1. Field of the Invention
The present invention relates to thermal reactors, and more specifically to thermal reactors for preparing thin films of Group IBIIIAVIA compound semiconductors for photovoltaic devices.
2. Description of the Related Art
Solar cells are photovoltaic (PV) devices that convert sunlight directly into electrical energy. Solar cells can be based on crystalline silicon or thin films of various semiconductor materials that are usually deposited on low-cost substrates, such as glass, plastic, or stainless steel.
Thin film based photovoltaic cells, such as amorphous silicon, cadmium telluride, copper indium diselenide or copper indium gallium diselenide based solar cells offer improved cost advantages by employing deposition techniques widely used in the thin film industry. Group IBIIIAVIA compound photovoltaic cells, including copper indium gallium diselenide (CIGS) based solar cells, have demonstrated the greatest potential for high performance, high efficiency, and low cost thin film PV products.
As illustrated in
After the absorber film 14 is formed, a transparent layer 15, for example, a CdS film, a ZnO film or a CdS/ZnO film-stack, is formed on the absorber film 14. Light enters the solar cell 10 through the transparent layer 15 in the direction of the arrows 16. The preferred electrical type of the absorber film is p-type, and the preferred electrical type of the transparent layer is n-type. However, an n-type absorber and a p-type window layer can also be formed. The above described conventional device structure is called a substrate-type structure. In the substrate-type structure light enters the device from the transparent layer side as shown in
Contrary to CIGS and amorphous silicon cells, which are fabricated on conductive substrates such as aluminum or stainless steel foils, standard silicon solar cells are not deposited or formed on a protective sheet. Such solar cells are separately manufactured, and the manufactured solar cells are electrically interconnected by a stringing or shingling process to form solar cell circuits. In the stringing or shingling process, the (+) terminal of one cell is typically electrically connected to the (−) terminal of the adjacent solar cell. Circuits may then be packaged in protective packages to form modules. Each module typically includes a plurality of strings of solar cells which are electrically connected to one another.
In a thin film solar cell employing a Group IBIIIAVIA compound absorber, the cell efficiency is a strong function of the molar ratio of IB/IIIA. If there are more than one Group IIIA materials in the composition, the relative amounts or molar ratios of these IIIA elements also affect the properties. For a Cu(In,Ga)(S,Se)2 absorber layer, for example, the efficiency of the device is a function of the molar ratio of Cu/(In+Ga). Furthermore, some of the important parameters of the cell, such as its open circuit voltage, short circuit current and fill factor, vary with the molar ratio of the IIIA elements, i.e. the Ga/(Ga+In) molar ratio. In general, for good device performance the Cu/(In+Ga) molar ratio is kept at around or below 1.0. On the other hand, as the Ga/(Ga+In) molar ratio increases, the optical bandgap of the absorber layer increases and therefore the open circuit voltage of the solar cell increases while the short circuit current may typically decrease. It is important for a thin film deposition process to have the capability of controlling both the molar ratio of IB/IIIA, and the molar ratios of the Group IIIA components in the composition.
As mentioned above, the second step or the reaction step of the two-step process involves the reaction process of the precursor stack that is formed at the first step of the two step process. The reaction process can be performed in radiation heating reactors or thermal reactors using, for example, resistance heaters. In general the thermal reactors can be atmospheric-pressure (AP) or Sub-Atmospheric (SA) thermal reactors. Such reactors are generally designed for thermal processing of thin-film solar cell materials deposited on a metallic substrate or foil.
During a thermal process, however, the metallic substrate expands as it is heated and contracts as it is cooled. Due to the inherent lack of rigidity of such structures, such expansion and contraction cause mechanical buckling of the substrate which manifests itself as bubbles, ridges and ripples. In addition, the metallic substrates may be produced with inherent distortions such as camber, scallops and quilting. Any distortion which causes the substrate to be in contact with the reactor bottom in some areas and not in others will naturally cause a different localized heating or cooling rate in the substrate and the material thereon. The areas in contact with the reactor walls will heat or cool more rapidly than those that are not in contact. For some types of processes such as the selenization of CIGS, this may cause significant variations in the properties of the synthesized solar cell absorber. Since it is not known how to enforce uniform heating or cooling by suppressing the aforementioned substrate distortions, it is best to enforce uniform heating or cooling through radiation transfer, convection and other means that do not require contact. A natural solution to these problems is to suspend the web at a distance over the bottom of the furnace.
