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| [[File:Illust poly thinfilm.gif|350px|thumb| Figure 1. Cross-section of thin film polycrystalline solar cell. The transparent conducting coating contacts the n-type semiconductor to draw current.]]
| | Phhhhzzz. A fuzzy yellow ball flys earlier you - you happen to be not confident when it passed you, but irrespective, you by some means know the male throughout the web won the level. You glance all over, and locate yourself hitting along with a overseas searching female - in fact, there are quite a few, probably fifty, children who are hitting below that look...diverse. They all hit the ball with a fluid, compact movement, whipping the ball around the courtroom like a engage in toy. Which it technically is. The manicured eco-friendly courts are surrounded by fences with windbreakers more than them, an occasional Babolat ad poster on the fence. There are South American young ones, Danish kids, Russian youngsters...there are Us citizens there, too. They all communicate the exact same language: tennis.<br><br> |
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| '''Transparent conducting films''' (TCFs) are optically transparent and [[electrical conductivity|electrically conductive]] in thin layers.
| | Glimpse at the dude across the internet. Even though you might not know it, he is Ryan Harrison, a indigenous of Shreveport, Louisiana, who happens to educate right here. His image may well not be acquainted to you, but it before long will. His deep blue eyes and filthy blond hair are not almost as piercing as his groundstrokes, but however, he stands out from the other children - typically simply because of his compact and impressive forehand, his consistant and driving backhand, and his in general courtroom sense. He has no immediate toughness that would make him stand out, but that's mainly because his entire match is very good.<br><br>Your switch is in excess of with him now, and as you stroll absent, you enjoy a Chinese child feed the ball to Ryan with some speed. Ryan smiles. He sets up almost flawlessly, his feet and coiling approximately fantastic, and unleashes a forehand winner to the corner. <br><br>"Feed it more difficult," Ryan says.<br><br>If you have a great ample creativity, you might have been able to see what I observed when I strike with him. And I know I'm not the only just one observing the expertise in Ryan. Chatting to the tennis professionals at John Newcombe's, who are, by the way, from many different nations (mainly Australia) and are ex-ATP players, I found out that Ryan had overwhelmed most of them six-, 6-. "Yeah, he is really very good," I recall Sal, a Mexican tennis pro, say. "Unquestionably likely to be top fifty a person working day." Ryan has trained for decades at Newk's, but he is originally from Shreveport, Louisiana. His father, Pat, was earlier a Head Tennis Pro and Tennis Director in Shreveport, LA, but immediately after 15 several years, he bought a position coaching at Newcombe's. Ryan was around 8 several years old, a promising junior and not particularly rooted to Louisiana, so they made the soar to Texas. Ryan has explained he had a very long discussion with his mothers and fathers about his job soon after their shift, and "he knew that he was heading to convert pro. University was not an challenge, but he didn't like it." mentioned the straight A pupil. At any time due to the fact then, Pat Harrison has been getting ready his two sons for the huge time. <br><br>Ryan is very gifted, but his very little brother, Christian, is just as excellent. He is fourth in the country for 14's, and thirty second for 16's boys singles, and has traveled internationally and gone deep in situations. <br><br>Useless to say, Pat and Phil Hendrie, the Academy Director, operate a good academy. Here's their routine (or at least the just one I was informed they had).<br><br><br><br>Physical fitness - 5:00 A.M.<br><br>Morning Hitting Session (Drills) - seven:00 A.M.-10:00 A.M.<br><br>Lunch - ten:30 A.M.-Noon<br><br>Absolutely free TIme - Midday -1:forty five P.M.<br><br>Evening Hitting Session (Drills/Match Engage in) - two:00 P.M.-five:00 P.M.<br><br>Dinner - 6:thirty P.M.<br><br>Totally free Time - 7:00-8:00 P.M.<br><br>Bedtime - Around 9:30 P.M.<br><br><br><br>At to start with look, not that hard, but have confidence in me, it kills you. Rather brief posting, hope you loved it.<br><br>Racquet: Babolat Pure Storm<br><br>Sponsor: Babolat, Nike<br><br>Born in: Shreveport, Louisiana<br><br>Birthdate: five/seven/92<br><br>Current Residence: New Braunfels, Texas<br><br>Performs: Right-handed, Two-handed backhand<br><br>Vocation Prize Funds: $1,796<br><br>Best Slam Outcomes: None (however)<br><br>Currently Ranked: 1277<br><br>Top: 6'0"<br><br> Pounds: one hundred sixty lbs.<br><br>Should you have any kind of issues regarding where and also how you can use [http://tinyurl.com/l4tujjg Nike Free Run], it is possible to e mail us on our own web page. |
