The invention relates generally to the field of photovoltaics. In particular, the invention relates to a group of layers used in solar cells and a solar cell made therefrom.
Solar energy is abundant in many parts of the world year around. Unfortunately, the available solar energy is not generally used efficiently to produce electricity. The cost of conventional solar cells, and electricity generated by these cells, is generally very high. For example, a typical solar cell achieves a conversion efficiency of less than 20 percent. Moreover, solar cells typically include multiple layers formed on a substrate, and thus solar cell manufacturing typically requires a significant number of processing steps. As a result, the high number of processing steps, layers, interfaces, and complexity increase the amount of time and money required to manufacture these solar cells.
Accordingly, there remains a need for an improved solution to the long-standing problem of inefficient and complicated solar energy conversion devices and methods of manufacture.
In one embodiment, a photovoltaic device is provided. The device comprises a transparent conducting layer. A p-type semiconductor window layer is disposed over the transparent conducting layer. An n-type semiconductor layer is disposed over the p-type semiconductor window layer. An n-type cadmium telluride absorber layer is disposed between the p-type semiconductor window layer and the n-type semiconductor layer.
In one embodiment, a photovoltaic device is provided. The device comprises an n-type transparent conducting layer. A p-type semiconductor window layer is disposed over the n-type transparent conducting layer. An n-type semiconductor layer is disposed over the p-type semiconductor window layer. An n-type cadmium telluride absorber layer is disposed between the p-type semiconductor window layer and the n-type semiconductor layer.
In another embodiment, is provided a photovoltaic device. The device comprises an n-type transparent conducting layer. A p-type transparent conducting layer is disposed over the n-type transparent conducting layer. A p-type magnesium telluride window layer is disposed over the p-type transparent conducting layer. An n-type cadmium telluride layer having a dopant density of greater than about 1×1017 per cubic centimeter is disposed over the p-type transparent conducting layer. An n-type cadmium telluride absorber layer having a dopant density in the range of about 1×1015 per cubic centimeter to about 1×1016 per cubic centimeter is disposed between the p-type magnesium telluride layer and the n-type cadmium telluride layer having a dopant density of greater than about 1×1017 per cubic centimeter.
In yet another embodiment, is provided a photovoltaic device. The device comprises an n-type transparent conducting layer. A p-type semiconductor window layer having a dopant density of greater than about 1×1018 per cubic centimeter is disposed over the n-type transparent conducting layer. An n-type semiconductor layer having a dopant density of greater than about 1×1017 per cubic centimeter is disposed over the p-type semiconductor window layer. An n-type cadmium telluride absorber layer having a dopant density in a range of about 1×1015 per cubic centimeter to about 1×1016 per cubic centimeter is disposed between the p-type semiconductor window layer and the n-type layer having a dopant density of greater than about 1×1017 per cubic centimeter.
In still yet another embodiment, is provided a photovoltaic device. The device comprises a first n-type transparent conducting layer. A p-type semiconductor window layer having a dopant density of greater than about 1×1018 per cubic centimeter is disposed over the first n-type transparent conducting layer. A second n-type transparent conducting layer is disposed over the p-type semiconductor window layer. An n-type cadmium telluride absorber layer having a dopant density in the range of about 1×1015 per cubic centimeter to about 1×1016 per cubic centimeter is disposed between the p-type semiconductor window layer and the second n-type transparent conducting layer.
In still yet another embodiment, a photovoltaic device is provided. The device comprises a p-type transparent conducting layer. A p-type semiconductor window layer is disposed over the p-type transparent conducting layer. An n-type semiconductor layer is disposed over the p-type semiconductor window layer. An n-type cadmium telluride absorber layer is disposed between the p-type semiconductor window layer and the n-type semiconductor layer.
These and other features, aspects, and advantages of the present invention will become better understood when the following detailed description is read with reference to the accompanying drawings in which like characters represent like parts throughout the drawings, wherein:
The invention relates generally to the field of photovoltaics. In particular, the invention relates to a group of layers used in solar cells and a solar cell made therefrom.