However, in a selenization process, the excess furnace volume required to suspend the substrate over a distance of hundreds of millimeters will reduce the concentration of reactive selenium vapor in the furnace. Such reduced concentration of selenium, in turn, reduces the quality of the CIGS semiconductor produced by such a process. Further problems can also arise when a large excess space exists under the suspended substrate. For example, the process gas containing selenium vapor is entrained by viscous drag on the top and bottom surfaces of the suspended substrate. This process gas can be dragged into the end of the ramp or cool zone and then is forced outward towards the web edge. The process gas then flows upwards and subsequently distorts gas flows above the substrate where the deposited precursor is located. This creates undesirable multidirectional gas flows which can create cross-web nonuniformity in the Selenium concentration and subsequent properties of the synthesized CIGS semiconductor
Internal design of the reactors is critical for the quality of the manufactured thin films. Deposition and growth of layers forming a thin film solar cell in a roll-to-roll or in-line process is attractive for higher throughput, lower cost and better yield of such approaches. There is a need, however, to develop roll-to-roll or in-line CIGS growth techniques in which the CIGS material composition and properties are tightly controlled.
The present invention provides a roll-to-roll thermal reactor including an elongated process chamber and a roll-to-roll reaction method for forming thin films from precursor materials deposited on substrates.
In an aspect of the present invention, the elongated chamber includes a bottom wall with a reduced contact surface region so as to minimize the physical contact between the substrate and the bottom wall of the elongated chamber of the reactor as the substrate including the precursor thereon is advanced on the reduced contact surface region. The reduced contact between the substrate and the bottom wall enables uniform heat transfer to the substrate without abrupt temperature changes when the substrate is heated and cooled.
In another aspect of the present invention, each heat zone within the elongated process chamber is lined with a high thermal conductivity layer terminating with low thermal conductivity separator regions that separate one heat zone from the next heat zone.
In one aspect, the aforementioned problems are addressed by a roll-to-roll thermal reactor to heat and react a precursor material disposed over a continuous workpiece to form a solar cell absorber. In this aspect, the reactor comprises an elongated process enclosure defined by a peripheral wall including a top wall, side walls and a bottom wall, wherein the continuous workpiece enters the elongated process enclosure from an entrance opening, advances through the elongated process chamber while contacting the bottom wall, and exits from an exit opening. In this aspect, the reactor further comprises at least one reduced contact surface region formed in an inner surface of the bottom wall so that the physical contact between the workpiece and the bottom wall is reduced, wherein the reduced contact surface region includes a plurality of fixed protrusions projecting upwardly from the inner surface of the bottom wall and wherein the workpiece touches topmost ends of the plurality of fixed protrusions.
In another aspect, the aforementioned problems are addressed by a solar cell processing system comprising a continuous workpiece containing a precursor material used to form a solar cell absorber. The system further comprises a reactor having a inlet and an outlet and a central chamber disposed between the inlet and the outlet, wherein the continuous workpiece is provided into the inlet of the reactor and extends through the central chamber and exits via the outlet wherein a portion of the reactor includes a reduced contact surface where the bottom surface of the continuous workpiece is intermittently supported by the reduced contact surface. The system further comprises a heating system that heats the reactor; and a gas supply system that provides reactive gas into the reactor so that the combination of the reactive gas and the heat from the heating system transforms the precursor material on the continuous workpiece in the solar cell absorber.
Embodiments of the present invention provide a roll-to-roll thermal reactor including an elongated process chamber or reactor chamber and a roll-to-roll reaction method for forming thin films from precursor materials deposited on substrates.
