electrode structure.
- the conductive layer 120 has regularly arranged pores and thus high porosity, which may make it easy to thickly coat the surface of the conductive layer 120 with the semiconductor oxide layer 122 . Because the conductive layer 120 is spaced apart from the semiconductor oxide layer 122 by merely several nanometers, the thickness of the electrode structure may be increased up to a distance that light can reach. As the thickness of the electrode structure becomes greater, the short-circuit current density becomes higher. That is, the semiconductor oxide layer 122 may serve as an energy barrier prohibiting the recombination of electrons and holes between the electrolyte 130 and the conductive layer 120 . Therefore, the photovoltaic energy conversion efficiency of the dye-sensitized solar cell can be remarkably increased.
- the electrode structure of the dye-sensitized solar cell having the above-described structure has regularly arranged pores, thus minimizing the recombination due to oxidation/reduction reaction occurring at a boundary between the electrode structure and the electrolyte. Moreover, the moving passage of electrons can be minimized in the electrode structure.
- FIG. 3 is a sectional view illustrating a dye-sensitized solar cell and a method of fabricating the same according to an embodiment of the present invention.
- a dye-sensitized solar cell may include a bottom electrode structure 110 , an electrode structure having a conductive layer 120 , a semiconductor oxide layer 122 and a dye layer 124 , an electrolyte layer 130 and a top electrode structure 140 .
- the bottom electrode structure 110 may include a transparent substrate with conductivity or a transparent substrate of which one side is coated with a conductive material.
- the electrode structure may be formed to contact the conductive side of the bottom electrode structure 110 .
- the electrolyte layer 130 is interposed between the electrode structure and the top electrode structure 140 , and fills the pores of the electrode structure.
- the electrolyte layer 130 has one state of liquid, solid and gel.
- the electrolyte layer 130 may include I 3 ⁇ /I ⁇ -based electrolyte.
- the top electrode structure 140 may include a transparent substrate with conductivity or a transparent substrate of which one side is coated with conductive material.
- the conductive one side of the top electrode structure 140 may be formed to contact the electrolyte layer 130 .
- the dye-sensitized solar cell may further include a catalyst layer 142 interposed between the electrolyte 130 and the top electrode structure 140 .
- the catalyst layer 142 may include platinum or carbon. Accordingly, it may be possible to form the dye-sensitized solar cell including the electrode structure having the pores regularly arranged.
- the dye-sensitized solar cell includes the electrode structure having the pores regularly arranged, thus making it possible to minimize the recombination due to oxidation/reduction reaction occurring at a boundary between the electrode structure and the electrolyte. Furthermore, it may be possible to minimize a moving passage of an electron in the electrode structure.
- FIG. 4 is a partial sectional view illustrating a flow of an electron created by sunlight in the dye-sensitized solar cell according to the embodiment of the present invention.
- the moving passage of the electrons may be minimized to a length of several nanometers to several tens of nanometers.
- the semiconductor oxide layer 122 between the dye layer 124 and the conductive layer 120 may serve as an energy barrier prohibiting the electrons transferred to the conductive layer 120 from reacting with the electrolyte layer 130 again. Consequently, the photovoltaic energy conversion efficiency may be maximized.
- a dye-sensitized solar cell includes an electrode structure having pores regularly arranged, thus making it possible to minimize the recombination due to oxidation/reduction reaction occurring at a boundary between the electrode structure and an electrolyte. Furthermore, it is possible to minimize a moving passage of an electron in the electrode structure. Consequently, the dye-sensitized solar cell can maximize its photovoltaic energy conversion efficiency.
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Abstract
Provided are a dye-sensitized solar cell and a method of fabricating the same. The dye-sensitized solar cell includes an electrode structure including a conductive layer having pores that are regularly arranged, a semiconductor oxide layer disposed on a surface of the conductive layer, and a dye layer disposed on a surface of the semiconductor oxide layer.
Description
- This U.S. non-provisional patent application claims priority under 35 U.S.C. § 119 of Korean Patent Application No. 10-2007-104023, filed on Oct. 16, 2007, the entire contents of which are hereby incorporated by reference.
- The present invention disclosed herein relates to a dye-sensitized solar cell and a method of fabricating the same, and more particularly, to a dye-sensitized solar cell including an electrode structure having a conductor with pores regularly formed, which is fabricated by the use of a template, and a method of fabricating the dye-sensitized solar cell.
