US20100275995A1 - Bifacial solar cells with back surface reflector - Google Patents
Bifacial solar cells with back surface reflector Download PDFInfo
- Publication number
- US20100275995A1 US20100275995A1 US12/456,398 US45639809A US2010275995A1 US 20100275995 A1 US20100275995 A1 US 20100275995A1 US 45639809 A US45639809 A US 45639809A US 2010275995 A1 US2010275995 A1 US 2010275995A1
- Authority
- US
- United States
- Prior art keywords
- back surface
- layer
- contact grid
- front surface
- depositing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Images
Classifications
-
- 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
- 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
- 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
- H10F10/148—Double-emitter photovoltaic cells, e.g. bifacial photovoltaic cells
-
- 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
-
- 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
- H10F77/206—Electrodes for devices having potential barriers
- H10F77/211—Electrodes for devices having potential barriers for photovoltaic 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
- Y02E10/547—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 generally to solar cells and, in particular, to an improved structure and manufacturing process for a bifacial solar cell.
- Bifacial solar cells may use any of a variety of different designs to achieve higher efficiencies than those typically obtained by a conventional, monofacial solar cell.
- One such design is shown in U.S. Pat. No. 5,665,175 which discloses a BSC configuration with first and second active regions formed on the front and back surfaces of the BSC, respectively, the two regions separated by a distance ⁇ .
- the distance ⁇ allows a leakage current to flow between the first and second active regions, thus allowing a solar cell panel utilizing such bifacial cells to continue to operate even if one or more individual solar cells become shaded or defective.
- U.S. Pat. No. 7,495,167 discloses an n + pp + structure and a method of producing the same.
- the p + layer formed by boron diffusion, exhibits a lifetime close to that of the initial level of the substrate.
- the '167 patent teaches that after phosphorous gettering, the cell must be annealed at a temperature of 600° C. or less for one hour or more.
- the cell then undergoes a final heat treatment step in which the cell is fired at a temperature of around 700° C. or less for one minute or less.
- U.S. Patent Application Publication No. 2005/0056312 discloses an alternative technique for achieving two or more p-n junctions in a single solar cell, the disclosed technique using transparent substrates (e.g., glass or quartz substrates).
- the BSC includes two thin-film polycrystalline or amorphous cells formed on opposing sides of a transparent substrate. Due to the design of the cell, the high temperature deposition of the absorber layers can be completed before the low temperature deposition of the window layers, thus avoiding degradation or destruction of the p-n junctions.
- the present invention provides a simplified manufacturing process and the resultant bifacial solar cell (BSC), the simplified manufacturing process reducing manufacturing costs.
- the BSC utilizes a combination of a back surface contact grid and an overlaid blanket metal reflector. Additionally, a doped amorphous silicon layer is interposed between the contact grid and the blanket layer.
- the manufacturing method is comprised of the steps of depositing a dopant of a first conductivity type onto the back surface of a silicon substrate to form a back surface doped region where the silicon substrate is of the same conductivity type as the dopant, depositing a back surface dielectric layer over the back surface doped region, forming an active area of a second conductivity type on the front surface of the silicon substrate, etching the active area, depositing a front surface passivation and AR dielectric layer onto the active area, applying and firing front and back surface contact grids, depositing a layer of doped amorphous silicon onto the back surface contact grid and the back surface dielectric, depositing a layer of metal over the doped amorphous silicon layer, and isolating the front active area.
- the method may further comprise the step of depositing a conductive interface layer between the doped amorphous silicon layer and the metal layer.
- a manufacturing method is provided that is comprised of the steps of depositing a boron doped layer onto the back surface of a p-type silicon substrate, depositing a back surface dielectric over the boron doped layer, diffusing phosphorous onto the front surface of the silicon substrate to form an n + layer and a front surface junction, removing the phosphor-silicate glass formed during the diffusion step (e.g., by etching with HF), depositing a front surface passivation and AR dielectric layer onto the n + layer, applying front and back surface contact grids, firing the front and back surface contact grids, depositing a boron doped layer of amorphous silicon onto the back surface grid and the back surface dielectric, depositing a metal layer onto the boron doped amorphous silicon layer, and isolating the front surface junction using, for example, a laser scriber.
- the method may further comprise the step of depositing a conductive interface layer, for example comprised of ITO or ZnO:Al, between the boron doped amorphous silicon layer and the metal layer.
- a conductive interface layer for example comprised of ITO or ZnO:Al
- the front and back surface contact grid firing steps may be performed simultaneously. Alternately, the back surface contact grid applying and firing steps may be performed prior to, or after, the front surface contact grid applying and firing steps.
- the boron doped layer depositing step can be formed by depositing a boron doped silicon dioxide layer using CVD, depositing a boron doped polysilicon layer using CVD, depositing a boron doped amorphous silicon layer using PE-CVD, spray coating a boric acid solution onto the back surface of the substrate, or spray/wipe coating a boron-doped spin-on glass onto the back surface of the substrate.
- the phosphorous diffusing step may be performed at a temperature of approximately 850° C. for a duration of approximately 10 to 20 minutes.
- the back surface dielectric depositing step may be performed after the step of applying the back surface contact grid.
- a bifacial solar cell is provided that is comprised of a silicon substrate of a first conductivity type with a front surface active region of a second conductivity type and a back surface doped region of the first conductivity type, dielectric layers deposited on the front surface active region and on the back surface doped region, a front surface contact grid applied to the front surface dielectric layer which alloys through the front surface dielectric to the active region during firing, a back surface contact grid applied to the back surface dielectric layer which alloys through the back surface dielectric to the back surface doped region during firing, an amorphous silicon layer doped with a dopant of a first conductivity type deposited on the back surface contact grid and back surface dielectric, and a blanket metal layer deposited on the doped amorphous silicon layer.
- the BSC may further comprise a groove on the front surface of the silicon substrate, the groove isolating the front surface junction.
- the BSC may further comprise a conductive interface layer, for example comprised of ITO or ZnO:Al, interposed between the doped amorphous silicon layer and the metal layer.
- the silicon substrate may be comprised of p-type silicon, the active region may be comprised of n + material resulting from a phosphorous diffusion step, and the doped region and the amorphous silicon layer may further comprise a boron dopant.
- the silicon substrate may be comprised of n-type silicon, the active region may be comprised of p + material resulting from a boron diffusion step, and the doped region and the amorphous silicon layer may further comprise a phosphorous dopant.
- the manufacturing method is comprised of the steps of forming an active area of a second conductivity type on the front surface of a silicon substrate of a first conductivity type, etching the front surface of the silicon substrate, depositing a front surface passivation and AR dielectric layer onto the active area, depositing a back surface dielectric layer over the back surface of the silicon substrate, applying and firing front and back surface contact grids, depositing a layer of doped amorphous silicon onto the back surface contact grid and the back surface dielectric, and depositing a layer of metal over the doped amorphous silicon layer.
- the method may further comprise the step of removing a back surface junction formed during the active area forming step.
- the method may further comprise the step of depositing a conductive interface layer between the doped amorphous silicon layer and the metal layer.
- the manufacturing method is comprised of the steps of diffusing phosphorous onto the front surface of a silicon substrate to form an n + layer and a front surface junction and onto the back surface to form a back surface junction, removing the phosphor-silicate glass formed during the diffusion step (e.g., by etching with HF), depositing a passivation and AR dielectric layer on the front surface and a back surface dielectric onto the back surface, applying and firing front and back surface contact grids, and depositing a metal layer onto the back surface contact grid and back surface dielectric.
- the front and back surface contact grid firing steps may be performed simultaneously.
- the back surface contact grid applying and firing steps may be performed prior to, or after, the front surface contact grid applying and firing steps.
- the method may further comprise the step of removing the back surface junction and isolating the front surface junction.
- a back surface metal grid may be applied, for example by screen printing or deposition using a shadow mask, after removing the back surface junction and prior to depositing the dielectric layer on the back surface.
- the back surface grid applying step may be performed after removing the back surface junction and prior to depositing the dielectric layer on the back surface.
- the manufacturing method is comprised of the steps of depositing a back surface dielectric onto the back surface of a silicon substrate of a first conductivity type, forming an active area of a second conductivity type on the front surface of the silicon substrate, etching the front surface of the silicon substrate, depositing a front surface passivation and AR dielectric layer onto the active area, applying and firing front and back surface contact grids, depositing a layer of doped amorphous silicon onto the back surface contact grid and the back surface dielectric, depositing a layer of metal over the doped amorphous silicon layer, and isolating the front surface junction, for example using a laser scriber.
- the method may further comprise the step of depositing a conductive interface layer between the doped amorphous silicon layer and the metal layer.
- the manufacturing method is comprised of the steps of depositing a dielectric layer on the back surface of a silicon substrate, diffusing phosphorous onto the front surface of the substrate to form an n + layer and a front surface junction, removing the phosphor-silicate glass formed during the diffusion step (e.g., by etching with HF), depositing a front surface passivation and AR dielectric layer, applying and firing front and back surface contact grids, depositing a boron doped layer of amorphous silicon onto the back surface contact grid and back surface dielectric, depositing a metal layer onto the boron doped amorphous silicon layer, and isolating the front surface junction, for example using a laser scriber.
- the method may further comprise the step of depositing a conductive interface layer, for example comprised of ITO or ZnO:Al, between the boron doped amorphous silicon layer and the metal layer.
- a conductive interface layer for example comprised of ITO or ZnO:Al
- the front and back surface contact grid firing steps may be performed simultaneously. Alternately, the back surface contact grid applying and firing steps may be performed prior to, or after, the front surface contact grid applying and firing steps.
- a bifacial solar cell (BSC) is provided that is comprised of a silicon substrate with a front surface active region of a first conductivity type, dielectric layers deposited on the front surface active region and on the back surface of the silicon substrate, a back surface contact grid applied to the back surface dielectric which alloys through the back surface dielectric to the back surface of the silicon substrate during firing, an amorphous silicon layer doped with a dopant of the first conductivity type deposited on the back surface contact grid and back surface dielectric, and a blanket metal layer deposited on the doped amorphous silicon layer.
- BSC bifacial solar cell
- the BSC may further comprise a conductive interface layer, for example comprised of ITO or ZnO:Al, interposed between the doped amorphous silicon layer and the metal layer.