In one embodiment, a roll-to-roll process of the present invention may be exemplified using a continuous workpiece or a workpiece including a multilayer Group IBIIIAVIA precursor deposited on a continuous substrate using various deposition methods. This workpiece may be processed in the elongated chamber of the present invention to manufacture Group IBIIIAVIA solar cell absorbers by reacting the CIGS precursor layer comprising copper (Cu), indium (In), gallium (Ga) and at least one Group VIA material such as selenium (Se). The roll-to-roll process reactor applies a process temperature to the workpiece at a predetermined rate and according to a predetermined temperature profile to convert the precursor layer into a CIGS thin film absorber as the workpiece is advanced through the reactor. The process involves heating the CIGS precursor layer to a temperature range of 300-700° C., preferably to a range of 400-600° C., in the presence of at least one of a reactive gas containing Se and an inert gas such as nitrogen (N2), while advancing the workpiece through the elongated process chamber and cooling the workpiece. Heat may preferably be transferred to the advancing workpiece from the elongated chamber walls which are heated. In one embodiment, the elongated chamber of the roll to roll reactor includes a bottom wall with a reduced contact surface region so as to reduce the physical contact between the substrate and the bottom wall of the elongated chamber of the reactor as the substrate, including the precursor thereon, is advanced on the reduced contact surface region. The reduced contact between the substrate and the bottom wall enables more uniform heat transfer to the substrate with less abrupt temperature changes as the substrate is heated and cooled. In another embodiment, each heat zone within the elongated process chamber is lined with a high thermal conductivity material separated by low thermal conductivity regions. For the various embodiments described below, a high thermal conductivity material may have a thermal conductivity of greater than 5 W/m-K, and a low thermal conductivity material may have a thermal conductivity of less than 2 W/m-K.
In one embodiment, the reduced contact surface region includes fixed protuberances that may make brief incidental contact with the continuous substrate to support the workpiece above the bottom wall without creating excess volume under the workpiece. In one embodiment, the fixed protuberances include, but are not limited to, widely spaced ridges, bumps, balls, nubs, bars or other small protruding features. This design supports the workpiece, reduces the time that the continuous substrate touches the bottom wall, and reduces or eliminates drastic changes in heating rate, especially in heat ramp-up and heat ramp-down zones of the elongated process chamber. Short incidental contact with these protuberances should not have a material influence on the localized heating rate, especially when these protuberances are fabricated from a low thermal conductivity material such as fused silica.
In one embodiment, the elongated chamber 100 includes a peripheral wall 104 defining an internal process space 106 or process space to heat, flow a process gas and to advance a continuous workpiece 102 in a process direction ‘P’ between an entrance opening 112A located at a first end 114A of the elongated chamber 100 and an exit opening 112B located at a second end 114B of the elongated chamber 100. At least a portion of the peripheral wall 104 is heated to a reaction temperature to provide heat for the reaction of the precursor. The peripheral wall 104 includes a top wall 104A, a bottom wall 104B and side walls 104C. The internal space 106 of the elongated chamber may be further defined by an inner surface 107 of the top wall 104A or the inner top surface 107, an inner surface 109 of the bottom wall 104B or the inner bottom surface 109, and inner surfaces 111 of the side walls 104C or the inner side wall surfaces 111. The internal space 106 may be divided into several sections or temperature zones of the elongated chamber 100. Accordingly, the axis of the elongated chamber 100 and the inner space 106 defined by the inner surfaces 107, 109 and 111 is preferably parallel to the x-axis, the transverse axis is parallel to the y-axis, and the vertical axis is parallel to the z-axis. As will be described below, the peripheral wall 104 of the elongated chamber 100 may include one or more inner layers called liner or insert which may be made of high thermal conductivity materials.
