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A solar cell (also called photovoltaic cell or photoelectric cell) is a solid state electrical device that converts the energy of light directly into electricity by the photovoltaic effect.
Assemblies of cells used to make solar modules which are used to capture energy from sunlight, are known as solar panels. The energy generated from these solar modules, referred to as solar power, is an example of solar energy.
Photovoltaics is the field of technology and research related to the practical application of photovoltaic cells in producing electricity from light, though it is often used specifically to refer to the generation of electricity from sunlight.
Cells are described as photovoltaic cells when the light source is not necessarily sunlight. These are used for detecting light or other electromagnetic radiation near the visible range, for example infrared detectors, or measurement of light intensity.
The term "photovoltaic" comes from the Greek φῶς (phōs) meaning "light", and "voltaic", from the name of the Italian physicist Volta, after whom a unit of electro-motive force, the volt, is named. The term "photo-voltaic" has been in use in English since 1849.
The photovoltaic effect was first recognized in 1839 by French physicist A. E. Becquerel. However, it was not until 1883 that the first photovoltaic cell was built, by Charles Fritts, who coated the semiconductor selenium with an extremely thin layer of gold to form the junctions. The device was only around 1% efficient. In 1888 Russian physicist Aleksandr Stoletov built the first photoelectric cell (based on the outer photoelectric effect discovered by Heinrich Hertz earlier in 1887). Albert Einstein explained the photoelectric effect in 1905 for which he received the Nobel prize in Physics in 1921. Russell Ohl patented the modern junction semiconductor solar cell in 1946, which was discovered while working on the series of advances that would lead to the transistor.
Solar cells were rescued from obscurity by the suggestion to add them to the Vanguard I satellite. In the original plans, the satellite would be powered only by battery, and last a short time while this ran down. By adding cells to the outside of the fuselage, the mission time could be extended with no major changes to the spacecraft or its power systems. There was some skepticism at first, but in practice the cells proved to be a huge success, and solar cells were quickly designed into many new satellites, notably Bell's own Telstar.
Improvements were slow over the next two decades, and the only widespread use was in space applications where their power-to-weight ratio was higher than any competing technology. However, this success was also the reason for slow progress; space users were willing to pay anything for the best possible cells, there was no reason to invest in lower-cost solutions if this would reduce efficiency. Instead, the price of cells was determined largely by the semiconductor industry; their move to integrated circuits in the 1960s led to the availability of larger boules at lower relative prices. As their price fell, the price of the resulting cells did as well. However these effects were limited, and by 1971 cell costs were estimated to be $100 a watt.
His first major effort was to canvas the potential market to see what possible uses for a new product were, and they quickly found that if the dollars per watt was reduced from then-current $100/watt to about $20/watt there was significant demand. Knowing that his ribbon concept would take years to develop, the team started looking for ways to hit the $20 price point using existing materials.
Putting all of these changes into practice, the company started buying up "reject" silicon from existing manufacturers at very low cost. By using the largest wafers available, thereby reducing the amount of wiring for a given panel area, and packaging them into panels using their new methods, by 1973 SPC was producing panels at $10 per Watt and selling them at $20 per Watt, a fivefold decrease in prices in two years.
The timing could not be better; the rapid increase in the number of offshore oil platforms and loading facilities produced an enormous market among the oil companies. As Tideland's fortunes improved, Automatic started looking for their own supply of solar panels. They found Bill Yerks of Solar Power International (SPI) in California, who was looking for a market. SPI was soon bought out by one of its largest customers, the ARCO oil giant, forming ARCO Solar. ARCO Solar's factory in Camarillo, California was the first dedicated to building solar panels, and has been in continual operation from its purchase by ARCO in 1977 to this day.
