The present invention relates to photovoltaic devices, and in particular, a 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. 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.
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 has greater cell efficiency than those manufactured by prior art processes.
Preferred embodiments of the present invention provide a hybrid transparent electrode assembly for a polyvoltaic cell and a method of manufacturing.
A photovoltaic cell comprising a top transparent electrode, a PV structure or layer, a semiconductor substrate, a bottom electrode, and a metal bus-bar grid assembly deposited on the top transparent electrode.
The method of manufacturing the PV device or cell includes the steps of: cleaning a preprocessed semiconductor bulk having a PV layer on its top surface; depositing a layer of a transparent conductive film over the top of said PV layer; depositing a metal bus-bar grid assembly over said transparent conductive film; and depositing a metal bottom layer on the bottom surface of said semiconductor bulk.
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.
The present invention describes a method to improve cell efficiency by means of optimizing cell top electrode design of a PC cell by using a hybrid top electrode assembly specifically designed for PV cells such as the one described in
Specific details of the fabrication of the preprocessed PV layer are disclosed in U.S. Provisional Application No. 61/715,283, filed 17 Oct. 2012 (docket number P 12); U.S. Provisional Application No. 61/715,286, filed 18 Oct. 2012 (docket number P 13); U.S. Provisional Application No. 61/715,287, filed 18 Oct. 2012 (docket number P 14); U.S. Provisional Application No. 61/761,342, filed 6 Feb. 2013 (docket number P7, sub case 002); and U.S. Provisional application Ser. No. 13/844,686, filed 15 Mar. 2013 (docket number P7, sub case 003); the entireties of which are incorporated by reference as if fully set forth herein.
As disclosed in U.S. Provisional application Ser. No. 13/844,686, filed 15 Mar. 2013 (docket number P7, sub case 003), the fabrication of a PV layer is done by a variety of heating methods, 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 PC layer have an effect 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 parameters. The overall parameters used during heating step include temperatures ranging from 852 to 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 transforms into a photovoltaic semiconductor material having a high-resistivity layer therein
The PV cell 100 described in
It has been found that adding a new component to the TCO electrode, a bus-bar and finger electrodes assembly, will greatly improve the overall electrode electric characteristics, while minimizing the TCO thickness, hence maximizing its transmittance, and therefore improving overall PV cell performance, or efficiency. Specifically, hybrid electrode design of the present invention consists of depositing a layer of a TCO layer over a layer of a metallic bus-bar and finger electrodes, that is been deposited on the PV structure shown in
Specifically in
A typical description of this hybrid top electrode assembly and its dimensions are described in TABLE 1 below.
A commercially available transparent conductive oxide film such as ITO, ZnO, AZO, GZO, IZO, and NbO2 or a stacked structure thereof may be used and the transparent conductive oxide film may be formed by PLD, MOCVD, or a coating method, not limited to the sputtering method.
The metal bus-bar grid may be stacked on top of the TCO surface by PLD, MOCVD, or a coating method, sputtering, screen printing and any other deposition method.
In the following, an embodiment of the present invention will be explained according to a process flowchart 500 of attached
First in PC cell preparation step 502, a preprocessed PV cell, as described in copending U.S. Provisional Application No. 61/715,283, filed 17 Oct. 2012 (docket number P 12) and the other provisional patent applications referred to above, is cleaned utilizing a 2% neutral detergent solution, commonly used for abrading agent removal in solar cell manufacturing process, in an ultrasonic bed for about 10 minutes.
Next in placement of ITO film step 504, a transparent conductive oxide (TCO) film, such as ITO, was formed over the top cell surface by a sputtering method. Several specimens with different ITO thickness were manufactured, varying from 85 nm to 700 nm.
While ITO was used in the present example, another transparent conductive oxide film such as ZnO, AZO, GZO, IZO, and NbO2 or a stacked structure thereof may be used and the transparent conductive oxide film may be formed by PLD, MOCVD, or a coating method, not limited to the sputtering method.
Transmittance properties of the ITO film deposited on the photovoltaic cell, for different ITO layer thicknesses, are shown in
Next in placement of metal bus-bar grid step 506, a metal bus-bar grid assembly was deposited on top of the ITO film, using silver paste, by screen printing method. Numerous geometries were tested, but typical mode results are shown in TABLE 2 below:
Next in placement of back electrode 508, silver paste was coated by screen printing on the rear surface of the cell, as back electrode. The thickness of this back-surface coating PC cell 108 was around 10 micrometers.
