US20160087115A1 - Solar cell structure and method for fabricating the same - Google Patents
Solar cell structure and method for fabricating the same Download PDFInfo
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- US20160087115A1 US20160087115A1 US14/495,048 US201414495048A US2016087115A1 US 20160087115 A1 US20160087115 A1 US 20160087115A1 US 201414495048 A US201414495048 A US 201414495048A US 2016087115 A1 US2016087115 A1 US 2016087115A1
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- 238000000034 method Methods 0.000 title claims description 20
- 239000004065 semiconductor Substances 0.000 claims abstract description 56
- 239000000758 substrate Substances 0.000 claims abstract description 52
- 229910052751 metal Inorganic materials 0.000 claims abstract description 42
- 239000002184 metal Substances 0.000 claims abstract description 42
- 238000002161 passivation Methods 0.000 claims description 31
- 238000004528 spin coating Methods 0.000 claims description 24
- 238000004519 manufacturing process Methods 0.000 claims description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 20
- 238000000137 annealing Methods 0.000 claims description 16
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 15
- 238000009792 diffusion process Methods 0.000 claims description 12
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 239000000377 silicon dioxide Substances 0.000 claims description 7
- 238000004544 sputter deposition Methods 0.000 claims description 7
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 5
- 229910052796 boron Inorganic materials 0.000 claims description 5
- 239000002245 particle Substances 0.000 claims description 5
- 229910052698 phosphorus Inorganic materials 0.000 claims description 5
- 239000011574 phosphorus Substances 0.000 claims description 5
- 235000012239 silicon dioxide Nutrition 0.000 claims description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 4
- 239000011368 organic material Substances 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 238000002207 thermal evaporation Methods 0.000 claims description 3
- 229910052786 argon Inorganic materials 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- CJNBYAVZURUTKZ-UHFFFAOYSA-N hafnium(iv) oxide Chemical compound O=[Hf]=O CJNBYAVZURUTKZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 238000002834 transmittance Methods 0.000 abstract description 3
- 239000000243 solution Substances 0.000 description 5
- 229910021421 monocrystalline silicon Inorganic materials 0.000 description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000003929 acidic solution Substances 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 229910021419 crystalline silicon Inorganic materials 0.000 description 2
- 230000000593 degrading effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 238000010248 power generation Methods 0.000 description 2
- 239000011265 semifinished product Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000002803 fossil fuel Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000003758 nuclear fuel Substances 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
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- H01L31/02168—
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- 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
- H10F77/30—Coatings
- H10F77/306—Coatings for devices having potential barriers
- H10F77/311—Coatings for devices having potential barriers for photovoltaic cells
- H10F77/315—Coatings for devices having potential barriers for photovoltaic cells the coatings being antireflective or having enhancing optical properties
-
- H01L31/02167—
-
- H01L31/02366—
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- H01L31/1804—
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- 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
- H10F10/10—Individual photovoltaic cells, e.g. solar cells having potential barriers
- H10F10/14—Photovoltaic cells having only PN homojunction potential barriers
-
- 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
- H10F71/121—The active layers comprising only Group IV materials
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- 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
- H10F77/30—Coatings
- H10F77/306—Coatings for devices having potential barriers
- H10F77/311—Coatings for devices having potential barriers for photovoltaic cells
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- 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
- H10F77/70—Surface textures, e.g. pyramid structures
- H10F77/703—Surface textures, e.g. pyramid structures of the semiconductor bodies, e.g. textured active layers
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- 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
- H10F77/70—Surface textures, e.g. pyramid structures
- H10F77/707—Surface textures, e.g. pyramid structures of the substrates or of layers on substrates, e.g. textured ITO layer on a glass substrate
-
- 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
- Y02E10/547—Monocrystalline silicon PV 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 relates to a solar cell structure, particularly to a surface structure of a crystalline silicon solar cell.
- monocrystalline silicon atoms are periodically arranged according to a specified rule.
- silicon metal having a purity of 99.999999999% (totally 11 digits of “9” used to express the purity) is fused in a quartz crucible.
- a seed crystal is inserted into the liquid silicon, rotated at a speed of 2-20 rpm and slowly pulled up at a speed of 0.3-10 mm per minute to form a monocrystalline silicon ingot having a diameter of 4-8 inches.
- the abovementioned process is the so-called Czochralski method.
- the monocrystalline silicon-based solar cell has high efficiency and high reliability and has been widely used nowadays.