The process direction ‘P’ is parallel to the axial direction of the elongated chamber 100. In this embodiment an axial length of the elongated chamber is greater than the width or transverse length of the elongated chamber 100. In a roll-to-roll process operation, the continuous workpiece 102 may be a sheet-shaped workpiece that enters the process space from the entrance opening 112A, advances though process space and leaves the process space from the exit opening 112B. In this embodiment, the front surface 103A of the continuous workpiece is exposed to the process space 106 and the process gas as the workpiece 102 is advanced therethrough while the back surface 103B is supported by the inner bottom surface 109 of the bottom wall 104B. The process gas, including at least one of a reactive gas such as selenium or a selenium-containing gas and an inert gas such as nitrogen, may be delivered into the process space 106 through the entrance opening 112A or a gas inlet adjacent to the entrance opening in the process direction ‘P’. An exhaust gas that is produced during the reaction may be removed through a gas exhaust located between the entrance opening 112A and the exit opening 112B. As mentioned above, the elongated chamber 100 and hence the internal process space 106 may be divided into several sections or zones including different heating and cooling characteristics to process the workpiece 102 as it is advanced therethrough. In one embodiment, the process space 106 of the elongated chamber may have a width in the range of 10-200 cm and a height in the range of 2-40 mm.
In one embodiment, the protuberances 122 may be formed as a part of the bottom wall using many manufacturing methods such as direct machining into the desired sections of the bottom wall material, such as silicon carbide, aluminum nitride, graphite, silicon nitride, aluminum oxide or using other known manufacturing methods to manufacture with the bottom wall material. When formed as the part of the bottom wall, both the protrusions and the bottom wall are made of the same material. However, a special surface coating layer including a low thermal conductive material, such as fused silica, and other amorphous ceramics, ceramoplastics, glass-ceramic, microporous ceramics, and the like, may be coated on such manufactured protuberances to make the protrusions less thermally conductive than the bottom wall material which may be a high thermal conductivity material. Alternatively, the protuberances may be manufactured as separate pieces which may include the same material as the bottom wall material or a different material from the bottom wall material. When separate pieces such as rods or balls are used, the protuberances may be made of low thermal conductivity materials, such as fused silica, whereas the bottom wall is made of high thermal conductivity material such as silicon carbide or aluminum nitride. The separate protuberance pieces may be attached or fastened to the bottom wall using many methods. For example, they may be inserted into recesses that are preformed in the desired sections of the bottom wall 104B. Best results may be obtained if such protuberances are thermal insulators and resistant to high temperature corrosion and mechanical wear applied by the workpiece.
The height of the protuberances above the inner bottom surface 109 of the bottom wall 104B can be quite small, for example on the order of a few millimeters, preferably 0.5-5 mm, and more preferably 1-3 mm. Such small protuberances elevate the workpiece 102 off the inner surface of the bottom wall 104A while minimizing the volume under the workpiece 102. In addition, the protuberances 122 may disrupt viscous process gas flow under the workpiece 102 and cause a series of small and uniform outward process gas flows which have a less disruptive effect than the sort of large non-uniform and multidirectional gas flows described above in the background section. The protuberances may be distributed as a pattern along rows extending along the transverse axis and/or columns extending along the axis on the bottom wall 104B. In this respect if the protuberances are laid out as rows, each row may include a single piece protuberance such as cylindrical rods, triangular rods, rectangular rods and the like. Each row may be made of multiple pieces of protuberances including more than one protuberance such as rows of hemispherical, pyramidal, conical, cylindrical or the like protuberances. A preferred distance between the uppermost ends of the protuberances along the axis and the transverse axis may be in the range of 25-50 mm.
An exemplary width for the protuberances may be less than 20 mm. The uppermost ends 124 of the protuberances may be coplanar. The protuberances may have the same height, for example, in the range of 1-10 mm. However, some of them may be made shorter to reduce the incidents of physical contact with the reduced contact surface region while still assisting to disrupt non-uniform gas flow under the workpiece. The protuberances 122 may preferably made of materials that are resistant to mechanical wear, especially, at high temperatures such as silicon carbide and aluminum nitride. When such hard materials are used to form the bottom wall of the elongated chamber, the protuberances or ribs may be formed in the bottom wall by directly machining the bottom wall. Exemplary materials for protuberances may be fused silica, silicon carbide, aluminum nitride, glass ceramics and zirconia.
