The subject matter described herein relates to photovoltaic devices. Some known photovoltaic devices include thin film solar modules having active portions of thin films of silicon. Light that is incident onto the modules passes into the active silicon films. If the light is absorbed by the silicon films, the light may generate electrons and holes in the silicon. The electrons and holes are used to create an electric potential and/or an electric current that may be drawn from the modules and applied to an external electric load.
Photons in the light excite electrons in the silicon films and cause the electrons to separate from atoms in the silicon films. In order for the photons to excite the electrons and cause the electrons to separate from the atoms in the films, the photons must have an energy that exceeds the energy band gap in the silicon films. The energy of the photons is related to the wavelengths of light that is incident on the films. Therefore, light is absorbed by the silicon films based on the energy band gap of the films and the wavelengths of the light.
Some known photovoltaic devices include tandem layer stacks that include two or more sets of silicon films deposited on top of one another and between a lower electrode and an upper electrode. The different sets of films may have different energy band gaps. Providing different sets of films with different band gaps may increase the efficiency of the devices as more wavelengths of incident light can be absorbed by the devices. For example, a first set of films may have a greater energy band gap than a second set of films. Some of the light having wavelengths associated with an energy that exceeds the energy band gap of the first set of films is absorbed by the first set of films to create electron-hole pairs. Some of the light having wavelengths associated with energy that does not exceed the energy band gap of the first set of films passes through the first set of films without creating electron-hole pairs. At least a portion of this light that passes through the first set of films may be absorbed by the second set of films if the second set of films has a lower energy band gap.
In order to provide different sets of films with different energy band gaps, the silicon films may be alloyed with germanium to change the band gap of the films. But, alloying the films with germanium tends to reduce the deposition rate that can be used in manufacturing. Furthermore, silicon films alloyed with germanium tend to be more prone to light-induced degradation than those with no germanium. Additionally, germane, the source gas used to deposit silicon-germanium alloy, is costly and hazardous.
As an alternative to alloying silicon films with germanium, the energy band gap of silicon films in a photovoltaic device may be reduced by depositing the silicon films as microcrystalline silicon films instead of amorphous silicon films. Amorphous silicon films typically have larger energy band gaps than silicon films that are deposited in a microcrystalline state. Some known photovoltaic devices include semiconductor layer stacks having amorphous silicon films stacked in series with a microcrystalline silicon films. In such devices, the amorphous silicon films are deposited in a relatively small thickness to reduce carrier transport-related losses in the junction. For example, the amorphous silicon films may be deposited with a small thickness to reduce the amount of electrons and holes that are excited from silicon atoms by incident light and recombine with other silicon atoms or other electrons and holes before reaching the top or bottom electrodes. The electrons and holes that do not reach the electrodes do not contribute to the voltage or current created by the photovoltaic device. But, as the thickness of the amorphous silicon junction is reduced, less light is absorbed by the amorphous silicon junction and the flow of photocurrent in the silicon films is reduced. As a result, the efficiency of the photovoltaic device in converting incident light into electric current can be limited by the amorphous silicon junction in the device stack.
In some photovoltaic devices having relatively thin amorphous silicon films, the surface area of photovoltaic cells in the device that have the active amorphous silicon films may be increased relative to inactive areas of the cells. The active areas include the silicon films that convert incident light into electricity while non-active or inactive areas include portions of the cells where the silicon film is not present or that do not convert incident light into electricity. The electrical power generated by photovoltaic devices may be increased by increasing the active areas of the photovoltaic cells in the device relative to the inactive areas in the device. For example, increasing the width of the cells in a monolithically-integrated thin film photovoltaic module having active amorphous silicon films increases the fraction or percentage of active photovoltaic material in the module that is exposed to sunlight. As the fraction of active photovoltaic material increases, the total photocurrent generated by the device may increase.
Increasing the width of the cells also increases the size or area of light-transmissive electrodes of the device. The light-transmissive electrodes are the electrodes that conduct electrons or holes created in the cells to create the voltage or current of the device. As the size or area of the light-transmissive electrodes increases, the electrical resistance (R) of the light-transmissive electrodes also increases. The electric current (I) that passes through the light-transmissive electrodes also may increase. As the current passing through the light-transmissive electrodes and the resistance of the light-transmissive electrodes increase, energy losses, such as I2R losses, in the photovoltaic device increase. As the energy losses increase, the photovoltaic device becomes less efficient and less power is generated by the device. Therefore, in monolithically-integrated thin film photovoltaic devices, there exists a trade-off between the fraction of active photovoltaic material in the devices and the energy losses incurred in the transparent conducting electrodes of the devices.
In some known photovoltaic devices, the photovoltaic cells are electrically coupled in series with each other. The series connection of the photovoltaic cells may risk damage to the device if one of the cells becomes reverse biased. For example, some known photovoltaic cells have become damaged or destroyed when one of several serially connected cells is shaded from incident light (e.g., “shaded cell”) while the adjacent cells are exposed to the light (e.g., “illuminated cells”). The illuminated cells generate electric current on opposite sides of the shaded cell and cause a voltage potential across the shaded cell. If the voltage potential is relatively large, the shaded cell may heat up and become damaged. For example, the shaded cell may ignite or combust and cause failure or destruction of the device.
Some known photovoltaic devices include bypass diodes that are joined to the cells. The bypass diodes permit electric current to bypass a shaded cell. For example, the voltage potential that would otherwise build up on opposite sides of a shaded cell is passed through the bypass diode between the illuminated cells and bypasses the shaded cell. These bypass diodes may be separately formed from the cells and are then coupled with the cells after the cells are formed. For example, the bypass diodes may be joined to the cells below the cells and/or substrate on which the cells are formed. Providing these bypass diodes requires additional equipment, processing steps, and/or components. For example, additional manufacturing equipment and/or processing may be required to form and/or couple the bypass diodes. Additional components may be added to the known cells to provide the bypass diode. The addition of more components to the cells may decrease the efficiency of the cells and/or provide increased failure rates of the cells.
A need exists for photovoltaic devices having increased efficiency in converting incident light into electric current and/or with decreased energy losses.
In one embodiment, a photovoltaic device includes: a substrate; lower and upper electrode layers disposed above the substrate; and a semiconductor layer disposed between the lower and upper electrode layers, the semiconductor layer absorbing incident light to excite electrons from the semiconductor layer, wherein the semiconductor layer includes a built-in bypass diode extending between and coupled with the lower and upper electrode layers, the bypass diode permitting electric current to flow through the bypass diode when a reverse bias is applied across the lower and upper electrode layers.
In another embodiment, a method for manufacturing a photovoltaic device includes: depositing a lower electrode layer above a substrate, a semiconductor layer above the lower electrode layer, and an upper electrode layer above the semiconductor layer, the semiconductor layer configured to absorb incident light to excite electrons from the semiconductor layer; and increasing at least one of a crystallinity or a diffusion of dopants in the semiconductor layer between the lower electrode layer and the upper electrode layer to form a built-in bypass diode, the bypass diode configured to permit electric current to flow through the bypass diode when a reverse bias is applied across the lower and upper electrode layers.
In another embodiment, a photovoltaic device includes: a substrate; and a plurality of electrically coupled photovoltaic cells disposed above the substrate in a direction that incident light is received by the photovoltaic cells, the photovoltaic cells generating electric current based on the light that is received by the photovoltaic cells, each of the photovoltaic cells including: lower and upper electrode layers disposed above the substrate; and a semiconductor layer disposed between the lower and upper electrode layers, the semiconductor layer absorbing the light to excite electrons from the semiconductor layer, wherein the semiconductor layer of at least one of the photovoltaic cells includes a built-in bypass diode extending between and coupled with the lower and upper electrode layers of the at least one of the photovoltaic cells, the bypass diode permitting the electric current to flow between neighboring ones of the photovoltaic cells through the bypass diode when the at least one of the photovoltaic cells is reverse biased.
The foregoing summary, as well as the following detailed description of certain embodiments of the presently described technology, will be better understood when read in conjunction with the appended drawings. For the purpose of illustrating the presently described technology, certain embodiments are shown in the drawings. It should be understood, however, that the presently described technology is not limited to the arrangements and instrumentality shown in the attached drawings. Moreover, it should be understood that the components in the drawings are not to scale and the relative sizes of one component to another should not be construed or interpreted to require such relative sizes.
Photons in the incident light that is absorbed by the upper and lower layer stacks 106, 108 excite electrons in the upper and lower layer stacks 106, 108 and cause the electrons to separate from atoms in the upper and lower layer stacks 106, 108. Complementary positive charges, or holes, are created when the electrons separate from the atoms. The upper and lower layer stacks 106, 108 have different energy band gaps that absorb different portions of the spectrum of wavelengths in the incident light. The electrons drift or diffuse through the upper and lower layer stacks 106, 108 and are collected at one of the upper and lower electrode layers 110, 112. The collection of the electrons at the upper or lower electrode layers 110, 112 generates an electric potential difference in the cell 100. The voltage difference in the cell 100 may be added to the potential difference that is generated in additional cells (not shown). The potential difference generated in a plurality of cells 100 serially coupled with one another may be added together to increase the total potential difference generated by the cells 100. Electric current is generated by the flow of electrons between neighboring cells 100. The current may be drawn from the cells 100 and applied to an external electric load.