- The present invention has been derived from research undertaken as a part of IT R & D program of the Ministry of Information and Communication and Institution of Information Technology Association (MIC/IITA) [2006-S-006-02], Components/Module technology for ubiquitous terminals.
- A dye-sensitized solar cell includes a dye molecule capable of receiving incident light with a visible wavelength to form electron-hole pairs, a semiconductor oxide capable of receiving excited electrons, and an electrolyte reacting with the electrons after working and returning to the solar cell, which significantly differs from a compound solar cell or a wafer type silicon solar cell using p-n junction.
- A dye-sensitized solar cell, which has been well known hitherto, was published by Michael Gratzel et al. (refer to U.S. Pat. No. 4,927,721). A photoelectrochemical solar cell published by Michael Gratzel et al. includes a photosensitive dye molecule capable of absorbing a visible light to generate electron-hole pairs, an electrode structure which is a semiconductor oxide formed of nanoparticle titanium oxide (TiO2) with dye molecules adsorbed, an opposite electrode coated with platinum (Pt) or carbon (C), and an electrolyte filled between the semiconductor oxide and the opposite electrode. Because such the photoelectrochemical solar cell can be fabricated with low fabrication cost per electrical power in comparison with the wafer type silicon solar cell that utilizes a p-n junction, so the photoelectrochemical solar cell is being in the limelight recently.
-
FIG. 1 is a partial sectional view illustrating a flow of electrons created by sunlight in a conventional dye-sensitized solar cell. - Referring to
FIG. 1 , dye molecules excited by light emitted from the sun eject electrons (e-) into a conduction band of asemiconductor oxide layer 20 formed of nanoparticle titanium oxide. The electrons ejected into the conduction band pass through the nanoparticle titanium oxide and arrive at aconductive substrate 10 formed of a glass coated with fluorine doped SnO2 (FTO). Thereafter, the electrons are transferred to an external circuit (not shown). The electrons, which come back after performing an electrical work in the external circuit, are injected into thesemiconductor oxide layer 20 formed of nanoparticle semiconductor oxide through an opposite electrode (not shown), e.g., platinum or carbon electrode, by means of the electron transfer function of an oxidation/reduction electrolyte 30. Finally, the electrons reduce thedye molecule 24 deficient in electrons. In this manner, the conventional dye-sensitized solar cell is operated. - However, before the electrons injected into the
semiconductor oxide layer 20 made of nanoparticle titanium oxide from thedye molecule 24 are transferred to the external circuit and perform an electrical work therein, some of the electrons injected into the conduction band stay in an unoccupied surface energy level of thesemiconductor oxide layer 20 on which thedye molecule 24 is not adsorbed while passing through thesemiconductor oxide layer 20 and theconductive substrate 10. At this time the electron and theelectrolyte 30 are recombined so that the electrons do not circulate in a circuit but vanished ineffectively. Accordingly, there is a loss in photovoltaic energy conversion efficiency. - Furthermore, in the dye-sensitized solar cell proposed by Michael Gratzel et al. where the semiconductor oxide layer is used as the electrode structure, a moving passage through which the electrons injected from the dye molecules to the semiconductor oxide layer move to the conductive substrate is also made of the nanoparticle titanium oxide. Accordingly, the electron encounters a strong electrical resistance while the electron moves to a 3-dimensional structured semiconductor oxide layer, leading to a decrease in short-circuit current density (Jsc). Resultingly, since the photovoltaic energy conversion efficiency is determined by multiplication of a current, a voltage and a fill factor of the solar cell, the current, the voltage and the fill factor should be improved to increase the photovoltaic energy conversion efficiency. Particularly, to increase the voltage significantly, there is a method of increasing the electron density of the nanoparticle semiconductor oxide by minimizing the recombination with the electrons.
- Example of a conventional method of minimizing the decrease of the photovoltaic energy conversion efficiency occurring in the semiconductor oxide, e.g., the titanium oxide, is as followings. In the conventional method, the semiconductor oxide formed of the titanium oxide is used as the electrode structure, and coated with a semiconductor oxide material having high band gap energy, for example, niobium oxide (Nb2O5) to form an energy barrier between the semiconductor oxide layer and the electrolyte, thus preventing the recombination. According to the conventional method, the photovoltaic energy conversion efficiency was somewhat enhanced. However, because the titanium oxide is basically used as a material for the electrode structure, there is a limitation in electron movement. Therefore, an increase in the photovoltaic energy conversion efficiency was limited. Adsorptive properties of the dye molecule on the niobium oxide are poorer than that of the dye molecule on the titanium oxide.
