Shockley–Queisser limit

In physics, the Shockley–Queisser limit or detailed balance limit refers to the maximum theoretical efficiency of a solar cell using a p-n junction to collect power from the cell. It was first calculated by William Shockley and Hans Queisser at Shockley Semiconductor in 1961.[1] The limit is one of the most fundamental to solar energy production, and is considered to be one of the most important contributions in the field.[2]

The limit places maximum solar conversion efficiency around 33.7% assuming a single p-n junction with a band gap of 1.1 eV (typical for silicon). That is, of all the power contained in sunlight falling on a silicon solar cell (about 1000 W/m²), only 33.7% of that could ever be turned into electricity (337 W/m²). Modern commercial mono-crystalline solar cells produce about 22% conversion efficiency, the losses due largely to practical concerns like reflection off the front surface and light blockage from the thin wires on its surface.

The Shockley–Queisser limit only applies to cells with a single p-n junction; cells with multiple layers can outperform this limit. In the extreme, with an infinite number of layers, the corresponding limit is 86% using concentrated sunlight.[3]

Contents

Background

In a traditional solid-state semiconductor, a solar cell is made from two doped crystals, one with a slight negative bias (n-type semiconductor), which has extra free electrons, and the other with a slight positive bias (p-type semiconductor), which is lacking free electrons. When placed in contact, some of the electrons in the n-type portion will flow into the p-type to "fill in" the missing electrons, also known as an electron hole. Eventually enough will flow across the boundary to equalize the Fermi levels of the two materials. The result is a region at the interface, the p-n junction, where charge carriers are depleted and/or accumulated on each side of the interface. In silicon, this transfer of electrons produces a potential barrier of about 0.6V to 0.7V.[4]

When placed in the sun, photons in the sunlight can strike the bound electrons in the p-type side of the semiconductor, giving them more energy, a process known technically as photoexcitation. In silicon, sunlight can provide enough energy to push an electron out of the lower-energy valence band into the higher-energy conduction band. As the name implies, electrons in the conduction band are free to move about the silicon. When a load is placed across the cell as a whole, these electrons will flow out of the p-type side into the n-type side, lose energy while moving through the external circuit, and then back into the p-type material where they can once again re-combine with the valence-band hole they left behind, producing a lower-energy photon. In this way, sunlight creates an electrical current.[4]

The Limit

The Shockley–Queisser limit is calculated by examining the amount of electrical energy that is extracted per photon of incoming sunlight. There are three primary considerations:

Blackbody radiation

Any material above absolute zero temperature will emit radiation through blackbody radiation. In the case of a solar cell at ambient room temperature, at 300 Kelvin, a baseline energy is always being emitted. This energy cannot be captured by the cell, and represents about 7% of the available incoming energy.

This radiation effect is dependent on cell temperature. Any energy lost in a cell is generally turned into heat, so any inefficiency in the cell increases the cell temperature when it is placed in sunlight. As the temperature of the cells increases, the blackbody radiation also increases, until an equilibrium is reached. In practice this equilibrium is normally reached at temperatures as high as 360 Kelvin, and cells normally operate at lower efficiencies than their room temperature rating. Module datasheets normally list this temperature dependancy as TNOTC.

Recombination

When an electron is ejected through photoexcitation, the atom it was formerly bound to is left with a net positive charge. Under normal conditions, the atom will pull off an electron from a surrounding atom in order to neutralize itself, a process known as recombination. That atom will then attempt to remove an electron from another atom, and so forth, producing an ionization chain reaction that moves through the cell. Since these can be viewed as the motion of a positive charge, it is useful to refer to them as "holes", a sort of virtual positive electron.

Like electrons, holes move around the material, and will be attracted towards a source of electrons. Normally these are provided through an electrode on the back surface of the cell. Meanwhile the photoelectrons are moving forward towards the electrodes on the front surface. For a variety of reasons, holes move much more slowly than electrons. This means that during the finite time while the electron is moving forward towards the p-n junction, it may meet a slowly moving hole left behind by a previous photoexcitation. When this occurs, the electron recombines at that atom, and the energy is lost (normally through the emission of a photon of that energy, but there are a variety of possible processes).

Recombination places an upper limit on the rate of production; past a certain rate there are so many holes in motion that new electrons will never make it to the p-n junction. In silicon this reduces the theoretical performance under normal operating conditions by another 10% over and above the thermal losses noted above. Materials with higher electron (or hole) mobility can improve on silicon's performance; gallium arsenide (GaAs) cells gain about 5% in real-world examples due to this effect alone. In brighter light, when it is concentrated by mirrors or lenses for example, this effect is magnified. Normal silicon cells quickly saturate, while GaAs continue to improve at concentrations as high as 1500 times.

