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.
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.
Initially, substrate 101 is prepared using any of a variety of well-known substrate preparatory processes (step 201). In general, during step 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 of substrate 101 is doped, thereby forming a back surface doped region 103 (step 203). Preferably 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. In at least one embodiment of the invention, 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.
After formation of region 103, a dielectric layer 105 is deposited on the back surface of substrate 101, specifically on top of doped region 103 as shown (step 205). Preferably 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. Next, an active region of a conductivity type different from that of the substrate is formed on the front surface of substrate 101. For example, assuming a p-type substrate, during step 207 phosphorous is diffused onto the front surface of substrate 101, creating n+ layer 107 and a p-n junction at the interface of substrate 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 the phosphorous diffusion step 207, 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). 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 while back 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, a contact 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 AR dielectric coating 109 to n+ layer 107. Similarly, contacts 113 alloy through dielectric coating 105 to layer 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 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 1019/cm3 or greater, with the same dopant type as substrate 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, 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. Typically layer 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 the reflective 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 in region 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 of layer 117 to further enable soldering of back contacts.
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 desired conductive interface layer 301 may be added between silicon layer 115 and back surface reflector layer 117.
In step 703, 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. 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 603 and 605 are preferably deposited at a temperature of 300° C. to 400° C.
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 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. As a result of this process, 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. As aluminum is a p-type dopant, 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. Although not shown in
In an alternate embodiment of that described above relative to
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.
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.
Number | Date | Country | |
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61215199 | May 2009 | US |