Thin film solar cell

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Thin film photovoltaic laminates being installed onto a roof.

A thin-film solar cell (TFSC), also called a thin-film photovoltaic cell (TFPV), is a solar cell that is made by depositing one or more thin layers (thin film) of photovoltaic material on a substrate. Film thickness varies from a few nanometers to tens of micrometers.

Thin film solar panels are commercially available for installation onto the roofs of buildings, either applied onto the finished roof, or integrated into the roof covering. Advantages over traditional PV panels include lower weight, wind resistance and (limited) resistance to foot traffic. Disadvantages include increased cost and reduced efficiency. Building integrated photovoltaics (BIPV) uses semi-transparent thin film cells that can be applied as window glazing. These cells act as window tinting while also generating electricity.

Films are deposited with various deposition methods on a variety of substrates. Thin-film solar cells are usually categorized by photovoltaic material:

History[edit]

Thin film cells initially appeared as small strips powering hand-held calculators.

It is now available in very large modules used in sophisticated building-integrated installations and vehicle charging systems. GBI Research projected thin film production to grow 24% from 2009 levels and to reach 22,214 MW in 2020. "Expectations are that in the long-term, thin-film solar PV technology would surpass dominating conventional solar PV technology, thus enabling the long sought-after grid parity objective."[1][2]

Materials[edit]

Cross-section of a thin-film polycrystalline solar cell.

Thin-film technologies reduce the amount of active material in a cell. Most sandwich active material between two panes of glass. Since silicon solar panels only use one pane of glass, thin film panels are approximately twice as heavy as crystalline silicon panels, although they have a smaller ecological impact (determined from life cycle analysis).[3] The majority of film panels have 2-3 percentage points lower conversion efficiencies than crystalline silicon.[4] Cadmium telluride (CdTe), copper indium gallium selenide (CIGS) and amorphous silicon (a-Si) are three thin-film technologies often used for outdoor applications. As of December 2013, CdTe cost per installed watt was $0.59 as reported by First Solar. CIGS technology laboratory demonstrations reached 20.4% as of December 2013. The lab efficiency of GaAs thin film technology topped 28%.[citation needed]


\begin{pmatrix}\mathrm{Cu}\\\mathrm{Ag}\\\mathrm{Au}\end{pmatrix}
\begin{pmatrix}\mathrm{Al}\\\mathrm{Ga}\\\mathrm{In}\end{pmatrix}
\begin{pmatrix}\mathrm{S} \\\mathrm{Se}\\\mathrm{Te}\end{pmatrix}_2
Possible combinations of Group-(XI, XIII, XVI) elements in the periodic table that yield a compound showing photovoltaic effect: Cu, Ag, AuAl, Ga, InS, Se, Te.

Cadmium telluride[edit]

Cadmium telluride is the only thin film material so far to rival crystalline silicon in cost/watt. However cadmium is a highly toxic and tellurium (anion: "telluride") supplies are limited.

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.[5] 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.[5]

Copper indium gallium selenide[edit]

Copper indium gallium selenide (CIGS) is a direct band gap material. It has the highest efficiency (~20%) among thin film materials (see CIGS solar cell). Traditional methods of fabrication involve vacuum processes including co-evaporation and sputtering. Recent developments at IBM and Nanosolar attempt to lower the cost by using non-vacuum solution processes.[citation needed]

Gallium arsenide[edit]

The Dutch Radboud University Nijmegen made a single junction GaAs cell that reached 25.8% in August 2008, using a 4 µm thick GaAs layer transferred from a wafer base to glass or plastic film. Recently, this increased to 28.8%.[6] The efficiency was attributed to high quality GaAs epitaxial growth, surface passivation by the AlGaAs[7] and the promotion of photon recycling.[8]

Amorphous silicon[edit]

Main article: Amorphous silicon

Amorphous silicon (a-Si) is a non-crystalline, allotropic form of silicon and the most well-developed thin film technology to-date.

