This disclosure relates generally to the field of semiconductors. More specifically, the present disclosure relates to solar cell manufacturing equipment and processes.
Crystalline silicon (including multi- and mono-crystalline silicon) is the most dominant absorber material for commercial photovoltaic applications. The relatively high efficiencies associated with mass-produced crystalline silicon solar cells, in conjunction with the abundance of material, garner appeal for continued use and advancement. But the relatively high cost of crystalline silicon material itself limits the widespread use of these solar modules. At present, the cost of “wafering,” or crystallizing silicon and cutting a wafer, accounts for about 40% to 60% of the finished solar module manufacturing cost. If a more direct way of making wafers were possible, great headway could be made in lowering the cost of solar cells.
There are different known methods of growing monocrystalline silicon and releasing or transferring the grown wafer. Regardless of the methods, a low cost epitaxial silicon deposition process and a high-volume, production-worthy low cost method of release layer formation may be prerequisites for wider use of silicon solar cells.
Porous semiconductor (PS) formation is a fairly new field with an expanding application landscape. The viability of this technology in solar applications may hinge on the ability to industrialize the process to large scale (at low cost), requiring development of very low cost-of-ownership, high-productivity porous silicon manufacturing equipment.
PS has been used in MEMS (micro-electro-mechanical systems) and related applications, where there is a higher tolerance for cost per unit area of the wafer than solar PV. The microelectronics industry achieves economy of scale through obtaining greater yield by increasing the number of die (or chips) per wafer, scaling the wafer size, and enhancing the chip functionality (or integration density) with each successive new product generation. In the solar industry, economy is achieved through the industrialization of solar cell and module manufacturing processes with low-cost, high-productivity equipment. Further economies are achieved through price reduction in raw materials through reduction of materials used per watt output of solar cells.
Some typical precursor chemistries for PS are: HF (49% in H2O typically), IPA (and/or acetic acid) and DI H2O. IPA (and/or acetic acid) serves as a surfactant and assists in the uniform creation of PS. Additional additives may be used to enhance the electrical conductivity of the electrolyte, thus reducing its heating through ohmic losses. Mixtures of HF and chemicals other than IPA can be readily employed by those skilled in the art.
In order to achieve the necessary economy for solar, process cost modeling is studied to identify and optimize equipment performance. Three categories of cost make up the total cost picture: fixed cost (FC), recurring cost (RC) and yield cost (YC). FC is made up of items such as equipment purchase price, installation cost and robotics or automation cost. RC is largely made up of electricity, gases, chemicals, operator salaries and maintenance technician support. YC may be interpreted as the total value of parts lost during production.
To achieve the cost-of-ownership (CoO) numbers required by the solar field, all aspects of the cost picture must be optimized. The qualities of a low cost process are (in order of priority): 1) high productivity, 2) high yield, 3) low RC, and 4) low FC.
Designing highly productive equipment requires a good understanding of the process requirements and reflecting those requirements in the equipment architecture. High yield requires a robust process and reliable equipment, and as equipment productivity increases, so too does yield cost. Low RC is also a prerequisite for overall low CoO. RC can impact plant site selection based on, for example, cost of local power or availability of bulk chemicals. FC, although important, is diluted by equipment productivity.
With the above said, in summary, high productivity, reliable, efficient manufacturing equipment may be a prerequisite for low cost solar cells.
Achieving low RC requires efficient use of chemicals. In wet processes, “drag out” or chemical carried out of the reaction chamber, must be rinsed off the wafer. With a greater amount of “drag out,” a correspondingly greater amount of rinse water is required to clean the wafer. Both of these factors add to CoO. Moreover, one must minimize the aging of chemicals so that they can be reused and/or recycled over an extended period.
In the field of photovoltaics, this disclosure enables high-productivity fabrication of semiconductor-based separation layers (made of porous semiconductors such as porous silicon), buried reflectors (made of multi-layer/multi-porosity porous semiconductors such as porous silicon), formation of porous semiconductor (such as porous silicon) for anti-reflection coatings, passivation layers, and multi junction, multi-band-gap solar cells (for instance, by forming a wider band gap porous silicon emitter on crystalline silicon thin film or wafer based solar cells).