- Taiwan The fossil fuel power plants and nuclear power plants dominate power generation in Taiwan. Therefore, Taiwan relies on the imported coal and nuclear fuel very much. Recently, the price of petroleum is growing higher and higher. Further, the safety of nuclear power is concerned by people because the nuclear power plants have been too old to operate safely in Taiwan. In order to reduce the dependence on imported coal and nuclear power generation, Taiwan pays much attention to renewable energies now.
- Taiwan is a subtropical country having abundant sunshine. Further, Taiwan has mature semiconductor industry and plays a significant role in the global solar cell production. Therefore, Taiwan is very suitable to develop solar energy.
- the current solar cell fabrication process includes the following steps: using the RCA process to clean the surface of the substrate; patterning the surface of the substrate; using an acidic solution to clean the patterned surface; using a diffusion process to fabricate a P-type or N-type semiconductor layer on the surface of the substrate; etching the edges of the substrate having experienced the abovementioned diffusion process; removing the oxide on the surface of the substrate; fabricating an antireflection layer on the surface of the substrate; and fabricating metal electrodes on the substrate. Whether a P-type or N-type semiconductor layer is fabricated in the abovementioned diffusion process depends on the conductivity type of the substrate. However, a P-type doped silicon substrate is normally used as the substrate, and a high-temperature diffusion process is used to fabricate an N-type doped semiconductor layer.
- a solar cell fabrication process includes many different fabrication processes. It is very important for solar cells to increase the efficiency and decrease fabrication cost in the fabrication process. It is particularly critical to enhance the antireflection performance.
- the antireflection function is usually achieved via etching the surface with an acidic solution or fabricating an antireflection layer on the surface, which needs many fabrication processes and increases the fabrication cost.
- Metal electrodes are fabricated after the antireflection layer is completed. However, the fabrication of the metal electrodes would decrease the performance of the antireflection layer, which should decrease light utilization and efficiency of the solar cell.
- the present invention fabricates a microsphere-roughened antireflection structure after the metal electrodes have been done to avoid degrading the antireflection function and promote the efficiency of the crystalline silicon solar cell.
- the present invention proposes a solar cell structure comprising a P-type metal contact electrode; a P-type semiconductor layer; a P-type monocrystalline substrate; an N-type semiconductor layer; an N-type metal contact electrode; and a microsphere-roughened antireflection layer, wherein the N-type semiconductor layer and the P-type semiconductor layer are respectively arranged on an upper surface and a lower surface of the P-type monocrystalline substrate.
- the P-type metal contact electrode is disposed below the P-type semiconductor layer, and the N-type metal contact electrode has a specified pattern and is connected with the N-type semiconductor layer.
- the microsphere-roughened antireflection layer is arranged on an upper surface of the N-type semiconductor layer, which is not cover the N-type metal contact electrode.
- the solar cell structure of the present invention further comprises a surface passivation layer disposed on the upper surface of the N-type semiconductor layer.
- the N-type metal contact electrode passes through the surface passivation layer to connect with the N-type semiconductor layer.
- the surface passivation layer is fabricated on the upper surface of the N-type semiconductor layer beforehand; next, the N-type metal contact electrode having a specified pattern is fabricated on an upper surface of the surface passivation layer; next, a baking process is undertaken to let the N-type metal contact electrode pass through the surface passivation layer to connect with the N-type semiconductor layer; then, the microsphere-roughened antireflection layer is fabricated on the upper surface of the surface passivation layer without covering the N-type metal contact electrode.
- the surface passivation layer can provide very good protection function, and the microsphere-roughened antireflection layer can reduce sunlight reflection and increase the transmittance of sunlight.
- the fabrication of the microsphere-roughened antireflection layer is undertaken in the last step to avoid degrading the performance of the microsphere-roughened antireflection layer and promote the efficiency of the solar cell.
- FIG. 1 is a diagram schematically showing a solar cell structure according to one embodiment of the present invention
- FIG. 2A is a diagram schematically showing a semi-finished product of a solar cell structure according to one embodiment of the present invention.
- FIG. 2B is a diagram schematically showing another semi-finished product of a solar cell structure according to one embodiment of the present invention.
- the solar cell structure of the present invention comprises a P-type metal contact electrode 10 ; a P-type semiconductor layer 20 ; a P-type monocrystalline substrate 30 ; an N-type semiconductor layer 40 ; an N-type metal contact electrode 50 ; a surface passivation layer 60 ; and a microsphere-roughened antireflection layer 70 .