The components and layers of the cell 100 are schematically illustrated in
The substrate 102 has a thickness that is sufficient to mechanically support the remaining layers of the cell 100 while providing mechanical and thermal stability to the cell 100 during manufacturing and handling of the cell 100. The substrate 102 is at least approximately 0.7 to 5.0 millimeters thick in one embodiment. By way of example only, the substrate 102 may be an approximately 2 millimeter thick layer of float glass. Alternatively, the substrate 102 may be an approximately 1.1 millimeter thick layer of borosilicate glass. In another embodiment, the substrate 102 may be an approximately 3.3 millimeter thick layer of low iron or standard float glass.
A textured template layer 114 may be deposited above the substrate 102. Alternatively, the template layer 114 is not included in the cell 100. The template layer 114 is a layer having a controlled and predetermined three dimensional texture that imparts the texture onto one or more of the layers and components in the cell 100 that are deposited onto or above the template layer 114. In one embodiment, the texture template layer 114 may be deposited and formed in accordance with one of the embodiments described in co-pending U.S. Nonprovisional patent application Ser. No. 12/762,880, entitled “Photovoltaic Cells And Methods To Enhance Light Trapping In Thin Film Silicon,” and filed Apr. 19, 2010 (the “'880 Application”). The entire disclosure of the '880 Application is incorporated by reference herein in its entirety. With respect to the '880 Application, the template layer 114 described herein may be similar to the template layer 136 described in the '880 Application and include an array of one or more of the structures 300, 400, 500 described and illustrated in the '880 Application.
The texture of the template layer 114 in the illustrated embodiment may be determined by the shape and dimensions of one or more structures 200, 300, 400 (shown in
The peak height (Hpk) 204 represents the average or median distance of the peaks 214 from the transitional shapes 208 between the peak structures 200. For example, the template layer 114 may be deposited as an approximately flat layer up to the bases 212 of the peaks 214, or to the area of the transitional shape 208. The template layer 114 may continue to be deposited in order to form the peaks 214. The distance between the bases 212 or transitional shape 208 to the peaks 214 may be the peak height (Hpk) 204.
The pitch 206 represents the average or median distance between the peaks 214 of the peak structures 200. The pitch 206 may be approximately the same in two or more directions. For example, the pitch 206 may be the same in two perpendicular directions that extend parallel to the substrate 102. In another embodiment, the pitch 206 may differ along different directions. Alternatively, the pitch 206 may represent the average or median distance between other similar points on adjacent peak structures 200. The transitional shape 208 is the general shape of the upper surface 202 of the template layer 114 between the peak structures 200. As shown in the illustrated embodiment, the transitional shape 208 can take the form of a flat “facet.” Alternatively, the flat facet shape may be a cone or pyramid when viewed in three dimensions. The base width (Wb) 210 is the average or median distance across the peak structures 200 at an interface between the peak structures 200 and the base 212 of the template layer 114. The base width (Wb) 210 may be approximately the same in two or more directions. For example, the base width (Wb) 210 may be the same in two perpendicular directions that extend parallel to the substrate 102. Alternatively, the base width (Wb) 210 may differ along different directions.
In general, the valley structures 300 include cavities that extend down into the template layer 114 from the upper surface 310 and toward the substrate 102. The valley structures 300 extend down to low points 312, or nadirs, of the template layer 114 that are located between the transition shapes 306. The peak height (Hpk) 302 represents the average or median distance between the upper surface 310 and the low points 312. The pitch 304 represents the average or median distance between the same or common points of the valley structures 300. For example, the pitch 304 may be the distance between the midpoints of the transition shapes 306 that extend between the valley structures 300. The pitch 304 may be approximately the same in two or more directions. For example, the pitch 304 may be the same in two perpendicular directions that extend parallel to the substrate 102. In another embodiment, the pitch 304 may differ along different directions. Alternatively, the pitch 304 may represent the distance between the low points 312 of the valley structures 300. Alternatively, the pitch 304 may represent the average or median distance between other similar points on adjacent valley structures 300.
The transitional shape 306 is the general shape of the upper surface 310 between the valley structures 300. As shown in the illustrated embodiment, the transitional shape 306 can take the form of a flat “facet.” Alternatively, the flat facet shape may be a cone or pyramid when viewed in three dimensions. The base width (Wb) 308 represents the average or median distance between the low points 312 of adjacent valley structures 300. Alternatively, the base width (Wb) 308 may represent the distance between the midpoints of the transition shapes 306. The base width (Wb) 308 may be approximately the same in two or more directions. For example, the base width (Wb) 308 may be the same in two perpendicular directions that extend parallel to the substrate 102. Alternatively, the base width (Wb) 308 may differ along different directions.
In general, the rounded structures 400 project upward from the base film 410 and away from the substrate 102 to rounded high points 412, or rounded apexes. The peak height (Hpk) 402 represents the average or median distance between the base film 410 and the high points 412. The pitch 404 represents the average or median distance between the same or common points of the rounded structures 400. For example, the pitch 404 may be the distance between the high points 412. The pitch 404 may be approximately the same in two or more directions. For example, the pitch 404 may be the same in two perpendicular directions that extend parallel to the substrate 102. Alternatively, the pitch 404 may differ along different directions. In another example, the pitch 404 may represent the distance between midpoints of the transition shapes 406 that extend between the rounded structures 400. Alternatively, the pitch 404 may represent the average or median distance between other similar points on adjacent rounded structures 400.
The transitional shape 406 is the general shape of the upper surface 414 between the rounded structures 400. As shown in the illustrated embodiment, the transitional shape 406 can take the form of a flat “facet.” Alternatively, the flat facet shape may be a cone or pyramid when viewed in three dimensions. The base width (Wb) 408 represents the average or median distance between the transition shapes 406 on opposite sides of a rounded structure 400. Alternatively, the base width (Wb) 408 may represent the distance between the midpoints of the transition shapes 406.
In accordance with one embodiment, the pitch 204, 302, 402 and/or base width (Wb) 210, 308, 408 of the structures 200, 300, 400 are approximately 400 nanometers to approximately 1500 nanometers. Alternatively, the pitch 204, 302, 402 of the structures 200, 300, 400 may be smaller than approximately 400 nanometers or larger than approximately 1500 nanometers. The average or median peak height (Hpk) 204, 302, 402 of the structures 200, 300, 400 may be approximately 25 to 80% of the pitch 206, 304, 404 for the corresponding structure 200, 300, 400. Alternatively, the average peak height (Hpk) 204, 302, 402 may be a different fraction of the pitch 206, 304, 404. The base width (Wb) 210, 308, 408 may be approximately the same as the pitch 206, 304, 404. In another embodiment, the base width (Wb) 210, 308, 408 may differ from the pitch 206, 304, 404. The base width (Wb) 210, 308, 408 may be approximately the same in two or more directions. For example, the base width (Wb) 210, 308, 408 may be the same in two perpendicular directions that extend parallel to the substrate 102. Alternatively, the base width (Wb) 210, 308, 408 may differ along different directions.
The parameters of the structures 200, 300, 400 in the template layer 114 may vary based on whether the PV cell 100 (shown in
In one embodiment, if the PV cell 100 (shown in
In another example, if the PV cell 100 (shown in
Returning to the discussion of the cell 100 shown in
The lower electrode layer 112 is deposited above the template layer 114. The lower electrode layer 112 is comprised of a conductive reflector layer 116 and a conductive buffer layer 118. The reflector layer 116 is deposited above the template layer 114. For example, the reflector layer 116 may be directly deposited onto the template layer 114. The reflector layer 116 has a textured upper surface 120 that is dictated by the template layer 114. For example, the reflector layer 116 may be deposited onto the template layer 114 such that the reflector layer 116 includes structures (not shown) that are similar in size and/or shape to the structures 200, 300, 400 (shown in
The reflector layer 116 may include, or be formed from, a reflective conductive material, such as silver and/or titanium. Alternatively, the reflector layer 116 may include, or be formed from, aluminum or an alloy that includes silver or aluminum. The reflector layer 116 is approximately 100 to 300 nanometers in thickness and may be deposited by sputtering the material(s) of the reflector layer 116 onto the template layer 114.
The reflector layer 116 provides a conductive layer and a reflective surface for reflecting light upward into the upper and lower active silicon layer stacks 106, 108. For example, a portion of the light that is incident on the cover layer 104 and that passes through the upper and lower active silicon layer stacks 106, 108 may not be absorbed by the upper and lower layer stacks 106, 108. This portion of the light may reflect off of the reflector layer 116 back into the upper and lower layer stacks 106, 108 such that the reflected light may be absorbed by the upper and/or lower layer stacks 106, 108. The textured upper surface 120 of the reflector layer 116 increases the amount of light that is absorbed, or “trapped” via partial or full scattering of the light into the upper and lower active silicon layer stacks 106, 108. The peak height (Hpk) 204, 302, 402, pitch 206, 304, 404, transitional shape 208, 306, 406, and/or base width (Wb) 210, 308, 408 (shown in
The buffer layer 118 is deposited above the reflector layer 116 and may be directly deposited onto the reflector layer 116. The buffer layer 118 provides an electric contact to the lower active silicon layer stack 108. For example, the buffer layer 118 may include, or be formed from, a transparent conductive oxide (TCO) material that is electrically coupled with the lower active silicon layer stack 108. In one embodiment, the buffer layer 118 includes aluminum doped zinc oxide, zinc oxide and/or indium tin oxide. In one embodiment, the buffer layer 118 includes SnO2:F. The buffer layer 118 may be deposited in a thickness of approximately 50 to 500 nanometers, although a different thickness may be used.