- As another conventional method, there has been an attempt to employ a nanowire-shaped semiconductor oxide as the electrode structure. However, unlike the expectation that the nanowire-shaped semiconductor oxide could increase the photovoltaic energy conversion efficiency because the nanowire itself is a single crystal and thus advantageous for electron diffusion, the electrode structure made of nanowire-, nanorod- and nanotube-shaped semiconductor oxide exhibits poorer photovoltaic energy conversion efficiency compared to the case of using the nanoparticle semiconductor oxide as the electrode structure. Possibly, this is ascribed to the fact that the electrode structure made of the nanowire-, nanorod- and nanotube-shaped semiconductor oxide has a smaller surface area than the nanoparticle semiconductor oxide. In addition to the aforesaid conventional methods, there have been attempts to form the electrode structure using a semiconductor oxide of zinc oxide (ZnO) or tin oxide instead of the titanium oxide. However, the solar cell achieved by this conventional method still exhibits a poorer photovoltaic energy conversion efficiency compared to the solar cell using the titanium oxide for the electrode structure.
- The present invention provides a dye-sensitized solar cell capable of maximizing photovoltaic energy conversion efficiency.
- The present invention also provides a method of fabricating a dye-sensitized solar cell capable of maximizing photovoltaic energy conversion efficiency.
- Embodiments of the present invention provide dye-sensitized solar cells including: an electrode structure including a conductive layer including pores which are regularly arranged; a semiconductor oxide layer disposed on a surface of the conductive layer; and a dye layer disposed on a surface of the semiconductor oxide layer.
- In some embodiments, the conductive layer includes at least one selected from the group consisting of tin oxide, indium doped tin oxide, antimony doped tin oxide, fluorine doped tin oxide, metal, conductive polymer and a nano carbon material.
- In other embodiments, the semiconductor oxide layer includes at least one selected from the group consisting of zinc oxide, tin oxide and titanium oxide.
- In still other embodiments, the dye-sensitized solar cells further include: a bottom electrode structure disposed one side of the electrode structure, and contacting the electrode structure; a top electrode structure disposed on the other side of the electrode structure; and an electrolyte layer interposed between the electrode structure and the top electrode structure, and filling the pores.
- In even other embodiments, the dye-sensitized solar cells further include a catalyst layer interposed between the electrode structure and the electrolyte layer. Herein, the catalyst layer includes platinum or carbon.
- In yet other embodiments, the electrolyte has one state of liquid, solid and gel.
- In further embodiments of the present invention, methods of fabricating a dye-sensitized solar cell include: forming an electrode structure including: preparing a template having pores that are regularly arranged; forming a conductive layer on a surface of the template; forming a semiconductor oxide layer on a surface of the conductive layer; and forming a dye layer on a surface of the semiconductor oxide layer.
- In still further embodiments, the methods further include removing the template.
- In even further embodiments, the template is formed of at least one material selected from the group consisting of polystyrene, poly methyl methacrylate (PMMA) and block co-polymer. Here, the template is burn out and removed during a thermal treatment of forming the electrode structure.
- In yet further embodiments, the template is formed of alumina. In this case, the template is removed after formation of the electrode structure.
- In other embodiments, the conductive layer is formed of at least one selected from the group consisting of tin oxide, indium doped tin oxide, antimony doped tin oxide, fluorine doped tin oxide, metal, conductive polymer and a nano carbon material.
- In still other embodiments, the forming of the semiconductor oxide layer is performed using at least one method selected from the group consisting of a deep coating method, an electrophoretic method, and an electroplating method.
- In even other embodiments, the forming of the semiconductor oxide layer includes anodizing or thermally oxidizing a metal or a metal precursor.
- In yet other embodiments, the semiconductor oxide layer includes at least one selected from the group consisting of zinc oxide, tin oxide and titanium oxide.
- According to the present invention, a dye-sensitized solar cell includes an electrode structure having pores regularly arranged, thus making it possible to minimize the recombination due to oxidation/reduction reaction occurring at a boundary between the electrode structure and an electrolyte. Furthermore, it is possible to minimize a moving passage of an electron in the electrode structure. Consequently, the dye-sensitized solar cell can maximize its photovoltaic energy conversion efficiency.
