1. Field of the Invention
Embodiments of the invention generally relate to the fabrication of photovoltaic cells.
2. Description of the Related Art
Solar cells are photovoltaic devices that convert sunlight directly into electrical power. The most common solar cell material is silicon, which is in the form of single or multicrystalline substrates, sometimes referred to as wafers. Because the amortized cost of forming silicon-based solar cells to generate electricity is higher than the cost of generating electricity using traditional methods, there has been an effort to reduce the cost to form solar cells.
Conventional silicon solar cells, such as crystalline-silicon solar cells, use a metal based contact structure for the front-surface current collection and for the rear surface contacting areas. The metal contact structures in connection with the substrate create an ohmic contact. Contact resistivity between the metal contact structures and the substrate is always desired to be low so as to maintain good electrical performance of the solar cell devices. Low charge recombination loss is also desired at the interface of the metal contacts and the substrate so as to keep high conversion efficiency of the solar cells.
Therefore, there exists a need for improved methods to form the metal contact structures formed on a surface of a substrate to form a solar cell with desired electric performances.
Embodiments of the invention contemplate the formation of a high efficiency solar cell using novel methods to form metal contact structures of the solar cell device. In one embodiment, a solar cell device includes a substrate comprising a doped semiconductor material, a surface formed on the substrate having a second doped semiconductor layer having a conductivity type opposite to the first doped semiconductor material, a dielectric layer disposed on the surface of the substrate, a metal contact structure formed in the dielectric layer with a first predetermined cross sectional area, and a metal line formed on the metal contact structure with a second predetermined cross sectional area, wherein the second predetermined cross sectional area is larger than the first predetermined cross sectional area.
In another embodiment, a method for manufacturing metal contact structures for a solar cell device includes providing a substrate having a dielectric layer disposed thereon, selectively disposing contact metal paste on the dielectric layer, firing the contact metal paste disposed on the dielectric layer to etch through the dielectric layer, forming contact openings in the dielectric layer, forming metal contact structures in the contact opening formed in the dielectric layer etched through the contact metal paste during the firing process, and selectively disposing a metal line over the contact structures formed in the dielectric layer.
In yet another embodiment, a method for manufacturing metal contact structures for a solar cell device includes providing a substrate having a dielectric layer disposed thereon, performing a contact opening process in the dielectric layer to selectively form a plurality of contact openings in the dielectric layer, disposing metal contacts in the contact openings formed in the dielectric layer, wherein the metal contacts include a top portion connecting to a low portion, wherein the top portion of the metal contacts has a first predetermined dimension larger than a second predetermined dimension of the low portion of the metal contacts formed within the contact openings.
So that the manner in which the above recited features of the present invention can be understood in detail, a more particular description of the invention, briefly summarized above, may be had by reference to embodiments, some of which are illustrated in the appended drawings.
For clarity, identical reference numerals have been used, where applicable, to designate identical elements that are common between figures. It is contemplated that features of one embodiment may be incorporated in other embodiments without further recitation.
Embodiments of the invention are about the formation of a high efficiency solar cell using methods to form metal contact structures of a solar cell device. The high efficiency solar cell may be obtained by maintaining minimum contact area between the metal contacts formed onto the silicon substrate so as to achieve low contact resistivity and low recombination loss. In one embodiment, the method includes depositing a dielectric material that is used to define the active regions and/or contact structure of a solar cell device. Various techniques may be used to form the active regions and/or contact structure of the solar cell. Solar cell substrates (e.g., substrate 150 in
The rotary actuator assembly 130 may be rotated and angularly positioned about the “F” axis by a rotary actuator (not shown) and a system controller 101. The rotation of the rotary actuator assembly 130 selectively positions the printing nests 131 within the system 100 (e.g., paths “D1” and “D2” illustrated in
In one embodiment, the rotary actuator assembly 130 includes four printing nests 131, or substrate supports, that are each adapted to support the substrate 150 during the screen printing process performed within the screen print chamber 102.