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| TCFs for [[photovoltaic]] applications have been fabricated from both inorganic and organic materials. Inorganic films typically are made up of a layer of transparent conducting oxide (TCO),<ref name="TCO">[http://materion.com/~/media/Files/PDFs/Microelectronics/TechnicalPapers/Transparent%20Conductive_All Conductive Oxide Thin Films] Materion Technical Paper, "Transparent Conductive Oxide Thin Films"</ref> generally in the form of [[indium tin oxide]] (ITO), fluorine doped tin oxide (FTO), and doped [[zinc oxide]]. Organic films are being developed using [[carbon nanotube]] networks and [[graphene]], which can be fabricated to be highly transparent to infrared light, along with networks of polymers such as [[poly(3,4-ethylenedioxythiophene)]] and its derivatives.
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| Transparent conducting films act as a window for light to pass through to the active material beneath (where carrier generation occurs), as an ohmic contact for carrier transport out of the photovoltaic, and can also act as transparent carrier for [[surface-mount technology|surface mount devices]] used between [[Ledglass|laminated glass]] or light transmissive [[LED Headliner|composites]]. Transparent materials possess [[bandgap]]s with energies corresponding to wavelengths which are shorter than the visible range of 380 nm to 750 nm. As such, photons with energies below the bandgap are not collected by these materials and thus visible light passes through. However, applications such as photovoltaics may require an even broader bandgap to avoid unwanted absorption of the solar spectra.
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| ==Transparent conducting oxides==
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| [[File:Solar cell.png|thumb|This solar cell, made of [[monocrystalline]] [[silicon]], has no transparent conducting film. Instead, it uses a "grid contact": a network of very thin metal wires.]]
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| ===Overview===
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| Transparent conductive oxides (TCO) are doped metal oxides used in optoelectronic devices such as flat panel displays and photovoltaics (including inorganic devices, organic devices, and [[dye-sensitized solar cell]]). Most of these films are fabricated with [[polycrystalline]] or [[amorphous]] microstructures. On average, these applications use electrode materials that have greater than 80% transmittance of incident light as well as conductivities higher than 10<sup>3</sup> [[Siemens (unit)|S]]/cm for efficient carrier transport. The transmittance of these films, just as in any [[transparent material]], is limited by light scattering at defects and [[grain boundaries]]. In general, TCOs for use as thin-film electrodes in solar cells should have a minimum carrier concentration on the order of 10<sup>20</sup> cm<sup>−3</sup> for low resistivity and a bandgap greater than 380 nm to avoid absorption of light over most of the solar spectra.<ref name = "Minami">{{cite journal|doi=10.1088/0268-1242/20/4/004|title=Transparent conducting oxide semiconductors for transparent electrodes|year=2005|last1=Minami|first1=Tadatsugu|journal=Semiconductor Science and Technology|volume=20|pages=S35|bibcode = 2005SeScT..20S..35M|issue=4 }}</ref> Mobility in these films is limited by ionized impurity scattering and is on the order of 40 cm<sup>2</sup>/(V·s). Current transparent conducting oxides used in industry are primarily n-type conductors, meaning their primary conduction is as donors of electrons. Suitable p-type transparent conducting oxides are still being researched.
