The present invention relates to photovoltaic devices, and in particular, an infrared photovoltaic device structure with improved photovoltaic properties and a simplified method of manufacture.
A solar cell (also called a photovoltaic cell) is an electrical device that converts the energy of light directly into electricity by the photovoltaic effect. Prior art solar cell technology typically utilizes crystalline silicon as a main ingredient, and in some other cases, inexpensive poly-crystalline silicon or other compound semiconductors. In addition, other technologies use organic materials for the so-called dye-sensitized solar cells. Prior art crystalline silicon solar cells are often fabricated by forming a high concentration n-type layer on a p-type silicon substrate. This high concentration n-type layer is generally formed by a process of ion implantation, or diffusion, introducing the n-type dopant phosphorous, to form a PN junction, followed by an annealing process. Once the PN junction is so formed, anode and cathode electrodes are formed to complete the photovoltaic cell.
Recently, the introduction of an intrinsic layer between the P and N layers to create a so-called PIN junction cell has also been introduced, to increase cell efficiency. However, in the same manner as the PN junction solar cell, the manufacturing process for PIN junction cells is based on impurity doping methods that are expensive and use toxic materials. It is highly desirable to have a manufacturing process for photovoltaic materials that reduces or eliminates toxic additives.
The conventional methods for manufacturing photovoltaic materials also require a multi-step process, or different processes, with each step possibly taking place at a different apparatus and at different times, and requiring its own management and resources. It is highly desirable to have a manufacturing process for photovoltaic (PV) materials that reduces the number of necessary processes or steps to reduce costs.
Currently available photovoltaic technology generally provides electric energy converted from sunlight only during the day. In addition, these legacy PV cells show best performance when the sun is high in the sky, and cell efficiency or performance drops drastically during morning and evening hours, as well as during overcast days. During cloudy or overcast days, the amount of energy that reaches solar cells is limited, since light is filtered by the cloud cover, therefore reducing the total amount of electric power generated by such solar cells in these conditions.
However, since prior art silicon-based PV cells are unable to produce electricity capturing infrared light, the performance of such cells will drop considerable in bad weather, despite the fact that the amount of infrared light (over 900 nm wavelength) reaching the earth's surface is practically unaffected by the weather or the amount of cloud cover. To overcome this issue, there are some prior art PV technologies able to capture infrared light, but using very expensive and toxic materials such as arsenic (As). It is highly desirable to have a manufacturing process for photovoltaic cell design that permits light to electricity conversion of a wide-range of light wavelengths, from the so-called visible light range to the infrared light range.
Preferred embodiments of the present invention provide a hybrid PV solar cell, one that generates electricity from both visible and infrared light (also called the infrared PV cell below), and a method of manufacturing the cell. The method of manufacturing the PV device is preferably a toxic material free process, which lowers the overall manufacturing cost.
The infrared PV solar cell is composed of a first electrode layer, a semiconductor substrate, a semiconductor PV layer, and a bottom electrode that forms a Shottcky junction between said bottom metal electrode and the PV layer.
Because of existence of the Shottcky junction, the PV cell of the present invention permits light to electricity conversion over a wide-range of light wavelengths, from the so-called visible light (between 350 nm to 900 nm wavelength) to the infrared light (over 900 nm wavelength). The PV structure only absorbs energy within the visible light spectrum, while the semiconductor/metal Shottcky interface absorbs energy in the infrared light wavelength or higher.
The method of manufacturing a photovoltaic (PV) device having a semiconductor substrate comprises performing the steps of: cleaning said substrate; introducing an inert gas under vacuum and a high temperature to form a semiconductor PV layer having a high resistivity on a first side of the substrate; forming a metal bottom layer on said semiconductor PV layer to create a Shottcky junction between the metal layer and said semiconductor PV layer; and forming a transparent electrode layer on the second side of said substrate.
In order to maximize the semiconductor/metal Shottcky contact surface area and therefore the infrared spectrum cell performance, the Shottcky interface was placed in the bottom of the cell. The top of the cell includes a transparent electrode. Both of these top and bottom layers are shown in
It is critical that the semiconductor substrate must be as thin a possible, in order to maximize the amount of light that penetrates into the wafer substrate and subsequently be absorbed by the bottom PV layer, and the Shottcky interface respectively.
Preferred embodiments of the present invention are illustrated by way of example, and not by way of limitation, in the figures of the accompanying drawings and in which like reference numerals refer to similar elements and in which:
In the following description, numerous specific details have been set forth to provide a more thorough understanding of embodiments of the present invention. It will be appreciated however, by one skilled in the art, that embodiments of the invention may be practiced without such specific details or with different implementations for such details. Additionally some well-known structures have not been shown in detail to avoid unnecessarily obscuring the present invention.
As seen in
The junction between the semiconductor and PV structure layers reacts to the visible-light spectrum, while the Schottky junction between the metal and PV structure layers reacts to the infrared light spectrum. These two combined junctions make a very powerful hybrid solar cell, capable of producing electricity from light of a very wide spectrum, from the visible through the infrared wavelengths.