Returning back to
The screen print chamber 102 is adapted to deposit material in a desired pattern on the surface of the substrate 150 positioned on the printing nest 131 in position “2” during the screen printing process. In one embodiment, the screen print chamber 102 includes a plurality of actuators, for example, actuators 102A (e.g., stepper motors or servomotors) that are in communication with the system controller 101 and are used to adjust the position and/or angular orientation of a screen printing mask 102B (
The system controller 101 facilitates the control and automation of the overall system 100 and may include a central processing unit (CPU) (not shown), memory (not shown), and support circuits (or I/O) (not shown). The CPU may be one of any form of computer processors that are used in industrial settings for controlling various chamber processes and hardware (e.g., conveyors, optical inspection assemblies, motors, fluid delivery hardware, etc.) and monitor the system and chamber processes (e.g., substrate position, process time, detector signal, etc.). The memory is connected to the CPU, and may be one or more of a readily available memory, such as random access memory (RAM), read only memory (ROM), floppy disk, hard disk, or any other form of digital storage, local or remote. Software instructions and data can be coded and stored within the memory for instructing the CPU. The support circuits are also connected to the CPU for supporting the processor in a conventional manner. The support circuits may include cache, power supplies, clock circuits, input/output circuitry, subsystems, and the like. A program (or computer instructions) readable by the system controller 101 determines which tasks are performable on a substrate. The program is software readable by the system controller 101, which includes code to generate and store at least substrate positional information, the sequence of movement of the various controlled components, substrate optical inspection system information, and any combination thereof.
The process sequence 300 starts at step 302 by providing a substrate, such as the substrate 150, to a screen print chamber, such as the screen print chamber 102 depicted in
The dielectric layer 404 disposed on the substrate 150 may be a silicon oxide layer, such as a silicon dioxide layer, a silicon nitride layer, a silicon oxynitride (SiON) layer, a composite layer including more than one dielectric layers, combination thereof, or the like, formed on the substrate 150. The dielectric layer 404 may be formed using a conventional thermal oxidation process a rapid thermal oxidation process, an atmospheric pressure or low pressure CVD process, a plasma enhanced CVD process, a PVD process, or applied using a sprayed-on, spin-on, roll-on, screen printed, or other similar type of deposition process. In one embodiment, the dielectric layer 404 is a silicon nitride layer that is between about 50 Å and about 3000 Å thick. In another embodiment, the dielectric layer 404 is a silicon nitride layer that is less than about 2000 Å thick. In one embodiment, the dielectric layer 404 is a silicon nitride layer having a thickness between about 100 Å and about 1000 Å, which is formed on the surface 420 of the doped silicon containing substrate 150. In another embodiment, the dielectric layer 404 is an aluminum oxide layer that is between about 30 Å and about 3000 Å thick. Aluminum is particularly useful for passivation of p-type as opposed to n-type surfaces. It should be noted that the discussion of the formation of a silicon nitride/silicon oxide type dielectric layer is not intended to be limiting as to the scope of the invention described herein since the dielectric layer 404 could also be formed using other conventional deposition processes (e.g., PECVD deposition) and/or be made of other dielectric materials.
In another embodiment, the dielectric layer 404 comprises a multilayer film stack, such as a silicon oxide/silicon nitride layer stack (e.g., a silicon oxide layer (e.g., layer(s) ˜20 Å to ˜3000 Å thick) and a silicon nitride layer (e.g., layer(s) ˜100 Å to ˜1000 Å thick)), an amorphous silicon/silicon oxide layer stack (e.g., amorphous silicon layer (e.g., ˜30 to 100 Å thick) and silicon oxide layer (e.g., ˜100 to 3000 Å thick)), or an amorphous silicon/silicon nitride stack (e.g., amorphous silicon layer (e.g., ˜30 to 100 Å thick) and silicon nitride layer (e.g., ˜100 to 1000 Å thick)). In one example, a 50 Å amorphous silicon layer is deposited on a silicon substrate using a CVD process, and then a 750 Å silicon nitride layer is deposited using a CVD or PVD process. In another example, a 50 Å silicon oxide layer is formed using a rapid thermal oxidation process on a silicon substrate, and then a 750 Å silicon nitride is deposited on the silicon oxide layer using a CVD or PVD process. In another example, the dielectric layer 404 comprises a multilayer film stack of aluminum oxide and silicon nitride. An example of a deposition chamber and/or process that may be adapted to form an amorphous silicon layer, silicon nitride, or silicon oxide discussed herein are further discussed in the commonly assigned and copending U.S. patent application Ser. Nos. 12/178,289, filed Jul. 23, 2008, and the commonly assigned U.S. patent application Ser. No. 12/202,213, filed Aug. 29, 2008, which are both herein incorporated by reference in their entirety.
In one embodiment, the silicon oxide or silicon nitride formation process is performed in a Vantage RadiancePlus™ RTP, Vantage RadOx™ RTP, or Applied Producer DARC®, or other similar chamber available from Applied Materials Inc. of Santa Clara, Calif. It is also contemplated that deposition equipment from other manufactures may also be utilized.