- the N-type semiconductor layer 40 and the P-type semiconductor layer 20 are respectively arranged on the upper surface and the lower surface of the P-type monocrystalline substrate 30 .
- the P-type metal contact electrode 10 is disposed below the P-type semiconductor layer 20 .
- the surface passivation layer 60 is disposed on the upper surface of the N-type semiconductor layer 40 .
- the N-type metal contact electrode 50 has a specified pattern and passes through the surface passivation layer 60 to connect with the N-type semiconductor layer 40 .
- the microsphere-roughened antireflection layer 70 is arranged on a portion of the upper surface of the surface passivation layer 60 which is free of the N-type metal contact electrode 50 . I.e., the microsphere-roughened antireflection layer 70 is arranged on the upper surface of the surface passivation layer 60 without covering the N-type metal contact electrode 50 .
- the upper surface of the P-type monocrystalline substrate 30 which contacts the N-type semiconductor layer 40 , is a serrated surface, so that the N-type semiconductor layer 40 , the surface passivation layer 60 and the microsphere-roughened antireflection layer 70 that are formed thereon also have a serrated shape, and whereby is enhanced the antireflection effect and increased the efficiency of the solar cell structure.
- a P-type monocrystalline substrate 30 In the fabrication of the solar cell structure of the present invention, provide a P-type monocrystalline substrate 30 firstly. Next, clean the P-type monocrystalline substrate 30 with acetone for 10 minutes. Next, clean the P-type monocrystalline substrate 30 with ethanol for 10 minutes. Next, clean the P-type monocrystalline substrate 30 with deionized water (DI water) for 10 minutes. Next, dry the P-type monocrystalline substrate 30 at a temperature of 100° C. for 10 minutes.
- DI water deionized water
- the spin-coating machine In the fabrication of the N-type semiconductor layer 40 on the P-type monocrystalline substrate 30 , use a spin-coating machine to spin-coat a phosphorus diffusion solution on the P-type monocrystalline substrate 30 uniformly to let the P-type monocrystalline substrate 30 coated with phosphorus.
- the spin-coating machine is set to respectively rotate at two different stages. During the first stage, the spin-coating machine rotates at a speed of 1000 rpm for 15 seconds. During the second stage, the spin-coating machine rotates at a speed of 3000 rpm for 20 seconds. Next, place the P-type monocrystalline substrate 30 in a high-temperature furnace tube filled with nitrogen, and bake the P-type monocrystalline substrate 30 at a temperature of 200° C.
- the upper surface of the P-type monocrystalline substrate 30 which is going to contact the N-type semiconductor layer 40 , is etched to form a serrated surface.
- the N-type semiconductor layer 40 , the surface passivation layer 60 and the microsphere-roughened antireflection layer 70 also have serrated surfaces.
- the spin-coating machine In the fabrication of the P-type semiconductor layer 20 on the P-type monocrystalline substrate 30 , use a spin-coating machine to spin-coat a boron diffusion solution on the P-type monocrystalline substrate 30 uniformly to let the P-type monocrystalline substrate 30 coated with boron.
- the spin-coating machine is set to respectively rotate at two different stages. During the first stage, the spin-coating machine rotates at a speed of 2000 rpm for 10 seconds. During the second stage, the spin-coating machine rotates at a speed of 3000 rpm for 20 seconds. Next, place the P-type monocrystalline substrate 30 in a high-temperature furnace tube filled with nitrogen, and bake the P-type monocrystalline substrate 30 at a temperature of 200° C.
- a sputtering system is used to deposit a hafnium dioxide (HfO 2 ) film, wherein the sputtering system is filled with 95% of argon and 5% of oxygen, and the pressure of a chamber of the sputtering system is controlled to 5 millitorr, and the radio frequency power for the sputtering system is controlled to 100-300 W for 4 minutes, whereby is obtained a surface passivation layer 60 having a thickness of about 80 nm.
- HfO 2 hafnium dioxide
- a thermal evaporation system is used to deposit aluminum having a thickness of about 150 nm on the upper surface of the surface passivation layer 60 to function as the N-type metal contact electrode 50 , as shown in FIG. 2A .
- a baking process is undertaken to let the N-type metal contact electrode 50 diffuse through the surface passivation layer 60 to connect with the N-type semiconductor layer 40 , as shown in FIG. 2B .
- a thermal evaporation system is used to deposit aluminum having a thickness of about 300 nm on the lower surface of the P-type semiconductor layer 20 to function as the P-type metal contact electrode 10 .