- The accompanying figures are included to provide a further understanding of the present invention, and are incorporated in and constitute a part of this specification. The drawings illustrate exemplary embodiments of the present invention and, together with the description, serve to explain principles of the present invention. In the figures:
-
FIG. 1 is a partial sectional view illustrating a flow of electrons created by sunlight in a conventional dye-sensitized solar cell; -
FIG. 2 is a plan view illustrating an electrode structure of a dye-sensitized solar cell and a method of fabricating the same according to an embodiment of the present invention; -
FIG. 3 is a sectional view illustrating a dye-sensitized solar cell and a method of fabricating the same according to an embodiment of the present invention; and -
FIG. 4 is a partial sectional view illustrating a flow of electrons created by sunlight in the dye-sensitized solar cell according to the embodiment of the present invention. - Preferred embodiments of the present invention will be described below in more detail with reference to the accompanying drawings. The present invention may, however, be embodied in different forms and should not be construed as limited to the embodiments set forth herein. Rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the present invention to those skilled in the art. In the figures, the dimensions of layers and regions are exaggerated for clarity of illustration. It will also be understood that when a layer (or film) is referred to as being ‘on’ another layer or substrate, it can be directly on the other layer or substrate, or intervening layers may also be present. Further, it will be understood that when a layer is referred to as being ‘under’ another layer, it can be directly under, and one or more intervening layers may also be present. In addition, it will also be understood that when a layer is referred to as being ‘between’ two layers, it can be the only layer between the two layers, or one or more intervening layers may also be present. Like reference numerals refer to like elements throughout.
- Hereinafter, an exemplary embodiment of the present invention will be described with the accompanying drawings.
-
FIG. 2 is a plan view illustrating an electrode structure of a dye-sensitized solar cell and a method of fabricating the same according to an embodiment of the present invention. - Referring to
FIG. 2 , the electrode structure of the dye-sensitized solar cell may include aconductive layer 120, asemiconductor oxide layer 122 and adye layer 124. - The
conductive layer 120 may have pores that are regularly arranged. Theconductive layer 120 may be formed by coating a surface of a template (not shown) having pores regularly arranged with a transparent and conductive material. The conductive material contained in theconductive layer 120 may include at least one material selected from the group consisting of tin oxide (SnO2), indium doped tin oxide (ITO), antimony doped tin oxide (ATO), fluorine doped tin oxide (FTO), metal, conductive polymer and a nano carbon material. Preferably, theconductive layer 120 may be formed of tin oxide. - The template used to form the
conductive layer 120 having pores regularly arranged may have a shape that allows a surface area of the electrode structure to be maximized, for example, a honeycomb, nanowire, nanorod, or nanotube shape. The template may include at least one material selected from the group consisting of polystyrene, poly methyl methacrylate (PMMA), block co-polymer and alumina. - The
semiconductor oxide layer 122 may be formed on a surface of theconductive layer 120. Thesemiconductor oxide layer 122 may be formed using one method selected from the group consisting of a deep coating method, an electrophoretic method, and an electroplating method. In addition, thesemiconductor oxide layer 122 may be formed by anodizing or thermally oxidizing a metal or a metal precursor. Thesemiconductor oxide layer 122 may include at least one selected from the group consisting of zinc oxide, tin oxide and titanium oxide. Preferably, thesemiconductor oxide layer 122 may include titanium oxide. - The
dye layer 124 may be formed on a surface of thesemiconductor oxide layer 122. Thedye layer 124 may be formed by adsorbing dye molecules on thesemiconductor oxide layer 122. Accordingly, it is possible to form the electrode structure having pores regularly arranged. - In the case of using an organic-based template such as polystyrene, PMMA and block co-polymer, the template may be burn out and removed during a thermal treatment process of forming the electrode structure. In contrast, in the case of using an inorganic-based template such as alumina, the template may be removed after the formation of the electrode structure. This is because the inorganic-based template is not sintered during the thermal process of forming the electrode structure.
