This invention relates to manufacturing a photovoltaic device with a vapor transport deposition process.
Manufacturing a photovoltaic device can include depositing a semiconductor layer. Some available deposition techniques (e.g. sputtering, evaporation) are line-of-sight depositions. As a result, these deposition techniques can be problematic for conformal coating of rough surface.
Photovoltaic devices can include multiple layers formed on a substrate (or superstrate). For example, a photovoltaic device can include a conducting layer, a semiconductor absorber layer, a buffer layer, a semiconductor window layer, and a transparent conductive oxide (TCO) layer, formed in a stack on a substrate. Each layer may in turn include more than one layer or film. For example, the semiconductor window layer and semiconductor absorber layer together can be considered a semiconductor layer. The semiconductor absorber layer can include copper-indium-gallium-(di)selenide (CIGS). The semiconductor layer can include a first film created (for example, formed or deposited) on the TCO layer and a second film created on the first film. Additionally, each layer can cover all or a portion of the device and/or all or a portion of the layer or substrate underlying the layer. For example, a “layer” can mean any amount of any material that contacts all or a portion of a surface.
Manufacturing a photovoltaic device can include depositing a semiconductor layer. For example, in manufacturing CIGS-based photovoltaic (PV) device, a buffer layer can be deposited by chemical bath deposition (CBD). Layers of In2S3, ZnS, or ZnSe can be deposited by various means. However, some available deposition techniques (e.g. sputtering, evaporation) are line-of-sight depositions. As a result, these deposition techniques can be problematic for conformal coating of a rough surface. A vapor transport deposition process and related deposition system are developed to achieve better results.
The present invention addresses aspects of manufacturability as well as a novel concept to deposit a semiconductor layer, such as In2S3, for applications which might include, but are not limited to, CIGS devices. Rather than depositing the compound layer via evaporation of its constituent elements In and S or directly evaporating from the compound onto the substrate, a vapor transport assisted growth process is developed.
In2S3 melts at 1050° C. and sublimes at lower temperatures to a vapor of In2S and S2. At the same time, the resulting evaporated pure In2S3 films result in an optical bandgap of approx. 2.0-2.2 eV. For use in PV devices, a larger bandgap is preferable in order to increase the device generated photocurrent. Controlled addition of oxygen can widen the direct optical band gap up to potentially that of In2O3 (3.6 eV).
Using an oxygen diluted transport gas in a vapor transport deposition (VTD) process can allow for partial oxidation and transport of the sublimed In2S3 vapor to the heated substrate for subsequent film growth. By practicing the composition and associated bandgap modification in the In-chalcogenide material system and their applications as buffer layers in CIGS devices, the films can be manufactured in the full bandgap range from In2Se3 to In2O3—i.e. In2(O,S,Se)3. However, due to the tendencies of chalcogenide displacement/stability of the individual chalcogenides, it is preferable to start with In2Se3 and facilitate the growing film to react with S vapor and O2 in reactive mode rather than in the transport gas.
In some embodiments, a further implementation of VTD for buffer layers in CIGS devices is the formation of ZnS, ZnSe, ZnO, and Zn (O,S,Se). The sublimation temperature of ZnS is about 1180° C. while ZnSe sublimation has been reported in the range of 850-1200° C. The same approach as has been described above in the case of In-based chalcogenide buffer films can be taken to prepare Zn(O,S,Se) layers via VTD, resulting in a tunable bandgap range of 2.67 to 3.7 eV.
In some embodiments, in a two step VTD process, VTD of In2(O,S,Se)3 and Zn(O,S,Se) can be combined to grade the buffer layer in composition and bandgap via both metal and chalcogenide content.
In one aspect, a method of manufacturing a photovoltaic device can include forming a semiconductor absorber layer adjacent to a substrate. The semiconductor absorber layer can include copper indium gallium diselenide. The method can include heating a deposition material to form a deposition material vapor. The deposition material can include a metal chalcogenide. The method can include transporting the deposition material vapor to a deposition chamber with a transport gas through a delivery pipe. The method can include forming a buffer layer including the deposition material adjacent to the semiconductor absorber layer.
The method can include forming a conducting layer adjacent to the substrate before forming the semiconductor absorber layer adjacent to the substrate. The method can include forming a transparent conductive oxide layer adjacent to the buffer layer. The method can include forming a semiconductor window layer adjacent to the buffer layer before forming a transparent conductive oxide layer adjacent to the buffer layer. The deposition material can include indium sulfide. The deposition material can include an indium chalcogenide. The deposition material can include indium selenide. The deposition material can include zinc sulfide. The deposition material can include a zinc chalcogenide. The deposition material can include zinc selenide. The step of heating the deposition material can occur in an environment including oxygen.
The buffer layer further can include oxygen. The step of heating the deposition material can include heating the deposition material to a temperature greater than about 800 degrees C. The step of heating the deposition material can include heating the deposition material to a temperature greater than about 1000 degrees C. The method can include distributing the deposition material vapor evenly over the width of the substrate. The method can include mixing the deposition material vapor and the transport gas to facilitate the reaction between the vapor and the transport gas before the vapor exits the distributor. The method can include mixing the deposition material vapor and the transport gas to facilitate the reaction between the vapor and the transport gas after the vapor exits the distributor. The method can include heating the delivery pipe. The transport gas can include helium.
In another aspect, a vapor transport deposition system for manufacturing a photovoltaic device can include a deposition material source including a deposition material. The deposition material can include a material including indium or zinc. The system can include a heater to heat the deposition material into a deposition material vapor. The system can include a structure including a substrate, a conducting layer, and a semiconductor absorber layer. The semiconductor absorber layer can include copper indium gallium diselenide. The system can include a transport gas source which can transport the deposition material vapor. The system can include a delivery pipe which can deliver the transport gas and deposition material vapor to a position adjacent to the structure, resulting in the deposition material vapor being deposited adjacent to the semiconductor absorber layer to form a buffer layer.