This type of thin-film cell is mostly fabricated by a technique called plasma-enhanced chemical vapor deposition. It uses a gaseous mixture of silane (SiH4) and hydrogen to deposit a very thin layer of silicon on a substrate, such as glass, plastic or metal, that has already been coated with a layer of transparent conducting oxide. Other methods used to deposit amorphous silicon on a substrate include sputtering and hot wire techniques. Thin-film silicon is an alternative to conventional wafer (or bulk) silicon (monocrystalline or polycrystalline).

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 than crystalline cells, the complete light spectrum can be absorbed with a very thin layer of photo-electrically active material. A film only 1 micrometer thick can absorb 90% of the usable solar energy.[9]

Amorphous silicon cells suffer from significant output loss (in the range 15-35%) from sun exposure due to the Staebler-Wronski effect. Thinner layers increase the electric field strength across the material, reducing degradation but also light absorption/efficiency. A laser scribing sequence enables the front and back of adjacent cells to be directly interconnected in series, without solder connection between cells, increasing voltage.[9] a-Si production is scaleable, due to its reduced material requirement and because large-area production systems are available.

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 higher energy infrared portion of the spectrum.

Its basic electronic structure is the p-i-n junction. A-Si's amorphous structure implies high inherent disorder and dangling bonds, making it a bad conductor for charge carriers. These dangling bonds act as recombination centers that severely reduce carrier lifetime and pin the Fermi level so that doping the material to n- or p- type is not possible.

A p-i-n structure is usually used, as opposed to an n-i-p structure. This is because the mobility of electrons in a-Si:H is roughly 1 or 2 orders of magnitude larger than that of holes, and thus the collection rate of electrons moving from the n- to p-type contact is better than holes moving from p- to n-type contact. Therefore, the p-type layer should be placed at the top where the light intensity is stronger, so that the majority of the charge carriers crossing the junction are electrons.[10]

Tandem-cell[edit]

A layer of amorphous silicon can be combined with layers of other allotropic forms of silicon to produce a multijunction photovoltaic cell. When only two layers (or p-n junctios) are combined, it is called a tandem-cell. By stacking these layers on top of one other, a broader range of the light spectra is absorbed, more photons are captured, improving the cell's overall efficiency.

In micromorphous silicon, a layer of a-Si is combined with a layer of nanocrystalline silicon creating a tandem cell. The top amorphous silicon layer absorbs the visible light, leaving the infrared part to the bottom nanocrystalline silicon layer.

Because all layers are made of silicon, they can be manufactured using PECVD. The band gap of a-Si is 1.7 eV and that of c-Si is 1.1 eV. The c-Si layer can absorb red and infrared light. The best efficiency can be achieved at transition between a-Si and c-Si. As nanocrystalline silicon (nc-Si) has about the same bandgap as c-Si, nc-Si can replace c-Si.[11]

Amorphous silicon can also be combined with protocrystalline silicon into a tandem-cell. Protocrystalline silicon with a low volume fraction of nanocrystalline silicon is optimal for high open-circuit voltage.[12] 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).

Black silicon ia another material used in thin-film technology.

Polymer[edit]

An organic solar cell uses a photovoltaic polymer to produce electricity. Current research devices display low efficiency and stability.

Chloride[edit]

Manufacturers usually apply a thin layer of cadmium chloride to increase the efficiency of solar cells. Magnesium chloride (extracted from seawater) performs just as well as cadmium chloride.[13]

Efficiencies, volumes and prices[edit]

Solar cell efficiencies of various cell technologies as tracked by NREL [14]

Since the invention of the first modern silicon solar cell in 1954, incremental improvements have resulted in modules capable of converting 12 to 18 percent of solar radiation into electricity.[15]

Cells made from these materials tend to be less efficient than bulk silicon, but are are less expensive to produce. Their quantum efficiency is also lower due to reduced number of collected charge carriers per incident photon.

