KR20130080143A - Grid electrode structure of dye-sensitized solar cell - Google Patents
Grid electrode structure of dye-sensitized solar cell Download PDFInfo
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- KR20130080143A KR20130080143A KR1020120000907A KR20120000907A KR20130080143A KR 20130080143 A KR20130080143 A KR 20130080143A KR 1020120000907 A KR1020120000907 A KR 1020120000907A KR 20120000907 A KR20120000907 A KR 20120000907A KR 20130080143 A KR20130080143 A KR 20130080143A
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- grid electrode
- electrode
- dye
- grid
- solar cell
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- 239000000758 substrate Substances 0.000 claims description 18
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 229910052709 silver Inorganic materials 0.000 claims description 6
- 239000004332 silver Substances 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 abstract description 7
- 239000000975 dye Substances 0.000 description 20
- 239000010410 layer Substances 0.000 description 17
- 239000004065 semiconductor Substances 0.000 description 13
- 239000003792 electrolyte Substances 0.000 description 12
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
- 230000027756 respiratory electron transport chain Effects 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 4
- 238000006479 redox reaction Methods 0.000 description 4
- 230000005611 electricity Effects 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 229910052697 platinum Inorganic materials 0.000 description 3
- 239000011241 protective layer Substances 0.000 description 3
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000008151 electrolyte solution Substances 0.000 description 2
- 229940021013 electrolyte solution Drugs 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 239000003566 sealing material Substances 0.000 description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- 229910001887 tin oxide Inorganic materials 0.000 description 2
- JBOIAZWJIACNJF-UHFFFAOYSA-N 1h-imidazole;hydroiodide Chemical compound [I-].[NH2+]1C=CN=C1 JBOIAZWJIACNJF-UHFFFAOYSA-N 0.000 description 1
- XZXYQEHISUMZAT-UHFFFAOYSA-N 2-[(2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound CC1=CC=C(O)C(CC=2C(=CC=C(C)C=2)O)=C1 XZXYQEHISUMZAT-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229920003182 Surlyn® Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 229940107816 ammonium iodide Drugs 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 239000002019 doping agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- 230000005281 excited state Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
Images
Classifications
-
- 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
- H01G9/2068—Panels or arrays of photoelectrochemical cells, e.g. photovoltaic modules based on photoelectrochemical cells
- H01G9/2081—Serial interconnection of 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
- 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
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- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Hybrid Cells (AREA)
- Photovoltaic Devices (AREA)
Abstract
Description
The present invention relates to a grid electrode structure of a dye-sensitized solar cell.
Dye-Sensitized Solar Cell (DSSC) is a solar cell developed by Michael Gratzel of the Swiss Federal Institute of Technology. It has lower manufacturing cost compared to conventional silicon solar cells, It is possible to manufacture a cell which is high in transparency and bendability and thus can be used in various applications.
Dye-sensitized solar cells serve as catalysts for photoelectrodes containing dye molecules that produce electron-hole pairs and semiconductor layers that deliver the generated electrons, electrolytes that supplement electrons with dye molecules, and redox reactions of electrolyte solutions. Made of a counter electrode coated with a platinum layer. When light is incident on the dye-sensitized solar cell, the dye that absorbs the light enters an excited state to send electrons to the conduction band of the semiconductor layer, and the transferred electrons flow along the electrode to an external circuit to transfer electrical energy. As it transfers electrical energy, it becomes a low energy state and moves to the counter electrode. The dye is supplied with electrons from the electrolyte solution as much as the number of electrons transferred to the semiconductor layer and returned to its original state. The electrolyte used serves to receive electrons from the counter electrode by a redox reaction and transfer them to the dye. The photoelectrode serving as a negative electrode of a dye-sensitized solar cell includes a semiconductor layer, such as titanium dioxide (TiO 2 ), on which a dye, which absorbs light in the visible region, generates an electron-hole pair. Electrolyte supplying electrons to dye is I - / I 3 - consists of a reduced species, I - - oxidation as a source of ions LiI, NaI, alkaline ammonium iodide, imidazolium iodide, etc. are used, I 3 - ions to produce an I 2 melt in a solvent. The counter electrode is made of platinum or the like and serves as a catalyst for the ion redox reaction to provide electrons to ions in the electrolyte through a redox reaction on the surface.