- the silicon substrate may be comprised of p-type silicon, the active region may be comprised of n + material resulting from a phosphorous diffusion step, and the amorphous silicon layer may further comprise a boron dopant.
- the silicon substrate may be comprised of n-type silicon, the active region may be comprised of p + material resulting from a boron diffusion step, and the amorphous silicon layer may further comprise a phosphorous dopant.
- the BSC may further comprise a metal grid pattern deposited directly onto the back surface of the silicon substrate and interposed between the silicon substrate and the back surface dielectric layer.
- the BSC may further comprise a groove on the front surface of the silicon substrate, the groove isolating the front surface junction.
- FIG. 1 illustrates a preferred embodiment of a BSC in accordance with the invention
- FIG. 2 illustrates the process flow for the BSC of FIG. 1 ;
- FIG. 3 illustrates an alternate embodiment of the BSC of FIG. 1 ;
- FIG. 4 illustrates the process flow for the BSC of FIG. 3 ;
- FIG. 5 illustrates an alternate fabrication process for the BSC of FIG. 1 ;
- FIG. 6 illustrates an alternate preferred embodiment of a BSC in accordance with the invention
- FIG. 7 illustrates the process flow for the BSC of FIG. 6 ;
- FIG. 8 illustrates an alternate preferred embodiment of a BSC in accordance with the invention
- FIG. 9 illustrates the process flow for the BSC of FIG. 8 ;
- FIG. 10 illustrates an alternate fabrication process for the BSC of FIG. 6 ;
- FIG. 11 illustrates an alternate embodiment of the BSC of FIG. 8 .
- FIG. 12 illustrates the process flow for the BSC of FIG. 11 .
- a conventional mono-facial solar cell includes a grid-shaped electrode on the front surface and a solid electrode covering the entire back surface.
- the electrode structure is designed to allow light to enter not only from the front surface, but also from the back surface.
- the solid electrode covering the back surface in the mono-facial cell is replaced by a grid electrode in the BSC.
- the grid-shaped back surface electrode allows light, e.g., indirect light, to enter from the rear.
- bifacial solar cells are provided that combine a non-continuous, e.g., grid-shaped, back surface electrode with a back surface reflector, thereby obtaining the advantage of improved efficiency.
- FIG. 1 illustrates a cross-sectional view of a preferred BSC structure fabricated in accordance with the procedure described in FIG. 2 .
- Silicon substrate 101 may be of either p- or n-type. In the exemplary device and process illustrated in FIGS. 1 and 2 , a p-type substrate is used.
- substrate 101 is prepared using any of a variety of well-known substrate preparatory processes (step 201 ).
- saw and handling induced damage is removed via an etching process, for example using a nitric and hydrofluoric (HF) acid mixture.
- the bottom surface of substrate 101 is doped, thereby forming a back surface doped region 103 (step 203 ).
- region 103 is doped with the same doping type as substrate 101 . Increasing the doping level of region 103 , compared to substrate 101 , lowers the contact resistance. Additionally, doped region 103 reduces back surface recombination, a problem that is exacerbated by the inclusion of a back surface reflector.
- region 103 is doped with a different doping type than that of substrate 101 .
- Region 103 can be formed using any of a variety of techniques. Exemplary techniques include, but are not limited to, chemical vapor deposition (CVD), plasma enhanced CVD (PE-CVD), spray coating, and spin coating. Accordingly, and assuming a p-type substrate and a p-type region 103 , this region can be formed by depositing a boron doped polysilicon layer using CVD; depositing a boron doped silicon dioxide or amorphous silicon layer using PE-CVD; spray/spin coating a boric acid solution or doped spin-on glass onto the back surface of substrate 101 ; or by other means.
- CVD chemical vapor deposition
- PE-CVD plasma enhanced CVD
- spray coating and spin coating. Accordingly, and assuming a p-type substrate and a p-type region 103 , this region can be formed by depositing a boron doped polysilicon layer using CVD; depositing a boron doped silicon dioxide or amorphous silicon layer using PE-CVD
- a dielectric layer 105 is deposited on the back surface of substrate 101 , specifically on top of doped region 103 as shown (step 205 ).
- layer 105 is comprised of silicon nitride or silicon dioxide or a silicon dioxide/silicon nitride stack, preferably deposited using PE-CVD techniques at a temperature of 300° C. to 400° C., and has a thickness of approximately 76 nanometers for silicon nitride or 100 nanometers for silicon oxide.
- an active region of a conductivity type different from that of the substrate is formed on the front surface of substrate 101 .
- n + layer 107 is formed using phosphoryl chloride (POCl 3 ), where the diffusion is performed at a diffusion temperature in the range of 825° C. to 890° C., preferably at a temperature of approximately 850° C., for 10 to 20 minutes in a nitrogen atmosphere (step 207 ).
- POCl 3 phosphoryl chloride
- boron from region 103 is diffused into the back surface of substrate 101 to form a back surface field (BSF).
- the phosphor-silicate glass (PSG) formed during diffusion step 207 is then etched away, for example using a hydrofluoric (HF) etch at or near room temperature for 1 to 5 minutes (step 209 ).
- the front side junction has a depth of 0.3 to 0.6 microns and a surface doping concentration of about 8 ⁇ 10 21 /cm 3 .
- a front surface passivation and anti-reflection (AR) dielectric layer 109 is deposited, preferably comprised of silicon nitride or silicon oxynitride or a stack of materials of the silicon oxide/silicon nitride system.
- layer 109 is comprised of an approximately 76 nanometer thick layer of silicon nitride.
- layer 109 is comprised of approximately 10 nanometers of SiO 2 under 70 nanometers of Si 3 N 4 .
- layer 109 is deposited at a temperature of 300° C. to 400° C.
- contact grids are applied to the front and back surfaces of BSC 100 (step 213 ), for example using a screen printing process.
- front contact grid 111 is comprised of silver while back contact grid 113 is comprised of an aluminum-silver mixture.
- both the front and back contact grids are aligned and use the same contact size and spacing, with electrodes being approximately 100 microns wide, 15 microns thick and spaced approximately 2.5 millimeters apart.
- the back contact grid uses a finer spacing in order to lessen resistance losses from lateral current flow in the substrate.
- a contact firing step 215 is performed, preferably at a peak temperature of 750° C.
- the back reflector may be deposited directly over back surface dielectric layer 105 and contacts 113 , preferably a layer 115 of amorphous silicon is applied first to the back surface (step 217 ).
- Layer 115 is preferably thin to minimize infrared absorption and series resistance, on the order of 5 to 40 nanometers thick, and deposited using a technique such as PE-CVD.
- Layer 115 is heavily doped, preferably at a level of 10 19 /cm 3 or greater, with the same dopant type as substrate 101 , i.e., p-type dopant in exemplary structure which uses a p-type substrate.
- boron is used as the dopant.
- the blanket metal layer 117 is deposited on the back surface of the structure (step 219 ), metal layer 117 providing both a back surface reflector and means for making an electrical connection with contacts 113 .
- metal layer 117 is 1 to 10 microns thick, with a thinner layer preferred to minimize wafer bowing.
- layer 115 is transparent to the long wavelength photons that reach the reflective layer 117 .
- the front junction is isolated, for example using a laser scriber to form a groove on the front cell surface around the periphery of the cell (step 221 ).
- Blanket metal layer 117 is preferably deposited using either physical vapor deposition (PVD) or screen printing, although it will be appreciated that other techniques can be used.
- layer 117 has a high red reflectance, thus extending the photon path length in region 101 and increasing the absorption of photons with a wavelength near the bandgap.
- low cost metals are preferred, such as aluminum.
- silver bus bars, a nickel vanadium coating or other materials can be added to the back surface of layer 117 to further enable soldering of back contacts.
- FIGS. 3 and 4 illustrate an alternate embodiment utilizing a minor modification of the previously described device structure and process.
- a thin conductive interface layer 301 is added between silicon layer 115 and back surface reflector layer 117 (step 401 ).
- Layer 301 prevents the metal of layer 117 , e.g., aluminum, mixing with the silicon of layer 115 , thereby helping to maintain the high reflectivity of layer 117 .
- Exemplary materials for layer 301 include indium tin oxide (ITO) and aluminum-doped zinc oxide (ZnO:Al).
- the thickness of layer 301 is chosen to provide an optical match between the back surface and the metal layer 117 in the near infrared when taken in combination with the thickness of back surface dielectric layer 105 .
- the thickness of a ZnO:Al layer 301 should be approximately 35 nanometers thick.
- FIG. 5 illustrates an alternate process for fabricating cell 100 .
- the phosphorous is diffused into the front surface of substrate 101 (step 207 ) to create the n + layer 107 and the p-n junction, thereby skipping back surface dielectric deposition step 205 .
- the PSG is etched away (step 209 ) and front surface dielectric 109 is deposited (step 211 ).
- the front surface contacts 111 and the back surface contacts are then applied (step 213 ), followed by the deposition of back surface dielectric layer 105 (step 501 ).
- back surface dielectric layer 105 is preferably comprised of silicon nitride or silicon dioxide or a silicon dioxide/silicon nitride stack. If desired, the order of steps 211 , 213 and 501 can be altered, for example applying the back contact grid 113 first, followed by deposition of back surface dielectric layer 105 , followed by the application of the front contact grid 111 , and then followed by the deposition of the front surface dielectric layer 109 .
- amorphous silicon layer 115 is deposited (step 217 ), followed by the deposition of blanket reflective layer 117 (step 219 ), all as previously described.
- blanket reflective layer 117 if desired conductive interface layer 301 may be added between silicon layer 115 and back surface reflector layer 117 .
- FIGS. 6 and 7 illustrate an alternate embodiment that eliminates doped region 103 .
- front and back surface junctions are formed.
- phosphorous is diffused onto the front surface of substrate 101 as previously described, creating n + layer 107 and a p-n junction at the interface of substrate 101 and n + layer 107 (step 701 ).
- phosphorous is also diffused onto the back surface of substrate 101 , creating n + layer 601 and a floating junction.
- step 701 is performed using phosphoryl chloride (POCl 3 ) with a diffusion temperature in the range of 825° C.
- Active region diffusing step 701 is followed by a PSG (assuming phosphorous) etching step 209 , preferably using an HF etch at or near room temperature for 1 to 5 minutes.
- PSG assuming phosphorous
- a front surface passivation and anti-reflection (AR) dielectric layer 603 is deposited as well as a back surface passivation and AR dielectric layer 605 .