The performance and potential of thin-film materials are high, reaching cell efficiencies of 12–20%; prototype module efficiencies of 7–13%; and production modules in the range of 9%.[16] The thin film cell prototype with the best efficiency yields 20.4% (First Solar), comparable to the best conventional solar cell prototype efficiency of 25.6% from Panasonic.[17][18]

NREL once predicted that costs would drop below $100/m2 in volume production, and could later fall below $50/m2.[19]

Absorption[edit]

Multiple techniques have been employed to increase the amount of light that enters the cell and reduce the amount that escapes without absorption. The most obvious technique is to minimizing the top contact coverage of the cell surface, reducing the area that blocks light from reaching the cell.

The weakly absorbed long wavelength light can be obliquely coupled into silicon and traverses the film several times to enhance absorption.[20][21]

Anti-reflective coatings can create destructive interference within the cell. This can be done by modulating the refractive index of the surface coating. Destructive interference eliminates the reflective wave and thus all incident light enters the cell.

Surface texturing is another option for increasing absorption, but increases costs. By applying a texture to the active material's surface, the reflected light can be refracted into striking the surface again, thus reducing reflectance. A textured backreflector can prevent light from escaping through the rear of the cell.

Thermal processing techniques can significantly enhance the crystal quality of the silicon and thereby increase efficiency.[22]

Further advancement into geometric considerations can exploit nanomaterial dimensionality. Large, parallel nanowire arrays enable long absorption lengths along the length of the wire while maintaining short minority carrier diffusion lengths along the radial direction. Adding nanoparticles between the nanowires allows conduction. The natural geometry of these arrays forms a textured surface that traps more light.

Production, cost and market[edit]

Crystalline silicon technologies continue to dominate the photovoltaic market, because of superior efficiency.[23] In July 2013 the price of Thin film a-Si dropped to €0.38/Wp,[24] about USD 0.502493.[25] using a micro crystalline silicon layer above the amorphous layer.[26] In 2011, GE announced plans to spend $600 million on a new CdTe solar cell plant and enter this market.[27]

Thin film manufacturers faced price competition from Chinese refiners of silicon and manufacturers of conventional solar panels. As of January, 2013, some thin film firms together with their patents were sold to Chinese firms below cost.[28]

Installations[edit]

First Solar, the CdTe thin-film manufacturer stated that "at the end of 2007, over 300 MW of First Solar PV modules had been installed worldwide." Below is a list of several early installations:[16]

  • Germany's largest thin-film pitched roof system, constructed by Riedel Recycling, opened in 2008 in Moers near Duisburg. Over eleven thousand First Solar CdTe modules deliver a total of 837 kW.[29]
  • A 2.4 MW First Solar rooftop installation was part of Southern California Edison program to install 250 MW of rooftop solar panels throughout Southern California by 2013.[30]
  • First Solar announced a 7.5 MW system to be installed in Blythe, CA, where the California Public Utilities Commission signed a 12 ¢/kWh power purchase agreement with First Solar (after incentives).[31]
  • Construction of a 10 MW plant in the Nevada desert began in July 2008.[32][33] First Solar is partnering with Sempra Generation, which will own and operate the PV power-plant, being built next to their natural gas plant.
  • Stadtwerke Trier (SWT) in Trier, Germany was expected to produce over 9 GWh annually.
  • A system by Juwi in Waldpolenz Solar Park, Germany was at the time of its announcement, both the largest and lowest cost PV system in the world at 40 MW. The price of 3.25 euros translated then (when the euro was equal to US$1.3) to $4.2 per installed watt.[34]
  • Denver-based Conergy Americas and officials at California's South San Joaquin Irrigation District (SSJID)[35] installed what they claimed to be the world's first single-axis solar tracking system featuring thin-film photovoltaic cells.[36]

Awards[edit]

Thin-film photovoltaic cells were included in Time Magazine's Best Inventions of 2008.[37]

See also[edit]

References[edit]