Fluorine doped tin oxide (FTO) is widely used as a transparent electrode constituting the photoelectrode or counter electrode of a dye-sensitized solar cell. Since the fluorine dopant tin oxide has a higher electrical resistance than a metal material, a grid electrode for collecting electrons may be further formed on the transparent electrode. In addition, a collecting electrode for connecting grid electrodes to each other is required to configure a solar cell module by connecting solar cells of a unit cell in parallel or in addition to a function of accumulating electrons. Silver (Ag) may be used as the grid electrode material. When silver is in direct contact with the electrolyte, silver may be oxidized by the electrolyte to lose the original function of the grid electrode. By-products generated by the oxidation reaction may be included in the electrolyte. Power generation efficiency may also be reduced. Therefore, in order to protect the grid electrode from the electrolyte, the surface of the metal electrode should be sealed with a sealing material such as surlyn.
1 illustrates a grid electrode of a dye-sensitized solar cell. Referring to FIG. 1, current collecting
FIG. 2 is a cross-sectional view of the dye-sensitized solar cell to which the grid electrode is applied (AA 'direction cross-section of FIG. 1). Referring to FIG. 2, the
Here, the electrons excited from the dye have a problem that the photoelectric conversion efficiency of the dye-sensitized solar cell is lowered as the electron transfer to the grid electrode is delayed as the resistance moves through the transparent electrode having a relatively larger size than the grid electrode.
Therefore, there is a need for a new grid electrode structure of a dye-sensitized solar cell that can quickly move electrons excited from the dye to the grid electrode by minimizing the path of migration on the transparent electrode.
The present invention has been made to solve the above-described problems, an object of the present invention is to minimize the distance that the electrons excited from the dye reaches the grid electrode and at the same time can reduce the resistance when moving from the grid electrode to the current collector electrode It is to provide a grid electrode structure of a dye-sensitized solar cell.
In order to solve the above problems, the grid electrode structure of the dye-sensitized solar cell of an embodiment of the present invention is a collector electrode for connecting the electrons excited from the dye to an external electrical circuit, at least one formed in the horizontal direction with the collector electrode And a second grid electrode intersecting with the first grid electrode and the first grid electrode, wherein at least one side is formed in a vertical direction so that one side thereof is electrically connected to the current collecting electrode.
According to one embodiment of the present invention, the aperture ratio is kept constant by adjusting the widths of the first grid electrode and the second grid electrode.
According to one embodiment of the present invention, the width of the second grid electrode is characterized in that it is wider than the width of the first grid electrode.
According to an aspect of an embodiment of the present invention, the width of the second grid electrode is characterized in that it gradually widens as it moves toward the current collecting electrode at a portion far from the current collecting electrode.
According to one embodiment of the present invention, the current collecting electrode is electrically connected to an external electrode, the external electrode is characterized in that formed by applying a silver paste on the side of the substrate.
According to the present invention as described above, while maintaining the same opening ratio (effective area) per unit area in the prior art, electrons excited from the dye are formed in the shortest path by forming a second grid electrode on the transparent electrode that intersects the first grid electrode perpendicularly. As the first grid electrode or the second grid electrode reaches, the electron transfer is quickly performed to the current collecting electrode, thereby improving the photoelectric conversion efficiency.
In addition, the width of the second grid electrode is formed to be wider than the width of the first grid electrode to reduce the resistance, so that electrons collected by the first grid electrode are quickly transferred to the current collecting electrode through the second grid electrode, thereby improving photoelectric conversion efficiency. There is an effect that can be improved.
1 illustrates a metal grid electrode of a dye-sensitized solar cell.
2 shows a cross section of a dye-sensitized solar cell to which a grid electrode is applied.