- a spin-coating machine is used to spin-coat a solution of silicon dioxide (SiO 2 ) particles which is a material of the microsphere-roughened antireflection layer 70 on the upper surface of the surface passivation layer 60 contacting the N-type metal contact electrode 50 .
- the spin-coating machine is set to respectively rotate at two different stages. During the first stage, the spin-coating machine rotates at a speed of 1000 rpm for 10 seconds. During the second stage, the spin-coating machine rotates at a speed of 1000-5000 rpm for 20-40 seconds. Then, the structure coated with the SiO 2 particles is placed in a high-temperature annealing furnace at a temperature of 300° C. for 10 minutes to enhance the cohesion of the crystalline structures inside the silicon dioxide particles.
- the present invention is characterized in fabricating a surface passivation layer and a microsphere-roughened antireflection layer in a solar cell to respectively provide a protection effect and increase transmittance of sunlight.
- the microsphere-roughened antireflection layer is fabricated after the P-type metal contact electrode and the N-type metal contact electrode have been done. Therefore, the present invention is superior in the antireflection function and able to promote the efficiency of solar cells.
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Abstract
Description
- The present invention relates to a solar cell structure, particularly to a surface structure of a crystalline silicon solar cell.
- In monocrystalline silicon, atoms are periodically arranged according to a specified rule. In fabricating monocrystalline silicon, silicon metal having a purity of 99.999999999% (totally 11 digits of “9” used to express the purity) is fused in a quartz crucible. Next, a seed crystal is inserted into the liquid silicon, rotated at a speed of 2-20 rpm and slowly pulled up at a speed of 0.3-10 mm per minute to form a monocrystalline silicon ingot having a diameter of 4-8 inches. The abovementioned process is the so-called Czochralski method. The monocrystalline silicon-based solar cell has high efficiency and high reliability and has been widely used nowadays.
- The fossil fuel power plants and nuclear power plants dominate power generation in Taiwan. Therefore, Taiwan relies on the imported coal and nuclear fuel very much. Recently, the price of petroleum is growing higher and higher. Further, the safety of nuclear power is worried by people because the nuclear power plants have been too old to operate safely in Taiwan. In order to reduce the dependence on imported coal and nuclear power generation, Taiwan pays much attention to renewable energies now.
- Taiwan is a subtropical country having abundant sunshine. Further, Taiwan has mature semiconductor industry and plays a significant role in the global solar cell production. Therefore, Taiwan is very suitable to develop solar energy.
- The current solar cell fabrication process includes the following steps: using the RCA process to clean the surface of the substrate; patterning the surface of the substrate; using an acidic solution to clean the patterned surface; using a diffusion process to fabricate a P-type or N-type semiconductor layer on the surface of the substrate; etching the edges of the substrate having experienced the abovementioned diffusion process; removing the oxide on the surface of the substrate; fabricating an antireflection layer on the surface of the substrate; and fabricating metal electrodes on the substrate. Whether a P-type or N-type semiconductor layer is fabricated in the abovementioned diffusion process depends on the conductivity type of the substrate. However, a P-type doped silicon substrate is normally used as the substrate, and a high-temperature diffusion process is used to fabricate an N-type doped semiconductor layer.
- From the abovementioned description, it is leaned that a solar cell fabrication process includes many different fabrication processes. It is very important for solar cells to increase the efficiency and decrease fabrication cost in the fabrication process. It is particularly critical to enhance the antireflection performance. The antireflection function is usually achieved via etching the surface with an acidic solution or fabricating an antireflection layer on the surface, which needs many fabrication processes and increases the fabrication cost. Metal electrodes are fabricated after the antireflection layer is completed. However, the fabrication of the metal electrodes would decrease the performance of the antireflection layer, which should decrease light utilization and efficiency of the solar cell.
- Considering the problems discussed above, the present invention fabricates a microsphere-roughened antireflection structure after the metal electrodes have been done to avoid degrading the antireflection function and promote the efficiency of the crystalline silicon solar cell.
- The present invention proposes a solar cell structure comprising a P-type metal contact electrode; a P-type semiconductor layer; a P-type monocrystalline substrate; an N-type semiconductor layer; an N-type metal contact electrode; and a microsphere-roughened antireflection layer, wherein the N-type semiconductor layer and the P-type semiconductor layer are respectively arranged on an upper surface and a lower surface of the P-type monocrystalline substrate. The P-type metal contact electrode is disposed below the P-type semiconductor layer, and the N-type metal contact electrode has a specified pattern and is connected with the N-type semiconductor layer. The microsphere-roughened antireflection layer is arranged on an upper surface of the N-type semiconductor layer, which is not cover the N-type metal contact electrode.