Spectrum losses

Since the act of moving an electron from the valence band to the conduction band requires energy, only photons with more than that amount of energy will produce a photoelectron. In silicon the conduction band is about 1.1 eV away from the valence band, which corresponds to red light. In other words, photons of red, yellow and blue light will all contribute to power production, whereas infrared, microwaves and radio waves will not.[5] This places an immediate limit on the amount of energy that can be extracted from the sun. Of the 1,000 W/m² in AM1.5 sunlight, about half of that has less than 1.1 eV of energy, and will not produce power in a silicon cell. That means there is a theoretical conversion efficiency of about 50% or less, ignoring all other factors.

Another important contributor to losses is that any energy above and beyond the bandgap energy is lost; while blue light has roughly twice the energy of red light, that energy is not captured by devices with a single p-n junction. The electron is ejected with higher energy when struck by a blue photon, but it loses this extra energy as it travels toward the p-n junction (the energy is converted into heat).[5]

All together

Considering the blackbody and recombination effects alone, a solar cell has a peak theoretical efficiency of 68%. Thus the spectrum losses represent the vast majority of lost power. Considering all three effects, a single-junction cell made of silicon will have a theoretical peak performance of about 33.7%, or about 337 W/m² in AM1.5.[1][5]

Other considerations

Shockley and Queisser's work considered the most basic physics only, there are a number of other factors that further reduce the theoretical power. Many of these have been explored since the 1980s. Landsberg and Baruch added various practical considerations like re-emission,[6] while a number of researchers have attempted to characterize other losses in the cell, like interstitial defects.

Exceeding the Limit

It is important to note that the limit makes several fundamental assumptions; that the cell contains a single p-n junction, that the junction is tuned to visible light, and that any extra energy in the photons is lost. None of these assumptions is necessarily true, and a number of different approaches have been used to significantly surpass the basic limit.

Tandem cells

The most widely explored path to higher efficiency solar cells has been to use multiple p-n junctions, each one tuned to a particular frequency of the spectrum. Since light will only react strongly with structures that contain roughly the same bandgap as their wavelength, as long as these layers are extremely thin they are almost transparent to lower frequencies. This allows the layers to be stacked, with the layers capturing higher frequencies (shortest wavelengths, bluish) on top, and the lower frequency light (longer wavelengths, reddish) traveling through them to the lower layers.

The calculation of the fundamental efficiency limits of these "tandem cells" (or "multi-junction cells") works in a fashion similar to those for single-junction cells, with the caveat that some of the light will be converted to other frequencies and re-emitted within the structure. Using methods similar to the original Shockley-Queisser analysis with these considerations in mind produces similar results; a two-layer cell can reach 42% efficiency, three-layer cells 49%, and a theoretical infinity-layer cell 68% in un-concentrated sunlight.[3]

The majority of tandem cells that have been produced to date use three layers, tuned to blue (on top), yellow (middle) and red (bottom). These cells require the use of semiconductors that can be tuned to specific frequencies, which has led to most of them being made of gallium arsenide (GaAs) compounds, often germanium for red, GaAs for yellow, and GaInP2 for blue. They are very expensive to produce, using techniques similar to microprocessor construction but with "chip" sizes on the scale of several centimeters. In cases where outright performance is the only consideration, these cells have become common; they are widely used in satellite applications for instance, where the power-to-weight ratio overwhelms practically every other consideration.

Gallium arsenide has higher electron mobility than silicon, which means the photoelectrons reach their p-n junctions more quickly. It also has many more charge carriers available, which means the ratio of electrons/holes to neutral atoms is lower. These effects reduce the chance that electrons and holes will meet during the journey to the junction, which allows more light to fall on the cell before they reach equilibrium. These cells have increasing efficiency under concentrated light; under the best possible conditions and perfect lighting, a two-layer cell can reach 55% efficiency, 63% for three-layer cells, and 86% for infinite layers.[3]

Using concentrations on the order of 500 to 1000, meaning that a 1 cm² square cell can use the light collected from a 1000 cm² area, produces the highest efficiencies seen to date. Three-layer cells are fundamentally limited to 63%, but existing commercial prototypes have already demonstrated over 40%.[7][8] These cells capture about 2/3 of their theoretical maximum performance, so assuming the same is true for a non-concentrated version of the same design, one might expect a three-layer cell of 30% efficiency under normal sunlight. This is not enough of an advantage over traditional silicon designs to make up for their extra production costs. For this reason, almost all tandem cell research for terrestrial use is dedicated to concentrator systems, normally using mirrors or fresnel lenses.