Despite significant academic and industrial research and development effort, the best efficiencies reported for cadmium telluride photovoltaic devices have been stagnant, for about decade, at about 16 percent. The efficiency of a cadmium telluride photovoltaic device module fabricated from such cadmium telluride photovoltaic devices, and designed to provide useful amounts of electricity (for household applications, for example), can be significantly lower. It has been estimated that a cadmium telluride photovoltaic device efficiency in excess of about 20 percent can be achieved. However, there are a few challenges in trying to achieve an efficiency of about 20 percent. One of the challenges includes achieving a high hole carrier concentration in p-type cadmium telluride either by using native or extrinsic dopants. Further, due to the large work function of p-type cadmium telluride it has so far been a serious challenge to form a stable and low contact resistance contact on the back of the cell.
Additional challenges may be associated with the cadmium sulfide window layer that is typically employed in combination with a p-type cadmium telluride absorber layer. Conventional explanation for the photovoltaic operation of a cadmium sulfide/cadmium telluride is based on the junction formation at the interface between the n-type cadmium sulfide and p-type cadmium telluride. Unfortunately, due to the presence of a host of secondary effects, for example, sulfur diffusion from the cadmium sulfide, presence of the piezo-effect, lattice mismatch, different crystal orientation between cadmium telluride and cadmium sulfide, and the presence of defect states at the interface, may result in a poor junction which translates in an open-circuit voltage that is lower than expected from theoretical calculations.
Embodiments of the invention described herein address the noted shortcomings of the state of the art. The device described herein fills the needs described above by employing an n-type cadmium telluride layer that will permit the addition of active dopants to the layer and hence result in higher open-circuit voltage, thereby providing a device with improved efficiency. In one embodiment, the device includes an n-type cadmium telluride absorber layer disposed between a p-type semiconductor window layer and an n-type semiconductor layer. Appreciating that this group of layers forms the required junctions in the device changes the concept of how one can improve these devices.
One or more specific embodiments of the present invention will be described below. In an effort to provide a concise description of these embodiments, all features of an actual implementation may not be described in the specification. It should be appreciated that in the development of any such actual implementation, as in any engineering or design project, numerous implementation-specific decisions must be made to achieve the developers' specific goals, such as compliance with system-related and business-related constraints, which may vary from one implementation to another. Moreover, it should be appreciated that such a development effort might be complex and time consuming, but would nevertheless be a routine undertaking of design, fabrication, and manufacture for those of ordinary skill having the benefit of this disclosure.
When introducing elements of various embodiments of the present invention, the articles “a,” “an,” “the,” and “said” are intended to mean that there are one or more of the elements. The terms “comprising,” “including,” and “having” are intended to be inclusive and mean that there may be additional elements other than the listed elements. Moreover, the use of “top,” “bottom,” “above,” “below,” and variations of these terms is made for convenience, but does not require any particular orientation of the components unless otherwise stated. As used herein, the terms “disposed over” or “deposited over” or “disposed between” refers to both secured or disposed directly in contact with and indirectly by having intervening layers therebetween.
As illustrated in
In one embodiment, the transparent conducting layer 110 comprises an n-type transparent conducting layer. In one embodiment, the n-type transparent conducting layer comprises at least one transparent conducting oxide selected from the group consisting of indium tin oxide, indium oxide, tin oxide, zinc oxide, aluminum doped zinc oxide, gallium doped zinc oxide, fluorine doped tin oxide, and indium zinc oxide.
In one embodiment, a dopant density within the n-type transparent conducting layer is in a range from about 1×1019 per cubic centimeter to about 1×1021 per cubic centimeter. In another embodiment, a dopant density within the n-type transparent conducting layer is greater than about 1×1020 per cubic centimeter.
In one embodiment, the n-type transparent conducting layer 110 has a thickness of less than or equal to about 500 nanometers. In another embodiment, the n-type transparent conducting layer 110 has a thickness of less than or equal to about 300 nanometers. In yet another embodiment, the n-type transparent conducting layer 110 has a thickness of less than or equal to about 200 nanometers.