In one embodiment, the buffer layer 118 provides a chemical buffer between the reflector layer 116 and the lower active silicon layer stack 108. For example, the buffer layer 118 may prevent chemical attack on the lower active silicon layer stack 108 by the reflector layer 116 during processing and manufacture of the cell 100. The buffer layer 118 impedes or prevents contamination of the silicon in the lower layer stack 108 and may reduce plasmon absorption losses in the lower layer stack 108.
The buffer layer 118 may provide an optical buffer between the reflector layer 116 and the lower active silicon layer stack 108. For example, the buffer layer 118 may be a light transmissive layer that is deposited in a thickness that is based on a predetermined range of wavelengths that is reflected off of the reflector layer 116. The thickness of the buffer layer 118 may permit certain wavelengths of light to pass through the buffer layer 118, reflect off of the reflector layer 116, pass back through the buffer layer 118 and into the lower layer stack 108. By way of example only, the buffer layer 118 may be deposited at a thickness of approximately 75 to 80 nanometers.
The lower active silicon layer stack 108 is deposited above, or directly onto, the buffer layer 118. In one embodiment, the lower layer stack 108 is deposited at a thickness of approximately 1 to 3 micrometers, although the lower layer stack 108 may be deposited at a different thickness. The lower layer stack 108 includes three sublayers 122, 124, 126 of silicon. In one embodiment, the sublayers 122, 124, 126 are n-doped, intrinsic and p-doped microcrystalline silicon films, respectively, that are deposited using plasma enhanced chemical vapor deposition (PECVD) at relatively low deposition temperatures. For example, the sublayers 122, 124, 126 may be deposited at a temperature in the range of approximately 160 to 250 degrees Celsius. The deposition of the sublayers 122, 124, 126 at relatively lower deposition temperatures may reduce interdiffusion of dopants from one sublayer 122, 124, 126 into another sublayer 122, 124, 126. In addition, use of lower deposition temperatures in a given sublayer 122, 124, 126 may help prevent hydrogen evolution from the underlying sublayers 122, 124, 126 in the upper and lower layer stacks 106, 108, respectively.
Alternatively, the lower layer stack 108 may be deposited at relatively high deposition temperatures. For example, the lower layer stack 108 may be deposited at a temperature in the range of approximately 250 to 350 degrees Celsius. As the deposition temperature increases, the average grain size of crystalline structure in the lower layer stack 108 may increase and may lead to an increase in the absorption of infrared light in the lower layer stack 108. Therefore, the lower layer stack 108 may be deposited at the higher temperatures in order to increase the average grain size of the silicon crystals in the lower layer stack 108. In addition, depositing the lower layer stack 108 at higher temperatures may make the lower layer stack 108 more thermally stable during the subsequent deposition of the upper layer stack 106. As described below, the top sublayer 126 of the lower layer stack 108 may be a p-doped silicon film. In such an embodiment, the bottom and middle sublayers 122, 124 of the lower layer stack 108 may be deposited at the relatively high deposition temperatures within the range of approximately 250 to 350 degrees Celsius while the top sublayer 126 is deposited at a relatively lower temperature within the range of approximately 150 to 250 degrees Celsius. Alternatively, the top sublayer 126 may be deposited at a temperature of at least 160 degrees Celsius. The p-doped sublayer 126 is deposited at the lower temperature to reduce the amount of interdiffusion between the p-doped top sublayer 126 and the intrinsic middle sublayer 124. Alternatively, the p-doped sublayer 126 is deposited at a higher deposition temperature, such as approximately 250 to 350 degrees Celsius, for example.
The sublayers 122, 124, 126 may have an average grain size of at least approximately 10 nanometers. In another embodiment, the average grain size in the sublayers 122, 124, 126 is at least approximately 20 nanometers. Alternatively, the average grain size of the sublayers 122, 124, 126 is at least approximately 50 nanometers. In another embodiment, the average grain size is at least approximately 100 nanometers. Optionally, the average grain size may be at least approximately 1 micrometer. The average grain size in the sublayers 122, 124, 126 may be determined by a variety of methods. For example, the average grain size can be measured using Transmission Electron Microscopy (“TEM”). In such an example, a thin sample of the sublayers 122, 124, 126 is obtained. For example, a sample of one or more of the sublayers 122, 124, 126 having a thickness of approximately 1 micrometer or less is obtained. A beam of electrons is transmitted through the sample. The beam of electrons may be rastered across all or a portion of the sample. As the electrons pass through the sample, the electrons interact with the crystalline structure of the sample. The path of transmission of the electrons may be altered by the sample. The electrons are collected after the electrons pass through the sample and an image is generated based on the collected electrons. The image provides a two-dimensional representation of the sample. The crystalline grains in the sample may appear different from the amorphous portions of the sample. Based on this image, the size of crystalline grains in the sample may be measured. For example, the surface area of several crystalline grains appearing in the image can be measured and averaged. This average is the average crystalline grain size in the sample in the location where the sample was obtained. For example, the average may be the average crystalline grain size in the sublayers 122, 124, 126 from which the sample was obtained.
The bottom sublayer 122 may be a microcrystalline layer of n-doped silicon. In one embodiment, the bottom sublayer 122 is deposited in a PECVD chamber with an operating frequency of approximately 13.56 MHz using a source gas combination of hydrogen (H), silane (SiH4) and phosphine, or phosphorus trihydride (PH3) at a vacuum pressure of approximately 2 to 3 ton and at an energy of approximately 500 to 1000 Watts. The ratio of source gases used to deposit the bottom sublayer 122 may be approximately 200 to 300 parts hydrogen gas to approximately 1 part silane to approximately 0.01 part phosphine.
The middle sublayer 124 may be a microcrystalline layer of intrinsic silicon. For example, the middle sublayer 124 may include silicon that is not doped or that has a dopant concentration that less than 1018/cm3. In one embodiment, the middle sublayer 124 is deposited in a PECVD chamber with an operating frequency of approximately 13.56 MHz using a source gas combination of hydrogen (H) and silane (SiH4) at a vacuum pressure of approximately 9 to 10 ton and at an energy of approximately 2 to 4 kilowatts. The ratio of source gases used to deposit the middle sublayer 124 may be approximately 50 to 65 parts hydrogen gas to approximately 1 part silane.
The top sublayer 126 may be a microcrystalline layer of p-doped silicon. Alternatively, the top sublayer 126 may be a protocrystalline layer of p-doped silicon. In one embodiment, the top sublayer 126 is deposited in a PECVD chamber with an operating frequency of approximately 13.56 MHz using a source gas combination of hydrogen (H), silane (SiH4) and trimethyl boron (B(CH3)3, or TMB) at a vacuum pressure of approximately 2 to 3 ton and at an energy of approximately 500 to 1000 Watts. The ratio of source gases used to deposit the top sublayer 126 may be approximately 200 to 300 parts hydrogen gas to approximately 1 part silane to approximately 0.01 part phosphine. TMB may be used to dope the silicon in the top sublayer 126 with boron. Using TMB to dope the silicon in the top sublayer 126 may provide better thermal stability than using a different type of dopant, such as boron trifluoride (BF3) or diborane (B2H6). For example, the use of TMB to dope silicon may result in less boron diffusing from the top sublayer 126 into adjacent layers, such as the middle sublayer 124, during the deposition of subsequent layers when compared to using trifluoride or diborane. By way of example only, using TMB to dope the top sublayer 126 may result in less boron diffusing into the middle sublayer 124 than when trifluoride or diborane is used to dope the top sublayer 126 during deposition of the upper layer stack 106.
The three sublayers 122, 124, 126 form an N-I-P junction or N-I-P stack of active silicon layers. As the lower layer stack 108, the three sublayers 122, 124, 126 have an energy band gap of approximately 1.1 eV. Alternatively, the lower layer stack 108 may have a different energy band gap. The lower layer stack 108 has a different energy band gap than the upper layer stack 106, as described below. The different energy band gaps of the upper and lower layer stacks 106, 108 permit the upper and lower layer stacks 106, 108 to absorb different wavelengths of incident light.
In one embodiment, an intermediate reflector layer 128 is deposited between the upper and lower layer stacks 106, 108. For example, the intermediate reflector layer 128 may be deposited directly on the lower layer stack 108. Alternatively, the intermediate reflector layer 128 is not included in the cell 100 and the upper layer stack 106 is deposited onto the lower layer stack 108. The intermediate reflector layer 128 partially reflects light into the upper layer stack 106 and permits some of the light to pass through the intermediate reflector layer 128 and into the lower layer stack 108. For example, the intermediate reflector layer 128 may reflect a subset of the spectrum of wavelengths of light that is incident on the cell 100 back up and into the upper layer stack 106.