The delivery pipe can be configured to mix the vapor and the transport gas and further facilitate the reaction between the vapor and the transport gas. The system can include a distributor in the deposition chamber for evenly distributing the vapor over the width of the substrate. The distributor can be configured to mix the vapor and the transport gas and further facilitate the reaction between the vapor and the transport gas. The system can include a conveyor for conveying a substrate adjacent to the distributor for deposition of the vapor as a layer on the substrate.
The deposition material can include indium sulfide. The deposition material can include an indium chalcogenide. The deposition material can include indium selenide. The deposition material can include zinc sulfide. The deposition material can include a zinc chalcogenide. The deposition material can include zinc selenide. The transport gas can include helium. The transport gas can include oxygen. The transport gas can include a mixture of helium and oxygen.
In another aspect, a method of depositing a material on a substrate can include heating a deposition material to form a deposition material vapor. The deposition material can include indium or zinc. The method can include transporting the deposition material vapor to a deposition chamber with a transport gas through a delivery pipe. The method can include forming a layer comprising the deposition material adjacent to the substrate. The deposition material can include indium sulfide. The deposition material can include an indium chalcogenide. The deposition material can include indium selenide. The deposition material can include zinc sulfide. The deposition material can include a zinc chalcogenide. The deposition material can include zinc selenide. The method can include reacting the deposition material vapor with oxygen present in the deposition chamber environment.
In another aspect, a photovoltaic device can include a substrate, a semiconductor absorber layer including copper indium gallium diselenide adjacent to the substrate, and a buffer layer including a metal chalcogenide adjacent to the semiconductor absorber layer. The photovoltaic device can include a conducting layer between the substrate and the semiconductor absorber layer. The photovoltaic device can include a transparent conductive oxide layer adjacent to the buffer layer. The photovoltaic device can include a semiconductor window layer between the buffer layer and the transparent conductive oxide layer. The buffer layer can include an indium chalcogenide. The buffer layer can include a zinc chalcogenide. The buffer layer can include oxygen.
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In some embodiments, tubular permeable member 24 can be made of silicon carbide although it could also be made of permeable carbon or any other permeable material that is preferably electrically conductive to provide the heating in the manner disclosed. Furthermore, distributor 22 can include shroud 34 of a generally tubular shape that receives the tubular permeable member 24 shown in
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Shroud 34 can also advantageously reduce radiant heat transfer from hot tubular permeable member 24 to glass substrate 100. Substrate 100 can be heated during the processing to a temperature of about 100° to 650° C., 300° to 750° C., or 300° to 850° C., or any suitable value. More specifically, the amount of energy shroud 34 radiates to glass substrate 100 can be reduced because its outside surface temperature is lower than that of hot tubular permeable member 24. Mullite has an adequately low emissivity and is relatively strong and easy to fabricate. In addition, coatings can be provided to lower the emissivity of the outer surface of shroud 34 such as Al2O3 or Y2O3 .
In some embodiments, the length of the slit-shaped opening 36 of the shroud 34 can be selected to control the extent of the width of the deposited layer on glass substrate 100. Thus, the length of split-shaped opening 36 can be selected to be less than the width of the glass sheet substrate to provide a strip of the deposited layer. Such control can also minimize waste of the vapors. When the entire width of the substrate is to be covered, one can ideally make the length of the slit-shaped opening 36 equal to or slightly less or more than the width of the substrate such that the substantially all of the vapors are deposited onto the substrate during the deposition.
In providing efficient deposition, shroud 34 has been spaced from the conveyed glass sheet substrate a distance in the range of 0.5 to 3.0 centimeters. Greater spacings can be utilized that would require lower system pressures and would result in vapor waste due to overspraying. Furthermore, smaller spacing could cause problems due to thermal warpage of the glass sheet substrate during conveyance. Smaller spacing can also caused the desired substrate temperature for the process to be exceeded.
Referring to
Each of material supplies 30 can include rotary screw 44 that receives semiconductor powder 40 from hopper 42 and can be rotatively driven by actuator 46. Delivery pipe 48 can extend from carrier gas source 38 to the adjacent end 28 of porous tubular member 24 in communication with rotary screw 44. Rotation of screw 44 at a controlled rate introduces semiconductor powder 40 into delivery pipe 48 so as to be entrained therein for flow into tubular permeable member 24 for the heating that provides the vapor.
In some embodiments, the deposition of a semiconductor layer of photovoltaic device, such as a buffer layer of CIGS modules, can be a two step VTD process. Referring to
Furthermore, in other embodiments, oxygen can be added to the transport gas or after the vapor exits the VTD source if only In2S3 (ZnS, In2Se3, ZnSe) is to be effluent from the distributor 24. In2S3 can be evaporated or otherwise vaporized in a partial oxygen ambient directing the vapor to the substrate without the use of a VTD source. In some embodiments, the deposition of a buffer layer of CIGS modules can be performed with a process evaporating from the elements In (Zn) and S in a partial oxygen ambient directing the vapor to the substrate without the use of a VTD source, such as reactive evaporation methods.
Referring to
A number of embodiments of the invention have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of the invention. It should also be understood that the appended drawings are not necessarily to scale, presenting a somewhat simplified representation of various preferred features illustrative of the basic principles of the invention.
This application claims priority under 35 U.S.C. §119(e) to Provisional U.S. Patent Application Ser. No. 61/367,121, filed on Jul. 23, 2010, which is hereby incorporated by reference.
Number | Date | Country | |
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61367121 | Jul 2010 | US |