This disclosure also enables formation of porous semiconductor layers on both sides of a substrate by alternating or modulating the voltage polarity and current direction to enable forming porous semiconductor layers on both sides. A process that is often used subsequent to porous silicon formation is silicon deposition, sometimes in epitaxial form. Dual side porous silicon formation enables dual side epitaxial layer deposition, thereby lowering the attainable cost of ownership of the silicon deposition process and fabrication cost of the resulting double side released thin silicon substrates.
In the semiconductor field, it enables fabrication of MEMS separation layers for die detachment, and shallow trench isolation (STI) porous silicon (using porous silicon formation with an optimal porosity and its subsequent oxidation). Other applications include the general fields of MEMS, including sensors and actuators, stand-alone, or integrated with integrated semiconductor microelectronics. Another range of applications pertains to high-surface-area reaction test-vehicles for food and drug evaluation.
These and other advantages of the disclosed subject matter, as well as additional novel features, will be apparent from the description provided herein. The intent of this summary is not to be a comprehensive description of the subject matter, but rather to provide a short overview of some of the subject matter's functionality. Other systems, methods, features and advantages here provided will become apparent to one with skill in the art upon examination of the following FIGURES and detailed description. It is intended that all such additional systems, methods, features and advantages included within this description, be within the scope of the claims.
The features, nature, and advantages of the disclosed subject matter will become more apparent from the detailed description set forth below when taken in conjunction with the accompanying drawings, wherein:
Although described with reference to specific embodiments, one skilled in the art could apply the principles discussed herein to other areas and/or embodiments.
Those with skill in the art will recognize that the disclosed embodiments have relevance to a wide variety of areas in addition to those specific examples described below.
The presently disclosed PS system design provides novel parallel or multi-wafer processing architecture, similar to low-cost, large-batch wet chemical processing in benches or tanks. Presently available PS tools rely on single wafer processing, which characteristically burdens each wafer with high capital cost, serial cumulative processing times, and excessive wafer handling/sealing, resulting in potential yield losses. The presently disclosed systems and methods may reduce the capital cost by a factor equal to the number of wafers in each stack or array. Furthermore, the proposed design may simplify automation, reduce the tool footprint, and enable downstream rinsing and drying.
One challenge with any PS chamber is handling H2 gas generated as a result of the anodic etch reaction that produces the PS. Hydrogen evolves from the surface of the wafer and each electrode. Since the electrolytic bath forms a part of the circuit, H2 gas may block current flow when it displaces the electrolyte; the supply of chemicals to the reaction surface thus may affect PS formation. It is therefore desirable to effectively and rapidly purge or sweep H2 byproducts from the surfaces of the wafer and electrodes. The wafer gap, fluid flow and design of the flow ports determine the effectiveness of the sweep. Hydrogen vent stacks 23 are provided to allow H2 to be released after the electrolyte flow has swept it from the surfaces of the wafers.
While sweeping H2 is fairly simple in terms of fluid mechanics, some consideration is warranted to mitigate the current loss from the fluid ports. Since the fluid lines are connected from wafer to wafer, depending on the geometry of the ports, line size and length, current can leak or bypass each wafer. For example reducing the line diameter and increasing the length results in greater electrical resistance, which reduces current losses or bypass losses. The current field lines are also influenced by the geometry adjacent to the wafer. So, large flow ports may be less desirable compared to multiple small ports.
The amount of wet chemical consumed during PS formation may be minimal compared to typical chamber flow rates. Therefore, if a more effective means of H2 mitigation were utilized, the flow capacity of the overall system could be reduced, which would enable further cost reduction. Some key advantages of the batch design shown in
The outcome of the PS tool is a clean and dry PS film. By stacking and transporting the wafers, one could envision a second chamber which clamps the wafer stack in a similar way followed by a rinse, purge and dry. Again, the ability to process multiple wafers simultaneously plays nicely into CoO reduction.
One of ordinary skill will understand that different current levels and polarities may be used in the embodiment of
While the upper chamber head space serves as the fluid “pressure head”, in actuality, it may be necessary to introduce a pump (not shown) to provide sufficient pressure and flow throughout the “n” stack. Furthermore, if the wafer “n” stack is increased, this may further necessitate a pump. It may be advantageous in this situation to insure an equal pressure drop from wafer to wafer. The pressure difference is necessary to seat each wafer against a seal. Without sufficient pressure holding each wafer against its seal, current may be allowed to leak around the wafers and adversely affect PS formation and uniformity.