These dimensions are shown only as an example. To obtain best results, the geometry and dimensions of this bus-bar grid assembly need to be optimized to type of TCO, type metal, and method of deposition used. For this particular example, commercially available low sintering temperature silver paste, were used. Deposition method use was screen printing.
Finally in firing step 510, the cell assembly was heated to 470° K for removing solvent containing binder, completing the PV cell or solar cell fabrication.
The remaining cell testing step 512 was conducted, the tests and the results are set forth below.
In order to illustrate the properties of the hybrid top electrode assembly, industry standard bias I-V curve characterization tests were performed on several specimens for various ITO film thicknesses and metal bus-bar geometries. Best results were obtained with cell manufactured using top hybrid electrode assembly with dimensions described in Table 2 above.
For evaluation purposes, cell's series resistance (RS) and fill factor (FF) were utilized in this example (see
The thinner the ITO layer on top of the cell, the higher the series resistance become. Cell efficiency will deteriorate as the RS value increases.
However, when a bus-bar grid is place on top of the ITO layer the RS values become unaltered, irrespective of the ITO layer thickness changes. Therefore, same cell efficiency values can be obtained when using ultra thin ITO layer thickness, as long as a metal bus-bar grid is placed on top of the ITO layer.
In addition, as shown in
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. application Ser. No. 13/844,298, filed Mar. 15, 2013 (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. application Ser. No. 13/844,521, filed Mar. 15, 2013 (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. 61/801,019, entitled Manufacturing Equipment for Photovoltaic Devices, filed 15 Mar. 2013 (Attorney Docket No. 44671-050 (P 32)); U.S. Provisional Application No. 61/800,912, entitled Infrared Photovoltaic Device, filed 15 Mar. 2013 (Attorney Docket No. 44671-049 (P 10)); 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 (P 17)), 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 application is related to copending U.S. Provisional Application No. 61/715,283, filed 17 Oct. 2012 (docket number P 12); U.S. Provisional Application No. 61/715,286, filed 18 Oct. 2012 (docket number P 13); U.S. Provisional Application No. 61/715,287, filed 18 Oct. 2012 (docket number P 14); U.S. Provisional Application No. 61/761,342, filed 6 Feb. 2013 (docket number P7); and U.S. application Ser. No. 13/844,686, filed 15 Mar. 2013 (docket number P7); the entireties of which are incorporated by reference as if fully set forth herein.
Filing Document | Filing Date | Country | Kind |
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PCT/US14/30079 | 3/15/2014 | WO | 00 |
Number | Date | Country | |
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61722693 | Nov 2012 | US | |
61738375 | Dec 2012 | US | |
61619410 | Apr 2012 | US | |
61722693 | Nov 2012 | US | |
61655449 | Jun 2012 | US | |
61722693 | Nov 2012 | US | |
61655449 | Jun 2012 | US | |
61619410 | Apr 2012 | US | |
61801145 | Mar 2013 | US | |
61722693 | Nov 2012 | US | |
61655449 | Jun 2012 | US | |
61619410 | Apr 2012 | US | |
61715280 | Oct 2012 | US | |
61761342 | Feb 2013 | US | |
61738375 | Dec 2012 | US | |
61715283 | Oct 2012 | US | |
61715286 | Oct 2012 | US | |
61715287 | Oct 2012 | US | |
61801244 | Mar 2013 | US | |
61800800 | Mar 2013 | US | |
61800912 | Mar 2013 | US | |
61801019 | Mar 2013 | US | |
61619410 | Apr 2012 | US |
Number | Date | Country | |
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Parent | 13844747 | Mar 2013 | US |
Child | 14777482 | US | |
Parent | 13844521 | Mar 2013 | US |
Child | PCT/US14/30079 | US | |
Parent | 13844428 | Mar 2013 | US |
Child | PCT/US14/30079 | US | |
Parent | 13844686 | Mar 2013 | US |
Child | PCT/US14/30079 | US | |
Parent | 13844298 | Mar 2013 | US |
Child | 13844686 | US |