- layers 603 and 605 are comprised of silicon nitride with an index of refraction of 2.07 and a layer thickness of approximately 76 nanometers.
- layers 603 and 605 are comprised of silicon oxynitride.
- layers 603 and 605 are comprised of a stack of two layers of different composition, for example 10 nanometers of silicon dioxide and 70 nanometers of silicon nitride. Layers 603 and 605 are preferably deposited at a temperature of 300° C. to 400° C.
- front and back surface contact grids are applied (step 213 ) and fired (step 215 ), followed by deposition of blanket reflective layer 117 (step 219 ), all as previously described.
- preferably front contact grid 111 is comprised of silver while back contact grid 113 is comprised of aluminum.
- Contact firing step 215 is preferably performed at a peak temperature of 750° C. for 3 seconds in air.
- contacts 111 alloy through passivation and AR dielectric coating 603 to n + layer 107 .
- Contacts 113 alloy through passivation and AR dielectric coating 605 and back diffused layer 601 to form contact to substrate 101 .
- a diode forms between back diffused layer 601 and contact 113 so that current does not flow from the back diffused layer into the contact and the back diffusion is floating. This isolates the back surface from the bulk 101 since there is zero current into a floating junction.
- conductive interface layer 301 may be added between silicon layer 115 and back surface reflector layer 117 . This embodiment can also separate the contact grid deposition process and firing of the front and back surface contact grids as previously described.
- FIGS. 8 and 9 illustrate an alternate embodiment in which the floating junction on the back surface of the substrate is removed.
- the back surface of substrate 101 is etched (step 901 ), thereby removing the back surface junction and providing isolation for the front junction.
- step 901 uses an isotropic wet silicon etch such as a mixture of nitric acid and HF acid.
- the back surface contact grid is comprised of an aluminum-silver mixture.
- FIG. 10 illustrates an alternate process for fabricating cell 600 .
- dielectric layer 605 is applied to the back surface of substrate 101 (step 1001 ).
- dielectric layer 603 is comprised of silicon nitride or silicon oxynitride. Applying dielectric layer 605 prior to diffusing the front surface n + layer 107 (step 701 ) prevents the formation of a back surface junction.
- front surface passivation and AR dielectric layer 603 is deposited (step 1003 ), followed by applying (step 213 ) and firing (step 215 ) of the contact grids, deposition of amorphous silicon layer 115 (step 217 ), and deposition of back surface reflector 117 (step 219 ).
- the front junction is isolated, for example using a laser scriber to form a groove on the front cell surface around the periphery of the cell (step 1005 ).
- This embodiment may also include conductive interface layer 301 between silicon layer 115 and back surface reflector layer 117 and, additionally, may separate the contact grid deposition and firing of the front and back surface contact grids as previously described.
- FIGS. 11 and 12 illustrate a variation of BFC 800 .
- a metal grid 1101 is applied directly onto the back surface of cell 101 (step 1201 ), thereby reducing contact resistance.
- Step 1201 is preferably performed after the back surface of substrate 101 has been etched to remove the back surface junction and isolate the front junction (step 901 ).
- Step 1201 is performed using either a deposition process with a shadow mask, or using a screen printing process.
- metal grid 1101 is comprised of aluminum.
- contact grids 111 and 113 are applied and fired, either together or separately as previously described. Back surface contact grid 113 is registered to metal grid 1101 .
- contact grid 113 alloys to metal grid 1101 .
- amorphous silicon layer 115 is deposited (step 217 ), followed by the deposition of blanket reflective layer 117 (step 219 ), all as previously described.
- blanket reflective layer 117 step 219
- conductive interface layer 301 may be added between silicon layer 115 and back surface reflector layer 117 .
- the process eliminates the steps of applying and firing the back surface contact grid 113 .
- metal grid 1101 fires through the overlaid dielectric layer, thereby allowing metal layer 117 to connect to metal grid 1101 .
- an n-type substrate may also be used with the invention.
- an n-type dopant such as phosphorous
- a p-type dopant such as boron
- an n-type dopant e.g., phosphorous
- identical element symbols used on multiple figures refer to the same component/processing step, or components/processing steps of equal functionality.
Landscapes
- Photovoltaic Devices (AREA)
- Electrodes Of Semiconductors (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
Abstract
Description
- This application claims the benefit of the filing date of U.S. Provisional Patent Application Ser. No. 61/215,199, filed May 1, 2009, the disclosure of which is incorporated herein by reference for any and all purposes.
- The present invention relates generally to solar cells and, in particular, to an improved structure and manufacturing process for a bifacial solar cell.
- Bifacial solar cells (BSC) may use any of a variety of different designs to achieve higher efficiencies than those typically obtained by a conventional, monofacial solar cell. One such design is shown in U.S. Pat. No. 5,665,175 which discloses a BSC configuration with first and second active regions formed on the front and back surfaces of the BSC, respectively, the two regions separated by a distance λ. The distance λ allows a leakage current to flow between the first and second active regions, thus allowing a solar cell panel utilizing such bifacial cells to continue to operate even if one or more individual solar cells become shaded or defective.
- U.S. Pat. No. 7,495,167 discloses an n+pp+ structure and a method of producing the same. In the disclosed structure, the p+ layer, formed by boron diffusion, exhibits a lifetime close to that of the initial level of the substrate. In order to achieve this lifetime, the '167 patent teaches that after phosphorous gettering, the cell must be annealed at a temperature of 600° C. or less for one hour or more. In order to retain the lifetime recovered by the phosphorous and low-temperature born gettering steps, the cell then undergoes a final heat treatment step in which the cell is fired at a temperature of around 700° C. or less for one minute or less.
- U.S. Patent Application Publication No. 2005/0056312 discloses an alternative technique for achieving two or more p-n junctions in a single solar cell, the disclosed technique using transparent substrates (e.g., glass or quartz substrates). In one disclosed embodiment, the BSC includes two thin-film polycrystalline or amorphous cells formed on opposing sides of a transparent substrate. Due to the design of the cell, the high temperature deposition of the absorber layers can be completed before the low temperature deposition of the window layers, thus avoiding degradation or destruction of the p-n junctions.
- Although there are a variety of BSC designs and techniques for fabricating the same, these designs and techniques tend to be relatively complex, and thus expensive. Accordingly, what is needed is a solar cell design that achieves the benefits associated with bifacial solar cells while retaining the manufacturing simplicity of a monofacial solar cell. The present invention provides such a design.
- The present invention provides a simplified manufacturing process and the resultant bifacial solar cell (BSC), the simplified manufacturing process reducing manufacturing costs. In accordance with the invention, the BSC utilizes a combination of a back surface contact grid and an overlaid blanket metal reflector. Additionally, a doped amorphous silicon layer is interposed between the contact grid and the blanket layer.
- In one embodiment of the invention, the manufacturing method is comprised of the steps of depositing a dopant of a first conductivity type onto the back surface of a silicon substrate to form a back surface doped region where the silicon substrate is of the same conductivity type as the dopant, depositing a back surface dielectric layer over the back surface doped region, forming an active area of a second conductivity type on the front surface of the silicon substrate, etching the active area, depositing a front surface passivation and AR dielectric layer onto the active area, applying and firing front and back surface contact grids, depositing a layer of doped amorphous silicon onto the back surface contact grid and the back surface dielectric, depositing a layer of metal over the doped amorphous silicon layer, and isolating the front active area. The method may further comprise the step of depositing a conductive interface layer between the doped amorphous silicon layer and the metal layer.
- In at least one embodiment of the invention, a manufacturing method is provided that is comprised of the steps of depositing a boron doped layer onto the back surface of a p-type silicon substrate, depositing a back surface dielectric over the boron doped layer, diffusing phosphorous onto the front surface of the silicon substrate to form an n+ layer and a front surface junction, removing the phosphor-silicate glass formed during the diffusion step (e.g., by etching with HF), depositing a front surface passivation and AR dielectric layer onto the n+ layer, applying front and back surface contact grids, firing the front and back surface contact grids, depositing a boron doped layer of amorphous silicon onto the back surface grid and the back surface dielectric, depositing a metal layer onto the boron doped amorphous silicon layer, and isolating the front surface junction using, for example, a laser scriber. The method may further comprise the step of depositing a conductive interface layer, for example comprised of ITO or ZnO:Al, between the boron doped amorphous silicon layer and the metal layer. The front and back surface contact grid firing steps may be performed simultaneously. Alternately, the back surface contact grid applying and firing steps may be performed prior to, or after, the front surface contact grid applying and firing steps. The boron doped layer depositing step can be formed by depositing a boron doped silicon dioxide layer using CVD, depositing a boron doped polysilicon layer using CVD, depositing a boron doped amorphous silicon layer using PE-CVD, spray coating a boric acid solution onto the back surface of the substrate, or spray/wipe coating a boron-doped spin-on glass onto the back surface of the substrate. The phosphorous diffusing step may be performed at a temperature of approximately 850° C. for a duration of approximately 10 to 20 minutes. The back surface dielectric depositing step may be performed after the step of applying the back surface contact grid.
- In at least one embodiment of the invention, a bifacial solar cell (BSC) is provided that is comprised of a silicon substrate of a first conductivity type with a front surface active region of a second conductivity type and a back surface doped region of the first conductivity type, dielectric layers deposited on the front surface active region and on the back surface doped region, a front surface contact grid applied to the front surface dielectric layer which alloys through the front surface dielectric to the active region during firing, a back surface contact grid applied to the back surface dielectric layer which alloys through the back surface dielectric to the back surface doped region during firing, an amorphous silicon layer doped with a dopant of a first conductivity type deposited on the back surface contact grid and back surface dielectric, and a blanket metal layer deposited on the doped amorphous silicon layer. The BSC may further comprise a groove on the front surface of the silicon substrate, the groove isolating the front surface junction. The BSC may further comprise a conductive interface layer, for example comprised of ITO or ZnO:Al, interposed between the doped amorphous silicon layer and the metal layer. The silicon substrate may be comprised of p-type silicon, the active region may be comprised of n+ material resulting from a phosphorous diffusion step, and the doped region and the amorphous silicon layer may further comprise a boron dopant. The silicon substrate may be comprised of n-type silicon, the active region may be comprised of p+ material resulting from a boron diffusion step, and the doped region and the amorphous silicon layer may further comprise a phosphorous dopant.