It also may be desirable to have voltage and current (or total power) be consistent from batch to batch. Since PS formation is an electrolytic process, as the wafer thickness changes (from template/substrate reuse) and the bath chemistry drifts (from HF consumption), the formation of PS may be affected. Real-time monitoring of the bath chemistry, combined with process characterization, may provide benefits in terms of determining the process robustness and insuring uniformity from batch to batch and within each batch.
The motivation for multi wafer processing is to reduce the capital cost per wafer and increase productivity, thereby reducing CoO. Another approach to achieving this goal is a planar array of wafers with a shared electrode.
The wafers shown in
A further refinement of the arrangement of
The substrates themselves, together with the compliant, impermeable seal, form individual sealed compartments of electrolyte, and the leakage of electrolyte and electric field between compartments may be minimized or even completely avoided. This may enable uniform formation of the desired porous silicon structures across the whole exposed surfaces of the substrates.
It is to be noted that in addition to the compliant, impermeable edge seal, it may be advantageous to stabilize the substrates in their vertical arrangement. This could be done, among other options, by the geometrical restriction (see
It may be advantageous to use either of the shown conforming edge seal embodiments for any of several reasons. In some applications, the wafers receiving the PS (porous semiconductor) layer may be reused a plurality of times, e.g. for the production of a thin film solar substrate that may be separated from the wafer by removal of the PS (porous semiconductor) layer. Under those circumstances, the exact dimensions of wafers 90 (thickness, diameter, shape, etc.) may vary slightly from one use to the next. For that reason, a conforming edge seal may be desirable to accommodate a range of slightly different shapes and sizes.
The embodiments of this disclosure may be used for formation of single sided and double sided porous semiconductor/porous silicon layers with either single or multi-porosity structures. The wafers with single sided porous semiconductor/porous silicon layers may be subsequently processed through single sided epitaxial semiconductor or silicon deposition, in order to generate thin epitaxial substrates from one side of such wafers, used as reusable templates.
Similarly, the wafers with double sided porous semiconductor/porous silicon layers may be subsequently processed through double sided epitaxial semiconductor or silicon deposition, in order to generate thin epitaxial substrates from both sides of such wafers, used as reusable templates, hence further reducing the cost of fabricating such thin epitaxial substrates.
The electrodes used in various porous semiconductor (silicon) equipment embodiments of this invention may be made of materials including, but not limited to, diamond, platinum, silicon, carbon, conductive materials coated with diamond or coated with diamond-like carbon, or other materials known in the art. Moreover, the electrode may be shaped as for instance, but not limited to, planar or curved discs, rods or rings. The electrode shape and size may be set to establish pre-specified electric field and current distribution.
The foregoing description of the exemplary embodiments is provided to enable any person skilled in the art to make and use the subject matter. Various modifications to these embodiments will be readily apparent to those skilled in the art, and the generic principles defined herein may be applied to other embodiments without the use of the innovative faculty. Thus, the subject matter claimed is not intended to be limited to the embodiments shown herein but is to be accorded the widest scope consistent with the principles and novel features disclosed herein.
It is intended that all such additional systems, methods, features and advantages that are included within this description, be within the scope of the claims.
This application claims priority to U.S. Provisional Patent Application Ser. No. 61/175,535, filed May 5, 2009, which is hereby incorporated by reference in its entirety for all purposes.