Using a concentrator also has the added benefit that the number of cells needed to cover a given amount of ground area is greatly reduced. A conventional system covering 1 m² would require 50 cells of 250 cm² (typical for modern cells), but for a concentrator system only a single cell is needed, along with a concentrator. The argument for concentrated tandem cells has been that the high cost of the cells themselves would be more than offset by the reduction in total number of cells and the much lower cost of the concentrators. The downside of the concentrator approach is that at high concentrations even small movements of the sun will cause the focussed sunlight to fall off the cell, so they need to be mounted in a machine that tracks the sun as it moves. Sun-tracking system are expensive, rising with the precision required, offsetting other advantages.

To date, no large-scale high-efficiency tandem cell commercial systems have been deployed, although one has been planned for Spain.[9] PV generator deployments using conventional cells are currently reaching about $5 per peak Watt for deployment and installation costs, a number the concentrator systems cannot yet match. However, Boeing's Spectrolab division claims to be aiming for $3 a Watt in the short term.[7] amorphous silicon solar cells for residential and commercial installations are often made as triple-junction tandem cells, and these are commercially available from Uni-Solar and other companies, but because single films of amorphous silicon solar cells tend to have low efficiency, triple-junction amorphous silicon solar cells can have a similar or even lower efficiency than a single-junction crystalline silicon solar cell. Note: The advantages of tandem amorphous-silicon solar cells (compared to conventional non-tandem solar cells) is not higher efficiency, but lower cost and the possibility of using flexible substrates.

Impurity photovoltaics

There has been some work on the use of deliberate impurities to produce mid-energy states within single crystal structures. These cells would combine some of the advantages of the multi-junction cell with the simplicity of existing silicon designs. A detailed limit calculation for these cells with a wide variety of impurities suggests a maximum efficiency of 77.2%[10] To date, no commercial cell using this technique has been produced.

Infrared capture

Approximately half of the solar energy reaching the Earth's surface is in the near and far infrared (IR). In silicon the energy of the bandgap is higher than the energy of these photons, and they do not contribute to energy production. Losing this energy limits cell efficiency to about 50% even if one ignores the other factors included in the Shockley–Queisser limit.

Various solutions to this problem have been proposed. The most obvious solution is to use a semiconductor with a lower bandgap that is suitable for capturing IR energy. This solution actually lowers efficiency, however, because it means more of the energy in the higher-frequency photons is lost. For this reason almost all IR-capture efforts are based on using two-layer cells with a conventional cell on top and an IR-sensitive one on the bottom. These cells have a fundamental limit the same as any other two-layer cell, at about 42%. Unlike the existing tandem cells, however, a conventional silicon cell can be used as the upper layer, which should be much less expensive to produce.

Although there have been a number of potential solutions to producing IR cells, none has reached commercial use.[11][12]

Recently the two-photon photovoltaic effect has been demonstrated in silicon. This phenomenon which occurs at very high optical intensities allows infrared photons to be captured in conventional silicon and can improve the efficiency of standard silicon solar cells if sun light can be sufficiently concentrated.[13]

Hot electron capture

Since much of the Shockley–Queisser limit is due to energy losses between the photon energy and the energy captured from the electrons they produce, it should be no surprise that there has been a considerable amount of research into ways to capture the energy of the electrons before they can lose it in the crystal structure.[14] A related concept is to use photoproducers that release more than one electron, instead of a single electron of greater energy. There has been a considerable amount of effort investigating quantum dots for both of these roles.[15]

Fluorescent downconversion

Another possibility for increased efficiency is to convert the frequency of light down towards the bandgap energy with a fluorescent material. Some fluorescent materials will convert a single high-energy photon into several lower-energy ones, although this conversion process tends to be relatively inefficient. On the upside, such a material could be painted on the front surface of an otherwise standard cell, boosting its efficiency for little cost. Overall operation of such a cell is similar to the quantum-dot case, releasing more electrons of lower energy and producing more energy overall.[16][17]

Recent studies have discovered a new class of materials that can be tuned to produce electrons of any energy from light across the entire solar spectrum.[18] In theory, these materials could capture all of the energy, and would be limited by optical issues (reflection off the front face, etc.), not the Shockley–Queisser limit.[19]

Even without these sorts of materials, another use of fluorescence is to produce a low-cost concentrator system. In this concept, sheets of clear plastic are dyed with fluorescent paint. When the dye re-radiates the light falling on the front of the plate, it is trapped within the plastic and travels fiber optic-like to the edges of the sheet. Cells on the edges will see about 40 times concentration, far from the area of peak efficiency of GaAs cells, but without any need for tracking - light falling on the plate from any angle will still be sent to the edges.[20]