At step 304, contact metal paste 406 is selectively deposited on the dielectric layer 404 in the screen print chamber 102 to form metal contacts by use of an ink jet printing, rubber stamping, stencil printing, screen printing, or other similar process to form and define a desired pattern where electrical contacts to the underlying substrate surface (e.g., silicon) are formed, as depicted in
As the contact metal paste 406 provides metal source to form metal contacts 408 on the substrate 150 during the subsequent firing process (further discussed below with reference to
In one embodiment, the contact metal paste 406 includes polymer resin having metal particles disposed therein. The polymer and particle mixture is commonly known as “pastes” or “inks”. The polymer resins act as a carrier to help enable printing of the metal paste 406 onto the dielectric layer 404. Other organic chemicals are added to tune the viscosity, surface wetting, or other properties of the paste. The polymer resin and other organics are removed from the dielectric layer 404 or from the substrate 150 during the subsequent firing process. Glass frits may also be included in the contact metal paste 406. Chemicals contained in the glass frits in the contact metal paste 406 can dissolve the dielectric layer 404 disposed on the substrate 150 to allow metal to dispose (e.g., firing through) within the dielectric layer 404 to form contact areas/contact holes 414 on the surface 420 of the substrate 150, as well as facilitating coalescence of the metal particles. Glass frits thus enables the contact metal paste 406 to pattern the dielectric layer 404 leaving metal particles in the dielectric layer 404 so as to print metal contacts 408 into the dielectric layer 404.
In one embodiment, metal particles included in the contact metal paste 406 may be selected from silver, silver alloy, copper (Cu), tin (Sn), cobalt (Co), rhenium (Rh), nickel (Ni), zinc (Zn), lead (Pb), and/or aluminum (Al), or other suitable metal particles to provide proper metal source for forming the metal contacts 408 in the dielectric layer 404. The contact metal paste 406 may include silver (Ag) particles formed in polymer resin having glass frits disposed therein to form silver metal contacts 408 (in
In another embodiment, the contact metal paste 406 may include an etchant material, such as ammonium fluoride (NH4F) containing material, having metal particles disposed therein. The ammonium fluoride (NH4F) containing material is formulated to etch the dielectric layer 404 by a subsequent firing process and be evaporated at the firing process. In one example, the contact metal paste 406 may contain 200 g/l of ammonium fluoride (NH4F), 50 g/l of 2000 MW polyethylene glycol (PEG) and 50 g/l of ethyl alcohol with the remainder of the 1 liter volume being DI water. Metal particles may be disposed in the contact metal paste. In another example, one liter of the contact metal paste may contain 90 milliliters of a 6:1 BOE etching solution, 5 g of 500 MW polyethylene glycol (PEG) and 5 g of ethyl alcohol with the remainder of the volume being DI water with a desired amount of metal particles dispensed or disposed therein. Additional components in the contact metal paste are generally selected so as to promote effective “wetting” of the dielectric layer 404 while minimizing the amount of spreading that can affect the formed feature/contact metal patterns in the dielectric layer 404. While polyethylene oxide (i.e., polyethylene glycol) based materials and other related materials work well as a surfactant in the contact metal paste, they also decompose at temperatures over 250 degrees Celsius to form volatile byproducts thereby avoiding the need for a post-rinse step to clean the substrate surface after heating the substrate in the next step.
In one embodiment, the contact metal paste 406 comprises an etchant material, ammonium fluoride (NH4F), having silver metal (Ag) disposed therein. Ammonium fluoride (NH4F) a solvent that forms a homogeneous mixture with ammonium fluoride, a pH adjusting agent (e.g., BOE, HF), and a surfactant/wetting agent. In one example, the solvent is dimethylamine, diethylamine, triethylamine or ethanolamine that are disposed in an aqueous solution. In one example, the surfactant/wetting agent may be polyethylene glycol (PEG), polypropylene glycol, polyethylene glycol-polypropylene glycol-block-copolymer, or glycerin. It is believed that one benefit of using an alkaline chemistry is that no volatile HF vapors will be generated until the subsequent heating process(es) begins to drive out the ammonia (NH3), thus reducing the need for expensive and complex ventilation and handling schemes prior to performing the heating process(es).