In one embodiment, the transparent conducting layer 110 comprises a p-type transparent conducting layer. In one embodiment, the p-type transparent conducting layer comprises BaCuEF, LaCuOD, MCuO(S1-y,Sey), strontium copper zinc oxy sulfide (Sr2Cu2ZnO2S2) or strontium copper gallium oxy sulfide (Sr2CuGaO3S), wherein ‘E’ comprises sulfur, selenium, or tellurium, wherein ‘D’ comprises sulfur, selenium, or tellurium, wherein ‘M’ comprises praseodymium, neodymium, or a lanthanide and wherein y has a value of 0 or less than or equal 1. In one embodiment, the p-type transparent conducting layer 110 comprises a class of materials called ‘delafossites’ which include copper aluminum oxide (CuAlO2) and strontium copper oxide (SrCu2O2).
In one embodiment, a dopant density within the p-type transparent conducting layer is in a range from about 1×1018 per cubic centimeter to about 1×1020 per cubic centimeter. In another embodiment, a dopant density within the p-type transparent conducting layer is in a range from about 1×1019 to 1×1020 per cubic centimeter.
In one embodiment, the p-type transparent conducting layer has a thickness of less than or equal to about 500 nanometers. In another embodiment, the p-type transparent conducting layer has a thickness of less than or equal to about 300 nanometers. In yet another embodiment, the p-type transparent conducting layer has a thickness of less than or equal to about 100 nanometers. In still yet another embodiment, the p-type transparent conducting layer has a thickness of less than or equal to about 50 nanometers.
In one embodiment, the p-type semiconductor window layer 112 and the n-type cadmium telluride layer 116 each have a corresponding band-gap. In one embodiment, the band-gap of the p-type semiconductor window layer 112 is greater than the band-gap of the n-type cadmium telluride layer 116. In one embodiment, the p-type semiconductor window layer 112 comprises a material having a band-gap in a range from about 1.5 electron Volts to about 3.7 electron Volts. In another embodiment, the p-type semiconductor window layer 112 comprises a material having a band-gap in a range from about 1.7 electron Volts to about 3.5 electron Volts. In yet another embodiment, the p-type semiconductor window layer 112 comprises a material having a band-gap in a range from about 2.1 electron Volts to about 3.4 electron Volts. Suitable examples of materials used for the p-type semiconductor window layer 112 include zinc telluride, magnesium telluride, magnesium selenide, zinc-magnesium-sulfide-selenide (ZnMgSSe), nitrogen doped zinc-magnesium-beryllium-selenide (ZnMgBeSe:N), copper oxide (Cu2O), hydrogenated amorphous silicon, amorphous silicon carbide (a-SiC:H), BaCuEF, LaCuOD, MCuO(S1-y,Sey), strontium copper zinc oxy sulfide (Sr2Cu2ZnO2S2) or strontium copper gallium oxy sulfide (Sr2CuGaO3S), wherein ‘E’ comprises sulfur, selenium, or tellurium, wherein ‘D’ comprises sulfur, selenium, or tellurium, wherein ‘M’ comprises praseodymium, neodymium, or a lanthanide and wherein y has a value of 0 or less than or equal 1. In one embodiment, the semiconductor window layer 112 comprises copper aluminum oxide (CuAlO2) or strontium copper oxide (SrCu2O2).
In one embodiment, a dopant density within the p-type semiconductor window layer 112 is in a range from about 1×1013 per cubic centimeter to about 1×1019 per cubic centimeter. In another embodiment, a dopant density within the p-type semiconductor window layer 112 is in a range from about 1×1014 per cubic centimeter to about 1×1018 per cubic centimeter. In yet another embodiment, a dopant density within the p-type semiconductor window layer 112 is in a range from about 1×1015 per cubic centimeter to about 1×1017 per cubic centimeter.