- In at least one embodiment of the invention, the manufacturing method is comprised of the steps of forming an active area of a second conductivity type on the front surface of a silicon substrate of a first conductivity type, etching the front surface of the silicon substrate, depositing a front surface passivation and AR dielectric layer onto the active area, depositing a back surface dielectric layer over the back surface of the silicon substrate, applying and firing front and back surface contact grids, depositing a layer of doped amorphous silicon onto the back surface contact grid and the back surface dielectric, and depositing a layer of metal over the doped amorphous silicon layer. The method may further comprise the step of removing a back surface junction formed during the active area forming step. The method may further comprise the step of depositing a conductive interface layer between the doped amorphous silicon layer and the metal layer.
- In at least one embodiment of the invention, the manufacturing method is comprised of the steps of diffusing phosphorous onto the front surface of a silicon substrate to form an n+ layer and a front surface junction and onto the back surface to form a back surface junction, removing the phosphor-silicate glass formed during the diffusion step (e.g., by etching with HF), depositing a passivation and AR dielectric layer on the front surface and a back surface dielectric onto the back surface, applying and firing front and back surface contact grids, and depositing a metal layer onto the back surface contact grid and back surface dielectric. The front and back surface contact grid firing steps may be performed simultaneously. Alternately, the back surface contact grid applying and firing steps may be performed prior to, or after, the front surface contact grid applying and firing steps. The method may further comprise the step of removing the back surface junction and isolating the front surface junction. A back surface metal grid may be applied, for example by screen printing or deposition using a shadow mask, after removing the back surface junction and prior to depositing the dielectric layer on the back surface. The back surface grid applying step may be performed after removing the back surface junction and prior to depositing the dielectric layer on the back surface.
- In at least one embodiment of the invention, the manufacturing method is comprised of the steps of depositing a back surface dielectric onto the back surface of a silicon substrate of a first conductivity type, forming an active area of a second conductivity type on the front surface of the silicon substrate, etching the front surface of the silicon substrate, depositing a front surface passivation and AR dielectric layer onto the active area, applying and firing front and back surface contact grids, depositing a layer of doped amorphous silicon onto the back surface contact grid and the back surface dielectric, depositing a layer of metal over the doped amorphous silicon layer, and isolating the front surface junction, for example using a laser scriber. The method may further comprise the step of depositing a conductive interface layer between the doped amorphous silicon layer and the metal layer.
- In at least one embodiment of the invention, the manufacturing method is comprised of the steps of depositing a dielectric layer on the back surface of a silicon substrate, diffusing phosphorous onto the front surface of the substrate to form an n+ layer and a front surface junction, removing the phosphor-silicate glass formed during the diffusion step (e.g., by etching with HF), depositing a front surface passivation and AR dielectric layer, applying and firing front and back surface contact grids, depositing a boron doped layer of amorphous silicon onto the back surface contact grid and back surface dielectric, depositing a metal layer onto the boron doped amorphous silicon layer, and isolating the front surface junction, for example using a laser scriber. The method may further comprise the step of depositing a conductive interface layer, for example comprised of ITO or ZnO:Al, between the boron doped amorphous silicon layer and the metal layer. The front and back surface contact grid firing steps may be performed simultaneously. Alternately, the back surface contact grid applying and firing steps may be performed prior to, or after, the front surface contact grid applying and firing steps.
- In at least one embodiment of the invention, a bifacial solar cell (BSC) is provided that is comprised of a silicon substrate with a front surface active region of a first conductivity type, dielectric layers deposited on the front surface active region and on the back surface of the silicon substrate, a back surface contact grid applied to the back surface dielectric which alloys through the back surface dielectric to the back surface of the silicon substrate during firing, an amorphous silicon layer doped with a dopant of the first conductivity type deposited on the back surface contact grid and back surface dielectric, and a blanket metal layer deposited on the doped amorphous silicon layer. The BSC may further comprise a conductive interface layer, for example comprised of ITO or ZnO:Al, interposed between the doped amorphous silicon layer and the metal layer. The silicon substrate may be comprised of p-type silicon, the active region may be comprised of n+ material resulting from a phosphorous diffusion step, and the amorphous silicon layer may further comprise a boron dopant. The silicon substrate may be comprised of n-type silicon, the active region may be comprised of p+ material resulting from a boron diffusion step, and the amorphous silicon layer may further comprise a phosphorous dopant. The BSC may further comprise a metal grid pattern deposited directly onto the back surface of the silicon substrate and interposed between the silicon substrate and the back surface dielectric layer. The BSC may further comprise a groove on the front surface of the silicon substrate, the groove isolating the front surface junction.
- A further understanding of the nature and advantages of the present invention may be realized by reference to the remaining portions of the specification and the drawings.
-
FIG. 1 illustrates a preferred embodiment of a BSC in accordance with the invention; -
FIG. 2 illustrates the process flow for the BSC ofFIG. 1 ; -
FIG. 3 illustrates an alternate embodiment of the BSC ofFIG. 1 ; -
FIG. 4 illustrates the process flow for the BSC ofFIG. 3 ; -
FIG. 5 illustrates an alternate fabrication process for the BSC ofFIG. 1 ; -
FIG. 6 illustrates an alternate preferred embodiment of a BSC in accordance with the invention; -
FIG. 7 illustrates the process flow for the BSC ofFIG. 6 ; -
FIG. 8 illustrates an alternate preferred embodiment of a BSC in accordance with the invention; -
FIG. 9 illustrates the process flow for the BSC ofFIG. 8 ; -
FIG. 10 illustrates an alternate fabrication process for the BSC ofFIG. 6 ; -
FIG. 11 illustrates an alternate embodiment of the BSC ofFIG. 8 ; and -
FIG. 12 illustrates the process flow for the BSC ofFIG. 11 . - A conventional mono-facial solar cell includes a grid-shaped electrode on the front surface and a solid electrode covering the entire back surface. In contrast, in a conventional bifacial solar cell (BSC), the electrode structure is designed to allow light to enter not only from the front surface, but also from the back surface. As such, the solid electrode covering the back surface in the mono-facial cell is replaced by a grid electrode in the BSC. In such a cell, the grid-shaped back surface electrode allows light, e.g., indirect light, to enter from the rear. Additionally, such a design provides improved efficiency due to the decreased contact area of the grid-shaped back surface electrode. In accordance with the present invention, bifacial solar cells are provided that combine a non-continuous, e.g., grid-shaped, back surface electrode with a back surface reflector, thereby obtaining the advantage of improved efficiency.
-
FIG. 1 illustrates a cross-sectional view of a preferred BSC structure fabricated in accordance with the procedure described inFIG. 2 .Silicon substrate 101 may be of either p- or n-type. In the exemplary device and process illustrated inFIGS. 1 and 2 , a p-type substrate is used. - Initially,
substrate 101 is prepared using any of a variety of well-known substrate preparatory processes (step 201). In general, duringstep 201 saw and handling induced damage is removed via an etching process, for example using a nitric and hydrofluoric (HF) acid mixture. After substrate preparation, the bottom surface ofsubstrate 101 is doped, thereby forming a back surface doped region 103 (step 203). Preferablyregion 103 is doped with the same doping type assubstrate 101. Increasing the doping level ofregion 103, compared tosubstrate 101, lowers the contact resistance. Additionally, dopedregion 103 reduces back surface recombination, a problem that is exacerbated by the inclusion of a back surface reflector. In at least one embodiment of the invention,region 103 is doped with a different doping type than that ofsubstrate 101. -
Region 103 can be formed using any of a variety of techniques. Exemplary techniques include, but are not limited to, chemical vapor deposition (CVD), plasma enhanced CVD (PE-CVD), spray coating, and spin coating. Accordingly, and assuming a p-type substrate and a p-type region 103, this region can be formed by depositing a boron doped polysilicon layer using CVD; depositing a boron doped silicon dioxide or amorphous silicon layer using PE-CVD; spray/spin coating a boric acid solution or doped spin-on glass onto the back surface ofsubstrate 101; or by other means. - After formation of
region 103, adielectric layer 105 is deposited on the back surface ofsubstrate 101, specifically on top of dopedregion 103 as shown (step 205). Preferablylayer 105 is comprised of silicon nitride or silicon dioxide or a silicon dioxide/silicon nitride stack, preferably deposited using PE-CVD techniques at a temperature of 300° C. to 400° C., and has a thickness of approximately 76 nanometers for silicon nitride or 100 nanometers for silicon oxide. Next, an active region of a conductivity type different from that of the substrate is formed on the front surface ofsubstrate 101. For example, assuming a p-type substrate, duringstep 207 phosphorous is diffused onto the front surface ofsubstrate 101, creating n+ layer 107 and a p-n junction at the interface ofsubstrate 101 and n+ layer 107. Preferably n+ layer 107 is formed using phosphoryl chloride (POCl3), where the diffusion is performed at a diffusion temperature in the range of 825° C. to 890° C., preferably at a temperature of approximately 850° C., for 10 to 20 minutes in a nitrogen atmosphere (step 207). It will be appreciated that during thephosphorous diffusion step 207, boron fromregion 103 is diffused into the back surface ofsubstrate 101 to form a back surface field (BSF). The phosphor-silicate glass (PSG) formed duringdiffusion step 207 is then etched away, for example using a hydrofluoric (HF) etch at or near room temperature for 1 to 5 minutes (step 209). In the preferred embodiment, the front side junction has a depth of 0.3 to 0.6 microns and a surface doping concentration of about 8×1021/cm3. - In
step 211, a front surface passivation and anti-reflection (AR)dielectric layer 109 is deposited, preferably comprised of silicon nitride or silicon oxynitride or a stack of materials of the silicon oxide/silicon nitride system. In one embodiment,layer 109 is comprised of an approximately 76 nanometer thick layer of silicon nitride. In another embodiment,layer 109 is comprised of approximately 10 nanometers of SiO2 under 70 nanometers of Si3N4. Preferably,layer 109 is deposited at a temperature of 300° C. to 400° C. - After deposition of the