3A and 3B are diagrams for comparing the aperture ratio between a conventional grid electrode structure and a grid electrode structure according to the present invention.
4 is a plan view of a grid electrode structure of a dye-sensitized solar cell according to another embodiment of the present invention.
5 is a cross-sectional view of the grid electrode structure of the dye-sensitized solar cell according to an embodiment of the present invention.
6 illustrates a module of a dye-sensitized solar cell by serial or parallel connection between unit cells according to an embodiment of the present invention.
7 is a plan view of a grid electrode structure of a dye-sensitized solar cell according to another embodiment of the present invention.
The following detailed description is only illustrative, and merely illustrates embodiments of the present invention. In addition, the principles and concepts of the present invention are provided for the purpose of explanation and most useful.
Accordingly, various forms that can be implemented by those of ordinary skill in the art, as well as not intended to provide a detailed structure beyond the basic understanding of the present invention through the drawings.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings.
The grid electrode may be formed in a predetermined pattern on the transparent electrode formed on the photoelectrode substrate and the counter electrode substrate. Herein, when light is absorbed by the dye molecules adsorbed on the semiconductor oxide layer, electrons are excited, and then the excited electrons move to the current collecting electrode through the semiconductor oxide layer and the transparent electrode. At this time, since the excited electrons are moved to the current collecting electrode along the grid electrode having a much lower electrical resistance than the transparent electrode made of a conductive oxide (ITO or FTO), the electron transfer is faster, thereby improving the efficiency of the dye-sensitized solar cell. Hereinafter, the grid electrode of the present invention may be formed with at least one protective layer that can prevent the corrosion by the penetration of the electrolyte to the outside. The grid electrode formation on the counter electrode substrate according to the present invention corresponds to the grid electrode formation on the photoelectrode substrate and thus will be omitted. In addition, the method of forming the semiconductor oxide layer, the catalyst layer and the sealing member of the dye-sensitized solar cell unit cell is obvious to those skilled in the art and will be omitted below.
3A and 3B are diagrams for comparing the aperture ratio (effective area) between the conventional grid electrode structure and the grid electrode structure according to the present invention.
As shown in FIG. 3A, a semiconductor oxide layer in which dye is adsorbed between the plurality of
Opening ratio = (unit area-total area of grid electrode) / unit area
= 1- (xyN 1 / AB).
Where x: grid electrode width, y: the length (A = B) of one side: the grid electrode length, N 1: number of the grid electrodes, A and B.
Here, if the unit area A * B is the same, the aperture ratio depends on the grid electrode area. If the grid electrode in the dye-sensitized solar cell, the length (y) and width (x) is N 1 gaeil grid electrode area is calculated as x * y * N 1. In FIG. 3A, six grid electrodes 610 are connected to the
Next, when the aperture ratio of FIG. 3B having the grid electrode structure of the present invention is compared with that of FIG. 3A, it is only necessary to determine whether the entire area of the grid electrode formed as described above is the same.
As shown in FIG. 3B, first, the grid electrode structure formed in the
First, in FIG. 3B, the grid electrode includes two
By the above calculation, since the total area 6xy of the grid electrode is the same in the same unit area (AB) in Figures 3a and 3b, it can be seen that the aperture ratio of the dye-sensitized solar cell is the same in Figures 3a and 3b.
Meanwhile, since the number of grid electrodes (6) of FIG. 3A disposed at the same distance A or B is smaller than the number of first grid electrodes (9) of FIG. 3B, the distance D 2 between the grid electrodes in FIG. It is smaller than the distance D 1 between the grid electrodes of FIG. 3A. Thus relatively
The rapid transfer of electrons can be interpreted as a decrease in the probability of electron recombination occurring when electrons excited from the dye pass through the semiconductor oxide layer and the transparent electrode, thereby increasing the photoelectric conversion efficiency. do.
Meanwhile, in the grid electrode structure according to the present invention, the
4 is a plan view of a grid electrode structure of a dye-sensitized solar cell according to another embodiment of the present invention.