- In one embodiment, the solar cell structure of the present invention further comprises a surface passivation layer disposed on the upper surface of the N-type semiconductor layer. The N-type metal contact electrode passes through the surface passivation layer to connect with the N-type semiconductor layer. In fabrication, the surface passivation layer is fabricated on the upper surface of the N-type semiconductor layer beforehand; next, the N-type metal contact electrode having a specified pattern is fabricated on an upper surface of the surface passivation layer; next, a baking process is undertaken to let the N-type metal contact electrode pass through the surface passivation layer to connect with the N-type semiconductor layer; then, the microsphere-roughened antireflection layer is fabricated on the upper surface of the surface passivation layer without covering the N-type metal contact electrode.
- Thus, the surface passivation layer can provide very good protection function, and the microsphere-roughened antireflection layer can reduce sunlight reflection and increase the transmittance of sunlight. In the present, the fabrication of the microsphere-roughened antireflection layer is undertaken in the last step to avoid degrading the performance of the microsphere-roughened antireflection layer and promote the efficiency of the solar cell.
-
FIG. 1 is a diagram schematically showing a solar cell structure according to one embodiment of the present invention; -
FIG. 2A is a diagram schematically showing a semi-finished product of a solar cell structure according to one embodiment of the present invention; and -
FIG. 2B is a diagram schematically showing another semi-finished product of a solar cell structure according to one embodiment of the present invention. - The technical contents of the present invention will be demonstrated in detail with embodiments. However, it should be understood: the embodiments are only to exemplify the present invention but not to limit the scope of the present invention.
- Refer to
FIG. 1 . The solar cell structure of the present invention comprises a P-typemetal contact electrode 10; a P-type semiconductor layer 20; a P-typemonocrystalline substrate 30; an N-type semiconductor layer 40; an N-typemetal contact electrode 50; asurface passivation layer 60; and a microsphere-roughenedantireflection layer 70. The N-type semiconductor layer 40 and the P-type semiconductor layer 20 are respectively arranged on the upper surface and the lower surface of the P-typemonocrystalline substrate 30. The P-typemetal contact electrode 10 is disposed below the P-type semiconductor layer 20. Thesurface passivation layer 60 is disposed on the upper surface of the N-type semiconductor layer 40. The N-typemetal contact electrode 50 has a specified pattern and passes through thesurface passivation layer 60 to connect with the N-type semiconductor layer 40. The microsphere-roughenedantireflection layer 70 is arranged on a portion of the upper surface of thesurface passivation layer 60 which is free of the N-typemetal contact electrode 50. I.e., the microsphere-roughenedantireflection layer 70 is arranged on the upper surface of thesurface passivation layer 60 without covering the N-typemetal contact electrode 50. - In one embodiment, the upper surface of the P-
type monocrystalline substrate 30, which contacts the N-type semiconductor layer 40, is a serrated surface, so that the N-type semiconductor layer 40, thesurface passivation layer 60 and the microsphere-roughenedantireflection layer 70 that are formed thereon also have a serrated shape, and whereby is enhanced the antireflection effect and increased the efficiency of the solar cell structure. - In the fabrication of the solar cell structure of the present invention, provide a P-type
monocrystalline substrate 30 firstly. Next, clean the P-typemonocrystalline substrate 30 with acetone for 10 minutes. Next, clean the P-typemonocrystalline substrate 30 with ethanol for 10 minutes. Next, clean the P-typemonocrystalline substrate 30 with deionized water (DI water) for 10 minutes. Next, dry the P-typemonocrystalline substrate 30 at a temperature of 100° C. for 10 minutes. - In the fabrication of the N-
type semiconductor layer 40 on the P-typemonocrystalline substrate 30, use a spin-coating machine to spin-coat a phosphorus diffusion solution on the P-typemonocrystalline substrate 30 uniformly to let the P-typemonocrystalline substrate 30 coated with phosphorus. The spin-coating machine is set to respectively rotate at two different stages. During the first stage, the spin-coating machine rotates at a speed of 1000 rpm for 15 seconds. During the second stage, the spin-coating machine rotates at a speed of 3000 rpm for 20 seconds. Next, place the P-typemonocrystalline substrate 30 in a high-temperature furnace tube filled with nitrogen, and bake the P-typemonocrystalline substrate 30 at a temperature of 200° C. for 15 minutes to dry the organic materials of the phosphorus diffusion solution. Next, place the P-typemonocrystalline substrate 30 in a fast-annealing furnace. Next, evacuate the fast-annealing furnace to a pressure of below 100 millitorr. Next, fill the fast-annealing furnace with nitrogen and maintain the pressure of nitrogen at 4-6 torr. Next, anneal the P-type monocrystalline substrate 30 at a temperature of 950° C. for about 60 seconds. Thus is completed the fabrication of the N-type semiconductor layer 40. - Before the N-