This market, combined with the 1973 oil crisis, led to a curious situation. Oil companies were now cash-flush due to their huge profits during the crisis, but were also acutely aware that their future success would depend on some other form of power. Over the next few years, the major oil companies started a number of solar firms, and were for decades the largest producers of solar panels. Exxon, ARCO, Shell, Amoco (later purchased by BP) and Mobil all had major solar divisions during the 1970s and 80s. Technology companies also had some investment, including General Electric, Motorola, IBM, Tyco and RCA.
As the semiconductor industry moved to ever-larger boules, older equipment became available at fire-sale prices. Cells have grown in size as older equipment became available on the surplus market; ARCO Solar's original panels used cells with 2 to 4 inch diameter. Panels in the 1990s and early 2000s generally used 5 inch wafers, and since 2008 almost all new panels use 6 inch cells. Another major change was the move to polycrystalline silicon. This material has less efficiency, but is less expensive to produce in bulk. The widespread introduction of flat screen televisions in the late 1990s and early 2000s led to the wide availability of large sheets of high-quality glass, used on the front of the panels.
Other technologies have also come to market. First Solar has grown to become the largest panel manufacturer, in terms of yearly power produced, using a thin-film cell sandwiched between two layers of glass. This was the first product to beat $1 a watt for production costs. Since then the rapid rise of Chinese manufacturing and the commensurate continuous improvement have pushed prices of the higher efficient crystalline silicon panels into the same range.
To make practical use of the solar-generated energy, the electricity is most often fed into the electricity grid using inverters (grid-connected photovoltaic systems); in stand-alone systems, batteries are used to store the energy that is not needed immediately. Solar panels can be used to power or recharge portable devices.
The solar cell works in three steps: # Photons in sunlight hit the solar panel and are absorbed by semiconducting materials, such as silicon. # Electrons (negatively charged) are knocked loose from their atoms, allowing them to flow through the material to produce electricity. Due to the special composition of solar cells, the electrons are only allowed to move in a single direction. # An array of solar cells converts solar energy into a usable amount of direct current (DC) electricity.
Due to the difficulty in measuring these parameters directly, other parameters are measured instead: thermodynamic efficiency, quantum efficiency, integrated quantum efficiency, VOC ratio, and fill factor. Reflectance losses are a portion of the quantum efficiency under "external quantum efficiency". Recombination losses make up a portion of the quantum efficiency, VOC ratio, and fill factor. Resistive losses are predominantly categorized under fill factor, but also make up minor portions of the quantum efficiency, VOC ratio.
Crystalline silicon devices are now approaching the theoretical limiting efficiency of 29%.
High-efficiency solar cells are of interest to decrease the cost of solar energy. Many of the costs of a solar power plant are proportional to the area of the plant; a higher efficiency cell may reduce area and plant cost, even if the cells themselves are more costly. Efficiencies of bare cells, to be useful in evaluating solar power plant economics, must be evaluated under realistic conditions. The basic parameters that need to be evaluated are the short circuit current, open circuit voltage.
The chart at the right illustrates the best laboratory efficiencies obtained for various materials and technologies, generally this is done on very small, i.e. one square cm, cells. Commercial efficiencies are significantly lower.
Grid parity, the point at which photovoltaic electricity is equal to or cheaper than grid power, can be reached using low cost solar cells. It is achieved first in areas with abundant sun and high costs for electricity such as in California and Japan. Grid parity has been reached in Hawaii and other islands that otherwise use diesel fuel to produce electricity. George W. Bush had set 2015 as the date for grid parity in the USA. Speaking at a conference in 2007, General Electric's Chief Engineer predicted grid parity without subsidies in sunny parts of the United States by around 2015.
The price of solar panels fell steadily for 40 years, until 2004 when high subsidies in Germany drastically increased demand there and greatly increased the price of purified silicon (which is used in computer chips as well as solar panels). One research firm predicted that new manufacturing capacity began coming on-line in 2008 (projected to double by 2009) which was expected to lower prices by 70% in 2015. Other analysts warned that capacity may be slowed by economic issues, but that demand may fall because of lessening subsidies. Other potential bottlenecks which have been suggested are the capacity of ingot shaping and wafer slicing industries, and the supply of specialist chemicals used to coat the cells.