A transparent top electrode is fabricated on top of the cell 100, allowing light to penetrate both photo-voltaic junctions. The metal layer 108 also functions as the bottom or back. ohmic electrode located at the bottom of cell 100.
Table 1 below describes the main parameters of the materials used to fabricate the photo-voltaic cell in the present invention.
One embodiment of the present invention to fabricate a hybrid PV cell 100 as shown in
First, a wafer heating process is used at step 202 to form the PV structure 9 on the semiconductor bulk layer 104.
Next is a PV cell preparation step 204, in which a neutral detergent is used in a wafer cleaning step and an organic neutral detergent is used for abrading agent removal.
Metal layer 206 is then formed, in which metal layer 108 is typically formed by sputtering.
Placement of top electrode step 208 is then performed, in which electrode TCO 102 is typically deposited by sputtering. This step is followed by the optional steps of applying a silver paste bus-bar on top of electrode 102 by screen printing and an anti-reflection coat on top of the bus-bar also by screen printing to complete the fabrication process.
Cell testing is performed at step 210, in which the PV device is run through a series of tests to determine its overall efficiency.
In other words, once the photo-voltaic layer in the semiconductor substrate is fabricated, a metal layer is placed on top of the PV layer. This metal layer functions as both the metal-semiconductor Shottcky junction as well as the photo-voltaic cell back electrode. The transparent conductive oxide layer is placed on top of the cell to complete the fabrication process.
More specifically, a 6-inch n-type silicon single crystal substrate having a resistivity of 1 to 5 (Ω cm), (100) crystal orientation is first cleaned by the use of a typical RCA cleaning method.
The substrate cleaning is performed in the following steps: removing organic material using sulfuric acid-hydrogen peroxide water cleaning for ten minutes at 350 K; pure water cleaning followed by nitrogen blow drying with infrared and ultraviolet light drying; cleaning using a 0.5% hydrofluoric acid solution; cleaning by ammonium-hydrogen peroxide water at 350 K for 10 minutes; removing heavy metal contamination by 80° C. hydrochloric acid-hydrogen peroxide water cleaning for ten minutes after pure water rinsing; and, lastly, pure water cleaning and nitrogen gas drying followed by paper IPA drying.
Next, a high resistivity layer, which is a first layer of the photo-voltaic generation layer, is preferably formed by the following method.
Inert gas is introduced into a quartz boat containing the semiconductor bulk wafer 304, which had been previously vacuumed to approximately 1 E-3 Pa. The quartz boat is then heated and kept at pre-determined annealing temperature (800K or more) for 30 minutes.
While vacuum of approximately 1 E-3 Pa was used in the present example, the degree of the vacuum may not be specified in particular at a vacuum of approximately 20 Pa or lower. Further, while argon gas was used as the inert gas in the present example, another inert gas such as helium gas and the like or a mixture of these inert gases may be used.
A variety of heating methods can be used to form intrinsic silicon layer 9, including but not limited to infrared heating, laser heating, and hot-wall furnace heating. In some embodiments, the particular heating methods used for treating the substrate layer have an effect on photovoltaic performance of the photovoltaic cell. In some embodiments, the cooling rate after the heating stage is a crucial factor to photovoltaic cell fabrication, whereas the heating rate is a less crucial factor to photovoltaic cell fabrication. Maximum photovoltaic cell performance can be obtained at heating temperatures above 1500° K, at heating times above 5 minutes, at approximately 1×10−3 Pa. The overall parameters used during heating step include temperatures ranging from 852 1700° Kelvin, heating times from one to 600 min., atmospheres from vacuum, argon, nitrogen or other inert gas at temperatures up to 1 atm. After the heating process is completed, the substrate is transformed into a photovoltaic semiconductor material having a high-resistivity layer therein.
Next, the substrate is preferably cleaned by the use of a typical RCA cleaning method, similar to the one mentioned above.
A 100 nm layer of gold is then formed on the PV structure by means of a sputtering method. While a sputtering method was used in this example, any other method may be utilized to fabricate the thin metal layer on top of the semiconductor photo-voltaic layer. While the thickness of 100 nm is used in the present example, the thickness is not limited to 100 nm, as long as it is sufficiently thick enough to block light, i.e., to reflect all light back to the cell.
Next, a 150 nm thick ZnO transparent conductive film is formed over the opposite side of the silicon substrate by a sputtering method.
An optional silver paste bus-bar is formed on top of the ZnO layer to improve overall top electrode electrical properties. Placement of the bus-bar is preferably performed by screen printing method.
While ZnO was used in the present example, another transparent conductive film such as ITO, SnO2, FTO, AZO, GZO, IZO, TNO, ATO, FeO2, and NbO2, or a stacked structure thereof may be used, and the transparent conductive film may be formed by PLD, MOCVD, a coating method, or the like, and not limited to the sputtering method.
Next, a silicon nitride film is preferably formed consecutively as an anti-reflection film. Lastly, a metal layer of aluminum is preferably added on top of the gold layer. This second metal layer is added by screen printing on the surface of the gold layer and heating of the second layer at 550 K to remove the binder, and complete the solar cell construction.