In one embodiment, the p-type semiconductor window layer 112 has a thickness of less than or equal to about 500 nanometers. In another embodiment, the p-type semiconductor window layer 112 has a thickness of less than or equal to about 300 nanometers. In yet another embodiment, the p-type semiconductor window layer 112 has a thickness of less than or equal to about 100 nanometers. In still yet another embodiment, the p-type semiconductor window layer 112 has a thickness of less than or equal to about 50 nanometers.
In one embodiment, the n-type cadmium telluride absorber layer comprises a dopant material comprising cadmium, aluminum, indium, iodine, or gallium. In one embodiment, a dopant density within the n-type cadmium telluride absorber layer is in a range from about 1×1015 per cubic centimeter to about 1×1017 per cubic centimeter. In one embodiment, the dopant density within the n-type cadmium telluride absorber layer is about 1×1016 per cubic centimeter.
CdTe is a prominent polycrystalline thin-film material, with a nearly ideal bandgap of about 1.45 electron volts to about 1.5 electron volts. CdTe also has a very high absorptivity. Although CdTe is most often used in photovoltaic devices without being alloyed, it can be alloyed with zinc, magnesium, manganese, and a few other elements to vary its electronic and optical properties. Films of CdTe can be manufactured using low-cost techniques.
The cadmium telluride may, in certain embodiments, comprise other elements from the Group II and Group VI or Group III and Group V that may not result in large bandgap shifts. In one embodiment, the bandgap shift is less than or equal to about 0.1 electron Volts for the absorber layer. In one embodiment, the atomic percent of zinc or magnesium in cadmium telluride is less than about 10 atomic percent. In another embodiment, the atomic percent of zinc or magnesium in cadmium telluride is up to about 8 atomic percent. In yet another embodiment, the atomic percent of zinc or magnesium in cadmium telluride is up to about 6 atomic percent.
In one embodiment, the n-type cadmium telluride absorber layer 116 has a thickness of less than or equal to about 6 micrometers. In another embodiment, the n-type cadmium telluride absorber layer 116 has a thickness of less than or equal to about 3 micrometers. In yet another embodiment, the n-type cadmium telluride absorber layer 116 has a thickness of less than or equal to about 2 micrometers.
In one embodiment, the n-type semiconductor layer 114 and the n-type cadmium telluride layer 116 each have a corresponding band-gap. The band-gap of the n-type semiconductor layer 114 is greater than or equal to the band-gap of the n-type cadmium telluride layer 116. In one embodiment, the n-type semiconductor layer comprises a material having a band-gap in a range from about 1.4 electron Volts to about 2.5 electron Volts. In another embodiment, the n-type semiconductor layer comprises a material having a band-gap in a range from about 1.5 electron Volts to about 2.4 electron Volts. In yet another embodiment, the n-type semiconductor layer comprises a material having a band-gap in a range from about 1.8 electron Volts to about 2.2 electron Volts. Suitable examples of materials used for the n-type semiconductor layer 114 include cadmium telluride, cadmium sulfide, cadmium zinc telluride, zinc telluride, cadmium selenide, zinc selenide, or n-type hydrogenated amorphous silicon.
In one embodiment, a dopant density within the n-type semiconductor layer 114 is in a range from about 1×1016 per cubic centimeter to about 1×1021 per cubic centimeter. In another embodiment, a dopant density within the n-type semiconductor layer 114 is in a range from about 1×1017 per cubic centimeter to about 1×1020 per cubic centimeter. In yet another embodiment, a dopant density within the n-type semiconductor layer 114 is in a range from about 1×1018 per cubic centimeter to about 1×1019 per cubic centimeter. In one embodiment, suitable dopant materials that can be used with an n-type semiconductor layer include cadmium, indium, gallium, or aluminum. In one embodiment, the n-type semiconductor layer 114 is an n-type cadmium telluride layer 516 with suitable dopant materials.
In one embodiment, the n-type semiconductor layer 114 has a thickness of less than or equal to about 500 nanometers. In another embodiment, the n-type semiconductor layer 114 has a thickness of less than or equal to about 300 nanometers. In yet another embodiment, the n-type semiconductor layer 114 has a thickness of less than or equal to about 200 nanometers. In still yet another embodiment, the n-type semiconductor layer 114 has a thickness of less than or equal to about 100 nanometers.