Many currently available solar cells are made from bulk materials that are cut into wafers between 180 to 240 micrometers thick that are then processed like other semiconductors.
Other materials are made as thin-films layers, organic dyes, and organic polymers that are deposited on supporting substrates. A third group are made from nanocrystals and used as quantum dots (electron-confined nanoparticles). Silicon remains the only material that is well-researched in both bulk and thin-film forms.
By far, the most prevalent bulk material for solar cells is crystalline silicon (abbreviated as a group as c-Si), also known as "solar grade silicon". Bulk silicon is separated into multiple categories according to crystallinity and crystal size in the resulting ingot, ribbon, or wafer.
#monocrystalline silicon (c-Si): often made using the Czochralski process. Single-crystal wafer cells tend to be expensive, and because they are cut from cylindrical ingots, do not completely cover a square solar cell module without a substantial waste of refined silicon. Hence most c-Si panels have uncovered gaps at the four corners of the cells. #Poly- or multicrystalline silicon (poly-Si or mc-Si): made from cast square ingots — large blocks of molten silicon carefully cooled and solidified. Poly-Si cells are less expensive to produce than single crystal silicon cells, but are less efficient. US DOE data shows that there were a higher number of multicrystalline sales than monocrystalline silicon sales. #Ribbon silicon is a type of multicrystalline silicon: it is formed by drawing flat thin films from molten silicon and results in a multicrystalline structure. These cells have lower efficiencies than poly-Si, but save on production costs due to a great reduction in silicon waste, as this approach does not require sawing from ingots.
Analysts have predicted that prices of polycrystalline silicon will drop as companies build additional polysilicon capacity quicker than the industry’s projected demand. On the other hand, the cost of producing upgraded metallurgical-grade silicon, also known as UMG Si, can potentially be one-sixth that of making polysilicon.
Manufacturers of wafer-based cells have responded to high silicon prices in 2004-2008 prices with rapid reductions in silicon consumption. According to Jef Poortmans, director of IMEC's organic and solar department, current cells use between eight and nine grams of silicon per watt of power generation, with wafer thicknesses in the neighborhood of 0.200 mm. At 2008 spring's IEEE Photovoltaic Specialists' Conference (PVS'08), John Wohlgemuth, staff scientist at BP Solar, reported that his company has qualified modules based on 0.180 mm thick wafers and is testing processes for 0.16 mm wafers cut with 0.1 mm wire. IMEC's roadmap, presented at the organization's recent annual research review meeting, envisions use of 0.08 mm wafers by 2015.
A cadmium telluride solar cell use a cadmium telluride (CdTe) thin film, a semiconductor layer to absorb and convert sunlight into electricity. Solarbuzz has reported that the lowest quoted thin-film module price stands at US$1.76 per watt-peak, with the lowest crystalline silicon (c-Si) module at $2.48 per watt-peak.
The cadmium present in the cells would be toxic if released. However, release is impossible during normal operation of the cells and is unlikely during fires in residential roofs. A square meter of CdTe contains approximately the same amount of Cd as a single C cell Nickel-cadmium battery, in a more stable and less soluble form. These multijunction cells consist of multiple thin films produced using metalorganic vapour phase epitaxy. A triple-junction cell, for example, may consist of the semiconductors: GaAs, Ge, and GaInP2. Each type of semiconductor will have a characteristic band gap energy which, loosely speaking, causes it to absorb light most efficiently at a certain color, or more precisely, to absorb electromagnetic radiation over a portion of the spectrum. The semiconductors are carefully chosen to absorb nearly all of the solar spectrum, thus generating electricity from as much of the solar energy as possible.