Thermophotovoltaic downconversion

Thermophotovoltaic cells are similar to phosphorescent systems, but use a plate to act as the downconvertor. Solar energy falling on the plate, typically black-painted metal, is re-emitted as lower-energy IR, which can then be captured in an IR cell. This relies on a practical IR cell being available, but the theoretical conversion efficiency can be calculated. For a converter with a bandgap of 0.92 eV, efficiency is limited to 54% with a single-junction cell, and 85% for concentrated light shining on ideal components with no optical losses and only radiative recombination.[21]

References

  1. ^ a b c William Shockley and Hans J. Queisser, "Detailed Balance Limit of Efficiency of p-n Junction Solar Cells", Journal of Applied Physics, Volume 32 (March 1961), pp. 510-519; DOI:10.1063/1.1736034
  2. ^ "Hans Queisser", Computer History Museum, 2004
  3. ^ a b c A. De Vos, "Detailed balance limit of the efficiency of tandem solar cells", Journal of Physics D: Applied Physics Volume 13, Issue 5 (14 May 1980), page 839-846 doi: 10.1088/0022-3727/13/5/018
  4. ^ a b "Photovoltaic Cells (Solar Cells), How They Work". specmat.com. http://www.specmat.com/Overview%20of%20Solar%20Cells.htm. Retrieved 22-May-07. 
  5. ^ a b c C. S. Solanki and G. Beaucarne, "Advanced Solar Cell Concepts", Interuniversity Microelectronics Center, Belgium
  6. ^ P T Landsberg and P Baruch, "The thermodynamics of the conversion of radiation energy for photovoltaics", Journal of Physics A: Mathematical and General, Volume 22 Issue 11 (7 June 1989), pp 1911-1926, doi: 10.1088/0305-4470/22/11/02
  7. ^ a b Michael Kanellos, "Solar cell breaks efficiency record", CNET News, 6 December 2006
  8. ^ "NREL Solar Cell Sets World Efficiency Record at 40.8 Percent", National Renewable Energy Laboratory, 13 August 2008
  9. ^ "Sun in Spain to fall on SolFocus", San Francisco Business Times, 3 November 2008
  10. ^ Andrew S. Brown and Martin A. Green, "Impurity photovoltaic effect: Fundamental energy conversion efficiency limits", Journal of Applied Physics, Volume 92, Issue 1 August 2002, pg. 1392, doi:10.1063/1.1492016
  11. ^ Stefan Lovgren, "Spray-On Solar-Power Cells Are True Breakthrough", National Geographic News, 14 January 2005
  12. ^ Jim Swenson, "Infrared Solar Cells", Ask A Scientist, US Department of Energy, 17 January 2005
  13. ^ Bahram Jalali, Sasan Fathpour, and Kevin Tsia, "Green Silicon Photonics", Optics and Photonics News, Vol. 20, Issue 6, pp. 18-23 (2009), doi:10.1364/OPN.20.6.000018
  14. ^ Gavin Conibeer et all, "Hot Carrier Solar Cell: Implementation of the Ultimate Photovoltaic Converter", Global Climate & Energy Project, Stanford University, September 2008
  15. ^ A. J. Nozik, "Quantum Dot Solar Cells", National Renewable Energy Laboratory, October 2001
  16. ^ Pattareeya Kittidachachan, "Photon collection efficiency of fluorescent solar collectors", CHIMIA International Journal for Chemistry, Volume 61 Issue 12 (December 2007), pp. 780-786, doi:10.2533/chimia.2007.780
  17. ^ "Sunovia, EPIR Demonstrate Optical Down-Conversion For Solar Cells"
  18. ^ Malcolm Chisholm et all, "The remarkable influence of M2δ to thienyl π conjugation in oligothiophenes incorporating MM quadruple bonds", Proceedings of the National Academy of Sciences, 14 August 2008
  19. ^ Pam Frost Gorder, "New Solar Energy Material Captures Every Color of the Rainbow", Research Communications, Ohio State, May 2008
  20. ^ Elizabeth A. Thomson, "MIT opens new 'window' on solar energy", MIT News, 10 July 2008
  21. ^ Nils-Peter Harder and Peter Würfel, "Theoretical limits of thermophotovoltaic solar energy conversion", Semiconductor Science and Technology, Volume 18 Issue 5 (May 2003), S151-S157, doi: 10.1088/0268-1242/18/5/303

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