While, a single crystal silicon having 1 to 5 (Ω-cm) and orientation (100) is used for the silicon substrate in the present example, the face orientation may be (110) or (111), and solar grade silicon or poly-crystalline silicon may be used. When a silicon substrate having a different resistivity is used, it is necessary to change heating temperature and time.
While a gold metal layer is used in the present example, any metal having a work function greater than that of n-type silicon semiconductor may be used, such as platinum (Pt), tungsten (W), nickel (Ni), iron (Fe), and palladium (Pd).
Example 2 was carried out to fabricate an infrared PV cell 500 as shown in
Note that all of the steps followed in example 2 are substantially the same as steps 402, 404, 406, 408, 410 and 412 of
The foregoing description of preferred embodiments of the present invention has been provided for the purposes of illustration and description. It is not intended to be exhaustive or to limit the invention to the precise forms disclosed. Various additions, deletions and modifications are contemplated as being within its scope. The scope of the invention is, therefore, indicated by the appended claims rather than the foregoing description. Further, all changes which may fall within the meaning and range of equivalency of the claims and elements and features thereof are to be embraced within their scope.
This application claims the benefit of U.S. application Ser. No. 13/844,686, filed Mar. 15, 2013 (Attorney Docket No. 44671-047 (P7)); U.S. Provisional Application No. 61/761,342, filed Feb. 6, 2013 (Attorney Docket No. 446714-047 (P7)); U.S. application Ser. No. 13/844,298, filed Mar. 15, 2013 (Attorney Docket No. 44671-033 (P2)); U.S. Provisional Application No. 61/619,410, filed Apr. 2, 2012 (Attorney Docket No. 44671-033 (P2)); U.S. application Ser. No. 13/844,428, filed Mar. 15, 2013 (Attorney Docket No. 44671-034 (P3)); U.S. Provisional Application No. 61/722,693, filed Nov. 5, 2012 (Attorney Docket No. 44671-034 (P3)); U.S. application Ser. No. 13/844,521, filed Mar. 15, 2013 (Attorney Docket No. 44671-035 (P4)); U.S. Provisional Application No. 61/655,449, filed Jun. 4, 2012 (Attorney Docket No. 44671-035 (P4)); U.S. application Ser. No. 13/844,747, filed Mar. 15, 2013 (Attorney Docket No. 44671-038 (P5)); U.S. Provisional Application No. 61/738,375, filed Dec. 17, 2012 (Attorney Docket No. 44671-038 (P5)); U.S. Provisional Application No. 61/715,283, filed Oct. 17, 2012 (Attorney Docket No. 44671-041 (P12)); U.S. Provisional Application No. 61/715,286, filed Oct. 18, 2012 (Attorney Docket No. 44671-043 (P13)); U.S. Provisional Application No. 61/715,287, filed Oct. 18, 2012 (Attorney Docket No. 44671-044 (P14)); U.S. Provisional Application No. 61/801,019, entitled Manufacturing Equipment for Photovoltaic Devices, filed 15 Mar. 2013 (Attorney Docket No. 44671-050 (P32)); U.S. Provisional Application No. 61/800,912, entitled infrared Photovoltaic Device, filed 15 Mar. 2013 (Attorney Docket No. 44671-049 (P10)); U.S. Provisional Application No. 61/800,800, entitled Hybrid Transparent Electrode Assembly for Photovoltaic Cell Manufacturing, filed 15 Mar. 2013 (Attorney Docket No. 44671-048 (P23)); U.S. Provisional Application No. 61/801,145, entitled PIN Photo-voltaic device and Manufacturing Method, filed 15 Mar. 2013 (Attorney Docket No. 44671-051 (P17)), and U.S. Provisional Application No. 61/801,244, entitled Infrared Photo-voltaic device and Manufacturing Method, filed 15 Mar. 2013 (Attorney Docket No. 44671-052 (P36)), the entireties of which are incorporated by reference as if fully set forth herein. This invention relates to copending U.S. patent application Ser. No. 13/844,686, filed 15 Mar. 2013 (docket number P7, sub case 003); the entirety of which is incorporated by reference as if fully set forth herein.
Number | Date | Country | |
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61801244 | Mar 2013 | US | |
61800800 | Mar 2013 | US | |
61800912 | Mar 2013 | US | |
61801019 | Mar 2013 | US | |
61801145 | Mar 2013 | US | |
61761342 | Feb 2013 | US | |
61722693 | Nov 2012 | US | |
61715283 | Oct 2012 | US | |
61715286 | Oct 2012 | US | |
61715287 | Oct 2012 | US | |
61619410 | Apr 2012 | US | |
61655449 | Jun 2012 | US | |
61738375 | Dec 2012 | US |
Number | Date | Country | |
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Parent | 13844686 | Mar 2013 | US |
Child | 14216540 | US | |
Parent | 13844428 | Mar 2013 | US |
Child | 13844686 | US | |
Parent | 13844298 | Mar 2013 | US |
Child | 13844428 | US | |
Parent | 13844521 | Mar 2013 | US |
Child | 13844298 | US | |
Parent | 13844747 | Mar 2013 | US |
Child | 13844521 | US |