GaAs based multijunction devices are the most efficient solar cells to date. In October 2010, triple junction metamorphic cell reached a record high of 42.3%.
This technology is currently being utilized in the Mars Exploration Rover missions which have run far past their 90 day design life.
Tandem solar cells based on monolithic, series connected, gallium indium phosphide (GaInP), gallium arsenide GaAs, and germanium Ge pn junctions, are seeing demand rapidly rise. Between December 2006 and December 2007, the cost of 4N gallium metal rose from about $350 per kg to $680 per kg. Additionally, germanium metal prices have risen substantially to $1000–$1200 per kg this year. Those materials include gallium (4N, 6N and 7N Ga), arsenic (4N, 6N and 7N) and germanium, pyrolitic boron nitride (pBN) crucibles for growing crystals, and boron oxide, these products are critical to the entire substrate manufacturing industry.
Triple-junction GaAs solar cells were also being used as the power source of the Dutch four-time World Solar Challenge winners Nuna in 2003, 2005 and 2007, and also by the Dutch solar cars Solutra (2005), Twente One (2007) and 21Revolution (2009).
The Dutch Radboud University Nijmegen set the record for thin film solar cell efficiency using a single junction GaAs to 25.8% in August 2008 using only 4 µm thick GaAs layer which can be transferred from a wafer base to glass or plastic film.
Dye-sensitized solar cells (DSSCs) are made of low-cost materials and do not need elaborate equipment to manufacture, so they can be made in a DIY fashion, possibly allowing players to produce more of this type of solar cell than others. In bulk it should be significantly less expensive than older solid-state cell designs. DSSC's can be engineered into flexible sheets, and although its conversion efficiency is less than the best thin film cells, its price/performance ratio should be high enough to allow them to compete with fossil fuel electrical generation. The DSSC has been developed by Prof. Michael Grätzel in 1991 at the Swiss Federal Institute of Technology (EPFL) in Lausanne (CH).
Typically a ruthenium metalorganic dye (Ru-centered) is used as a monolayer of light-absorbing material. The dye-sensitized solar cell depends on a mesoporous layer of nanoparticulate titanium dioxide to greatly amplify the surface area (200–300 m2/g TiO2, as compared to approximately 10 m2/g of flat single crystal). The photogenerated electrons from the light absorbing dye are passed on to the n-type TiO2, and the holes are absorbed by an electrolyte on the other side of the dye. The circuit is completed by a redox couple in the electrolyte, which can be liquid or solid. This type of cell allows a more flexible use of materials, and is typically manufactured by screen printing and/or use of Ultrasonic Nozzles, with the potential for lower processing costs than those used for bulk solar cells. However, the dyes in these cells also suffer from degradation under heat and UV light, and the cell casing is difficult to seal due to the solvents used in assembly. In spite of the above, this is a popular emerging technology with some commercial impact forecast within this decade. The first commercial shipment of DSSC solar modules occurred in July 2009 from G24i Innovations.
Organic solar cells and polymer solar cells are built from thin films (typically 100 nm) of organic semiconductors including polymers, such as polyphenylene vinylene and small-molecule compounds like copper phthalocyanine (a blue or green organic pigment) and carbon fullerenes and fullerene derivatives such as PCBM. Energy conversion efficiencies achieved to date using conductive polymers are low compared to inorganic materials. However, it has improved quickly in the last few years and the highest NREL (National Renewable Energy Laboratory) certified efficiency has reached 8.3% for the Konarka Power Plastic. In addition, these cells could be beneficial for some applications where mechanical flexibility and disposability are important.
These devices differ from inorganic semiconductor solar cells in that they do not rely on the large built-in electric field of a PN junction to separate the electrons and holes created when photons are absorbed. The active region of an organic device consists of two materials, one which acts as an electron donor and the other as an acceptor. When a photon is converted into an electron hole pair, typically in the donor material, the charges tend to remain bound in the form of an exciton, and are separated when the exciton diffuses to the donor-acceptor interface. The short exciton diffusion lengths of most polymer systems tend to limit the efficiency of such devices. Nanostructured interfaces, sometimes in the form of bulk heterojunctions, can improve performance.