The intermediate reflector layer 128 includes, or is formed from, a partially reflective material. For example, the intermediate reflector layer 128 may be formed from titanium dioxide (TiO2), zinc oxide (ZnO), aluminum doped zinc oxide (AZO), indium tin oxide (ITO), doped silicon oxide or doped silicon nitride. In one embodiment, the intermediate reflector layer 128 is approximately 10 to 200 nanometers in thickness, although a different thickness may be used.
The upper active silicon layer stack 106 is deposited above the lower active silicon layer stack 108. For example, the upper layer stack 106 may be directly deposited onto the intermediate reflector layer 128 or onto the lower layer stack 108. In one embodiment, the upper layer stack 106 is deposited at a thickness of approximately 200 to 400 nanometers, although the upper layer stack 106 may be deposited at a different thickness. The upper layer stack 106 includes three sublayers 130, 132, 134 of silicon.
In one embodiment, the sublayers 130, 132, 134 are n-doped, intrinsic, and p-doped amorphous silicon (a-Si:H) films, respectively, that are deposited using plasma enhanced chemical vapor deposition (PECVD) at relatively low deposition temperatures. For example, the sublayers 130, 132, 134 may be deposited at a temperature of approximately 185 to 250 degrees Celsius. In another example, the sublayers 130, 132, 134 may be deposited at temperatures between 185 and 225 degrees Celsius. Alternatively, the p-doped sublayer 134 is deposited at a temperature that is lower than the temperatures at which the n-doped and intrinsic sublayers 130, 132 are deposited. For example, the p-doped sublayer 134 may be deposited at a temperature of approximately 120 to 200 degrees Celsius while the intrinsic and/or n-doped sublayers 132, 130 are deposited at temperatures of at least 200 degrees Celsius. By way of example only, the intrinsic and/or n-doped sublayers 132, 130 may be deposited at a temperature of approximately 250 to 350 degrees Celsius.
The deposition of one or more of the sublayers 130, 132, 134 at relatively lower deposition temperatures may reduce interdiffusion of dopants between sublayers 122, 124, 126 in the lower layer stack 108 and/or between sublayers 130, 132, 134 in the upper layer stack 106. The diffusion of dopants in and between the sublayers 122, 124, 126 and in and between the sublayers 130, 132, 134 may be based on the temperature at which the sublayers 122, 124, 126 and 130, 132, 134 are heated. For example, the interdiffusion of dopants between the sublayers 122, 124, 126, 130, 132, 134 can increase with exposure to increasing temperatures. Using lower deposition temperatures may reduce the amount of dopant diffusion in the sublayers 122, 124, 126 and/or in the sublayers 130, 132, 134. Use of lower deposition temperatures in a given sublayer 122, 124, 126, 130, 132, 134 may reduce hydrogen evolution from the underlying sublayers 122, 124, 126, 130, 132, 134 in the upper and lower layer stacks 106, 108, respectively.
The deposition of the sublayers 130, 132, 134 at relatively lower deposition temperatures may increase the energy band gap of the upper layer stack 106 relative to amorphous silicon layers that are deposited at higher deposition temperatures. For example, depositing the sublayers 130, 132, 134 as amorphous silicon layers at temperatures between approximately 185 to 250 degrees Celsius may cause the band gap of the upper layer stack 106 to be approximately 1.85 to 1.95 eV. Increasing the band gap of the upper layer stack 106 may cause the sublayers 130, 132, 134 to absorb a smaller subset of the spectrum of wavelengths in the incident light, but may increase the electric potential difference generated in the cell 100.
Alternatively, the upper layer stack 106 may be deposited at relatively high deposition temperatures. For example, the upper layer stack 106 may be deposited at a temperature in the range of approximately 250 to 350 degrees Celsius. As the deposition temperature of amorphous silicon increases, the energy band gap of the silicon decreases. For example, depositing the sublayers 130, 132, 134 as amorphous silicon layers with relatively little to no germanium in the layers at temperatures between approximately 250 and 350 degrees Celsius may cause the band gap of the upper layer stack 106 to be at least 1.65 eV. In one embodiment, the band gap of the upper layer stack 106 formed from amorphous silicon with a germanium content in the silicon being 0.01% or less is 1.65 to 1.80 eV. The germanium content may represent the fraction or percentage of germanium in the upper layer stack 106 relative to other materials, such as silicon, in the upper layer stack 106. Decreasing the band gap of the upper layer stack 106 may cause the sublayers 130, 132, 134 to absorb a larger subset of the spectrum of wavelengths in the incident light and may result in a greater electric current to be generated by a plurality of cells 100 electrically interconnected in a series.
Deposition of the upper layer stack 106 at relatively high deposition temperatures may be verified by measuring the hydrogen content of the upper layer stack 106. In one embodiment, the final hydrogen content of the upper layer stack 106 is less than approximately 8 atomic percent if the upper layer stack 106 was deposited at temperatures above approximately 250 degrees Celsius. The final hydrogen content in the upper layer stack 106 may be measured using Secondary Ion Mass Spectrometer (SIMS). A sample of the upper layer stack 106 is placed into the SIMS. The sample is then sputtered with an ion beam. The ion beam causes secondary ions to be ejected from the sample. The secondary ions are collected and analyzed using a mass spectrometer. The mass spectrometer then determines the molecular composition of the sample. The mass spectrometer can determine the atomic percentage of hydrogen in the sample.
Alternatively, the final hydrogen concentration in upper layer stack 106 may be measured using Fourier Transform Infrared spectroscopy (“FTIR”). In FTIR, a beam of infrared light is then sent through a sample of the upper layer stack 106. Different molecular structures and species in the sample may absorb the infrared light differently. Based on the relative concentrations of the different molecular species in the sample, a spectrum of the molecular species in the sample is obtained. The atomic percentage of hydrogen in the sample can be determined from this spectrum. Alternatively, several spectra are obtained and the atomic percentage of hydrogen in the sample is determined from the group of spectra.
As described below, the top sublayer 134 may be a p-doped silicon film. In such an embodiment, the bottom and middle sublayers 130, 132 may be deposited at the relatively high deposition temperatures within the range of approximately 250 to 350 degrees Celsius while the top sublayer 134 is deposited at a relatively lower temperature within the range of approximately 150 to 200 degrees Celsius. The p-doped top sublayer 134 is deposited at the lower temperature to reduce the amount of interdiffusion between the p-doped top sublayer 134 and the intrinsic middle sublayer 132. Depositing the p-doped top sublayer 134 at a lower temperature may increase the band gap of the sublayer 134 and/or makes the sublayer 134 more transmissive of visible light.
The bottom sublayer 130 may be an amorphous layer of n-doped silicon. In one embodiment, the bottom sublayer 130 is deposited in a PECVD chamber with an operating frequency of approximately 13.56 MHz using a source gas combination of hydrogen (H2), silane (SiH4) and phosphine, or phosphorus trihydride (PH3) at a vacuum pressure of approximately 2 to 3 ton and at an energy of approximately 500 to 1000 Watts. The ratio of source gases used to deposit the bottom sublayer 130 may be approximately 200 to 300 parts hydrogen gas to approximately 1 part silane to approximately 0.01 part phosphine.
The middle sublayer 132 may be an amorphous layer of intrinsic silicon. Alternatively, the middle sublayer 132 may be a polymorphous layer of intrinsic silicon. In one embodiment, the middle sublayer 132 is deposited in a PECVD chamber with an operating frequency of approximately 13.56 MHz using a source gas combination of hydrogen (H) and silane (SiH4) at a vacuum pressure of approximately 1 to 3 ton and at an energy of approximately 200 to 400 Watts. The ratio of source gases used to deposit the middle sublayer 132 may be approximately 4 to 12 parts hydrogen gas to approximately 1 part silane.
In one embodiment, the top sublayer 134 may be a protocrystalline layer of p-doped silicon. Alternatively, the top sublayer 134 is an amorphous layer of p-doped silicon. In one embodiment, the top sublayer 134 is deposited in a PECVD chamber with an operating frequency of approximately 13.56 MHz using a source gas combination of hydrogen (H), silane (SiH4), and boron trifluoride (BF3), TMB, or diborane (B2H6) at a vacuum pressure of approximately 2 to 3 ton and at an energy of approximately 500 to 1000 Watts. The ratio of source gases used to deposit the top sublayer 126 may be approximately 200 to 300 parts hydrogen gas to approximately 1 part silane to approximately 0.01 part dopant gas.
The three sublayers 130, 132, 134 form an NIP junction of active silicon layers. The three sublayers 130, 132, 134 have an energy band gap that differs from the energy band gap of the lower layer stack 108. For example, the energy band gap of the upper layer stack 106 may be at least about 50% greater than the lower layer stack 108. In another example, the upper layer stack 106 may have an energy band gap that is at least about 60% greater than the energy band gap of the lower layer stack 108. Alternatively, the energy band gap of the upper layer stack 106 may be at least about 40% greater than the energy band gap of the lower layer stack 108. The different energy band gaps of the upper and lower layer stacks 106, 108 permit the upper and lower layer stacks 106, 108 to absorb different wavelengths of incident light and may increase the efficiency of the cell 100 in converting incident light into electric potential and/or current.