In one implementation, the reduced contact surface comprise a plurality of parallel spaced apart ridges or rods that are approximately 25-50 mm apart and extend substantially across the width of the chamber. These ridges define a contact surface that is approximately between 0.25 mm wide to 1 mm wide in the direction of the process direction P that contact with the bottom surface 103B of the workpiece. In this implementation, the ridges inhibit gas flow in the direction parallel to the direction of process direction P. There may be 20-40 ridges per linear meter. In another implementation, the discrete protrusions, such as fixed balls, pyramids, cylinders etc., may define a contact surface of approximately 1 mm2 that contacts the bottom surface of the workpiece 102 and the protrusions are formed to a density of about 2500 protrusions per square m.
To aid transfer of heat to the process space, it is best to construct or line the elongated chamber of the reactors with materials which have high thermal conductivity such as silicon carbide, graphite, aluminum nitride, and the like high thermal conductivity ceramics or dielectric materials. However such materials can inhibit the maintenance of thermal gradients or profiles configured for the reactor. Because when the entire elongated chamber walls are constricted or lined with such materials and a specific section is heated to a temperature that is different than the neighboring sections have, the applied heat may transfer not only towards this heated zone, but also towards the neighboring zones maintained at different temperature thereby disturbing the desired thermal gradient. An example may be a reaction zone surrounded by heating and cooling zones which need to be maintained at temperatures other than the hotter reaction zones. Furthermore, as it is advanced through the reactor, the heated workpiece or web also transports heat in the direction of motion or the process direction ‘P’. Such transportation of heat with the workpiece may also make precise temperature control or implementing a temperature profile within the reactor more difficult, especially when the process space is heated through the heat transferred from the walls of the reactor chamber. As will be described more fully below, one solution to such problems is to construct the walls of the elongated chamber or inserts (liners) out of materials which have high thermal conductivity but disrupt the liner walls on a periodic basis with sections that have low thermal conductivity such as fused silica and other amorphous ceramics, ceramoplastics, glass-ceramic board, microporous, ceramics, and the like.
As also shown in
In
In one embodiment, the protuberances 122A of the insert may be formed as a part of the bottom plate 130B using, for instance, direct machining into the desired sections of the bottom plate material, such as silicon carbide or aluminum nitride, or using other known manufacturing methods to manufacture with the bottom plate material. When formed as the part of the bottom plate, both the protrusions 122A and the bottom plate 130B are made of the same material. However, a special surface coating layer including a low thermal conductivity material, such as fused silica, amorphous ceramics and flame sprayed ceramics such as alumina, zirconia, yttria-stabilized zirconia, and the like may be coated on such manufactured protuberances to make protrusions less thermally conductive than the bottom plate material which may be a high thermal conductive material. Alternatively, the protuberances 122A may be manufactured as separate pieces which may include the same material as the bottom plate material or a different material from the bottom wall material. When separate pieces such as rods or balls are used, the protuberances may be made of low thermal conductivity materials, such as fused silica, whereas the bottom plate of the insert is made of high thermal conductivity materials such as silicon carbide or aluminum nitride. The separate protuberance pieces may be attached or fastened to the bottom plate 130B using many methods. For example, they may be inserted into recesses that are preformed in the desired sections of the bottom plate 130B or may be glued to the bottom plate using appropriate adhesives.
Referring to
The embodiment shown in
Although the present invention is described with respect to certain preferred embodiments, modifications thereto will be apparent to those skilled in the art. Hence, the scope of the present invention should not be limited to the foregoing description but should be defined by the appended claims.
This application claims the benefit of U.S. Provisional Application No. 61/453,470 filed on Mar. 16, 2011, which is hereby incorporated by reference in its entirety herein.
Number | Date | Country | |
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61453470 | Mar 2011 | US |