It has been found that protocrystalline silicon with a low volume fraction of nanocrystalline silicon is optimal for high open circuit voltage. These types of silicon present dangling and twisted bonds, which results in deep defects (energy levels in the bandgap) as well as deformation of the valence and conduction bands (band tails). The solar cells made from these materials tend to have lower energy conversion efficiency than bulk silicon, but are also less expensive to produce. The quantum efficiency of thin film solar cells is also lower due to reduced number of collected charge carriers per incident photon.
An amorphous silicon (a-Si) solar cell is made of amorphous or microcrystalline silicon and its basic electronic structure is the p-i-n junction. a-Si is attractive as a solar cell material because it is abundant and non-toxic (unlike its CdTe counterpart) and requires a low processing temperature, enabling production of devices to occur on flexible and low-cost substrates. As the amorphous structure has a higher absorption rate of light than crystalline cells, the complete light spectrum can be absorbed with a very thin layer of photo-electrically active material. A film only 1 micron thick can absorb 90% of the usable solar energy. This reduced material requirement along with current technologies being capable of large-area deposition of a-Si, the scalability of this type of cell is high. However, because it is amorphous, it has high inherent disorder and dangling bonds, making it a bad conductor for charge carriers. These dangling bonds act as recombination centers that severely reduce the carrier lifetime and pin the Fermi energy level so that doping the material to n- or p- type is not possible. Amorphous Silicon also suffers from the Staebler-Wronski effect, which results in the efficiency of devices utilizing amorphous silicon dropping as the cell is exposed to light. The production of a-Si thin film solar cells uses glass as a substrate and deposits a very thin layer of silicon by plasma-enhanced chemical vapor deposition (PECVD). A-Si manufacturers are working towards lower costs per watt and higher conversion efficiency with continuous research and development on Multijunction solar cells for solar panels. Anwell Technologies Limited recently announced its target for multi-substrate-multi-chamber PECVD, to lower the cost to USD0.5 per watt.
Amorphous silicon has a higher bandgap (1.7 eV) than crystalline silicon (c-Si) (1.1 eV), which means it absorbs the visible part of the solar spectrum more strongly than the infrared portion of the spectrum. As nc-Si has about the same bandgap as c-Si, the nc-Si and a-Si can advantageously be combined in thin layers, creating a layered cell called a tandem cell. The top cell in a-Si absorbs the visible light and leaves the infrared part of the spectrum for the bottom cell in nc-Si.
Recently, solutions to overcome the limitations of thin-film crystalline silicon have been developed. Light trapping schemes where the weakly absorbed long wavelength light is obliquely coupled into the silicon and traverses the film several times can significantly enhance the absorption of sunlight in the thin silicon films. Minimizing the top contact coverage of the cell surface is another method for reducing optical losses; this approach simply aims at reducing the area that is covered over the cell to allow for maximum light input into the cell. Anti-reflective coatings can also be applied to create destructive interference within the cell. This can by done by modulating the Refractive index of the surface coating; if destructive interference is achieved, there will be no reflective wave and thus all light will be transmitted into the semiconductor cell. Surface texturing is another option, but may be less viable because it also increases the manufacturing price. By applying a texture to the surface of the solar cell, the reflected light can be refracted into striking the surface again, thus reducing the overall light reflected out. Light trapping as another method allows for a decrease in overall thickness of the device; the path length that the light will travel is several times the actual device thickness. This can be achieved by adding a textured backreflector to the device as well as texturing the surface. If both front and rear surfaces of the device meet this criteria, the light will be 'trapped' by not having an immediate pathway out of the device due to internal reflections. Thermal processing techniques can significantly enhance the crystal quality of the silicon and thereby lead to higher efficiencies of the final solar cells. Further advancement into geometric considerations of building devices can exploit the dimensionality of nanomaterials. Creating large, parallel nanowire arrays enables long absoprtion lengths along the length of the wire while still maintaining short minority carrier diffusion lengths along the radial direction. Adding nanoparticles between the nanowires will allow for conduction through the device. Because of the natural geometry of these arrays, a textured surface will naturally form which allows for even more light to be trapped. A further advantage of this geometry is that these types of devices require about 100 times less material than conventional wafer-based devices.