The energy band gaps of the upper and lower layer stack 106, 108 may be measured using ellipsometry. Alternatively, an external quantum efficiency (EQE) measurement may be used to obtain the energy band gaps of the upper and lower layer stacks 106, 108. The EQE measurement is obtained by varying wavelengths of light that are incident upon a semiconductor layer or layer stack and measuring the efficiency of the layer or layer stack in converting incident photons into electrons that reach the external circuit. Based on the efficiencies of the upper and lower layer stacks 106, 108 in converting incident light into electrons at different wavelengths, the energy band gaps of the upper and lower layer stacks 106, 108 may be derived. For example, each of the upper and lower layer stacks 106, 108 may be more efficient in converting incident light having an energy that is greater than the band gap of the upper or lower layer stack 106, 108 than in converting light of a different energy.
The upper electrode layer 110 is deposited above the upper layer stack 106. For example, the upper electrode layer 110 may be directly deposited onto the upper layer stack 106. The upper electrode layer 110 includes, or is formed from, a conductive and light transmissive material. For example, the upper electrode layer 110 may be formed from a transparent conductive oxide. Examples of such materials include zinc oxide (ZnO), tin oxide (SnO2), fluorine doped tin oxide (SnO2:F), tin-doped indium oxide (ITO), titanium dioxide (TiO2), and/or aluminum-doped zinc oxide (Al:ZnO). The upper electrode layer 110 can be deposited in a variety of thicknesses. In some embodiments, the upper electrode layer 110 is approximately 50 nanometers to 2 micrometers thick.
In one embodiment, the upper electrode layer 110 is formed from a 60 to 90 nanometer thick layer of ITO or Al:ZnO. The upper electrode layer 110 may function as both a conductive material and a light transmissive material with a thickness that creates an anti-reflection (AR) effect in the upper electrode layer 110 of the cell 100. For example, the upper electrode layer 110 may permit a relatively large percentage of one or more wavelengths of incident light to propagate through the upper electrode layer 110 while reflecting a relatively small percentage of the wavelength(s) of light to be reflected by the upper electrode layer 110 and away from the active layers of the cell 100. By way of example only, the upper electrode layer 110 may reflect approximately 5% or less of one or more wavelengths of incident light. In another example, the upper electrode layer 110 may reflect approximately 3% or less of the light. In another embodiment, the upper electrode layer 110 may reflect approximately 2% or less of the light. In yet another example, the upper electrode layer 110 may reflect approximately 0.5% or less of the light.
The thickness of the upper electrode layer 110 may be adjusted to increase the amount of incident light that propagates through the upper electrode layer 110 and down into the upper and lower layer stacks 106, 108. Although the sheet resistance of relatively thin upper electrode layers 110 may be relatively high, such as approximately 20 to 50 ohms per square, the relatively high sheet resistance of the upper electrode layer 110 may be compensated for by decreasing a width of the upper electrode layers 110, as described below.
An adhesive layer 136 is deposited above the upper electrode layer 110. For example, the adhesive layer 136 may be deposited directly on the upper electrode layer 110. Alternatively, the adhesive layer 136 is not included in the cell 100. The adhesive layer 136 secures the cover layer 104 to the upper electrode layer 110. The adhesive layer 136 may prevent moisture ingress into the cell 100. The adhesive layer 136 may include a material such as a polyvinyl butyral (“PVB”), surlyn, or ethylene-vinyl acetate (“EVA”) copolymer, for example.
The cover layer 104 is placed above the adhesive layer 136. Alternatively, the cover layer 104 is placed on the upper electrode layer 110. The cover layer 104 includes or is formed from a light transmissive material. In one embodiment, the cover layer 104 is a sheet of tempered glass. The use of tempered glass in the cover layer 104 may help to protect the cell 100 from physical damage. For example, a tempered glass cover layer 104 may help protect the cell 100 from hailstones and other environmental damage. In another embodiment, the cover layer 104 is a sheet of soda-lime glass, low-iron tempered glass, or low-iron annealed glass. The use of a highly transparent, low-iron glass cover layer 104 can improve the transmission of light to the silicon layer stacks 106 and 108. Optionally, an AR coating (not shown) may be provided on the top of the cover layer 104.
As described above, each of the cells 504 includes several layers. For example, each cell 504 includes a substrate 512 that is similar to the substrate 102 (shown in
The upper electrode layer 518 of one cell 504 is electrically coupled with the lower electrode layer 514 in a neighboring, or adjacent, cell 100. As described above, the collection of the electrons and holes at the upper and lower electrode layers 518, 514 generates a voltage difference in each of the cells 504. The voltage difference in the cells 504 may be additive across multiple cells 504 in the device 500. The electrons and holes flow through the upper and lower electrode layers 518, 514 in one cell 504 to the opposite electrode layer 518, 514 in a neighboring cell 504. For example, if the electrons in a first cell 504 flow to the lower electrode layer 514 in a when light strikes the tandem layer stack 516, then the electrons flow through the lower electrode layer 514 of the first cell 504 to the upper electrode layer 518 in a second cell 504 that is adjacent to the first cell 504. Similarly, if the holes flow to the upper electrode layer 518 in the first cell 504, then the holes flow from the upper electrode layer 518 in the first cell 504 to the lower electrode layer 514 in the second cell 504. Electric current and voltage is generated by the flow of electrons and holes through the upper and lower electrode layers 518, 514. The current is applied to the external load 542.
The device 500 may be a monolithically integrated solar module similar to one or more of the embodiments described in co-pending U.S. Nonprovisional patent application Ser. No. 12/569,510, filed Sep. 29, 2009, and entitled “Monolithically-Integrated Solar Module” (“'510 Application”). The entire disclosure of the '510 Application is incorporated by reference herein. For example, in order to create the shapes of the lower and upper electrode layers 514, 518 and the tandem layer stack 516 in the device 500, the device 500 may be fabricated as a monolithically integrated module as described in the '510 Application. In one embodiment, portions of the lower electrode layer 514 are removed to create lower separation gaps 524. The portions of the lower electrode layer 514 may be removed using a patterning technique on the lower electrode layer 514. For example, a laser light that scribes the lower separation gaps 524 in the lower electrode layer 514 may be used to create the lower separation gaps 524. After removing portions of the lower electrode layer 514 to create the lower separation gaps 524, the remaining portions of the lower electrode layer 514 are arranged as linear strips extending in directions transverse to the plane of the magnified view 502.
The tandem layer stack 516 is deposited on the lower electrode layer 514 such that the tandem layer stack 516 fills in the volumes in the lower separation gaps 524. The tandem layer stack 516 is then exposed to a focused beam of energy, such as a laser beam, to remove portions of the tandem layer stack 516 and provide inter-layer gaps 526 in the tandem layer stack 516. The inter-layer gaps 526 separate the tandem layer stacks 516 of adjacent cells 504. After removing portions of the tandem layer stacks 516 to create the inter-layer gaps 526, the remaining portions of the tandem layer stacks 516 are arranged as linear strips extending in directions transverse to the plane of the magnified view 502.
The upper electrode layer 518 is deposited on the tandem layer stack 516 and on the lower electrode layer 514 in the inter-layer gaps 526. In one embodiment, the conversion efficiency of the device 500 may be increased by depositing a relatively thin upper electrode layer 518 with a thickness that is adjusted or tuned to provide an anti-reflection effect. For example, a thickness 538 of the upper electrode layer 518 may be adjusted to increase the amount of visible light that is transmitted through the upper electrode layer 518 and into the tandem layer stack 516. The amount of visible light that is transmitted through the upper electrode layer 518 may vary based on the wavelength of the incident light and the thickness of the upper electrode layer 518. One thickness of the upper electrode layer 518 may permit more light of one wavelength to propagate through the upper electrode layer 518 than light of other wavelengths. By way of example only, the upper electrode layer 518 may be deposited at a thickness of approximately 60 to 90 nanometers.
In terms of increasing the total power generated by the PV device 500, the increased power output arising from the anti-reflection effect provided by a thin upper electrode layer 518 may be sufficient to overcome at least some, if not all, of energy losses that may occur in the upper electrode layer 518. For example, some I2R losses of the photocurrent that is generated by the cell 504 may occur in the relatively thin upper electrode layer 518 due to the resistance of the upper electrode layer 518. But, an increased amount of photocurrent may be generated due to the thickness of the upper electrode layer 518 being based on a wavelength of the incident light to increase the amount of incident light that passes through the upper electrode layer 518. The increased amount of photocurrent may result from an increased amount of light passing through the upper electrode layer 518. The increased photocurrent may overcome or at least partially compensate for the I2R power loss associated with the relatively high sheet resistance of a thin upper electrode layer 518.
By way of example only, in a cell 504 having one amorphous silicon junction layer stack and one microcrystalline silicon junction stacked in series in the tandem layer stack 516, an output voltage in the range of approximately 1.25 to 1.5 volts and an electric current density in the range of approximately 10 to 15 milliamps per square centimeter may be achieved. I2R losses in a thin upper electrode layer 518 of the cell 504 may be sufficiently small that a width 540 of the cell 504 may be increased even if the upper electrode layer 518 has a relatively high sheet resistance. For example, the width 540 of the cell 504 may be increased to as large as approximately 0.4 to 1 centimeter even if the sheet resistance of the upper electrode layer 518 is at least 10 ohms per square, such as a sheet resistance of at least approximately 15 to 30 ohms/square. Because the width 540 of the cell 504 can be controlled in the device 500, the I2R power loss in the upper electrode layer 518 may be reduced without the use or addition of a conducting grid on top of a thin upper electrode layer 518.