type semiconductor layer 40 is fabricated on the P-type monocrystalline substrate 30, the upper surface of the P-type monocrystalline substrate 30, which is going to contact the N-type semiconductor layer 40, is etched to form a serrated surface. Thereby, the N-type semiconductor layer 40, thesurface passivation layer 60 and the microsphere-roughenedantireflection layer 70 also have serrated surfaces. - In the fabrication of the P-
type semiconductor layer 20 on the P-type monocrystalline substrate 30, use a spin-coating machine to spin-coat a boron diffusion solution on the P-type monocrystalline substrate 30 uniformly to let the P-type monocrystalline substrate 30 coated with boron. The spin-coating machine is set to respectively rotate at two different stages. During the first stage, the spin-coating machine rotates at a speed of 2000 rpm for 10 seconds. During the second stage, the spin-coating machine rotates at a speed of 3000 rpm for 20 seconds. Next, place the P-type monocrystalline substrate 30 in a high-temperature furnace tube filled with nitrogen, and bake the P-type monocrystalline substrate 30 at a temperature of 200° C. for 15 minutes to dry the organic materials of the boron diffusion solution. Next, place the P-type monocrystalline substrate 30 in a fast-annealing furnace. Next, evacuate the fast-annealing furnace to a pressure of below 100 millitorr. Next, fill the fast-annealing furnace with nitrogen and maintain the pressure of nitrogen at 4-6 torr. Next, anneal the P-type monocrystalline substrate 30 at a temperature of 950° C. for about 60 seconds. Thus is completed the fabrication of the P-type semiconductor layer 20. - In the fabrication of the
surface passivation layer 60, a sputtering system is used to deposit a hafnium dioxide (HfO2) film, wherein the sputtering system is filled with 95% of argon and 5% of oxygen, and the pressure of a chamber of the sputtering system is controlled to 5 millitorr, and the radio frequency power for the sputtering system is controlled to 100-300 W for 4 minutes, whereby is obtained asurface passivation layer 60 having a thickness of about 80 nm. - Refer to
FIG. 2A andFIG. 2B . In the fabrication of the N-typemetal contact electrode 50, a thermal evaporation system is used to deposit aluminum having a thickness of about 150 nm on the upper surface of thesurface passivation layer 60 to function as the N-typemetal contact electrode 50, as shown inFIG. 2A . After the deposition of the N-typemetal contact electrode 50, a baking process is undertaken to let the N-typemetal contact electrode 50 diffuse through thesurface passivation layer 60 to connect with the N-type semiconductor layer 40, as shown inFIG. 2B . - Similarly, in the fabrication of the P-type
metal contact electrode 10, a thermal evaporation system is used to deposit aluminum having a thickness of about 300 nm on the lower surface of the P-type semiconductor layer 20 to function as the P-typemetal contact electrode 10. - In the fabrication of the microsphere-roughened
antireflection layer 70, a spin-coating machine is used to spin-coat a solution of silicon dioxide (SiO2) particles which is a material of the microsphere-roughenedantireflection layer 70 on the upper surface of thesurface passivation layer 60 contacting the N-typemetal contact electrode 50. The spin-coating machine is set to respectively rotate at two different stages. During the first stage, the spin-coating machine rotates at a speed of 1000 rpm for 10 seconds. During the second stage, the spin-coating machine rotates at a speed of 1000-5000 rpm for 20-40 seconds. Then, the structure coated with the SiO2 particles is placed in a high-temperature annealing furnace at a temperature of 300° C. for 10 minutes to enhance the cohesion of the crystalline structures inside the silicon dioxide particles. - In conclusion, the present invention is characterized in fabricating a surface passivation layer and a microsphere-roughened antireflection layer in a solar cell to respectively provide a protection effect and increase transmittance of sunlight. In the present invention, the microsphere-roughened antireflection layer is fabricated after the P-type metal contact electrode and the N-type metal contact electrode have been done. Therefore, the present invention is superior in the antireflection function and able to promote the efficiency of solar cells.
Claims (8)
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