This application claims the benefit of Korean Patent Application No. 2008-0033912, filed Apr. 11, 2008, the disclosure of which is hereby incorporated herein by reference in its entirety.
1. Field of the Invention
The present invention relates to a solar cell, and more particularly, to an organic solar cell.
2. Description of the Related Art
Fossil fuels currently used as a main energy source are gradually decreasing in production. Further, fossil fuels emit carbon dioxide during combustion of the fossil fuel, which contributes to global warming. For this reason, research on conversion technology for environment-friendly energy as a substitute for the fossil fuels is actively progressing. Examples of the environment-friendly energy include hydraulic, wind power, and solar energies.
A solar cell is a device for converting solar light into electrical energy, and most commercial solar cells are fabricated using silicon. However, because of low light absorption of silicon, silicon solar cells are fabricated thick, and equipped outside buildings because of their large size.
To overcome the limitation of such a silicon solar cell, a polymer solar cell using a conjugated polymer is being investigated. While the polymer solar cell absorbs more light than the silicon solar cell, it does not reach a sufficient level yet. A polymer active layer may be formed thick in order to improve the light absorption of the polymer solar cell. However, this increases series resistance.
The present invention is directed to an organic solar cell, which does not increase a thickness of an active layer, and greatly improves light absorption, and a method of fabricating the same.
According to an embodiment of the present invention, an organic solar cell is provided. The organic solar cell includes a first electrode and a second electrode. An organic active layer is disposed between the first electrode and the second electrode. The organic active layer includes a concave-convex pattern in one surface adjacent to the second electrode.
The first electrode may be a transparent electrode, and the second electrode may be a reflective electrode. The unevenness may be a diffraction grating, and specifically, a blazed diffraction grating. The organic active layer may be a polymer active layer, and specifically, a bulk heterojunction active layer. A buffer layer may be disposed between the organic active layer and the transparent electrode.
According to another embodiment of the present invention, a method of fabricating an organic solar cell is provided. First, a first electrode is formed on a cell substrate. An organic active layer is formed on the first electrode. An concave-convex pattern is formed in a top surface of the organic active layer. A second electrode is formed on the organic active layer having the concave-convex pattern.
The concave-convex pattern may be formed by contacting an elastomer stamp and the top surface of the organic active layer. The elastomer stamp may be formed by molding using a template having a surface relief grating (SRG). The template may include a photoisomerization polymer layer, and the surface relief grating may be formed by irradiating interference light onto the photoisomerization polymer layer. The surface relief grating may be a blazed diffraction grating.
These and/or other aspects and advantages of the invention will become apparent and more readily appreciated from the following description of the embodiments, taken in conjunction with the accompanying drawings of which:
Reference will now be made in detail to the present embodiments of the present invention, examples of which are shown in the accompanying drawings. This invention may, however, be embodied in different forms and should not be construed as limited to the embodiments set forth herein. In the drawings, when a layer is described as being formed on another layer or substrate, the layer may be formed on the other layer or substrate, or a third layer may be interposed between the layer and the other layer or substrate.
Referring to
The first electrode 12 may be a transparent electrode. The transparent electrode may be formed of indium tin oxide (ITO), indium oxide (IO), tin oxide (TO), indium zinc oxide (IZO) or zinc oxide (ZO). The first electrode 12 may be formed by vacuum deposition, sol-gel deposition or metal organic deposition. For example, the first electrode 12 may be formed by RF magnetron sputtering.
Before forming the first electrode 12, an antireflection layer 11 may be formed on a lower surface of the cell substrate 10.
An organic active layer 16 may be formed on the first electrode 12. Before forming the organic active layer 16, a buffer layer 14 may be formed on the first electrode 12. The buffer layer 14 may improve an adhesive strength between the first electrode 12 and the organic active layer 16, and serve as a charge transport layer. The buffer layer 14 may be a poly(3,4-ethylenedioxythiophene) (PEDOT): poly(styrene sulfonate) (PSS) layer.
The organic active layer 16 is a photoelectric conversion layer containing an organic material, which absorbs light and generates excitons. The organic active layer 16 may be a donor/acceptor double layer, in which a donor layer is separated from an acceptor layer, or a bulk-heterojunction (BHJ) layer, in which a donor and an acceptor are mixed. In the structure of the donor/acceptor double layer, an electrode is spaced apart from an interface between the donor layer and the acceptor layer, and thus the excitons generated at the interface may be recombined with each other during transfer to the electrode, which may result in low photoelectric conversion efficiency. However, in the bulk-heterojunction layer, the donor and the acceptor are mixed together in the organic active layer 16, so that an electrode is relatively close to a junction interface between the donor and the acceptor, thus reducing probability of recombination of the exciton. Therefore, when the organic active layer 16 is the bulk-heterojunction layer, the photoelectric conversion efficiency may be improved.
The donor may be an organic monomer such as phthalocyanine, a phthalocyanine derivative, merocyanine or a merocyanine derivative, or a polymer such as poly(phenylenevinylene) (PPV), a PPV derivative, polythiophene or a polythiophene derivative. The PPV derivative may be poly(2-methoxy-5-(2-ethyhexoxy)-1,4-phenylenevinylene) (MEH-PPV) or 2-methoxy-5-(3,7-dimethyloctyloxy)-1,4-phenylenevinylene (MDMO-PPV), and the polythiophene derivative may be poly(3-hexylthiophene) (P3HT) or poly(3-octylthiophene) (P3OT). The acceptor may be fullerene, a fullerene derivative, perylene or a perylene derivative. The fullerene derivative may be phenyl-C61-butyric acid methyl ester (PCBM).