Portions of the upper electrode layer 518 are removed to create upper separation gaps 528. The upper separation gaps 528 electrically separate portions of the upper electrode layer 518 that are in adjacent cells 504. The upper separation gaps 528 may be created by exposing the upper electrode layer 518 to a focused beam of energy, such as a laser light. The focused beam of energy may locally increase the crystallinity of the tandem layer stack 516 proximate to the upper separation gaps 528. For example, a crystalline fraction of the tandem layer stack 516 in a vertical portion 530 that extends between the upper electrode layer 518 and the lower electrode layer 514 may be increased by exposure to the focused beam of energy. Additionally, the focused beam of energy may cause diffusion of dopants within the tandem layer stack 516. The vertical portion 530 of the tandem layer stack 516 is disposed between the upper and lower electrode layers 518, 514 and below a left edge 534 of the upper electrode layer 518. As shown in
The crystalline fraction of the tandem layer stack 516 and the vertical portion 530 may be determined by a variety of methods. For example, Raman spectroscopy can be used to obtain a comparison of the relative volume of noncrystalline material to crystalline material in the tandem layer stack 516 and the vertical portion 530. One or more of the tandem layer stack 516 and the vertical portion 530 sought to be examined can be exposed to monochromatic light from a laser, for example. Based on the chemical content and crystal structure of the tandem layer stack 516 and the vertical portion 530, the monochromatic light may be scattered. As the light is scattered, the frequency (and wavelength) of the light changes. For example, the frequency of the scattered light can shift. The frequency of the scattered light is measured and analyzed. Based on the intensity and/or shift in the frequency of the scattered light, the relative volumes of amorphous and crystalline material of the tandem layer stack 516 and the vertical portion 530 being examined can be determined. Based on these relative volumes, the crystalline fraction in the tandem layer stack 516 and the vertical portion 530 being examined may be measured. If several samples of the tandem layer stack 516 and the vertical portion 530 are examined, the crystalline fraction may be an average of the several measured crystalline fractions.
In another example, one or more TEM images can be obtained of the tandem layer stack 516 and the vertical portion 530 to determine the crystalline fraction of the tandem layer stack 516 and the vertical portion 530. One or more slices of the tandem layer stack 516 and the vertical portion 530 being examined are obtained. The percentage of surface area in each TEM image that represents crystalline material is measured for each TEM image. The percentages of crystalline material in the TEM images can then be averaged to determine the crystalline fraction in the tandem layer stack 516 and the vertical portion 530 being examined.
In one embodiment, the increased crystallinity and/or the diffusion of the vertical portion 530 relative to a remainder of the tandem layer stack 516 forms a built-in bypass diode 532 that vertically extends through the thickness of the tandem layer stack 516 in the view shown in
Without the built-in bypass diodes 532, a cell 504 that is shaded or no longer exposed to light while the other cells 504 continue to be exposed to light may become reverse biased by the electric potential generated by the exposed cells 504. For example, the electric potential generated by the light-exposed cells 504 may be built up across the shaded cell 504 at the upper and lower electrode layers 518, 514 of the shaded cell 504. As a result, the shaded cell 504 may increase in temperature and, if the shaded cell 504 significantly increases in temperature, the shaded cell 504 may become permanently damaged and/or incinerate. In addition, a shaded cell 504 that does not have a built-in bypass diode 532 may prevent electric potential or current from being generated by the entire device 500.
With the built-in bypass diodes 532, the electric potential generated by the exposed cells 504 may bypass the shaded cell 504 through the bypass diodes 532 formed at the edges of the upper separation gaps 528 of the shaded cell 504. The increased crystallinity of the portion 530 of the tandem layer stack 516 and/or interdiffusion between the upper electrode layer 518 and the portion 530 in the tandem layer stack 516 provides a path for electric current to pass through when the shaded cell 504 is reverse biased. For example, the reverse bias across the shaded cell 504 may be dissipated through the bypass diodes 532 as the bypass diodes 532 have a lower electrical resistance characteristic under reverse bias than the bulk of the shaded cell 504.
The presence of built-in bypass diodes 532 may be determined by comparing the electrical output of the device 500 before and after shading an individual cell 504. For example, the device 500 may be illuminated and the electrical potential generated by the device 500 is measured. One or more cells 504 may be shaded from the light while the remaining cells 504 are illuminated. The device 500 may be short circuited by joining the leads 506, 508 together. The device 500 may then be exposed to light for a predetermined time period, such as one hour. Both the shaded cells 504 and the unshaded cells 504 are then once again illuminated and the electrical potential generated by the device 500 is measured. If the electrical potential before and after the shading of the cells 504 is within approximately 100 millivolts of one another, then the device 500 may include built-in bypass diodes 532. Alternatively, if the electrical potential after the shading of the cells 504 is approximately 200 to 1500 millivolts lower than the electrical potential prior to the shading of the cells 504, then the device 500 likely does not include the built-in bypass diodes 532. In another embodiment, the presence of a built-in bypass diode 532 for a particular cell 504 may be determined by electrically probing the cell 504. If the cell 504 demonstrates a reversible, non-permanent diode breakdown when the cell 504 is reverse biased without illumination, then the cell 504 includes the built-in bypass diode 532. For example, if the cell 504 demonstrates greater than approximately 10 milliamps per square centimeter of leakage current when a reverse bias of approximately −5 to −8 volts is applied across the upper and lower electrode layers 514, 518 of the cell 504 without illumination, then the cell 504 includes the built-in bypass diode 532.
At 610, portions of the lower electrode layer are removed to separate the lower electrode layer of each cell in the device from one another. As described above, portions of the lower electrode layer may be removed using a focused beam of energy, such as a laser beam. At 612, a lower active silicon layer stack is deposited. For example, the lower layer stack 108 (shown in
At 620, portions of the upper and lower layer stacks are removed between adjacent cells in the device. For example, sections of the upper and lower layer stacks 106, 108 (shown in
At 626, conductive leads are electrically joined to the outermost cells in the device. For example, the leads 506, 508 (shown in
The device 700 may include many cells 704 electrically coupled with one another in series. By way of example only, the device 700 may have twenty-five, fifty, or one hundred or more cells 704 connected with one another in a series. Each of the outermost cells 704 also may be electrically connected with one of a plurality of leads 706, 708. The leads 706, 708 may be similar to the leads 506, 508 (shown in
The cells 704 include several layers stacked on or above each other along a deposition direction 732 of the photovoltaic device 700. The deposition direction 732 may represent the direction in which the various layers or components of the photovoltaic device 700 are deposited and/or the direction in which light is received into the photovoltaic device 700. In the illustrated embodiment, these layers include a substrate 712, a lower electrode layer 714, a semiconductor layer 716, an upper electrode layer 718, an adhesive layer 720, and a cover layer 722. The substrate 712 may be similar to the substrate 102 (shown in
Similar to the device 500 (shown in
The semiconductor layer 716 is deposited above the lower electrode layer 714 such that the semiconductor layer 716 fills in the volumes in the lower separation gaps 724, as shown in
The laser light removes portions of the semiconductor layer stack 716 to divide the semiconductor layer stack 716 into sections that are separate from each other, with each section of the semiconductor layer stack 716 being present in a different cell 704. In the illustrated embodiment, after removing portions of the semiconductor layer stack 716 to create the inter-layer separation gaps 736, the remaining sections of the semiconductor layer stack 716 are arranged in linear strips that extend in directions that are parallel to the length direction 724.
The upper electrode layer 718 is deposited above the semiconductor layer 716 and on the lower electrode layer 714 in the inter-layer gaps 736. In one embodiment, a thickness dimension 738 of the upper electrode layer 718 is based on one or more wavelengths of incident light that is received by the device 700. For example, the thickness dimension 738 of the upper electrode layer 718 that is measured in a direction parallel to the deposition direction 732 may be based on the wavelengths of light that are to be absorbed by the semiconductor layer 716. In one embodiment, the semiconductor layer 716 may include one or more films having one or more energy band gaps that absorb wavelengths of incident light. As a result, the thickness dimension 738 may be based on the band gap(s) of the semiconductor layer 716.
The upper electrode layer 718 may be deposited above the semiconductor layer 716 such that the upper electrode layer 718 fills in the volumes in the inter-layer separation gaps 736, as shown in
In
The scribe lines 808 are referred to as “continuous” because, in one embodiment, the scribe lines 808 are elongated along at least one direction. For example, the scribe lines 808 may extend from the back side 712 of the photovoltaic device to the front side 710 of the photovoltaic device 700 in directions that are generally parallel to the length direction 724. Alternatively, the continuous scribe lines 808 may be elongated and extend a smaller distance between the sides 710, 712 and/or along different directions. In another embodiment, the scribe lines 808 may be non-continuous. For example, the scribe lines 808 may not extend from one side 710 to the other side 712 or may not be elongated in one direction more than one or more other directions.