dielectric layer 109, contact grids are applied to the front and back surfaces of BSC 100 (step 213), for example using a screen printing process. In the exemplary embodiment,front contact grid 111 is comprised of silver whileback contact grid 113 is comprised of an aluminum-silver mixture. In the preferred embodiment, both the front and back contact grids are aligned and use the same contact size and spacing, with electrodes being approximately 100 microns wide, 15 microns thick and spaced approximately 2.5 millimeters apart. In at least one alternate embodiment, the back contact grid uses a finer spacing in order to lessen resistance losses from lateral current flow in the substrate. Next, acontact firing step 215 is performed, preferably at a peak temperature of 750° C. for 3 seconds in air. As a result of this process,contacts 111 alloy through passivation and ARdielectric coating 109 to n+ layer 107. Similarly,contacts 113 alloy throughdielectric coating 105 tolayer 103. It should be understood that either a single firing step can be performed as shown, or the front surface and back surface contact grids can be applied and fired separately, thereby allowing different firing conditions to be used for each grid. - Although the back reflector may be deposited directly over back
surface dielectric layer 105 andcontacts 113, preferably alayer 115 of amorphous silicon is applied first to the back surface (step 217).Layer 115 is preferably thin to minimize infrared absorption and series resistance, on the order of 5 to 40 nanometers thick, and deposited using a technique such as PE-CVD.Layer 115 is heavily doped, preferably at a level of 1019/cm3 or greater, with the same dopant type assubstrate 101, i.e., p-type dopant in exemplary structure which uses a p-type substrate. For the exemplary embodiment, boron is used as the dopant. Lastly, theblanket metal layer 117 is deposited on the back surface of the structure (step 219),metal layer 117 providing both a back surface reflector and means for making an electrical connection withcontacts 113. Typicallylayer 117 is 1 to 10 microns thick, with a thinner layer preferred to minimize wafer bowing. Given the bandgap of amorphous silicon, i.e., 1.75 eV,layer 115 is transparent to the long wavelength photons that reach thereflective layer 117. Lastly, the front junction is isolated, for example using a laser scriber to form a groove on the front cell surface around the periphery of the cell (step 221). -
Blanket metal layer 117 is preferably deposited using either physical vapor deposition (PVD) or screen printing, although it will be appreciated that other techniques can be used. Preferably,layer 117 has a high red reflectance, thus extending the photon path length inregion 101 and increasing the absorption of photons with a wavelength near the bandgap. Additionally, low cost metals are preferred, such as aluminum. Although not shown, silver bus bars, a nickel vanadium coating or other materials can be added to the back surface oflayer 117 to further enable soldering of back contacts. -
FIGS. 3 and 4 illustrate an alternate embodiment utilizing a minor modification of the previously described device structure and process. Instructure 300, a thinconductive interface layer 301 is added betweensilicon layer 115 and back surface reflector layer 117 (step 401).Layer 301 prevents the metal oflayer 117, e.g., aluminum, mixing with the silicon oflayer 115, thereby helping to maintain the high reflectivity oflayer 117. Exemplary materials forlayer 301 include indium tin oxide (ITO) and aluminum-doped zinc oxide (ZnO:Al). Optimally, the thickness oflayer 301 is chosen to provide an optical match between the back surface and themetal layer 117 in the near infrared when taken in combination with the thickness of backsurface dielectric layer 105. Thus, for example, iflayer 105 is 50 nanometers thick, then the thickness of a ZnO:Al layer 301 should be approximately 35 nanometers thick. -
FIG. 5 illustrates an alternate process for fabricatingcell 100. In this process, after the formation of region 103 (step 203), the phosphorous is diffused into the front surface of substrate 101 (step 207) to create the n+ layer 107 and the p-n junction, thereby skipping back surfacedielectric deposition step 205. Next, the PSG is etched away (step 209) andfront surface dielectric 109 is deposited (step 211). Thefront surface contacts 111 and the back surface contacts are then applied (step 213), followed by the deposition of back surface dielectric layer 105 (step 501). As previously noted, backsurface dielectric layer 105 is preferably comprised of silicon nitride or silicon dioxide or a silicon dioxide/silicon nitride stack. If desired, the order ofsteps back contact grid 113 first, followed by deposition of backsurface dielectric layer 105, followed by the application of thefront contact grid 111, and then followed by the deposition of the frontsurface dielectric layer 109. - After firing the front and back surface contact grids (step 215),
amorphous silicon layer 115 is deposited (step 217), followed by the deposition of blanket reflective layer 117 (step 219), all as previously described. Although not shown, if desiredconductive interface layer 301 may be added betweensilicon layer 115 and backsurface reflector layer 117. -
FIGS. 6 and 7 illustrate an alternate embodiment that eliminates dopedregion 103. In this embodiment, aftersubstrate preparation step 201, front and back surface junctions are formed. Assuming the p-type substrate of the exemplary embodiments, phosphorous is diffused onto the front surface ofsubstrate 101 as previously described, creating n+ layer 107 and a p-n junction at the interface ofsubstrate 101 and n+ layer 107 (step 701). Duringstep 701, phosphorous is also diffused onto the back surface ofsubstrate 101, creating n+ layer 601 and a floating junction. Preferably step 701 is performed using phosphoryl chloride (POCl3) with a diffusion temperature in the range of 825° C. to 890° C., preferably at a temperature of approximately 850° C., for 10 to 20 minutes in a nitrogen atmosphere. Activeregion diffusing step 701 is followed by a PSG (assuming phosphorous)etching step 209, preferably using an HF etch at or near room temperature for 1 to 5 minutes. - In
step 703, a front surface passivation and anti-reflection (AR)dielectric layer 603 is deposited as well as a back surface passivation and ARdielectric layer 605. In an exemplary embodiment, layers 603 and 605 are comprised of silicon nitride with an index of refraction of 2.07 and a layer thickness of approximately 76 nanometers. In an alternate embodiment, layers 603 and 605 are comprised of silicon oxynitride. In another alternate embodiment, layers 603 and 605 are comprised of a stack of two layers of different composition, for example 10 nanometers of silicon dioxide and 70 nanometers of silicon nitride.Layers - Next, the front and back surface contact grids are applied (step 213) and fired (step 215), followed by deposition of blanket reflective layer 117 (step 219), all as previously described. In this embodiment, preferably
front contact grid 111 is comprised of silver whileback contact grid 113 is comprised of aluminum. Contact firingstep 215 is preferably performed at a peak temperature of 750° C. for 3 seconds in air. As a result of this process,contacts 111 alloy through passivation and ARdielectric coating 603 to n+ layer 107.Contacts 113 alloy through passivation and ARdielectric coating 605 and back diffusedlayer 601 to form contact tosubstrate 101. As aluminum is a p-type dopant, a diode forms between back diffusedlayer 601 and contact 113 so that current does not flow from the back diffused layer into the contact and the back diffusion is floating. This isolates the back surface from thebulk 101 since there is zero current into a floating junction. Although not shown inFIGS. 6 and 7 , if desiredconductive interface layer 301 may be added betweensilicon layer 115 and backsurface reflector layer 117. This embodiment can also separate the contact grid deposition process and firing of the front and back surface contact grids as previously described. -
FIGS. 8 and 9 illustrate an alternate embodiment in which the floating junction on the back surface of the substrate is removed. Instructure 800, after formation of the front junction and PSG etching, the back surface ofsubstrate 101 is etched (step 901), thereby removing the back surface junction and providing isolation for the front junction. In a preferred embodiment, step 901 uses an isotropic wet silicon etch such as a mixture of nitric acid and HF acid. After removal of the back surface floating junction, the process continues as previously described relative toFIGS. 6 and 7 . Preferably in this embodiment the back surface contact grid is comprised of an aluminum-silver mixture. -
FIG. 10 illustrates an alternate process for fabricatingcell 600. In this process, after preparation of substrate 101 (step 201),dielectric layer 605 is applied to the back surface of substrate 101 (step 1001). As previously described, preferablydielectric layer 603 is comprised of silicon nitride or silicon oxynitride. Applyingdielectric layer 605 prior to diffusing the front surface n+ layer 107 (step 701) prevents the formation of a back surface junction. After the front surface diffusion (step 701) and the PSG etch (step 209), front surface passivation and ARdielectric layer 603 is deposited (step 1003), followed by applying (step 213) and firing (step 215) of the contact grids, deposition of amorphous silicon layer 115 (step 217), and deposition of back surface reflector 117 (step 219). Lastly, the front junction is isolated, for example using a laser scriber to form a groove on the front cell surface around the periphery of the cell (step 1005). This embodiment may also includeconductive interface layer 301 betweensilicon layer 115 and backsurface reflector layer 117 and, additionally, may separate the contact grid deposition and firing of the front and back surface contact grids as previously described. -
FIGS. 11 and 12 illustrate a variation ofBFC 800. As shown in the BFC cross-sectional view ofBFC 1100, ametal grid 1101 is applied directly onto the back surface of cell 101 (step 1201), thereby reducing contact resistance.Step 1201 is preferably performed after the back surface ofsubstrate 101 has been etched to remove the back surface junction and isolate the front junction (step 901).Step 1201 is performed using either a deposition process with a shadow mask, or using a screen printing process. Preferably,metal grid 1101 is comprised of aluminum. After depositingdielectric layers 603 and 605 (step 703),contact grids surface contact grid 113 is registered tometal grid 1101. During the firing step,contact grid 113 alloys tometal grid 1101. Next,amorphous silicon layer 115 is deposited (step 217), followed by the deposition of blanket reflective layer 117 (step 219), all as previously described. Although not shown, if desiredconductive interface layer 301 may be added betweensilicon layer 115 and backsurface reflector layer 117. - In an alternate embodiment of that described above relative to
FIGS. 11 and 12 , the process eliminates the steps of applying and firing the backsurface contact grid 113. In this embodiment,metal grid 1101 fires through the overlaid dielectric layer, thereby allowingmetal layer 117 to connect tometal grid 1101. - As previously noted, an n-type substrate may also be used with the invention. In such an embodiment, an n-type dopant, such as phosphorous, is used in those regions which were previously described as using a p-type dopant such as boron. Similarly, in those regions which previously used a p-type dopant (e.g., boron), an n-type dopant (e.g., phosphorous) is used. Lastly, it should be understood that identical element symbols used on multiple figures refer to the same component/processing step, or components/processing steps of equal functionality.
- As will be understood by those familiar with the art, the present invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. Accordingly, the disclosures and descriptions herein are intended to be illustrative, but not limiting, of the scope of the invention.