As shown in FIG. 4, the grid electrode structure may be formed by crossing the
It can be seen that the distance between the grid electrodes in FIG. 4 is D 3 , which is smaller than the distance between the grid electrodes when the number of grid electrodes in FIG. 3B is 10, from which the
In addition, the width of the
The grid electrode structure according to the present invention is not limited to the number of first grid electrodes and the number of second grid electrodes, and is variously modified according to a process applied in a dye-sensitized solar cell capable of minimizing the width of the first grid electrode. Can be.
5 is a cross-sectional view (a-a 'direction) of a grid electrode structure of a dye-sensitized solar cell according to an embodiment of the present invention.
As shown in FIG. 5, the
In this case, the dye-sensitized solar
6 illustrates a module of a dye-sensitized solar cell by serial or parallel connection between unit cells according to an embodiment of the present invention.
As shown in (a) of FIG. 6, the unit cells of the dye-sensitized solar cell are
Meanwhile, as shown in (b) of FIG. 6, the unit cells of the dye-sensitized solar cell are connected to the
Therefore, panelization can be achieved on a large area by electrically connecting unit cells of a dye-sensitized solar cell having a predetermined size in series, parallel, series, and parallel.
7 is a plan view of a grid electrode structure of a dye-sensitized solar cell according to another embodiment of the present invention.
As shown in FIG. 7, the
Since the electrons collected from the first grid electrode move along the
That is, the portion of the
Therefore, in the grid electrode structure according to the present invention, electrons excited from the dye are transparent through a plurality of first grid electrodes formed to intersect with the second grid electrode while maintaining a constant aperture ratio by the same as the total area of the conventional grid electrode. In order to minimize the distance to move on the electrode and to transfer the electrons to the current collecting electrode, the width of the second grid electrode is gradually widened as it moves toward the current collecting electrode at a part far from the current collecting electrode to reduce the resistance. Conversion efficiency can be improved.
The present invention has been described in detail with reference to exemplary embodiments, but those skilled in the art to which the present invention pertains can make various modifications without departing from the scope of the present invention. Will understand.
Therefore, the scope of the present invention should not be limited to the above-described embodiments, but should be determined by equivalents to the appended claims, as well as the appended claims.
300: photoelectrode unit cell 320: current collector electrode
330: semiconductor oxide layer 341: first grid electrode
342, 700:
381,382: transparent electrode 510: conductive adhesive
520,521 Wire 1000: Dye-sensitized solar cell unit cell
Claims (5)
At least one first grid electrode formed in a horizontal direction with the current collecting electrode;
The grid electrode structure of the dye-sensitized solar cell comprising a second grid electrode crossing the first grid electrode, one side is formed at least one in the vertical direction to be electrically connected to the current collecting electrode.
The grid electrode structure of the dye-sensitized solar cell, characterized in that the aperture ratio is kept constant by adjusting the widths of the first grid electrode and the second grid electrode.
The grid electrode structure of the dye-sensitized solar cell, characterized in that the width of the second grid electrode is wider than the width of the first grid electrode.
The width of the second grid electrode is a grid electrode structure of the dye-sensitized solar cell, characterized in that gradually widens as it moves toward the current collecting electrode at a portion far from the current collecting electrode.
The current collecting electrode is electrically connected to an external electrode,
The external electrode is a grid electrode structure of a dye-sensitized solar cell, characterized in that formed by applying a silver paste on the side of the substrate.
Priority Applications (1)
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KR1020120000907A KR20130080143A (en) | 2012-01-04 | 2012-01-04 | Grid electrode structure of dye-sensitized solar cell |
Applications Claiming Priority (1)
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KR1020120000907A KR20130080143A (en) | 2012-01-04 | 2012-01-04 | Grid electrode structure of dye-sensitized solar cell |
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2012
- 2012-01-04 KR KR1020120000907A patent/KR20130080143A/en not_active Application Discontinuation
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