In
The scribe marks 902 are referred to as “discrete” because, in one embodiment, the scribe marks 902 are separated from each other in directions that are parallel to the length direction 724. For example, in contrast to the scribe lines 808, which are continuous and elongated along the length direction 724, the scribe marks 902 are not continuous or elongated along the length direction 724 and are separated from each other along the length direction 724. In another example, the scribe lines 808 are separated from each other along directions that are parallel to the width direction 726 and are elongated along the length direction 724 while the scribe marks 902 are separated from each other along both the perpendicular length and width directions 724, 726.
In the illustrated embodiment, the scribe lines 808 are continuous in that the scribe lines 808 define outer edges of neighboring photovoltaic cells 704. For example, the scribe lines 808 are disposed between photovoltaic cells 704, such as photovoltaic cells 704A and 704B, that are next to each other along the width direction 726 of the photovoltaic device 700. A single scribe line 808 separates neighboring photovoltaic cells 704 in one embodiment. Conversely, multiple scribe marks 902 may be disposed between neighboring photovoltaic cells 704. For example, in the illustrated embodiment, five scribe marks 902 are disposed between the photovoltaic cells 704A, 704B. Alternatively, multiple scribe lines 808 and/or a single scribe mark 902 may separate neighboring photovoltaic cells 704. The number of scribe lines 808 and scribe marks 902 shown in
The beam of energy 900 increases a crystallinity of the semiconductor layer 716 at and/or near the scribe marks 902. The beam of energy 900 may locally increase the level, amount, percentage, or fraction of crystalline material in the semiconductor layer 716. For example, the beam of energy 900 may locally convert amorphous semiconductor material in the semiconductor layer 716 below the scribe mark 902 to poly-, micro-, or proto-crystalline material. The beam of energy 900 may increase the crystallinity of the semiconductor layer 716 by heating the semiconductor layer 716 and thereby causing the crystallinity of the semiconductor material in the semiconductor layer 716 to increase. The crystallinity of the semiconductor layer 716 may be increased in a volume that generally extends from the scribe mark 902 at an exposed upper surface 904 of the semiconductor layer 716 to a lower interface 906 between the semiconductor layer 716 and a layer disposed below the semiconductor layer 716, such as the lower electrode layer 716.
The beam of energy 900 may cause diffusion of dopants within the semiconductor layer 716 in the volume that generally extends from the scribe mark 902 at the upper surface 904 to the lower interface 906. For example, the semiconductor layer 716 may include one or more NIP or PIN junctions or stacks of semiconductor films. The beam of energy 900 heats the NIP or PIN junctions and causes n-type and/or p-type dopants in the junctions to diffuse into the intrinsic layers or films of the junctions in one embodiment.
The localized regions 1000 have greater amounts, fractions, or percentages of crystallinity than volumes of the semiconductor layer 716 disposed outside of the localized regions 1000. For example, the amount, fraction, or percentage of poly-, micro, or proto-crystalline material in the localized regions 1000 may be 5%, 10%, 15%, 20%, 25%, 35%, 50%, or 75% or more than the amount, fraction, or percentage of the same material in the volumes of the semiconductor layer 716 disposed outside of the localized regions 1000.
The diffusion of dopants within the localized regions 1000 of the semiconductor layer 716 may be greater than the diffusion of dopants within volumes of the semiconductor layer 716 disposed outside of the localized regions 1000. For example, the amount of n- and/or p-type dopants in the intrinsic layers of NIP and/or PIN junctions in the localized regions 1000 of the semiconductor layer 716 may be 10, 100, or 1000 or more times greater than the amount of n- and/or p-type dopants in the intrinsic layers of NIP and/or PIN junctions in volumes of the semiconductor layer 716 that are outside of the localized regions 1000.
The crystallinity of the localized regions 1000 may be determined by a variety of methods. For example, Raman spectroscopy can be used to obtain a comparison of the relative volume of noncrystalline material to crystalline material in samples of the localized regions 1000 and the volumes of the semiconductor layer 716 that are outside of the localized regions 1000. In one embodiment, laser light is directed into a volume of the semiconductor layer 716 that is outside the localized regions 1000 and another laser light of the same or similar wavelength is directed into the localized region 1000. The laser lights may have less energy than the focused beams of energy 806, 900 (shown in
Based on the chemical content and crystal structure of the volumes outside of the localized regions 1000 and within the localized regions 1000, the monochromatic laser light may be scattered. As the laser light is scattered, the frequency (and wavelength) of the laser light changes. For example, the frequency of the scattered light can shift. The frequency of the scattered light is measured and analyzed. Based on the intensity and/or shift in the frequency of the scattered light, the relative volumes of amorphous and crystalline material of the semiconductor layer 716 outside of the localized regions 1000 and inside the localized regions 1000 may be determined. Based on these relative volumes of amorphous and crystalline material, the crystalline fraction or percentage of the semiconductor layer 716 and the localized regions 1000 may be measured.
In another example, one or more TEM images can be obtained of samples of the localized regions 1000 and samples of the semiconductor layer 716 outside of the localized regions 1000 to determine the crystalline fraction of the semiconductor layer 716 and the localized regions 1000. For example, one or more slices of the semiconductor layer 716 and the localized regions 1000 being examined may be obtained and TEM images may be obtained of the samples. The percentage of surface area in each TEM image that represents crystalline material is measured for each TEM image. The percentages of crystalline material in the TEM images can then be averaged to determine the crystalline fraction or percentage in the semiconductor layer 716 and the localized regions 1000.
The increased crystallinity and/or diffusion of dopants within the localized regions 1000 of the semiconductor layer 716 forms built-in bypass diodes 1002 in the semiconductor layer 716. The bypass diode 1002 is schematically shown in one of the localized regions 1000 of the semiconductor layer 716 in
Without the built-in bypass diodes 1002 between neighboring photovoltaic cells 704, a shaded photovoltaic cell 704 that is disposed between and electrically coupled in series with illuminated photovoltaic cells 704 may become reverse biased by the electric potential generated by the illuminated cells 704. For example, in
In operation, if the photovoltaic cell 704B is shaded while the photovoltaic cells 704A, 704C are illuminated, a reverse bias can develop across the photovoltaic cell 704B. For example, the lower electrode layer 714 of the photovoltaic cell 704B is electrically coupled with the upper electrode layer 718 of the photovoltaic cell 704A and the upper electrode layer 718 of the photovoltaic cell 704B is electrically coupled with the lower electrode layer 714 of the photovoltaic cell 704C. As a result, the current that is generated in the photovoltaic cells 704A, 704C creates a reverse bias voltage between the upper and lower electrode layers 718, 714 of the photovoltaic cell 704B. The bypass diode 1002 has a breakdown voltage that, when the reverse bias across the bypass diode 1002 exceeds the breakdown voltage, the bypass diode 1002 becomes conductive and allows the reverse bias to flow through the bypass diode 1002. The bypass diode 1002 permits current to flow through the localized region 1000 at a lower reverse bias voltage than the volumes of the semiconductor layer 716 located outside of the localized region 1000. For example, the increased crystallinity and/or interdiffusion of dopants in the localized region 1000 provides a path having a lower electrical resistance characteristic under reverse bias than the semiconductor layer 716 outside of the localized region 1000 within the photovoltaic cell 704.
In one example, if the reverse bias across the bypass diode 1002 exceeds the breakdown voltage of the bypass diode 1002, then electric current may flow through the bypass diode 1002 from the lower electrode layer 714 to the upper electrode layer 716 (or vice-versa) within the photovoltaic cell 704B. As a result, the photovoltaic cell 704B allows the reverse bias caused by the illuminated photovoltaic cells 704A, 704C to bypass the semiconductor layer 716 of the photovoltaic cell 704B and flow between the upper and lower electrode layers 718, 714 of the photovoltaic cell 704B. The photovoltaic cell 704B thereby can be protected from incinerating or being otherwise damaged by the reverse bias. Moreover, as a shaded photovoltaic cell may otherwise block electric current generated in a photovoltaic device from being extracted from the device, the bypass diodes 1002 may permit the photovoltaic device 700 to continue generating electric current to power the external load 702 (shown in
The presence of the bypass diodes 1002 and/or localized regions 1000 may be determined by comparing the electrical output of the photovoltaic device 700 before and after shading an individual photovoltaic cell 704. For example, the photovoltaic device 700 may be illuminated and the current generated by the photovoltaic device 700 is measured (referred to as the “pre-shading current”). Then, one or more of the photovoltaic cells 704 may be shaded from the light while the remaining photovoltaic cells 704 are illuminated. The photovoltaic device 700 may then be short-circuited by electrically coupling the leads 706, 708 (shown in
The presence of the bypass diode 1002 in one or more of the photovoltaic cells 704 may be determined by electrically probing the photovoltaic cell 704. If the photovoltaic cell 704 demonstrates a reversible, non-permanent diode breakdown when the photovoltaic cell 704 is reverse biased without illumination, then the photovoltaic cell 704 may include the bypass diode 1002. For example, if the photovoltaic cell 704 demonstrates greater than approximately 10 milliamps per square centimeter of leakage current when a reverse bias of approximately −5 to −8 volts is applied across the upper and lower electrode layers 718, 714 of the photovoltaic cell 704 without illuminating the photovoltaic cell 704, then the photovoltaic cell 704 may include the bypass diode 1002 and/or localized region 1000.