Number | Name | Date | Kind |
---|---|---|---|
4043894 | Gibbs | Aug 1977 | A |
4070206 | Kressel et al. | Jan 1978 | A |
4082570 | House et al. | Apr 1978 | A |
4165252 | Gibbs | Aug 1979 | A |
4249959 | Jebens | Feb 1981 | A |
4251679 | Zwan | Feb 1981 | A |
4348254 | Lindmayer | Sep 1982 | A |
4361950 | Amick | Dec 1982 | A |
4409423 | Holt | Oct 1983 | A |
4427839 | Hall | Jan 1984 | A |
4461922 | Gay et al. | Jul 1984 | A |
4479847 | McCaldin et al. | Oct 1984 | A |
4626613 | Wenham et al. | Dec 1986 | A |
4672023 | Leung | Jun 1987 | A |
4922277 | Carlson | May 1990 | A |
5024953 | Uematsu et al. | Jun 1991 | A |
5073230 | Maracas et al. | Dec 1991 | A |
5112453 | Behr et al. | May 1992 | A |
5208068 | Davis | May 1993 | A |
5248621 | Sano | Sep 1993 | A |
5316593 | Olson et al. | May 1994 | A |
5348618 | Canham et al. | Sep 1994 | A |
5397400 | Matsuno et al. | Mar 1995 | A |
5458755 | Fujiyama et al. | Oct 1995 | A |
5459099 | Hsu | Oct 1995 | A |
5494832 | Lehmann et al. | Feb 1996 | A |
5538564 | Kaschmitter | Jul 1996 | A |
5645684 | Keller | Jul 1997 | A |
5660680 | Keller | Aug 1997 | A |
5681392 | Swain | Oct 1997 | A |
5882988 | Haberern et al. | Mar 1999 | A |
5928438 | Salami | Jul 1999 | A |
5951833 | Yamagata | Sep 1999 | A |
6091021 | Ruby | Jul 2000 | A |
6096229 | Shahid | Aug 2000 | A |
6114046 | Hanoka | Sep 2000 | A |
6127623 | Nakamura et al. | Oct 2000 | A |
6143629 | Sato | Nov 2000 | A |
6204443 | Kiso et al. | Mar 2001 | B1 |
6294725 | Hirschberg et al. | Sep 2001 | B1 |
6331208 | Nishida et al. | Dec 2001 | B1 |
6399143 | Chong | Jun 2002 | B1 |
6416647 | Dordi et al. | Jul 2002 | B1 |
6428620 | Yamagata et al. | Aug 2002 | B1 |
6429037 | Wenham et al. | Aug 2002 | B1 |
6441297 | Keller et al. | Aug 2002 | B1 |
6448155 | Iwasaki et al. | Sep 2002 | B1 |
6461932 | Wang | Oct 2002 | B1 |
6524880 | Moon et al. | Feb 2003 | B2 |
6534336 | Iwane | Mar 2003 | B1 |
6551908 | Ukiyo et al. | Apr 2003 | B2 |
6555443 | Artmann et al. | Apr 2003 | B1 |
6566235 | Nishida et al. | May 2003 | B2 |
6602760 | Poortmans et al. | Aug 2003 | B2 |
6602767 | Nishida et al. | Aug 2003 | B2 |
6613148 | Rasmussen | Sep 2003 | B1 |
6624009 | Green et al. | Sep 2003 | B1 |
6645833 | Brendel | Nov 2003 | B2 |
6649485 | Solanki et al. | Nov 2003 | B2 |
6653722 | Blalock | Nov 2003 | B2 |
6664169 | Iwasaki et al. | Dec 2003 | B1 |
6756289 | Nakagawa et al. | Jun 2004 | B1 |
6818104 | Iwasaki et al. | Nov 2004 | B2 |
6881644 | Malik et al. | Apr 2005 | B2 |
6946052 | Yanagita et al. | Sep 2005 | B2 |
6964732 | Solanki | Nov 2005 | B2 |
7014748 | Matsumura et al. | Mar 2006 | B2 |
7022585 | Solanki et al. | Apr 2006 | B2 |
7026237 | Lamb | Apr 2006 | B2 |
7368756 | Bruhns et al. | May 2008 | B2 |
7402523 | Nishimura | Jul 2008 | B2 |
20020106874 | Iwane et al. | Aug 2002 | A1 |
20020153039 | Moon et al. | Oct 2002 | A1 |
20020168592 | Vezenov | Nov 2002 | A1 |
20020179140 | Toyomura | Dec 2002 | A1 |
20030017712 | Brendel | Jan 2003 | A1 |
20030039843 | Johnson | Feb 2003 | A1 |
20030124761 | Baert | Jul 2003 | A1 |
20040028875 | Van Rijn | Feb 2004 | A1 |
20040173790 | Yeo | Sep 2004 | A1 |
20040259335 | Narayanan | Dec 2004 | A1 |
20040265587 | Koyanagi | Dec 2004 | A1 |
20050160970 | Niira | Jul 2005 | A1 |
20050172998 | Gee et al. | Aug 2005 | A1 |
20050176164 | Gee et al. | Aug 2005 | A1 |
20050177343 | Nagae | Aug 2005 | A1 |
20050199279 | Yoshimine et al. | Sep 2005 | A1 |