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| To date, the industry standard in TCO is ITO, or [[indium tin oxide|tin-doped indium-oxide]]. This material boasts a low resistivity of ~10<sup>−4</sup> Ω·cm and a transmittance of greater than 80%.{{Citation needed|date=August 2010}} However ITO has the drawback of being expensive. [[Indium]], the film’s primary metal, is rare (6000 metric tons worldwide in 2006), and its price fluctuates due to market demand (over $800 per kg in 2006).<ref name = "Indium">[http://geology.com/articles/indium.shtml Indium Price Supported by LCD Demand and New Uses for the Metal]</ref> For this reason, doped binary compounds such as [[aluminum-doped zinc-oxide]] (AZO) and indium-doped [[cadmium oxide|cadmium-oxide]] have been proposed as alternative materials. AZO is composed of aluminum and zinc, two common and inexpensive materials, while indium-doped cadmium oxide only uses indium in low concentrations.
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| Binary compounds of metal oxides without any intentional impurity doping have also been developed for use as TCOs. These systems are typically n-type with a carrier concentration on the order of 10<sup>20</sup> cm<sup>−3</sup>, provided by interstitial metal ions and oxygen vacancies which both act as donors. However, these simple TCOs have not found practical use due to the high dependence of their electrical properties on temperature and oxygen partial pressure.<ref name = "Minami"/>
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| ===Fabrication===
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| Doped metal oxides for use as transparent conducting layers in photovoltaic devices are typically grown on a [[glass]] substrate. This glass substrate, apart from providing a support that the oxide can grow on, has the additional benefit of blocking most infrared wavelengths greater than 2 µm for most silicates, and converting it to heat in the glass layer. This in turn helps maintain a low temperature of the active region of the solar cell, which degrades in performance as it heats up. TCO films can be deposited on a substrate through various deposition methods, including [[Metalorganic vapour phase epitaxy|metal organic chemical vapor deposition]] (MOCVD), metal organic molecular beam deposition (MOMBD), spray pyrolysis, and [[pulsed laser deposition]] (PLD), however conventional fabrication techniques typically involve magnetron [[sputtering]] of the film. The sputtering process is very inefficient, with only 30% of planar target material available for deposition on the substrate. Cylindrical targets offer closer to 80% utilization. In the case of ITO recycling of unused target material is required for economic production. For AZO or ZnAl sputtering target material is sufficiently inexpensive that recovery of materials use is of no concern. There is some concern that there is a physical limit to the available indium for ITO<ref name = "USGS">[http://minerals.usgs.gov/minerals/pubs/commodity/indium/mcs-2009-indiu.pdf Indium], USGS report</ref> Growth typically is performed in a reducing environment to encourage oxygen vacancy formation within the film, which contribute to the carrier concentration (if n-type).<ref name = "Minami"/>
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| ===Theory===
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| Charge carriers in these oxides arise from three fundamental sources: interstitial metal ion impurities, oxygen vacancies, and doping ions. The first two sources always act as electron donors; indeed, some TCOs are fabricated solely using these two intrinsic sources as carrier generators. When an oxygen vacancy is present in the lattice it acts as a doubly charged electron donor. In ITO, for example, each oxygen vacancy causes the neighboring In<sup>3+</sup> ion 5s orbitals to be stabilized from the 5s conduction band by the missing bonds to the oxygen ion, while two electrons are trapped at the site due to charge neutrality effects. This stabilization of the 5s orbitals causes a formation of a donor level for the oxygen ion, determined to be 0.03 eV below the conduction band.<ref name = "Edwards">{{cite journal|doi=10.1039/b408864f|title=Basic materials physics of transparent conducting oxides|pmid=15452622|year=2004|last1=Edwards|first1=P. P.|last2=Porch|first2=A.|last3=Jones|first3=M. O.|last4=Morgan|first4=D. V.|last5=Perks|first5=R. M.|journal=Dalton Transactions|issue=19|pages=2995–3002}}</ref> Thus these defects act as shallow donors to the bulk crystal. Common notation for this doping is [[Kröger–Vink notation]] and is written as:
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| ::<math> O_{O}^{x} \leftrightarrow V_{O}^{\bullet\bullet} + 0.5O_{2} (g) + 2e'</math>
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| Here “O” in the subscripts indicates that both the initially bonded oxygen and the vacancy that is produced lie on an oxygen lattice site, while the superscripts on the oxygen and vacancy indicate charge. Thus to enhance their electrical properties, ITO films and other transparent conducting oxides are grown in reducing environments, which encourage oxygen vacancy formation.