Claims (62)
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/456,398 US20100275995A1 (en) | 2009-05-01 | 2009-06-15 | Bifacial solar cells with back surface reflector |
PCT/US2010/001175 WO2010126572A2 (en) | 2009-05-01 | 2010-04-19 | Bifacial solar cells with back surface reflector |
JP2012508467A JP2012525703A (en) | 2009-05-01 | 2010-04-19 | Double-sided solar cell with back reflector |
EP10770047.8A EP2425457A4 (en) | 2009-05-01 | 2010-04-19 | BIFACEE SOLAR CELLS COMPRISING A REAR FACE REFLECTOR |
CN201080019116XA CN102549765A (en) | 2009-05-01 | 2010-04-19 | Bifacial solar cells with back surface reflector |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US21519909P | 2009-05-01 | 2009-05-01 | |
US12/456,398 US20100275995A1 (en) | 2009-05-01 | 2009-06-15 | Bifacial solar cells with back surface reflector |
Publications (1)
Publication Number | Publication Date |
---|---|
US20100275995A1 true US20100275995A1 (en) | 2010-11-04 |
Family
ID=43029508
Family Applications (5)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US12/456,398 Abandoned US20100275995A1 (en) | 2009-05-01 | 2009-06-15 | Bifacial solar cells with back surface reflector |
US12/456,378 Expired - Fee Related US8298850B2 (en) | 2009-05-01 | 2009-06-15 | Bifacial solar cells with overlaid back grid surface |
US12/456,404 Expired - Fee Related US8404970B2 (en) | 2009-05-01 | 2009-06-15 | Bifacial solar cells with back surface doping |
US13/662,242 Abandoned US20130056061A1 (en) | 2009-05-01 | 2012-10-26 | Bifacial solar cells with overlaid back grid surface |
US13/849,813 Abandoned US20130217169A1 (en) | 2009-05-01 | 2013-03-25 | Bifacial solar cells with back surface doping |
Family Applications After (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US12/456,378 Expired - Fee Related US8298850B2 (en) | 2009-05-01 | 2009-06-15 | Bifacial solar cells with overlaid back grid surface |
US12/456,404 Expired - Fee Related US8404970B2 (en) | 2009-05-01 | 2009-06-15 | Bifacial solar cells with back surface doping |
US13/662,242 Abandoned US20130056061A1 (en) | 2009-05-01 | 2012-10-26 | Bifacial solar cells with overlaid back grid surface |
US13/849,813 Abandoned US20130217169A1 (en) | 2009-05-01 | 2013-03-25 | Bifacial solar cells with back surface doping |
Country Status (5)
Country | Link |
---|---|
US (5) | US20100275995A1 (en) |
EP (3) | EP2425455A4 (en) |
JP (3) | JP2012525702A (en) |
CN (3) | CN102668114A (en) |
WO (3) | WO2010126572A2 (en) |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100275984A1 (en) * | 2009-05-01 | 2010-11-04 | Calisolar, Inc. | Bifacial solar cells with back surface doping |
US20120048365A1 (en) * | 2010-08-27 | 2012-03-01 | Daeyong Lee | Solar cell and manufacturing method thereof |
US20120318345A1 (en) * | 2011-06-20 | 2012-12-20 | Yoonsil Jin | Solar cell |
US20130133741A1 (en) * | 2010-10-05 | 2013-05-30 | Mitsubishi Electric Corporation | Photovoltaic device and manufacturing method thereof |
US20130139881A1 (en) * | 2010-10-20 | 2013-06-06 | Mitsubishi Electric Corporation | Photovoltaic device and manufacturing method thereof |
US20130199606A1 (en) * | 2012-02-06 | 2013-08-08 | Applied Materials, Inc. | Methods of manufacturing back surface field and metallized contacts on a solar cell device |
CN103247715A (en) * | 2012-02-10 | 2013-08-14 | 信越化学工业株式会社 | Solar cell and method of manufacturing the same |
US20140057413A1 (en) * | 2012-08-23 | 2014-02-27 | Michael Xiaoxuan Yang | Methods for fabricating devices on semiconductor substrates |
US20140158193A1 (en) * | 2011-08-09 | 2014-06-12 | Solexel, Inc. | Structures and methods of formation of contiguous and non-contiguous base regions for high efficiency back-contact solar cells |
US20140230894A1 (en) * | 2012-02-29 | 2014-08-21 | Bakersun | Bifacial crystalline silicon solar panel with reflector |
WO2016122731A1 (en) * | 2015-01-26 | 2016-08-04 | 1366 Technologies, Inc. | Method for creating a semiconductor wafer having profiled doping and wafers and solar cell components having a profiled field, such as drift and back surface |
CN107104161A (en) * | 2012-02-29 | 2017-08-29 | 贝克阳光公司 | Two-sided crystal silicon solar plate with reflector |
US11145509B2 (en) | 2019-05-24 | 2021-10-12 | Applied Materials, Inc. | Method for forming and patterning a layer and/or substrate |
US11189739B1 (en) * | 2020-11-19 | 2021-11-30 | Jinko Green Energy (shanghai) Management Co., Ltd. | Solar cell |
Families Citing this family (40)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102247785B1 (en) * | 2009-09-18 | 2021-05-20 | 신에쓰 가가꾸 고교 가부시끼가이샤 | Solar cell, method for manufacturing solar cell, and solar cell module |
TW201121066A (en) * | 2009-12-14 | 2011-06-16 | Ind Tech Res Inst | Bificial solar cell |
DE102010025983A1 (en) * | 2010-03-03 | 2011-09-08 | Centrotherm Photovoltaics Ag | Solar cell with dielectric backside mirroring and process for its production |
KR101661768B1 (en) | 2010-09-03 | 2016-09-30 | 엘지전자 주식회사 | Solar cell and manufacturing method thereof |
KR101699300B1 (en) * | 2010-09-27 | 2017-01-24 | 엘지전자 주식회사 | Solar cell and manufacturing method thereof |
KR20120084104A (en) * | 2011-01-19 | 2012-07-27 | 엘지전자 주식회사 | Solar cell |
CN102169923B (en) * | 2011-03-05 | 2013-03-27 | 常州天合光能有限公司 | Method for passivating P-type doping layer of N-type silicon solar cell and cell structure |
KR101699299B1 (en) | 2011-03-29 | 2017-01-24 | 엘지전자 주식회사 | Bifacial solar cell |
KR101103501B1 (en) * | 2011-05-30 | 2012-01-09 | 한화케미칼 주식회사 | Solar cell and manufacturing method thereof |
TWI584485B (en) * | 2011-10-29 | 2017-05-21 | 西瑪奈米技術以色列有限公司 | a network aligned on a substrate |
CN102437238A (en) * | 2011-11-30 | 2012-05-02 | 晶澳(扬州)太阳能科技有限公司 | Method for boron doping of crystalline silicon solar cell |
CN102437246B (en) * | 2011-12-20 | 2013-12-25 | 日地太阳能电力股份有限公司 | Preparation method of crystalline silicon solar cell |
KR101776874B1 (en) * | 2011-12-21 | 2017-09-08 | 엘지전자 주식회사 | Solar cell |
KR101838278B1 (en) * | 2011-12-23 | 2018-03-13 | 엘지전자 주식회사 | Solar cell |
KR101329855B1 (en) * | 2012-01-31 | 2013-11-14 | 현대중공업 주식회사 | Method for fabricating bi-facial solar cell |
KR101335082B1 (en) * | 2012-02-01 | 2013-12-03 | 현대중공업 주식회사 | Method for fabricating bi-facial solar cell |
KR20130096822A (en) | 2012-02-23 | 2013-09-02 | 엘지전자 주식회사 | Solar cell and method for manufacturing the same |
KR20140022515A (en) * | 2012-08-13 | 2014-02-25 | 엘지전자 주식회사 | Solar cell |
CN103633157B (en) * | 2012-08-24 | 2016-03-09 | 财团法人工业技术研究院 | Solar cell and solar cell module |
TWI484115B (en) * | 2012-08-31 | 2015-05-11 | George Uh-Schu Liau | A photovoltaic case |
KR101372305B1 (en) * | 2012-09-21 | 2014-03-14 | 영남대학교 산학협력단 | Solar cell and the fabrication method thereof |
US20140238478A1 (en) * | 2013-02-28 | 2014-08-28 | Suniva, Inc. | Back junction solar cell with enhanced emitter layer |
EP4092764A1 (en) | 2013-04-03 | 2022-11-23 | Lg Electronics Inc. | Solar cell |
US20140361407A1 (en) * | 2013-06-05 | 2014-12-11 | SCHMID Group | Silicon material substrate doping method, structure and applications |
CN103367545A (en) * | 2013-07-08 | 2013-10-23 | 浙江晶科能源有限公司 | Method for synchronously implementing local contact and local doping at back of solar cell by utilizing laser |
US10217893B2 (en) * | 2013-09-16 | 2019-02-26 | Special Materials Research And Technology, Inc. (Specmat) | Methods, apparatus, and systems for passivation of solar cells and other semiconductor devices |
KR101627028B1 (en) * | 2014-02-20 | 2016-06-03 | 제일모직주식회사 | The method for preparing the bifacial solar cell |
KR101627029B1 (en) * | 2014-02-20 | 2016-06-03 | 제일모직주식회사 | The method for preparing the ibc solar cell |
DE102014105358A1 (en) * | 2014-04-15 | 2015-10-15 | Solarworld Innovations Gmbh | Solar cell and method for producing a solar cell |
US20160072000A1 (en) * | 2014-09-05 | 2016-03-10 | David D. Smith | Front contact heterojunction process |
CN105405924B (en) * | 2014-11-28 | 2017-11-03 | 南昌大学 | A kind of preparation method of the high square resistance doping crystal silicon layer of crystal silica-based solar cell |
CN106159022B (en) * | 2015-03-27 | 2018-03-27 | 比亚迪股份有限公司 | A kind of crystal silicon solar cell sheet and preparation method thereof |
US9525081B1 (en) * | 2015-12-28 | 2016-12-20 | Inventec Solar Energy Corporation | Method of forming a bifacial solar cell structure |
US10741703B2 (en) | 2016-07-29 | 2020-08-11 | Sunpower Corporation | Shingled solar cells overlapping along non-linear edges |
CN106876519A (en) * | 2017-01-20 | 2017-06-20 | 广东爱康太阳能科技有限公司 | A kind of alundum (Al2O3) is passivated the two-sided crystal silicon solar batteries preparation method of N-type |
CN107910398B (en) * | 2017-10-12 | 2020-08-04 | 环晟光伏(江苏)有限公司 | Manufacturing method of P-type PERC double-sided solar cell |