20050274410 | Yuuki et al. | Dec 2005 | A1 |
20050281982 | Li | Dec 2005 | A1 |
20060021565 | Zahler et al. | Feb 2006 | A1 |
20060043495 | Uno | Mar 2006 | A1 |
20060054212 | Fraas et al. | Mar 2006 | A1 |
20060070884 | Momoi et al. | Apr 2006 | A1 |
20060105492 | Veres et al. | May 2006 | A1 |
20060105912 | Konle et al. | May 2006 | A1 |
20060196536 | Fujioka | Sep 2006 | A1 |
20060231031 | Dings et al. | Oct 2006 | A1 |
20060266916 | Miller et al. | Nov 2006 | A1 |
20060283495 | Gibson | Dec 2006 | A1 |
20070077770 | Wang et al. | Apr 2007 | A1 |
20070082499 | Jung et al. | Apr 2007 | A1 |
20080047601 | Nag et al. | Feb 2008 | A1 |
20080157283 | Moslehi | Jul 2008 | A1 |
20080210294 | Moslehi | Sep 2008 | A1 |
20080264477 | Moslehi | Oct 2008 | A1 |
20080289684 | Moslehi | Nov 2008 | A1 |
20080295887 | Moslehi | Dec 2008 | A1 |
20090042320 | Wang et al. | Feb 2009 | A1 |
20090107545 | Moslehi | Apr 2009 | A1 |
20090301549 | Moslehi | Dec 2009 | A1 |
20100022074 | Wang et al. | Jan 2010 | A1 |
20100116316 | Moslehi et al. | May 2010 | A1 |
Number | Date | Country |
---|---|---|
06-260670 | Sep 1994 | JP |
2002-2299661 | Oct 2002 | JP |
PCTEP9908573 | May 2000 | WO |
WO 2002055760 | Jul 2002 | WO |
Entry |
---|
Alvin D. Compaan, Photovoltaics: Clean Power for the 21st Century, Solar Energy Materials & Solar Cells, 2006, pp. 2170-2180, vol. 90, Elsevier B.V. |
C.Berge, 150-mm Layer Transfer for Monocrystalline Silicon Solar Cells, Solar Energy Materials & Solar Cells, 2006, pp. 3102-3107, vol. 90, Elsevier B.V. |
C.Oules et al, Silicon on Insulator Structures Obtained by Epitaxial Growth of Silicon over Porous Silicon, Journal of the Electrochemical Society, Inc., 1992, p. 3595, vol. 139, No. 12, Meylan Cedex, France. |
C.S.Solanki, et al, Porous Silicon Layer Transfer Processes for Solar Cells, Solar Energy Materials & Solar Cells, 2004, pp. 101-113, vol. 83, Elsevier B.V., Leuven, Belgium. |
C.S.Solanki, et al, Self-Standing Porous Silicon Films by One-Step Anodizing, Journal of Electrochemical Society, 2004, pp. C307-C314, vol. 151, The Electrochemical Society, Inc., Leuven, Belgium. |
F.Duerinckx, et al, Reorganized Porous Silicon Bragg Reflectors for Thin-Film Silicon Solar Cells, IEEE Electron Device Letters, Oct. 2006, vol. 27, No. 10. |
Francois J. Henley, Layer-Transfer Quality Cleave Principles, SiGen, Jul. 8, 2005 pp. 1-6, The Silicon Genesis Corporation, San Jose, California. |
H.J.Kim, et al, Large-Area Thin-Film Free-Standing Monocrystalline Si Solar cells by Layer Transfer, Leuven, Belgium, IEEE, 2006. |
J.H.Werner et al, From Polycrystalline to Single Crystalline Silicon on Glass, Thin Solid Films, 2001, pp. 95-100, vol. 383, Issue 1-2, Elsevier Science B.V., Germany. |
J.J. Schermer et al., Epitaxial Lift-Off for large area thin film III/V devices, phys. Stat. sol. (a) 202, No. 4, 501-508 (2005). |
Jianhua Zhao, et al, A 19.8% Efficient Honeycomb Multicrystalline Silicon Solar Cell with Improved Light Trapping, IEEE Transactions on Electron Devices, 1999, vol. 46, No. 10. |
K. Van Nieuwenhuysen et al., Progress in epitaxial deposition on low-cost substrates for thin-film crystalline silicon solar cells at IMEC, Journal of Crystal Growth, 2006, pp. 438-441, vol. 287, Elsevier B.V., Leuven, Belgium. |
K.L. Chopra et al., Thin-Film Solar Cells: An Overview, Progress in Photovoltaics: Research and Applications, 2004, pp. 69-92, vol. 12, John Wiley & Sons, Ltd. |