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| Dopant ionization within the oxide occurs in the same way as in other semiconductor crystals. Shallow donors near the conduction band (n-type) allow electrons to be thermally excited into the conduction band, while acceptors near the valence band (p-type) allow electrons to jump from the valence band to the acceptor level, populating the valence band with holes. It is important to note that carrier scattering in these oxides arises primarily from ionized impurity scattering. Charged impurity ions and point defects have scattering cross-sections that are much greater than their neutral counterparts. Increasing the scattering decreases the mean-free path of the carriers in the oxide, which leads to poor device performance and a high resistivity. These materials can be modeled reasonably well by the [[free electron gas]] theory assuming a parabolic conduction band and doping levels above the [[Mott Criterion]]. This criterion states that an insulator such as an oxide can experience a composition-induced transition to a metallic state given a minimum doping concentration n<sub>c</sub>, determined by:
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| ::<math> n_{c}^{1/3} a_{H}^{*} = 0.26 \pm 0.05</math>
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| where a<sub>H</sub>* is the mean ground state [[Bohr radius]]. For ITO, this value requires a minimum doping concentration of roughly 10<sup>19</sup> cm<sup>−3</sup>. Above this level, the typically electrically insulating material becomes metallic and is capable of allowing carrier flow.<ref name = "Edwards"/>
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| ==Transparent conducting polymers==
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| [[File:Polymercell.JPG|350px|thumb| Figure 2. Polymer photovoltaic cell using transparent conducting polymers.]]
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| [[Conductive polymer]]s were reported in the mid the 20th century as derivatives of polyaniline.<ref>[http://nobelprize.org/nobel_prizes/chemistry/laureates/2000/chemadv.pdf The Nobel Prize in Chemistry, 2000: Conductive polymers]</ref> Research continued on such polymers in the 1960s and 70s and continued into the turn of the 21st century.<ref>"Historical Background (or there is nothing new under the Sun)" in György Inzelt “Conducting Polymers” Springer, 2008, Berlin, Heidelberg. {{doi|10.1007/978-3-540-75930-0}}</ref><ref>{{cite journal|doi=10.1196/annals.1292.016|title=An Overview of the First Half-Century of Molecular Electronics|year=2003|last1=Hush|first1=Noel S.|journal=Annals of the New York Academy of Sciences|volume=1006|pages=1–20|pmid=14976006|bibcode = 2003NYASA1006....1H }}</ref> Most conductive polymers are derivatives of [[polyacetylene]], [[polyaniline]], [[polypyrrole]] or [[polythiophene]]s.<ref name = "Skotheim">Skotheim, Terje A. Reynold, John [http://books.google.com/books?id=6GRovXHas_MC&printsec=frontcover “Handbook of Conducting Polymers”] CRC Press, 1998 ISBN 0-8247-0050-3</ref> These polymers have [[conjugated system|conjugated double bonds]] which allow for conduction. By manipulating the band structure, polythiophenes have been modified to achieve a [[HOMO/LUMO|HOMO-LUMO]] separation ([[bandgap]]) that is large enough to make them transparent to visible light. <!-- excess detail: In a polymer, the band structure is determined by the molecular orbitals. The effective bandgap is the separation between the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO). This gap can be approximated with understanding of the [[Huckel method]]. -->
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| ===Applications===
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| Transparent conductive polymers are used as electrodes on light emitting diodes and photovoltaic devices.<ref>Pregan, B; Gratzel, M. ''Nature'' '''1991''', ''353'', 737. http://www.nature.com/nature/journal/v353/n6346/abs/353737a0.html</ref> They have conductivity below that of transparent conducting oxides but have low absorption of the visible spectrum allowing them to act as a transparent conductor on these devices. However, because transparent conductive polymers do absorb some of the visible spectrum and significant amounts of the mid to near IR, they lower the efficiency of photovoltaic devices.{{Citation needed|date=March 2011}}
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| The transparent conductive polymers can be made into ''flexible'' films making them desirable despite their lower conductivity. This makes them useful in the development of [[flexible electronics]] where traditional transparent conductors will fail.