In certain embodiments, the device includes a back contact layer 218. Referring to
In one embodiment, the photovoltaic device 300 comprises a substrate 320 disposed over a back contact layer 318. In the illustrated embodiment in
The configuration of the layers illustrated in
As illustrated in
The configuration of the layers illustrated in
As used herein the term “dopant materials” means that the dopant employed comprises a foreign material different to the material in the bulk of a semiconductor material. The foreign material may be considered as impurities willfully introduced in the material. The dopant materials in a layer render the layers either p-type or n-type. As used herein the phrase “dopant density” means the resultant doping concentration of a layer based on both the acceptor states and the donor states that are present in the layer on account of various types of defects and willfully introduced impurities present in the layer. In one embodiment, the defects are inherent in the layers based on the method of manufacturing while the impurities may be introduced in the layers during the manufacturing process as discussed herein.
In one embodiment, a p-type transparent conducting layer 512 is disposed between the n-type transparent conducting layer 510 and the p-type semiconductor window layer 514. The advantage of disposing a p-type transparent conducting layer 512 between the n-type transparent conducting layer 510 and the p-type semiconductor window layer 514 is that doing so allows for optimizing the p-type semiconductor with respect to the n-type cadmium telluride interface. For example, magnesium telluride or magnesium cadmium telluride may be used as the p-type transparent conducting layer 512. Magnesium telluride cannot be doped to render it more p-type i.e., a p+-type. But magnesium telluride has a good lattice match with cadmium telluride. Thus the defects at the interface of the p-type semiconductor window layer and the n-type cadmium telluride absorber layer are minimized The more p-type the layer, the better is the capability of the layer to cancel out the gap in work-function of the layer and the cadmium telluride absorber layer. The p+-type transparent conducting layer may completely deplete the p-type semiconductor layer and generate the field into the n-type cadmium telluride absorber layer, though physically the charge is separated at the defect free interface. As used herein the term “p+-type” implies a p-type semiconductor layer in which there is excess mobile hole concentration.
As illustrated in
In one embodiment, a dopant density within the p-type transparent conducting layer 512 is in a range from about 1×1018 per cubic centimeter to about 1×1020 per cubic centimeter. In another embodiment, a dopant density within the p-type transparent conducting layer 512 is in a range from about 1×1019 to 1×1020 per cubic centimeter.
In one embodiment, the p-type transparent conducting layer 512 comprises BaCuEF, LaCuOD, MCuO(S1-y,Sey), strontium copper zinc oxy sulfide (Sr2Cu2ZnO2S2) or strontium copper gallium oxy sulfide (Sr2CuGaO3S), wherein ‘E’ comprises sulfur, selenium, or tellurium, wherein ‘D’ comprises sulfur, selenium, or tellurium, wherein ‘M’ comprises praseodymium, neodymium, or a lanthanide and wherein y has a value of 0 or less than or equal 1. In one embodiment, the p-type transparent conducting layer 512 comprises copper aluminum oxide (CuAlO2) and strontium copper oxide (SrCu2O2).
In one embodiment, the p-type transparent conducting layer 512 has a thickness of less than or equal to about 500 nanometers. In another embodiment, the p-type transparent conducting layer 512 has a thickness of less than or equal to about 300 nanometers. In yet another embodiment, the p-type transparent conducting layer 512 has a thickness of less than or equal to about 100 nanometers. In still yet another embodiment, the p-type transparent conducting layer 512 has a thickness of less than or equal to about 50 nanometers.