At step 306, a metal line 410 is formed on the metal contacts 408 to balance the overall area coverage of metal structures required to be formed in the solar cell devices 400 so as to maintain desired conductivity formed in the solar cell devices 400, as shown in
In one embodiment, the metal paste selected to be disposed on the metal contacts 408 is a metal containing metal paste configured to form the metal line 410 containing a desired metal element on the substrate 150. Suitable examples of the metal elements that may be used to form the metal paste include copper (Cu), silver (Ag), tin (Sn), cobalt (Co), rhenium (Rh), nickel (Ni), zinc (Zn), lead (Pb), and/or aluminum (Al). In one embodiment depicted here, silver (Ag) or copper (Cu) is used as the metal source material to form the metal paste. After the metal paste is disposed, printed, or pasted on the metal contacts 408, a “non-fire-through” firing process is performed to assist melting the metal paste, thereby leaving the silver metal adhering on the metal contacts 408 without damaging the dielectric layer 404. In one embodiment, the “non-fire-through” firing process is performed a temperature within a range between about 600 degrees Celsius and about 900 degrees Celsius for a time period between about 8 second and about 12 seconds. Additionally, the “non-fire-through” firing process may also assist forming a good electrical contact among the dielectric layer 404 and the metal contacts 408.
In another embodiment, the metal line 410 may also be formed by a CVD process, a PVD process, a sputter process, a plating process, or any suitable processes. An etching process or material removal process, such as laser ablation, patterning, dry/wet etching, or other similar techniques is then followed to form desired patterns or metal grid on the metal line 410.
In one embodiment, the metal line 410 may have a width 424 of between about 50 μm and about 1000 μm so as to compensate the area coverage reduced from width 412 of the metal contacts 408 formed in the dielectric layer 404. In another embodiment, the metal line 410 may be configured to have a cross sectional area between about 10 percent and about 200 percent, such as between about 100 percent and about 200 percent, greater than the cross sectional area of the metal contacts 408 formed in the dielectric layer 404. It is noted that the term “cross sectional area” described herein generally refers to a plane parallel to the surface 420 of the substrate 150. In another embodiment, the width 424 of the metal line 410 may be configured to be between about 10 percent and about 200 percent, such as between about 100 percent and about 200 percent, wider than the width of the metal contacts 408 formed thereunder. In one embodiment, the width 424 of the metal line 410 is between about 10 μm and about 200 μm wider than the width 412 of the metal contacts 408.
At step 308, a thermal process, such as a firing and/or a sintering process, is performed on the substrate 150 to form metal contacts 408 in the dielectric layer 404 using a “fire-through” metallization process, as shown in
In another embodiment, the metal contacts 408 may be formed by a drop-in replacement process, double print process, or other suitable process to place silver metals into the contact holes/features 414 to form the desired metal contacts 408 as needed.
As discussed above, as the metal contacts 408 formed in the dielectric layer 404 may create ohmic contact at the surface 420 of the substrate 150, accordingly, the dimension of the features/contact holes 414 for the metal contacts 408 to be disposed therein is controlled to be formed as small as possible to reduce contact resistivity. However, small dimension of the metal contact 408 may affect the conductivity and/or the area coverage (also cross sectional area) of the metal contacts 408 as required to be formed in the solar cell devices 400, thereby adversely reducing the overall electric performance or conversion efficiency of the solar cell devices 400 formed on the substrate 150.
It is noted that the sequence of performing the step 306 and 308 may be switched, cycled, repeated or in any order until desired thickness, profile, structures are formed on the substrate.
The process sequence 500 starts at step 502 by providing a substrate, such as the substrate 150 having a dielectric layer 404 disposed thereon, as depicted in
At step 504, a contact opening process is performed on the substrate 150 to form contact holes 602 in the dielectric layer 404, as depicted in
In one embodiment, the contact holes 602 are formed in the dielectric layer 404 by an etching process. The etching process may be performed by a conventional etching process utilizing a mask layer during the etching process to form the contact holes 602 with desired patterns, features, dimensions, shapes, or configurations in the dielectric layer 404. In one embodiment, the etching process utilized to form the contact hole 602 is a dry plasma etching process utilizing a halogen containing gas, such as SF6, as the active etchants to etch the dielectric layer 404.
In another embodiment, the contact holes 602 are formed by an etchant material selectively pasted on the dielectric layer 404 to form contact holes 602 therein. The etchant material may include an etching solution to be selectively pasted on the dielectric layer 404 by use of a conventional ink jet printing, rubber stamping, screen printing, or other similar process to form and define the contact holes 602. The etching solution as used here may be similar or the same as the solution discussed above utilized to etch the dielectric layer 404 at step 304. In one embodiment, the etchant material is disposed on the dielectric layer 404 by a screen printing process performed in a screen printing tool, such as the tool depicted in
As discussed above, dimension of the contact holes 602 formed in the dielectric layer 404 is desired to be small so as to maintain a minimum contact resistivity. Accordingly, contact holes 602 formed in the dielectric layer 404 is controlled having a mean diameter or width 604 less than about 50 μm. In one example, the features the contact holes 602 are circular holes, slots, rectangular shaped holes, hexagonal shaped holes, or other desirable shape.