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| ===Poly(3,4-ethylenedioxythiophene) (PEDOT)===
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| [[Poly(3,4-ethylenedioxythiophene)]] (PEDOT) has conductivity of up to around 1,000 S/cm.<ref name = "Hu">{{cite journal|doi=10.1063/1.3075067|title=Infrared transparent carbon nanotube thin films|year=2009|last1=Hu|first1=Liangbing|last2=Hecht|first2=David S.|last3=Grüner|first3=George|journal=Applied Physics Letters|volume=94|pages=081103|bibcode = 2009ApPhL..94h1103H|issue=8 }}</ref> Thin oxidized PEDOT films have approx. 10% or less absorption in the visible spectrum and excellent stability.<ref name = "Groenendaal">{{cite journal|last1=Groenendaal|first1=L.|last2=Jonas|first2=F.|last3=Freitag|first3=D.|last4=Pielartzik|first4=H.|last5=Reynolds|first5=J. R.|title=Poly(3,4-ethylenedioxythiophene) and Its Derivatives: Past, Present, and Future|journal=Advanced Materials|volume=12|pages=481|year=2000|doi=10.1002/(SICI)1521-4095(200004)12:7<481::AID-ADMA481>3.0.CO;2-C|issue=7}}</ref> However, PEDOT is insoluble in water making processing more difficult and costly.
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| The bandgap of PEDOT can be varied between 1.4 and 2.5 eV by varying the degree of π-overlap along the backbone.<ref name = "Groenendaal"/> This can be done by adding substituents along the chain, which result in steric interactions preventing π-overlap. Substituents can also be electron-accepting or donating which will modify the electronic character and thus modify the bandgap. This allows for the formation of a wide bandgap conductor which is transparent to the visible spectrum.
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| PEDOT is prepared by mixing EDT monomer with an oxidizing agent such as [[Iron(III) chloride|FeCl<sub>3</sub>]]. The oxidizing agent acts as an initiator for polymerization. Research has shown that increasing the ratio of [FeCl<sub>3</sub>]/[monomer] decreases the solubility of the PEDOT.<ref name = "Groenendaal"/> This is thought to be a result of increased [[Cross-link|crosslinking]] in the polymer making it more difficult to dissolve in a solvent.
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| ===Poly(3,4-ethylenedioxythiophene) PEDOT: poly(styrene sulfonate) PSS===
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| Doping PEDOT with poly(styrene sulfonate) can improve the properties over the unmodified PEDOT. This PEDOT:PSS compound has become the industry leader in transparent conductive polymers. [[PEDOT:PSS]] is water soluble making processing easier. PEDOT:PSS has a conductivity ranging from 400 to 600 S/cm while still transmitting ~80% of visible light.<ref name = "Louwet">{{cite journal|doi=10.1016/S0379-6779(02)00518-0|title=PEDOT/PSS: synthesis, characterization, properties and applications|year=2003|last1=Louwet|first1=F|journal=Synthetic Metals|volume=135-136|pages=115|last2=Groenendaal|first2=L.|last3=Dhaen|first3=J.|last4=Manca|first4=J.|last5=Van Luppen|first5=J.|last6=Verdonck|first6=E.|last7=Leenders|first7=L.}}</ref> Treatment in air at 100 °C for over 1000 hours will result in a minimal change in conductivity.<ref name = "Ouyang">{{cite journal|doi=10.1002/adfm.200400016|title=High-Conductivity Poly(3,4-ethylenedioxythiophene):Poly(styrene sulfonate) Film and Its Application in Polymer Optoelectronic Devices|year=2005|last1=Ouyang|first1=J.|last2=Chu|first2=C.-W.|last3=Chen|first3=F.-C.|last4=Xu|first4=Q.|last5=Yang|first5=Y.|journal=Advanced Functional Materials|volume=15|pages=203|issue=2}}</ref> Recently, it was reported that the conductivity of PEDOT:PSS can be improved to be more than 3000 S/cm.<ref>Yijie Xia, Kuan Sun, Jianyong Ouyang, Solution-Processed Metallic Conducting Polymer Films as Transparent Electrode of Optoelectronic Devices, Advanced Materials, 24 (2012) 2436-2440.</ref>
