This invention relates to a method for making solar cells. More particularly, the present invention relates to selective etching of a porous silicon layer to under-cut and release a silicon-based device layer that is then used for making solar cells.
Solar cells are semiconductor devices that are usually manufactured from silicon-based material. Some solar cells are made from screen printed poly-crystalline silicon. Single crystalline wafers can be used to make very efficient solar cells. However, high manufacturing costs for making single crystalline materials makes the large scale production of solar cells from these materials impractical.
Poly-crystalline silicon wafers used to manufacture solar cells are made by cutting 180 to 350 micrometer thick wafers from block-cast silicon ingots. The wafers are usually lightly p-type doped. To make a solar cell from the wafer, a surface diffusion of n-type dopants is performed on the front side of the wafer. This forms a p-n junction a few hundred nanometers below the surface. Solar cells usually also include anti-reflective coatings, such as silicon nitride or titanium dioxide and/or have textured surfaces increase efficiency of light absorption. This method is disadvantageous in that the crystal takes an exceptionally long time to grow on the silicon ingot.
Metal contacts are formed on the back and front surfaces of poly-crystalline silicon wafers by screen-printing metal pastes, such as silver paste or aluminum paste. After the metal contacts are formed, the solar cells are assembled into panels and are sandwiched between glass and polymer resins.
As mentioned above, solar cells and solar panels that are formed from single crystal silicon are preferred because of the efficiency of the solar cells and panels made from single crystal silicon.
The present invention is direct to a method of making a solar cell. In accordance with the method of the present invention, a silicon-based device layer is formed on a base wafer. The base wafer includes a single crystal silicon wafer and a sacrificial porous silicon layer that is deposited thereon. The sacrificial porous silicon layer is formed using thermal deposition or any other suitable coating or deposition technique. Preferably, the porous silicon layer has a porosity of 30 percent or more. The sacrificial porous silicon layer comprises, for example, carbon doped oxide, spin-on-glass (SOG), fluoridated silicon glass (FSG) or a combination thereof. The thickness of the porous silicon layer is preferably in a range of several nanometers to several microns.
The silicon-based device layer is preferably crystalline or semi-crystalline, as opposed to being amorphous, and is epitaxially grown on top of the sacrificial porous silicon layer. The silicon-based device layer is preferably a p-doped silicon-based device layer that has a thickness of several microns to several hundred microns. The silicon-based device layer is formed using any suitable growth or deposition technique, such as chemical vapor deposition. A working wafer that includes the single crystal silicon wafer, the silicon-based device layer and the sacrificial porous silicon layer sandwiched between the single crystal silicon wafer and the silicon-based device layer is referred to herein as a composited wafer.
In accordance with the embodiments of the invention, after the composite wafer is formed the sacrificial layer is selectively etched thereby releasing the silicon-based device layer, or a portion thereof and the single crystal wafer, or a portion thereof. The released silicon-based device layer, or the portion thereof, is then provided with the appropriate electrical contacts and anti-reflective coatings and is coupled to one or more substrates to form a solar cell. The released single crystal wafer, or the portion thereof, is then used to make additional composite wafers and additional solar cells, such as described above.
In order to accomplish release of the silicon-based device layer, or the portion thereof, the etch rate of the porous silicon layer needs to be significantly faster than the etch rates of either the single crystal wafer or of the silicon-based device layer. Selective etching of the sacrificial porous silicon layer has been observed by treating the composite wafer to an aqueous etchant that is maintained at temperatures in a range of 0 to 10 degrees Celsius. The aqueous etchant preferably includes one or more etchants such as potassium hydroxide, sodium hydroxide and hydrogen fluoride in a concentration of 5% or less by weight. In further embodiments of the invention the aqueous etchant includes an alcohol, such as isopropyl alcohol, in a concentration of 10% or less by weight. In still further embodiments of the invention the etchant includes a surfactant in a concentration of 1% or less by weight. Also, to further control etch rates during the selective etching step, the composite wafer and the aqueous etchant are treated with ultrasonic energy.
As described above, the sacrificial porous silicon layer 103 preferably has a porosity of 30 percent or more and is several nanometers to several microns thick. The sacrificial porous silicon layer 103 is formed from any suitable porous silicon material including, but not limited to carbon doped oxide, spin-on-glass (SOG), fluoridated silicon glass (FSG) or a combination thereof.