The bulk-heterojunction layer may be MEH-PPV:PCBM, MDMO-PPV:PCBM, P3HT:PCBM or P3OT:PCBM.
Referring to
The stamp concave-convex pattern 22a may be a linear one-dimensional or island-shaped two-dimensional diffraction grating, and preferably, a blazed diffraction grating structure.
Referring to
The organic concave-convex pattern 16a may correspond to the stamp concave-convex pattern 20a to form a linear one-dimensional or island-shaped two-dimensional diffraction grating, and preferably, a blazed diffraction grating structure.
Referring to
Referring to
When the organic concave-convex pattern 16a is a diffraction grating, a diffraction equation for the reflective light (Ld) will be given by Formula 1.
mλ=n
active
·P(sin θi+sin θd)
In Formula 1, m is a diffraction order, λ is a wavelength of incident light, nactive is a refractive index of an organic active layer, P is a period of an organic concave-convex pattern, θ1 is an incident angle, and θd is a diffraction angle.
Further, the reflective light (Ld) reflected at the interface between the organic concave-convex pattern 16a and the second electrode 18 is not emitted into air, and a condition for total reflection at an interface between the cell substrate 10 and the external air will be given by Formula 2.
In Formula 2, θc is an incident angle when light reflected from an interface between an organic concave-convex pattern and a second electrode is incident to an interface between a cell substrate and air, nactive is a refractive index of an organic active layer, and nair is a refractive index of air.
When the light (Li) is incident to the solar cell in a vertical direction, sin θi may be 0 and θc may be the same as θd. In this case, under the condition given by Formula 3, the light (Ld) reflected from the interface between the organic concave-convex pattern 16a and the second electrode 18 may be totally reflected at the interface between the cell substrate 10 and the air, and then incident to the organic active layer 16. Thus, a path of the light passing through the organic active layer 16 may be increased, which results in improved light absorption.
In Formula 3, m is a diffraction order, λ is a wavelength of incident light, and P is a period of an organic concave-convex pattern.
Referring to
Referring to
A method of forming the surface relief grating will be described with reference to
The laser source 41 may be a laser source generating light having a wavelength of about 400 to 500 nm, for example, an argon laser source. Light emitted from the laser source 41 is reflected from the reflection mirrors 42 and 43 and incident to the polarizer 44 or the wave plate 45, which polarizes the light. After that, the polarized light is converted into collimated light while passing through the spatial filter 46 and the collimating lens 47. After that, a part of the collimated and polarized light is directly incident to the photoisomerization polymer layer 32 (
The period of the surface relief grating 32a (
nλ=2d sin θ [Formula 4]
In Formula 4, n is an integer, λ is a wavelength of a laser source, d is a period of a surface relief grating, and θ is an incident angle of light incident to a photoisomerization polymer layer.
The method of forming the surface relief grating 32a (
Referring again to
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Hereinafter, preferable examples will be provided to aid in understanding the present invention. However, it will be understood that the examples set forth herein are provided merely to aid in understanding the present invention, and not to limit the present invention.
A surface relief grating was formed in a top surface of a photoisomerization polymer layer PDO3 using a 100 mW/cm2, 488 nm Argon laser. An elastomer stamp was formed using the PDO3 layer having the surface relief grating as a template. To be specific, the elastomer stamp was formed by pouring a polysiloxane acid prepolymer, which is a 10:1 (wt/wt) mixture of PDMS and a curing agent (Sylgard 184, Dow Corning) on the PDO3 layer having the surface relief grating, curing the polymer at 60□, and then separating the hardened polymer from the PDO3 layer.
A glass substrate (Samsung Corning) coated with a transparent electrode ITO having a sheet resistance of 10 Ω/sq or less was cleaned, and PEDOT:PSS (Baytron P VPAI 4083, H.C. Starck) was spin-coated to a thickness of 20 nm on the ITO layer. A mixture solution prepared by dissolving 30 mg P3HT (Rieke Metals) and 24 mg PCBM (Nano-C) in 2 ml chlorobenzene was spin-coated on the PEDOT:PSS layer to form an 80 nm organic active layer. The elastomer stamp fabricated in Fabrication Example 1 was conformally disposed on the organic active layer, and annealed for 20 minutes at 110□ in a nitrogen atmosphere, thereby forming an organic concave-convex pattern. After that, the elastomer stamp was separated, and a 20 nm calcium layer and a 100 nm aluminum layer were thermally deposited in sequence in a 10−6 torr vacuum, thereby forming a reflective electrode.
An organic solar cell was fabricated by the same method as described in Fabrication Example 1, except that an elastomer stamp was not in contact with an organic active layer.
An organic solar cell was fabricated by the same method as described in Fabrication Example 1, except that an elastomer stamp without a stamp concave-convex pattern was formed on an organic active layer.
Referring to
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An open circuit voltage (Voc), a short circuit current density (Jsc) and a fill factor (FF) are extracted from
Referring to
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According to the present invention, as an organic concave-convex pattern is formed in one surface of an organic active layer, an optical path passing through the organic active layer can be increased, and light absorption can be significantly improved without any change in thickness of the organic active layer. Also, as the organic concave-convex pattern has a blazed diffraction grating structure, the optical path passing through the organic active layer can be further increased.
Although a few embodiments of the present invention have been shown and described, it would be appreciated by those skilled in the art that changes may be made in these embodiments without departing from the principles and spirit of the invention, the scope of which is defined in the claims and their equivalents.
Number | Date | Country | Kind |
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10-2008-0033912 | Apr 2008 | KR | national |