In one embodiment, a back contact layer 622 may be disposed on the n-type semiconductor layer 616. As illustrated in
In one embodiment, a substrate 724 may be disposed over the back contact layer 722. As discussed above, the configuration of the layers when the substrate is disposed over the back contact layer is a “substrate” configuration. As illustrated in
In one embodiment, an n-type transparent conducting layer 810 may be disposed over a substrate 824. As discussed above, the configuration of the layers when the n-type transparent conducting layer is disposed over the substrate is a “superstrate” configuration. As illustrated in
In one embodiment, the photovoltaic device described in
As illustrated in
In certain embodiments, the n-type semiconductor layer 114 comprises at least one transparent conducting oxide selected from the group consisting of indium tin oxide, indium oxide, tin oxide, zinc oxide, aluminum doped zinc oxide, gallium doped zinc oxide, fluorine doped tin oxide, and indium zinc oxide. As illustrated in
As illustrated in
In still yet another embodiment, a photovoltaic device 1300 is provided. The device 1300 comprises a p-type transparent conducting layer 1310. A p-type semiconductor window layer 1312 is disposed over the p-type transparent conducting layer 1310. An n-type semiconductor layer 1314 is disposed over the p-type semiconductor window layer 1312. An n-type cadmium telluride absorber layer 1316 is disposed between the p-type semiconductor window layer 1312 and the n-type semiconductor layer 1314. Light 1318 enters the device 1300 through the p-type transparent conducting layer 1310 and the p-type semiconductor window layer 1312. In some embodiments, where the device comprises a p-type transparent conducting layer 1310, the p-type transparent conducting layer 1310 may assist in relaxing the requirement on the p-type semi-conducting layer 1312 with regard to minimizing the bather for charge to cross the interface between the p-type transparent conducting layer 1310 and the p-type semiconductor window layer 1312.
Yet another embodiment is a method for making the devices described above. The method comprises disposing layers such as layers 110, 112, 114, and 116 in a photovoltaic device 100. The layers may be disposed using a wide variety of methods including closed-space sublimation, electro chemical deposition, chemical bath deposition, vapor transport deposition, and other physical or chemical vapor deposition.
Referring to
Referring to
Typically, the efficiency of a solar cell is defined as the electrical power that can be extracted from a module divided by the power density of the solar energy incident on the cell surface. Using
η=JSCVOCFF/PS
with (4) PS being the incident solar power. The relationship shown in the equation does an excellent job of determining the performance of a solar cell. However, the three terms in the numerator are not totally independent factors and typically, specific improvements in the device processing, materials, or design may impact all three factors.
Photovoltaic properties of any heterojunction-based solar cells considerably depend on the recombination centres present in the components of the heterojunction, and especially in the presence of recombination centres at the interface of the heterojunction. These recombination centres can be due to structural defects of the crystal lattice in the vicinity of the interface or in the bulk of the junction. Detailed electrical characterization of the heterojunctions can reveal recombination centres due to different defects or impurities and can potentially their influence on solar cell performance. With a direct energy band gap of 1.45 electron Volts and a high optical absorption coefficient, cadmium telluride is a very suitable absorber material for photovoltaic cells, especially, thin film solar cells. As mentioned earlier, conventional thin film p-type cadmium telluride/n-type cadmium sulfide photovoltaic cells with a small area have shown long-term stable performance and high conversion efficiency up to about 16 percent. However, the efficiencies of industrial, polycrystalline p-type cadmium telluride/n-type cadmium sulfide modules with large areas are still less than 11 percent. An alternative approach as discussed herein, includes in one embodiment, a heterojunction formed between the p-type semiconductor window layer 112 and the n-type cadmium telluride layer 116. The better lattice match resulting at the heterojunction may result in a reduction in the number of recombination centres in the junction area and thus assist in providing a solar cell with an improved performance. One other difference between a cadmium sulfide window layer and the p-type semiconductor window layer includes the inherent existence of the cadmium sulfide window layer as an n-type layer. Since cadmium telluride may be easily doped to form an n-type cadmium telluride, it may be associated with the p-type semiconductor window layer.
While only certain features of the invention have been illustrated and described herein, many modifications and changes will occur to those skilled in the art. It is, therefore, to be understood that the appended claims are intended to cover all such modifications and changes as fall within the true spirit of the invention.