The silicon-based device layer 105 is preferably a p-doped silicon-based device layer that has a thickness of several microns to several hundred microns. The sacrificial porous silicon layer 103 and the silicon-based device layer 105 are formed using any suitable coating, growth and/or deposition techniques including, but not limited to, thermal deposition and chemical vapor deposition.
Referring to
After the sacrificial porous silicon layer 103 is formed in the step 202, in the step 204 the device layer 105 is formed over the sacrificial porous silicon layer 103. The device layer 105 is preferably formed using any suitable technique, but is preferably formed by epitaxially growing a crystalline or semi-crystalline silicon device layer using vapor deposition techniques. The device layer 105 that is formed in the step 204 is preferably a p-doped device layer. The device layer 105 is formed, for example, by vapour depositing silicon-based precursors that includes a p-dopant or p-dopants, herein referred to as p-doped silicon-based precursors. Suitable p-doped silicon-based precursors include trivalent atoms typically from group IIIA of the periodic table, such as boron or aluminum. Alternatively to using p-doped silicon-based precursors to form the device layer 105, the device layer 105 may be doped after its formation using ion implantation techniques. In some cases, it can be useful to form the device layer 105 by using p-doped silicon-based precursors, such as described above, and further doping the device layer 105 with the same or different dopants using ion implantation techniques.
Now referring to
In accordance with the embodiments of the invention, the device layer 105 is patterned with access groves or holes in the step 206 by using photo-resist masking and etching techniques. It will be clear to one skilled in the art that while patterning the device layer 105 with access groves or holes, such as described above, can be beneficial, it is not necessary to implement the present invention. Regardless of whether the step 206 of patterning the device layer 105 with access groves or holes is performed, in the step 208 the composite wafer 100 is treated with an etchant to form a released silicon-based device layer 105′ and a release single crystal silicon wafer 101′, such as shown in
Still referring to
1) Anionic Surfactants, such as, for example, Perfluorooctanoate (PFOA or PFO), Perfluorooctanesulfonate (PFOS), Sodium dodecyl sulfate (SDS), ammonium lauryl sulfate, Sodium laureth sulfate and Alkyl benzene sulfonate;
2) Soap or fatty acid salt surfactants;
3) Cationic Surfactants, such as, for example, Cetyl trimethylammonium bromide (CTAB), a.k.a. hexadecyl trimethyl ammonium bromide, Cetylpyridinium chloride (CPC), Polyethoxylated tallow amine (POEA), Benzalkonium chloride (BAC) and Benzethonium chloride (BZT);
4) Zwitterionic (amphoteric) Surfactants, such as, for example Dodecyl betaine, Cocamidopropyl betaine, Coco ampho glycinate; and
5) Nonionic Surfactants, such as, for example Alkyl poly(ethylene oxide), Alkylphenol poly(ethylene oxide) Copolymers of poly(ethylene oxide) and poly(propylene oxide), Octyl glucoside, Decyl maltoside, Fatty alcohols, Cetyl alcohol, Oleyl alcohol, Cocamide MEA, cocamide DEA, Polysorbates and Dodecyl dimethylamine oxide.
In still further embodiments of the invention, during the selective etching step 208 the composite wafer 100 and the aqueous etchant are treated with ultrasonic energy. After the release, silicon-based device layer 105′ is formed in the step 203. In the step 205 the released silicon-based device layer 105′ is attached to a suitable substrate 101″, such as, for example, a glass substrate, and provided with all the appropriate inter-connects to form a solar cell.
Referring now to
With reference to
The present invention has been described in terms of specific embodiments incorporating details to facilitate the understanding of the principles of construction and operation of the invention. As such, references herein to specific embodiments and details thereof are not intended to limit the scope of the claims appended hereto. It will be apparent to those skilled in the art that modifications can be made in the embodiments chosen for illustration without departing from the spirit and scope of the invention.
The present application is a continuation of U.S. patent application Ser. No. 12/716,785, filed Mar. 3, 2010, which claims priority under 35 U.S.C. §119(e) to U.S. Provisional Patent Application Ser. No. 61/157,195, filed on Mar. 3, 2009, and titled “METHOD FOR SELECTIVE UNDER-ETCHING OF POROUS SILICON,” the entirety of which is hereby incorporated by reference.
Number | Date | Country | |
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61157195 | Mar 2009 | US |
Number | Date | Country | |
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Parent | 12716785 | Mar 2010 | US |
Child | 14667157 | US |