In another embodiment, the localized regions 1000 in the semiconductor layer 716 may be formed by the focused beam of energy 806 (shown in
In one embodiment, the I-V curve 1100 represents the relationship between the current (I) flowing through the bypass diode 1002 (shown in
In one embodiment, the I-V curve 1200 represents the relationship between the current (I) flowing through the bypass diode 1002 (shown in
At 1302, a substrate is provided. For example, a substrate such as the substrate 102 (shown in
At 1304, a template layer is deposited above the substrate. For example, the template layer 134 (shown in
At 1306, a lower electrode layer is deposited above the template layer or the substrate. For example, the lower electrode layer 132, 514, or 714 (shown in
At 1308, portions of the lower electrode layer are removed. For example, scribe lines such as the scribe lines 808 (shown in
At 1310, a semiconductor layer is deposited above the lower electrode layer. For example, one or more semiconductor layers or films may be deposited above the lower electrode layer 132, 514, 714 (shown in
At 1312, portions of the semiconductor layer are removed. For example, scribe lines such as the scribe lines 808 (shown in
At 1314, an upper electrode layer is deposited above the semiconductor layer. For example, the upper electrode layer 130, 518, or 718 (shown in
At 1316, portions of the upper electrode layer are removed. For example, scribe lines such as the scribe lines 808 (shown in
At 1318, the crystallinity and/or interdiffusion of dopants within the semiconductor layer deposited at 1310 are increased. The crystallinity and/or interdiffusion of dopants may be increased in discrete areas, such as the localized regions 1000 (shown in
At 1320, conductive leads are electrically joined to the outermost photovoltaic cells in the photovoltaic device. For example, the leads 506, 508 and/or the leads 706, 708 (shown in
At 1322, an adhesive layer is deposited above the upper electrode layer. For example, the adhesive layer 136, 520, or 720 (shown in
At 1324, a cover layer is affixed to the adhesive layer. For example, the cover layer 104, 522, or 722 (shown in
At 1326, a junction box is mounted to the device. For example, a junction box that is configured to deliver electric potential and/or current from the photovoltaic device 100, 500, 700 (shown in
In one embodiment, a photovoltaic device includes: a substrate; lower and upper electrode layers disposed above the substrate; and a semiconductor layer disposed between the lower and upper electrode layers, the semiconductor layer absorbing incident light to excite electrons from the semiconductor layer, wherein the semiconductor layer includes a built-in bypass diode extending between and coupled with the lower and upper electrode layers, the bypass diode permitting electric current to flow through the bypass diode when a reverse bias is applied across the lower and upper electrode layers.
In another aspect, the bypass diode extends from an upper surface of the semiconductor layer to an opposite interface of the semiconductor layer.
In another aspect, the bypass diode is disposed within the semiconductor layer between the upper and lower electrode layers.
In another aspect, a localized region of the semiconductor layer that includes the bypass diode has a greater crystallinity than volumes of the semiconductor layer that are outside of the localized region.
In another aspect, the bypass diode has a smaller breakdown voltage than other volumes of the semiconductor layer.
In another aspect, the bypass diode extends through the semiconductor layer from the lower electrode layer to a scribe line disposed above the semiconductor layer along a direction that light is received into the semiconductor layer and that separates the upper electrode layer into sections.
In another aspect, the bypass diode permits the electric current to flow through the bypass diode instead of through the semiconductor layer.
In another embodiment, a method for manufacturing a photovoltaic device includes: depositing a lower electrode layer above a substrate, a semiconductor layer above the lower electrode layer, and an upper electrode layer above the semiconductor layer, the semiconductor layer configured to absorb incident light to excite electrons from the semiconductor layer; and increasing at least one of a crystallinity or a diffusion of dopants in the semiconductor layer between the lower electrode layer and the upper electrode layer to form a built-in bypass diode, the bypass diode configured to permit electric current to flow through the bypass diode when a reverse bias is applied across the lower and upper electrode layers.
In another aspect, the increasing operation comprises exposing the semiconductor layer to a focused beam of energy.
In another aspect, the increasing operation comprises exposing the semiconductor layer to a focused beam of energy that also separates the upper electrode layer into separate sections.
In another aspect, the increasing operation comprises forming a scribe line in the upper electrode layer and directing a focused beam of energy into the semiconductor layer within the scribe line.
In another aspect, the scribe lines are formed as elongated lines that separate the upper electrode layer into sections and the focused beam of energy is directed at separate scribe marks on the semiconductor layer that are spaced apart from each other.
In another aspect, the increasing operation comprises exposing the semiconductor layer to a plurality of laser lights.
In another aspect, the increasing operation comprises exposing the semiconductor layer to an initial focused beam of energy that increases the at least one of the crystallinity or the diffusion of dopants in a localized region of the semiconductor layer and exposing the semiconductor layer to a subsequent focused beam of energy that further increases the at least one of the crystallinity or the diffusion of dopants in the localized region.
In another aspect, the increasing operation comprises forming the bypass diode in the semiconductor layer by exposing the semiconductor layer to a first focused beam of energy and reducing a reverse breakdown voltage of the bypass diode by exposing the semiconductor layer to a second focused beam of energy.
In another embodiment, a photovoltaic device includes: a substrate; and a plurality of electrically coupled photovoltaic cells disposed above the substrate in a direction that incident light is received by the photovoltaic cells, the photovoltaic cells generating electric current based on the light that is received by the photovoltaic cells, each of the photovoltaic cells including: lower and upper electrode layers disposed above the substrate; and a semiconductor layer disposed between the lower and upper electrode layers, the semiconductor layer absorbing the light to excite electrons from the semiconductor layer, wherein the semiconductor layer of at least one of the photovoltaic cells includes a built-in bypass diode extending between and coupled with the lower and upper electrode layers of the at least one of the photovoltaic cells, the bypass diode permitting the electric current to flow between neighboring ones of the photovoltaic cells through the bypass diode when the at least one of the photovoltaic cells is reverse biased.
In another aspect, the bypass diode is disposed within the semiconductor layer of the at least one of the photovoltaic cells between the upper and lower electrode layers.
In another aspect, a localized region of the semiconductor layer of the at least one of the photovoltaic cells that includes the bypass diode has a greater crystallinity than volumes of the semiconductor layer that are outside of the localized region.
In another aspect, the upper electrode layers of the photovoltaic cells are separated by a scribe line, the bypass diode extending from the scribe line to the lower electrode layer of the semiconductor layer in the at least one of the photovoltaic cells.
In another aspect, the bypass diode permits the electric current to flow through the bypass diode instead of through the semiconductor layer of the at least one of the photovoltaic cells.
It is to be understood that the above description is intended to be illustrative, and not restrictive. For example, the above-described embodiments (and/or aspects thereof) may be used in combination with each other. In addition, many modifications may be made to adapt a particular situation or material to the teachings of the subject matter described herein without departing from its scope. Dimensions, types of materials, orientations of the various components, and the number and positions of the various components described herein are intended to define parameters of certain embodiments, and are by no means limiting and are merely exemplary embodiments. Many other embodiments and modifications within the spirit and scope of the claims will be apparent to those of skill in the art upon reviewing the above description. The scope of the subject matter disclosed herein should, therefore, be determined with reference to the appended claims, along with the full scope of equivalents to which such claims are entitled. In the appended claims, the terms “including” and “in which” are used as the plain-English equivalents of the respective terms “comprising” and “wherein.” Moreover, in the following claims, the terms “first,” “second,” and “third,” etc. are used merely as labels, and are not intended to impose numerical requirements on their objects. Further, the limitations of the following claims are not written in means—plus-function format and are not intended to be interpreted based on 35 U.S.C. §112, sixth paragraph, unless and until such claim limitations expressly use the phrase “means for” followed by a statement of function void of further structure.
This application is a continuation-in-part of co-pending U.S. application Ser. No. 12/796,378, entitled “Photovoltaic Modules And Methods For Manufacturing Photovoltaic Modules Having Tandem Semiconductor Layer Stacks,” and filed on Jun. 8, 2010 (the “'378 Application”). The '378 Application is a nonprovisional patent application of, and claims priority benefit from, U.S. Provisional Patent Application Ser. No. 61/185,770, entitled “Photovoltaic Devices Having Tandem Semiconductor Layer Stacks” (the “'770 Application”), and filed on Jun. 10, 2009; U.S. Provisional Patent Application Ser. No. 61/221,816, entitled “Photovoltaic Devices Having Multiple Semiconductor Layer Stacks” (the “'816 Application”), and filed on Jun. 30, 2009; and U.S. Provisional Patent Application Ser. No. 61/230,790, entitled “Photovoltaic Devices Having Multiple Semiconductor Layer Stacks” (the “'790 Application”), and filed on Aug. 3, 2009. The entire disclosure of the above listed applications (the '378, '770, '816, and '790 Applications) are incorporated by reference herein in their entirety.
Number | Date | Country | |
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61185770 | Jun 2009 | US | |
61221816 | Jun 2009 | US | |
61230790 | Aug 2009 | US |
Number | Date | Country | |
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Parent | 12796378 | Jun 2010 | US |
Child | 12963424 | US |