CN107946390A (en) * | 2017-12-04 | 2018-04-20 | 孙健春 | It is a kind of that there is the solar cell and production method for changing power grid |
CN109545886B (en) * | 2018-10-22 | 2020-08-25 | 浙江光隆能源科技股份有限公司 | Preparation method of half-chip polycrystalline solar cell |
AU2020284180A1 (en) * | 2019-05-29 | 2022-01-27 | Solaround Ltd. | Bifacial photovoltaic cell manufacturing process |
TWI718703B (en) * | 2019-10-09 | 2021-02-11 | 長生太陽能股份有限公司 | Solar cell and manufacturing method thereof |
Citations (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4468853A (en) * | 1982-05-13 | 1984-09-04 | Tokyo Shibaura Denki Kabushiki Kaisha | Method of manufacturing a solar cell |
US4994879A (en) * | 1988-11-25 | 1991-02-19 | Agency Of Industrial Science & Technology | Photoelectric transducer with light path of increased length |
US5665175A (en) * | 1990-05-30 | 1997-09-09 | Safir; Yakov | Bifacial solar cell |
US6096968A (en) * | 1995-03-10 | 2000-08-01 | Siemens Solar Gmbh | Solar cell with a back-surface field |
US20040063326A1 (en) * | 2002-07-01 | 2004-04-01 | Interuniversitair Microelektronica Centrum (Imec) | Semiconductor etching paste and the use thereof for localized etching of semiconductor substrates |
US20050016585A1 (en) * | 2001-11-26 | 2005-01-27 | Adolf Munzer | Manufacturing a solar cell with backside contacts |
US20050022863A1 (en) * | 2003-06-20 | 2005-02-03 | Guido Agostinelli | Method for backside surface passivation of solar cells and solar cells with such passivation |
US20050056312A1 (en) * | 2003-03-14 | 2005-03-17 | Young David L. | Bifacial structure for tandem solar cells |
US20050133084A1 (en) * | 2003-10-10 | 2005-06-23 | Toshio Joge | Silicon solar cell and production method thereof |
US20070137699A1 (en) * | 2005-12-16 | 2007-06-21 | General Electric Company | Solar cell and method for fabricating solar cell |
US20070175508A1 (en) * | 2005-11-08 | 2007-08-02 | Lg Chem, Ltd. | Solar cell of high efficiency and process for preparation of the same |
US20080257399A1 (en) * | 2007-04-19 | 2008-10-23 | Industrial Technology Research Institute | Bifacial thin film solar cell and method for making the same |
US20090211627A1 (en) * | 2008-02-25 | 2009-08-27 | Suniva, Inc. | Solar cell having crystalline silicon p-n homojunction and amorphous silicon heterojunctions for surface passivation |
US20100027598A1 (en) * | 2007-02-13 | 2010-02-04 | Yusuke Kanahashi | Software radio transceiver |
US20100275983A1 (en) * | 2009-05-01 | 2010-11-04 | Calisolar, Inc. | Bifacial solar cells with overlaid back grid surface |
US20120000517A1 (en) * | 2008-02-25 | 2012-01-05 | Ju-Hwan Yun | Solar cell and method for manufacturing the same |
Family Cites Families (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4166919A (en) * | 1978-09-25 | 1979-09-04 | Rca Corporation | Amorphous silicon solar cell allowing infrared transmission |
DE3815512C2 (en) * | 1988-05-06 | 1994-07-28 | Deutsche Aerospace | Solar cell and process for its manufacture |
JP2994735B2 (en) * | 1990-11-27 | 1999-12-27 | シャープ株式会社 | Solar cell |
JPH08111537A (en) * | 1994-10-07 | 1996-04-30 | Sharp Corp | Solar battery |
JP3342339B2 (en) * | 1997-02-28 | 2002-11-05 | 三洋電機株式会社 | Semiconductor integrated circuit and method of manufacturing the same |
JP2999985B2 (en) * | 1997-11-25 | 2000-01-17 | シャープ株式会社 | Solar cell |
JP2000138386A (en) * | 1998-11-04 | 2000-05-16 | Shin Etsu Chem Co Ltd | Solar cell manufacturing method and solar cell manufactured by this method |
JP2001044470A (en) * | 1999-07-30 | 2001-02-16 | Hitachi Ltd | Solar cell, method of manufacturing solar cell, and concentrating solar cell module |
JP4812147B2 (en) * | 1999-09-07 | 2011-11-09 | 株式会社日立製作所 | Manufacturing method of solar cell |
JP2002076400A (en) * | 2000-08-30 | 2002-03-15 | Shin Etsu Handotai Co Ltd | Solar cell and method for manufacturing solar cell |
JP2002198546A (en) * | 2000-12-27 | 2002-07-12 | Kyocera Corp | Method of forming solar cell element |
JP2002353475A (en) * | 2001-05-29 | 2002-12-06 | Kyocera Corp | Solar cell element |
JP2003209271A (en) * | 2002-01-16 | 2003-07-25 | Hitachi Ltd | Solar cell and method of manufacturing the same |
JP4593980B2 (en) * | 2004-03-29 | 2010-12-08 | 京セラ株式会社 | Photoelectric conversion device, solar cell element using the same, and solar cell module |
EP1763086A1 (en) * | 2005-09-09 | 2007-03-14 | Interuniversitair Micro-Elektronica Centrum | Photovoltaic cell with thick silicon oxide and silicon nitride passivation and fabrication method |
US7375378B2 (en) * | 2005-05-12 | 2008-05-20 | General Electric Company | Surface passivated photovoltaic devices |
US7824579B2 (en) * | 2005-06-07 | 2010-11-02 | E. I. Du Pont De Nemours And Company | Aluminum thick film composition(s), electrode(s), semiconductor device(s) and methods of making thereof |
JP2007096040A (en) * | 2005-09-29 | 2007-04-12 | Sharp Corp | Solar cell and method of manufacturing solar cell |
US20070107773A1 (en) | 2005-11-17 | 2007-05-17 | Palo Alto Research Center Incorporated | Bifacial cell with extruded gridline metallization |
CN101336465B (en) * | 2005-11-24 | 2011-07-06 | 新南创新私人有限公司 | Low area screen printed metal contact structure and method |
NL2000248C2 (en) | 2006-09-25 | 2008-03-26 | Ecn Energieonderzoek Ct Nederl | Process for the production of crystalline silicon solar cells with improved surface passivation. |
US20110132423A1 (en) * | 2006-10-11 | 2011-06-09 | Gamma Solar | Photovoltaic solar module comprising bifacial solar cells |
DE102007012277A1 (en) * | 2007-03-08 | 2008-09-11 | Gebr. Schmid Gmbh & Co. | Process for producing a solar cell and solar cell produced therewith |
JP2009059833A (en) * | 2007-08-31 | 2009-03-19 | Hitachi Ltd | Solar cell |
CN100573928C (en) * | 2007-10-08 | 2009-12-23 | 苏州阿特斯阳光电力科技有限公司 | A kind of phosphorus diffusion method of making solar cell |
WO2009052511A2 (en) * | 2007-10-18 | 2009-04-23 | Belano Holdings, Ltd. | Mono-silicon solar cells |
-
2009
- 2009-06-15 US US12/456,398 patent/US20100275995A1/en not_active Abandoned
- 2009-06-15 US US12/456,378 patent/US8298850B2/en not_active Expired - Fee Related
- 2009-06-15 US US12/456,404 patent/US8404970B2/en not_active Expired - Fee Related
-
2010
- 2010-04-19 CN CN2010800190909A patent/CN102668114A/en active Pending
- 2010-04-19 WO PCT/US2010/001175 patent/WO2010126572A2/en active Application Filing
- 2010-04-19 JP JP2012508466A patent/JP2012525702A/en active Pending
- 2010-04-19 JP JP2012508467A patent/JP2012525703A/en active Pending
- 2010-04-19 EP EP10770045.2A patent/EP2425455A4/en not_active Withdrawn
- 2010-04-19 EP EP10770047.8A patent/EP2425457A4/en not_active Withdrawn
- 2010-04-19 WO PCT/US2010/001174 patent/WO2010126571A2/en active Application Filing
- 2010-04-19 JP JP2012508465A patent/JP2012525701A/en active Pending
- 2010-04-19 CN CN201080019116XA patent/CN102549765A/en active Pending
- 2010-04-19 CN CN2010800190896A patent/CN102656704A/en active Pending
- 2010-04-19 WO PCT/US2010/001173 patent/WO2010126570A2/en active Application Filing
- 2010-04-19 EP EP10770046.0A patent/EP2425456A4/en not_active Withdrawn
-
2012
- 2012-10-26 US US13/662,242 patent/US20130056061A1/en not_active Abandoned
-
2013
- 2013-03-25 US US13/849,813 patent/US20130217169A1/en not_active Abandoned
Patent Citations (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4468853A (en) * | 1982-05-13 | 1984-09-04 | Tokyo Shibaura Denki Kabushiki Kaisha | Method of manufacturing a solar cell |
US4994879A (en) * | 1988-11-25 | 1991-02-19 | Agency Of Industrial Science & Technology | Photoelectric transducer with light path of increased length |
US5665175A (en) * | 1990-05-30 | 1997-09-09 | Safir; Yakov | Bifacial solar cell |
US6096968A (en) * | 1995-03-10 | 2000-08-01 | Siemens Solar Gmbh | Solar cell with a back-surface field |
US20050016585A1 (en) * | 2001-11-26 | 2005-01-27 | Adolf Munzer | Manufacturing a solar cell with backside contacts |
US20040063326A1 (en) * | 2002-07-01 | 2004-04-01 | Interuniversitair Microelektronica Centrum (Imec) | Semiconductor etching paste and the use thereof for localized etching of semiconductor substrates |
US20050056312A1 (en) * | 2003-03-14 | 2005-03-17 | Young David L. | Bifacial structure for tandem solar cells |
US20050022863A1 (en) * | 2003-06-20 | 2005-02-03 | Guido Agostinelli | Method for backside surface passivation of solar cells and solar cells with such passivation |
US20050133084A1 (en) * | 2003-10-10 | 2005-06-23 | Toshio Joge | Silicon solar cell and production method thereof |
US7495167B2 (en) * | 2003-10-10 | 2009-02-24 | Hitachi, Ltd. | Silicon solar cell and production method thereof |