  1. ^ Renewable Energy Magazine[dead link]
  2. ^ GBI Research (2011). "Thin Film Photovoltaic PV Cells Market Analysis to 2020 CIGS Copper Indium Gallium Diselenide to Emerge as the Major Technology by 2020". gbiresearch.com. Retrieved 29 January 2011. 
  3. ^ Pearce, J.; Lau, A. (2002). "Net Energy Analysis for Sustainable Energy Production from Silicon Based Solar Cells". Solar Energy. p. 181. doi:10.1115/SED2002-1051. ISBN 0-7918-1689-3.  edit
  4. ^ Datasheets of the market leaders: First Solar for thin film, Suntech and SunPower for crystalline silicon
  5. ^ a b Fthenakis, Vasilis M. (2004). "Life cycle impact analysis of cadmium in CdTe PV production" (PDF). Renewable and Sustainable Energy Reviews 8 (4): 303–334. doi:10.1016/j.rser.2003.12.001. 
  6. ^ Yablonovitch, Eli; Miller, Owen D.; Kurtz, S. R. (2012). "The opto-electronic physics that broke the efficiency limit in solar cells". 2012 38th IEEE Photovoltaic Specialists Conference. p. 001556. doi:10.1109/PVSC.2012.6317891. ISBN 978-1-4673-0066-7. 
  7. ^ Schnitzer, I.; Yablonovitch, E.; Caneau, C.; Gmitter, T. J. (1993). "Ultrahigh spontaneous emission quantum efficiency, 99.7% internally and 72% externally, from Al Ga As/Ga As/Al Ga As double heterostructures". Applied Physics Letters 62 (2): 131. doi:10.1063/1.109348.  edit
  8. ^ Wang, X.; Khan, M. R.; Gray, J. L.; Alam, M. A.; Lundstrom, M. S. (2013). "Design of Ga As Solar Cells Operating Close to the Shockley–Queisser Limit". IEEE Journal of Photovoltaics 3 (2): 737. doi:10.1109/JPHOTOV.2013.2241594.  edit
  9. ^ a b Photovoltaics. Engineering.Com (9 July 2007). Retrieved on 19 January 2011.
  10. ^ "Amorphes Silizium für Solarzellen" (in German). 
  11. ^ J. M. Pearce, N. Podraza, R. W. Collins, M.M. Al-Jassim, K.M. Jones, J. Deng, and C. R. Wronski (2007). "Optimization of Open-Circuit Voltage in Amorphous Silicon Solar Cells with Mixed Phase (Amorphous + Nanocrystalline) p-Type Contacts of Low Nanocrystalline Content". Journal of Applied Physics 101: 114301. doi:10.1063/1.2714507. 
  12. ^ Pearce, J. M.; Podraza, N.; Collins, R. W.; Al-Jassim, M. M.; Jones, K. M.; Deng, J.; Wronski, C. R. (2007). "Optimization of open circuit voltage in amorphous silicon solar cells with mixed-phase (amorphous+nanocrystalline) p-type contacts of low nanocrystalline content". Journal of Applied Physics 101 (11): 114301. doi:10.1063/1.2714507.  edit
  13. ^ Karen Field. "Bean Curd Component Could Slash Solar Panel Costs". EE Times. 2014.
  14. ^ "NREL: Best PV research cell efficiencies". Retrieved 25 November 2012. 
  15. ^ Steve Heckeroth (February–March 2010). "The Promise of Thin-Film Solar". Mother Earth News. Retrieved 2010-03-23. 
  16. ^ a b Utility-Scale Thin-Film: Three New Plants in Germany Total Almost 50 MW
  17. ^ Yet Another Solar Cell Efficiency Record For First Solar
  18. ^ Panasonic HIT Solar Cell Sets World Efficiency Record
  19. ^ "NREL: Photovoltaics Research - Thin Film Photovoltaic Partnership Project". Nrel.gov. 2012-06-28. Retrieved 2014-06-26. 
  20. ^ Widenborg, Per I.; Aberle, Armin G. (2007). "Polycrystalline Silicon Thin-Film Solar Cells on AIT-Textured Glass Superstrates". Advances in OptoElectronics 2007: 1. doi:10.1155/2007/24584. 
  21. ^ [1]
  22. ^ Terry, Mason L.; Straub, Axel; Inns, Daniel; Song, Dengyuan; Aberle, Armin G. (2005). "Large open-circuit voltage improvement by rapid thermal annealing of evaporated solid-phase-crystallized thin-film silicon solar cells on glass". Applied Physics Letters 86 (17): 172108. Bibcode:2005ApPhL..86q2108T. doi:10.1063/1.1921352. 
  23. ^ "ANWELL produces its first solar panel". NextInsight. 2008-09-01. 
  24. ^ "Service | PVX spot market price index solar PV modules - SolarServer". Solarserver.com. 2014-06-20. Retrieved 2014-06-26. 
  25. ^ (Mid-market rates: 2013-08-31 21:20 UTC 1 EUR = 1.32235 USD)
  26. ^ "Photovoltaics: Thin-film technology about to make its breakthrough". Solar server. 2008-08-07. 
  27. ^ Peralta, Eyder. (2011-04-07) GE Unveils Plans To Build Largest Solar Panel Factory In U.S. : The Two-Way. NPR. Retrieved on 2011-05-05.
  28. ^ Diane Cardwell; Keith Bradsher (January 9, 2013). "Chinese Firm Buys U.S. Solar Start-Up". The New York Times. Retrieved January 10, 2013. 
  29. ^ "Germany’s largest thin-film pitched roof system begins production". PV-tech. 28 October 2008. 
  30. ^ "California Utility to Install 250MW of Roof-Top Solar". SustainableBusiness.com. 2008-03-27. 
  31. ^ "First Solar announces two solar projects with Southern California Edison". Semiconductor-Today.com. 2008-07-17. 
  32. ^ First Solar to Build 10 MW Solar PV Power Plant for Sempra Generation
  33. ^ Wenzel, Elsa. (2008-07-24) First Solar and Sempra plan thin-film solar plant | Green Tech – CNET News. News.cnet.com. Retrieved on 2011-05-05.
  34. ^ "Report at juwi.de". 
  35. ^ the homepage of the South San Joaquin Irrigation District
  36. ^ Conergy Brings World's First Known Thin-Film Solar Energy Tracking System – and $400,000 In Annual Utility Bill Savings – to California's South San Joaquin Irrigation District
  37. ^ "25. Thin-Film Solar Panels". Time. 2008-10-29. TIME's Best Inventions of 2008. Retrieved 2010-05-25. 