- The
conductive layer 120 has regularly arranged pores and thus high porosity, which may make it easy to thickly coat the surface of theconductive layer 120 with thesemiconductor oxide layer 122. Because theconductive layer 120 is spaced apart from thesemiconductor oxide layer 122 by merely several nanometers, the thickness of the electrode structure may be increased up to a distance that light can reach. As the thickness of the electrode structure becomes greater, the short-circuit current density becomes higher. That is, thesemiconductor oxide layer 122 may serve as an energy barrier prohibiting the recombination of electrons and holes between theelectrolyte 130 and theconductive layer 120. Therefore, the photovoltaic energy conversion efficiency of the dye-sensitized solar cell can be remarkably increased. - The electrode structure of the dye-sensitized solar cell having the above-described structure has regularly arranged pores, thus minimizing the recombination due to oxidation/reduction reaction occurring at a boundary between the electrode structure and the electrolyte. Moreover, the moving passage of electrons can be minimized in the electrode structure.
-
FIG. 3 is a sectional view illustrating a dye-sensitized solar cell and a method of fabricating the same according to an embodiment of the present invention. - Referring to
FIG. 3 , a dye-sensitized solar cell may include abottom electrode structure 110, an electrode structure having aconductive layer 120, asemiconductor oxide layer 122 and adye layer 124, anelectrolyte layer 130 and atop electrode structure 140. - The
bottom electrode structure 110 may include a transparent substrate with conductivity or a transparent substrate of which one side is coated with a conductive material. The electrode structure may be formed to contact the conductive side of thebottom electrode structure 110. - The
electrolyte layer 130 is interposed between the electrode structure and thetop electrode structure 140, and fills the pores of the electrode structure. Theelectrolyte layer 130 has one state of liquid, solid and gel. Preferably, theelectrolyte layer 130 may include I3 −/I−-based electrolyte. - The
top electrode structure 140 may include a transparent substrate with conductivity or a transparent substrate of which one side is coated with conductive material. The conductive one side of thetop electrode structure 140 may be formed to contact theelectrolyte layer 130. The dye-sensitized solar cell may further include acatalyst layer 142 interposed between theelectrolyte 130 and thetop electrode structure 140. Thecatalyst layer 142 may include platinum or carbon. Accordingly, it may be possible to form the dye-sensitized solar cell including the electrode structure having the pores regularly arranged. - Because the dye-sensitized solar cell includes the electrode structure having the pores regularly arranged, thus making it possible to minimize the recombination due to oxidation/reduction reaction occurring at a boundary between the electrode structure and the electrolyte. Furthermore, it may be possible to minimize a moving passage of an electron in the electrode structure.
-
FIG. 4 is a partial sectional view illustrating a flow of an electron created by sunlight in the dye-sensitized solar cell according to the embodiment of the present invention. - Referring to
FIG. 4 , because electrons (e-) transferred from thedye layer 124 to theconductive layer 120 move to thebottom electrode structure 110 through the honeycombedconductive layer 120 in the electrode structure of the dye-sensitized solar cell, the moving passage of the electrons may be minimized to a length of several nanometers to several tens of nanometers. Thesemiconductor oxide layer 122 between thedye layer 124 and theconductive layer 120 may serve as an energy barrier prohibiting the electrons transferred to theconductive layer 120 from reacting with theelectrolyte layer 130 again. Consequently, the photovoltaic energy conversion efficiency may be maximized. - As described above, according to the present invention, a dye-sensitized solar cell includes an electrode structure having pores regularly arranged, thus making it possible to minimize the recombination due to oxidation/reduction reaction occurring at a boundary between the electrode structure and an electrolyte. Furthermore, it is possible to minimize a moving passage of an electron in the electrode structure. Consequently, the dye-sensitized solar cell can maximize its photovoltaic energy conversion efficiency.
- The above-disclosed subject matter is to be considered illustrative, and not restrictive, and the appended claims are intended to cover all such modifications, enhancements, and other embodiments, which fall within the true spirit and scope of the present invention. Thus, to the maximum extent allowed by law, the scope of the present invention is to be determined by the broadest permissible interpretation of the following claims and their equivalents, and shall not be restricted or limited by the foregoing detailed description.
Claims (13)
1. A dye-sensitized solar cell comprising:
an electrode structure including:
a conductive layer including pores which are regularly arranged;
a semiconductor oxide layer disposed on a surface of the conductive layer; and
a dye layer disposed on a surface of the semiconductor oxide layer.
2. The dye-sensitized solar cell of claim 1 , wherein the conductive layer comprises at least one selected from the group consisting of tin oxide, indium doped tin oxide, antimony doped tin oxide, fluorine doped tin oxide, metal, conductive polymer and a nano carbon material.
3. The dye-sensitized solar cell of claim 1 , wherein the semiconductor oxide layer comprises at least one selected from the group consisting of zinc oxide, tin oxide and titanium oxide.