At step 506, after the contact holes 602 are formed in the dielectric layer 404, contact metal paste is selectively disposed in the dielectric layer 404, filling the contact holes 602 formed in the dielectric layer 404, as shown in
In one embodiment, the contact metal paste includes polymer resin to act as a carrier to help enable printing of the metal contact 606 into the dielectric layer 404. The polymer resin, such as ethylcellulose, and various chemicals, and other organics are removed from the contact areas/contact holes 414 during the subsequent thermal process. The firing process creates an ohmic contact between the metal contacts 408 and the surface 420 of the substrate 150.
In one embodiment, the contact metal paste may include metal particles disposed therein to provide proper metal source for filling the metal contacts 606 in the contact holes 602 formed in the dielectric layer 404. In one embodiment, metal particles included in the contact metal paste may be selected from silver, silver alloy, copper (Cu), tin (Sn), cobalt (Co), rhenium (Rh), nickel (Ni), zinc (Zn), lead (Pb), and/or aluminum (Al), or other suitable metal particles to provide proper metal source for forming the metal contacts 606 in the dielectric layer 404. The contact metal paste may include silver (Ag) particles formed therein to form silver metal contacts 606 in the dielectric layer 404.
As discussed above, as the metal contacts 606 formed in the dielectric layer 404 may create ohmic contact at the surface 420 of the substrate 150, accordingly, the width 604 of the contact holes 602 are small to reduce contact recombination losses. However, small dimension of the metal contacts 606 formed in the contact holes 602 may affect the conductivity and/or the area coverage (also cross sectional area) of the metal contacts 606 as required to be formed in the solar cell devices 600, thereby adversely reducing the overall electric performance of the solar cell devices 600 formed on the substrate 150. Accordingly, the metal contacts 606 formed in the contact holes 602 are configured to have a top portion 610 having a larger (i.e. wider) width 608 than a width 604 (e.g., or a cross sectional area of the top portion 610 larger than a cross sectional area of the metal contacts 606) formed in a lower portion 612 of the metal contacts 606 filling in the contact holes 602. The wider width 608 of the top portion 610 of the metal contacts 606 may assist balancing the overall area coverage of metal structures required to form in the solar cell devices 600 so as to maintain desired conductivity formed in the solar cell devices 600. In one embodiment, the top portion 610 of the metal contacts 606 may have a mean diameter or width 608 of between about 50 μm and about 1000 μm so as to compensate the area coverage reduced from width 608 of the lower portion 612 of the metal contacts 606 formed in the dielectric layer 404. In another embodiment, the width 608 of the top portion 610 of the metal contacts 606 may be configured to be between about 10 percent and about 200 percent wider than the width 604 of the lower portion 612 of the metal contacts 606 formed thereunder. In one embodiment, the width 608 of the top portion 610 of the metal contacts 606 are between about 10 μm and about 100 μm wider than the width 604 of the lower portion 612 of the metal contacts 606. In another embodiment, the top portion 610 may be configured to have a cross sectional area between about 10 percent and about 200 percent, such as between about 100 percent and about 200 percent, greater than the cross sectional area of the lower portion 612 formed in the dielectric layer 404. It is noted that the term “width” is a mean diameter of the structures (holes, vias, trenches, openings, conductive lines and the like) formed on the substrate and is used to determine a cross sectional area of the structures. It is noted that the term “cross sectional area” as utilized herein refers to the sectional area taken in a plane parallel to the surface 420 of the substrate 150.
At step 508, after the metal contacts 606 are filled in the contact holes 602 in the dielectric layer 404, a thermal annealing process (e.g., a firing process) may be performed to assist densifying, melting and adhering the metal source from the contact metal paste onto the substrate 150. The thermal annealing process as performed in this step is a so called “non-fire through” process so that the metal contacts 606 disposed in the dielectric layer 404 is thermally proceeded to be melt and adhered on the substrate surface 420 without damaging or etching through the dielectric layer 404. The thermal annealing process or the firing process may also assist evaporating the polymer or organic material in the contact metal paste from the dielectric layer 404, leaving a clean surface of the metal contacts 606 to be disposed in the dielectric layer 404. In one embodiment, the thermal annealing/firing temperature may be controlled between about 600 degrees Celsius and about 900 degrees Celsius, such as about 800 degrees Celsius for short time period, such as between about 8 seconds and about 12 seconds, for example, about 10 seconds.
While the foregoing is directed to embodiments of the present invention, other and further embodiments of the invention may be devised without departing from the basic scope thereof, and the scope thereof is determined by the claims that follow.