Poly-crystalline silicon wafers are made by wire-sawing block-cast silicon ingots into very thin (180 to 350 micrometer) slices or wafers. The wafers are usually lightly p-type doped. To make a solar cell from the wafer, a surface diffusion of n-type dopants is performed on the front side of the wafer. This forms a p-n junction a few hundred nanometers below the surface.
Antireflection coatings, to increase the amount of light coupled into the solar cell, are typically next applied. Silicon nitride has gradually replaced titanium dioxide as the antireflection coating because of its excellent surface passivation qualities. It prevents carrier recombination at the surface of the solar cell. It is typically applied in a layer several hundred nanometers thick using plasma-enhanced chemical vapor deposition (PECVD). Some solar cells have textured front surfaces that, like antireflection coatings, serve to increase the amount of light coupled into the cell. Such surfaces can usually only be formed on single-crystal silicon, though in recent years methods of forming them on multicrystalline silicon have been developed.
The wafer then has a full area metal contact made on the back surface, and a grid-like metal contact made up of fine "fingers" and larger "busbars" are screen-printed onto the front surface using a silver paste. The rear contact is also formed by screen-printing a metal paste, typically aluminium. Usually this contact covers the entire rear side of the cell, though in some cell designs it is printed in a grid pattern. The paste is then fired at several hundred degrees celsius to form metal electrodes in ohmic contact with the silicon. Some companies use an additional electro-plating step to increase the cell efficiency. After the metal contacts are made, the solar cells are interconnected in series (and/or parallel) by flat wires or metal ribbons, and assembled into modules or "solar panels". Solar panels have a sheet of tempered glass on the front, and a polymer encapsulation on the back.
Solar cells are manufactured primarily in Japan, Germany, Mainland China, Taiwan and the United States, though numerous other nations have or are acquiring significant solar cell production capacity. While technologies are constantly evolving toward higher efficiencies, the most effective cells for low cost electrical production are not necessarily those with the highest efficiency, but those with a balance between low-cost production and efficiency high enough to minimize area-related balance of systems cost. Those companies with large scale manufacturing technology for coating inexpensive substrates may, in fact, ultimately be the lowest cost net electricity producers, even with cell efficiencies that are lower than those of single-crystal technologies.
In late September 2008, Sanyo Electric Company, Ltd. announced its decision to build a manufacturing plant for solar ingots and wafers in Salem, Oregon. The plant began operating in October 2009 and reached its full production capacity of 70 megawatts (MW) of solar wafers per year in April 2010.
In early October 2008, First Solar, Inc. broke ground on an expansion of its Perrysburg, Ohio, facility that will add enough capacity to produce another 57 MW per year of solar modules at the facility, bringing its total capacity to roughly 192 MW per year. The company expects to complete construction early next year and reach full production by mid-2010.
In mid-October 2008, SolarWorld AG opened a manufacturing plant in Hillsboro, Oregon, that is currently producing 500 MW of solar cells per year in 2011.
Solyndra has a manufacturing facility for its unique tubular CIGS technology in California.
In March 2010, SpectraWatt, Inc. began production at its manufacturing plant in Hopewell Junction, NY, which was expected to produce 120 MW of solar cells per year when it reached full production in 2011. However, the closure of this plant was announced in late 2010 due to deteriorating market conditions coupled with demand drops from Europe.
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