Sources[edit]

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  • Green, Martin A. “Consolidation of thin-film photovoltaic technology: the coming decade of opportunity.” Progress in Photovoltaics: Research and Applications 14, no. 5 (2006): 383–392.
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  • Ullal, H. S., and B. von Roedern. “Thin Film CIGS and CdTe Photovoltaic Technologies: Commercialization, Critical Issues, and Applications; Preprint” (2007).
  • Hegedus, S. “Thin film solar modules: the low cost, high throughput and versatile alternative to Si wafers.” Progress in Photovoltaics: Research and Applications 14, no. 5 (2006): 393–411.
  • Poortmans, J., and V. Arkhipov. Thin Film Solar Cells: Fabrication, Characterization and Applications. Wiley, 2006.
  • Wronski, C.R., B. Von Roedern, and A. Kolodziej. “Thin-film Si:H-based solar cells.” Vacuum 82, no. 10 (June 3, 2008): 1145–1150.
  • Chopra, K. L., P. D. Paulson, and V. Dutta. “Thin-film solar cells: an overview.” Progress in Photovoltaics: Research and Applications 12, no. 2-3 (2004): 69–92.
  • Hamakawa, Y. Thin-Film Solar Cells: Next Generation Photovoltaics and Its Applications. Springer, 2004.
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External links[edit]