US20070175508A1 (en) * | 2005-11-08 | 2007-08-02 | Lg Chem, Ltd. | Solar cell of high efficiency and process for preparation of the same |
US20070137699A1 (en) * | 2005-12-16 | 2007-06-21 | General Electric Company | Solar cell and method for fabricating solar cell |
US20100027598A1 (en) * | 2007-02-13 | 2010-02-04 | Yusuke Kanahashi | Software radio transceiver |
US20080257399A1 (en) * | 2007-04-19 | 2008-10-23 | Industrial Technology Research Institute | Bifacial thin film solar cell and method for making the same |
US20090211627A1 (en) * | 2008-02-25 | 2009-08-27 | Suniva, Inc. | Solar cell having crystalline silicon p-n homojunction and amorphous silicon heterojunctions for surface passivation |
US20120000517A1 (en) * | 2008-02-25 | 2012-01-05 | Ju-Hwan Yun | Solar cell and method for manufacturing the same |
US20100275983A1 (en) * | 2009-05-01 | 2010-11-04 | Calisolar, Inc. | Bifacial solar cells with overlaid back grid surface |
US8298850B2 (en) * | 2009-05-01 | 2012-10-30 | Silicor Materials Inc. | Bifacial solar cells with overlaid back grid surface |
US20130056061A1 (en) * | 2009-05-01 | 2013-03-07 | Silicor Material Inc. | Bifacial solar cells with overlaid back grid surface |
US8404970B2 (en) * | 2009-05-01 | 2013-03-26 | Silicor Materials Inc. | Bifacial solar cells with back surface doping |
Non-Patent Citations (1)
Title |
---|
Kim et al. "Advanced front and rear metallization for thin and high efficiency crystalline silicon solar cells". Presentation 2CV.4.15. 22nd European photovoltaic solar energy conference and exhibition, Milan, 2007. * |
Cited By (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100275984A1 (en) * | 2009-05-01 | 2010-11-04 | Calisolar, Inc. | Bifacial solar cells with back surface doping |
US20100275983A1 (en) * | 2009-05-01 | 2010-11-04 | Calisolar, Inc. | Bifacial solar cells with overlaid back grid surface |
US8298850B2 (en) | 2009-05-01 | 2012-10-30 | Silicor Materials Inc. | Bifacial solar cells with overlaid back grid surface |
US8404970B2 (en) * | 2009-05-01 | 2013-03-26 | Silicor Materials Inc. | Bifacial solar cells with back surface doping |
US20120048365A1 (en) * | 2010-08-27 | 2012-03-01 | Daeyong Lee | Solar cell and manufacturing method thereof |
US10121915B2 (en) * | 2010-08-27 | 2018-11-06 | Lg Electronics Inc. | Solar cell and manufacturing method thereof |
US20130133741A1 (en) * | 2010-10-05 | 2013-05-30 | Mitsubishi Electric Corporation | Photovoltaic device and manufacturing method thereof |
US20130139881A1 (en) * | 2010-10-20 | 2013-06-06 | Mitsubishi Electric Corporation | Photovoltaic device and manufacturing method thereof |
US20120318345A1 (en) * | 2011-06-20 | 2012-12-20 | Yoonsil Jin | Solar cell |
US20140158193A1 (en) * | 2011-08-09 | 2014-06-12 | Solexel, Inc. | Structures and methods of formation of contiguous and non-contiguous base regions for high efficiency back-contact solar cells |
US20130199606A1 (en) * | 2012-02-06 | 2013-08-08 | Applied Materials, Inc. | Methods of manufacturing back surface field and metallized contacts on a solar cell device |
US9871156B2 (en) * | 2012-02-10 | 2018-01-16 | Shin-Etsu Chemical Co., Ltd. | Solar cell and method of manufacturing the same |
CN103247715A (en) * | 2012-02-10 | 2013-08-14 | 信越化学工业株式会社 | Solar cell and method of manufacturing the same |
US20130206229A1 (en) * | 2012-02-10 | 2013-08-15 | Shin-Etsu Chemical Co., Ltd. | Solar cell and method of manufacturing the same |
US20220278246A1 (en) * | 2012-02-29 | 2022-09-01 | Bakersun | Bifacial crystalline silicon solar panel with reflector |
US20140230894A1 (en) * | 2012-02-29 | 2014-08-21 | Bakersun | Bifacial crystalline silicon solar panel with reflector |
US9379270B2 (en) * | 2012-02-29 | 2016-06-28 | Bakersun | Bifacial crystalline silicon solar panel with reflector |
CN107104161A (en) * | 2012-02-29 | 2017-08-29 | 贝克阳光公司 | Two-sided crystal silicon solar plate with reflector |
US9196503B2 (en) * | 2012-08-23 | 2015-11-24 | Michael Xiaoxuan Yang | Methods for fabricating devices on semiconductor substrates |
US20140057413A1 (en) * | 2012-08-23 | 2014-02-27 | Michael Xiaoxuan Yang | Methods for fabricating devices on semiconductor substrates |
WO2016122731A1 (en) * | 2015-01-26 | 2016-08-04 | 1366 Technologies, Inc. | Method for creating a semiconductor wafer having profiled doping and wafers and solar cell components having a profiled field, such as drift and back surface |
US10439095B2 (en) | 2015-01-26 | 2019-10-08 | 1366 Technologies, Inc. | Methods for creating a semiconductor wafer having profiled doping and wafers and solar cell components having a profiled field, such as drift and back surface |
US10770613B2 (en) | 2015-01-26 | 2020-09-08 | 1366 Technologies Inc. | Methods for creating a semiconductor wafer having profiled doping and wafers and solar cell components having a profiled field, such as drift and back surface |
US11145509B2 (en) | 2019-05-24 | 2021-10-12 | Applied Materials, Inc. | Method for forming and patterning a layer and/or substrate |
US12183578B2 (en) | 2019-05-24 | 2024-12-31 | Applied Materials, Inc. | Method for forming and patterning a layer and/or substrate |
US11189739B1 (en) * | 2020-11-19 | 2021-11-30 | Jinko Green Energy (shanghai) Management Co., Ltd. | Solar cell |
US11990555B2 (en) | 2020-11-19 | 2024-05-21 | Jinko Green Energy (shanghai) Management Co., Ltd. | Solar cell |
Also Published As
Publication number | Publication date |
---|---|
EP2425457A4 (en) | 2013-07-24 |
EP2425456A4 (en) | 2013-07-31 |
CN102668114A (en) | 2012-09-12 |
WO2010126571A3 (en) | 2011-01-20 |
EP2425456A2 (en) | 2012-03-07 |
US20130217169A1 (en) | 2013-08-22 |
JP2012525703A (en) | 2012-10-22 |
US20100275983A1 (en) | 2010-11-04 |
CN102549765A (en) | 2012-07-04 |
US8404970B2 (en) | 2013-03-26 |
US20100275984A1 (en) | 2010-11-04 |
US8298850B2 (en) | 2012-10-30 |
US20130056061A1 (en) | 2013-03-07 |
WO2010126571A2 (en) | 2010-11-04 |
EP2425455A4 (en) | 2013-08-07 |
JP2012525701A (en) | 2012-10-22 |
WO2010126570A2 (en) | 2010-11-04 |
JP2012525702A (en) | 2012-10-22 |
EP2425457A2 (en) | 2012-03-07 |
WO2010126572A2 (en) | 2010-11-04 |
EP2425455A2 (en) | 2012-03-07 |
CN102656704A (en) | 2012-09-05 |
WO2010126572A3 (en) | 2011-01-27 |
WO2010126570A3 (en) | 2011-02-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20100275995A1 (en) | Bifacial solar cells with back surface reflector | |
US20250006851A1 (en) | Front contact solar cell with formed emitter | |
JP3722326B2 (en) | Manufacturing method of solar cell | |
US10658529B2 (en) | Solar cell and manufacturing method thereof | |
US20090260681A1 (en) | Solar cell and method for manufacturing the same | |
KR101225978B1 (en) | Sollar Cell And Fabrication Method Thereof | |
WO2013039158A1 (en) | Solar cell module | |
JP2008529265A (en) | Semiconductor device having heterojunction and interfinger structure | |
WO2011093360A1 (en) | Process for production of back-electrode-type solar cell, back-electrode-type solar cell, and back-electrode-type solar cell module | |
JP4486622B2 (en) | Manufacturing method of solar cell | |
KR20190079622A (en) | Method for manufacturing high photoelectric conversion efficiency solar cell and high photoelectric conversion efficiency solar cell | |
KR101321538B1 (en) | Bulk silicon solar cell and method for producing same | |
JP2005167291A (en) | Method for manufacturing solar cell and method for manufacturing semiconductor device | |
KR20160034062A (en) | Solar cell and method for manufacturing the same | |
KR20120021793A (en) | Solar cell and method for manufacturing the same | |
KR101976753B1 (en) | Solar cell manufacturing method and solar cell | |
KR20130113002A (en) | Selective emitter solar cells and fabrication method using acid solution protection layer |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: CALISOLAR, INC., CALIFORNIA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:KAES, MARTIN;BORDEN, PETER;OUNADJELA, KAMEL;AND OTHERS;SIGNING DATES FROM 20090611 TO 20090613;REEL/FRAME:022880/0419 |
|
AS | Assignment |
Owner name: GOLD HILL CAPITAL 2008, LP, CALIFORNIA Free format text: SECURITY AGREEMENT;ASSIGNOR:CALISOLAR INC.;REEL/FRAME:027119/0928 Effective date: 20111025 |
|
AS | Assignment |
Owner name: SILICON VALLEY BANK, CALIFORNIA Free format text: SECURITY AGREEMENT;ASSIGNOR:CALISOLAR INC.;REEL/FRAME:027131/0042 Effective date: 20111025 |
|
AS | Assignment |
Owner name: SILICOR MATERIALS INC., CALIFORNIA Free format text: CHANGE OF NAME;ASSIGNOR:CALISOLAR INC.;REEL/FRAME:029397/0001 Effective date: 20120223 |
|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |
|
AS | Assignment |
Owner name: SILICOR MARTERIALS, INC. FKA CALISOLAR INC., CALIF Free format text: RELEASE;ASSIGNOR:SILICON VALLEY BANK;REEL/FRAME:036448/0613 Effective date: 20150812 |