Lammert et al., The Interdigitated Back Contact Solar Cell: A Silicon Solar Cell for Use in Concentrated Sunlight, IEEE Transactions on Electron Devices, pp. 337-342. Apr. 1977. |
MacDonald et al., “Design and Fabrication of Highly Topographic Nano-imprint Template for Dual Damascene Full 3-D Imprinting,” Dept. of Chemical Eng., University of Texas at Austin, Oct. 24, 2005. |
Martin A. Green, Consolidation of Thin-Film Photovoltaic Technology: The Coming Decade of Opportunity, Progress in Photovoltaics: Research and Applications, 2006, pp. 383-392, vol. 14, John Wiley & Sons, Ltd. |
Martin A. Green, Silicon Photovoltaic Modules: A Brief History of the First 50 Years, Progress in Photovoltaics: Research and Applications, 2005, pp. 447-455, vol. 13, John Wiley & Sons, Ltd. |
Nobuhiko Sato et al, Epitaxial Growth on Porous Si for a New Bond and Etchback Silicon-on-Insulator, Journal of Electrochemical Society, Sep. 1995, vol. 142, No. 9, The Electrochemical Society, Inc., Hiratsuka, Japan. |
P.J.Verlinden, et al, Sliver® Solar Cells: A New Thin-Crystalline Silicon Photovoltaic Technology, Solar Energy Materials & Solar Cells, 2006, pp. 3422-3430, vol. 90, Elsevier B.V. |
P.R. Hageman et al., Large Area, Thin Film Epitaxial Lift Off III/V Solar Cells, 25th PVSC, May 13-17, 1996 Washington D.C., IEEE. |
Photovoltaic Technology Research Advisory Council, A Vision for Photovoltaic Technology, 2005, pp. 1-41, European Commision Publications Office. |
Prometheus Institute, U.S. Solar Industry Year in Review: U.S. Solar Energy Industry Charging Ahead, (SEIA) the Solar Energy Industry Association, 2006. |
R.Brendel, et al, Sol-Gel Coatings for Light Trapping in Crystalline Thin Film Silicon Solar Cells, Journal of Non-Crystalline Solids, 1997, pp. 391-394, vol. 218, Elsevier Science B.V., Germany. |
Richard Auer et al, Simplified Transfer Process for High-Current Thin-Film Crystalline Si Solar Modules, 3rd World Conference on Photovoltaic Energy Conversion, May 11-18, 2003, Osaka, Japan. |
Richard M. Swanson, A Vision for Crystalline Silicon Photovoltaics, Progress in Photovoltaics: Research and Applications, 2006, pp. 443-453, vol. 14, John Wiley & Sons, Ltd. |
Rolf Brendel, A Novel Process for Ultrathin Monocrystalline Silicon Solar Cells on Glass, 14th European Photovolaic Solar Energy Conference, Jun. 30-Jul. 4, 1997, Barcelona, Spain. |
Rolf Brendel, Review of Layer Transfer Processes for Cystalline Thin-Film Silicon Solar Cells, The Japan Journal of Applied Physics, 2001, pp. 4431-4439, vol. 40, Part 1, No. 7, The Japan Society of Applied Physics, Japan. |
Rolf Brendel, Thin-Film Crystalline Silicone Mini-Modules Using Porous Si for Layer Transfer, Solar Energy, 2004, pp. 969-982, vol. 77, Elsevier Ltd., Germany. |
S. Hegedus, Thin Film Solar Modules: The Low Cost, High Throughput and Versatile Alternative to Si Wafers, Progress in Photvoltaics: Research and Applications, 2006, pp. 393-411, vol. 14, John Wiley & Sons, Ltd. |
Takao Yonehara, et al, Epitaxial Layer Transfer by Bond and Etch Back of Porous Si, Applied Physics Letter 64, Apr. 18, 1994, vol. 16, American Institute of Physics. |
Toshiki Yagi, et al, Ray-Trace Simulation of Light Trapping in Silicon Solar Cell with Texture Structures, Solar Energy Materials & Solar Cells, 2006, pp. 2647-2656, vol. 90, Elsevier B.V. |
Number | Date | Country | |
---|---|---|---|
20110030610 A1 | Feb 2011 | US |
Number | Date | Country | |
---|---|---|---|
61175535 | May 2009 | US |