4. A method of fabricating a dye-sensitized solar cell, the method comprising:
forming an electrode structure including:
preparing a template having pores that are regularly arranged;
forming a conductive layer on a surface of the template;
forming a semiconductor oxide layer on a surface of the conductive layer; and
forming a dye layer on a surface of the semiconductor oxide layer.
5. The method of claim 4 , further comprising removing the template.
6. The method of claim 5 , wherein the template is formed of at least one material selected from the group consisting of polystyrene, poly methyl methacrylate (PMMA) and block co-polymer.
7. The method of claim 6 , wherein the template is burn out and removed during a thermal treatment of forming the electrode structure.
8. The method of claim 5 , wherein the template is formed of alumina.
9. The method of claim 4 , wherein the conductive layer is formed of at least one selected from the group consisting of tin oxide, indium doped tin oxide, antimony doped tin oxide, fluorine doped tin oxide, metal, conductive polymer and a nano carbon material.
10. The method of claim 4 , wherein the forming of the semiconductor oxide layer is performed using at least one method selected from the group consisting of a deep coating method, an electrophoretic method, and an electroplating method.
11. The method of claim 10 , wherein the semiconductor oxide layer comprises at least one selected from the group consisting of zinc oxide, tin oxide and titanium oxide.
12. The method of claim 4 , wherein the forming of the semiconductor oxide layer comprises anodizing or thermally oxidizing a metal or a metal precursor.
13. The method of claim 12 , wherein the semiconductor oxide layer comprises at least one selected from the group consisting of zinc oxide, tin oxide and titanium oxide.
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| US13/870,046 US8809104B2 (en) | 2007-10-16 | 2013-04-25 | Dye-sensitized solar cell and method of fabricating the same |
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| KR1020070104023A KR100927660B1 (en) | 2007-10-16 | 2007-10-16 | Dye-Sensitized Solar Cells and Manufacturing Method Thereof |
| KR10-2007-0104023 | 2007-10-16 |
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Cited By (2)
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|---|---|---|---|---|
| US20100144083A1 (en) * | 2008-06-24 | 2010-06-10 | Sony Corporation | Method of manufacturing photoelectric conversion device |
| US20140322921A1 (en) * | 2013-04-26 | 2014-10-30 | Iftikhar Ahmad | Method and apparatus for microwave treatment of dielectric films |
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| KR101682575B1 (en) | 2009-08-24 | 2016-12-06 | 삼성전자주식회사 | Electrochromic device and method of manufacturing the same |
| KR101034657B1 (en) | 2010-02-25 | 2011-05-16 | 주식회사 하나디에스 | Metal Electrode Dye Solar Cell and Manufacturing Method Thereof |
| KR101179005B1 (en) | 2010-12-24 | 2012-08-31 | 부산대학교 산학협력단 | Hybrid Nano Structure And Electrode Using It And Manufacturing Method Thereof |
| KR101458444B1 (en) * | 2012-02-27 | 2014-11-10 | 서강대학교산학협력단 | Porous transition metal oxide structure, preparing method of the same, photoelectrode including the same, and dye-sensitized solar cell including the photoelectrode |
| KR101665637B1 (en) * | 2012-06-29 | 2016-10-12 | 서강대학교산학협력단 | Photoelectrode for dye-sensitized solar cell, preparing method of the same, and dye-sensitized solar cell having the same |
| KR101451114B1 (en) * | 2012-11-12 | 2014-10-17 | 서강대학교산학협력단 | Photoelectrode for dye-sensitized solar cell, preparing method of the same, and dye-sensitized solar cell including the same |
| SE537836C2 (en) | 2014-02-06 | 2015-11-03 | Exeger Sweden Ab | A transparent dye-sensitized solar cell and a way of producing it |
| KR102534569B1 (en) | 2019-12-30 | 2023-05-22 | 한국전자통신연구원 | Semiconductor material and manufacturing method thereof |
| DE102022108893A1 (en) | 2022-04-12 | 2023-10-12 | Universität Siegen, Körperschaft des öffentlichen Rechts | Solar capsule for a dye solar cell |
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Also Published As
| Publication number | Publication date |
|---|---|
| US20130237006A1 (en) | 2013-09-12 |
| US8809104B2 (en) | 2014-08-19 |
| KR100927660B1 (en) | 2009-11-20 |
| KR20090038631A (en) | 2009-04-21 |
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