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| PEDOT:PSS is prepared by polymerizing EDT monomer in an aqueous solution of PSS using Na<sub>2</sub>S<sub>2</sub>O<sub>8</sub> as the oxidizing agent. This aqueous solution is then spin coated and dried to make a film.<ref name = "Ouyang"/>
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| ===Poly(4,4-dioctylcyclopentadithiophene)===
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| Poly(4,4-dioctylcyclopentadithiophene) can be doped with [[iodine]] or [[2,3-dichloro-5,6-dicyano-1,4-benzoquinone]] (DDQ) to form a transparent conductor. The doped polymer has low absorption of the visible spectrum with an absorption band centered around 1050 nm. When doped with iodine, a conductivity of 0.35 S/cm can be achieved. However, the iodine has a tendency to diffuse out in air, making the iodine-doped poly(4,4-dioctylcyclopentadithiophene) unstable.<ref name = "Coppo">{{cite journal|doi=10.1016/j.synthmet.2003.12.001|title=Investigation of solution processed poly(4,4-dioctylcyclopentadithiophene) thin films as transparent conductors|year=2004|last1=Coppo|first1=P|journal=Synthetic Metals|volume=143|pages=203|last2=Schroeder|first2=Raoul|last3=Grell|first3=Martin|last4=Turner|first4=Michael L|issue=2}}</ref>
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| DDQ itself has a conductivity of 1.1 S/cm. However, DDQ-doped poly(4,4-dioctylcyclopentadithiophene) also tends to decrease its conductivity in air. DDQ-doped polymer has better stability than the iodine-doped polymer, but the stability is still below that of PEDOT. In summary, poly(4,4-dioctylcyclopentadithiophene) has inferior properties relative to PEDOT and PEDOT:PSS, which need to be improved for realistic applications.
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| Poly(4,4-dioctylcyclopentadithiophene) is solution polymerized by combining monomer with [[iron(III) chloride]]. Once the polymerization is complete the doping is done by exposing the polymer to iodine vapor or DDQ solution.<ref name = "Coppo"/>
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| ==Carbon nanotubes==
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| ===Advantages===
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| Transparent conductors are fragile and tend to break down due to fatigue. The most commonly used TCO is Indium-Tin-Oxide (ITO) because of its good electrical properties and ease of fabrication. However, these thin films are usually fragile and such problems as lattice mismatch and stress-strain constraints lead to restrictions in possible uses for TCFs. ITO has been shown to degrade with time when subject to mechanical stresses. Recent increases in cost are also forcing many to look to carbon nanotube films as a potential alternative.
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| [[Carbon nanotubes]] (CNTs) have attracted much attention because of their materials properties, including a high elastic modulus (~1–2 TPa), a high tensile strength (~13–53 GPa), and a high conductivity (metallic tubes can theoretically carry an electrical current density of 4×10<sup>9</sup> A/cm<sup>2</sup>, which is ~1000 times higher than for other metals such as [[copper]]).<ref name = "Hong">{{cite journal|doi=10.1038/nnano.2007.89|pmid=18654263|title=Nanotube Electronics: A flexible approach to mobility|year=2007|last1=Hong|first1=Seunghun|last2=Myung|first2=Sung|journal=Nature Nanotechnology|volume=2|issue=4|pages=207–8|bibcode = 2007NatNa...2..207H }}</ref> CNT thin films have been used as transparent electrodes in TCFs because of these good electronic properties.
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| ===Preparation of CNT thin films===
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| [[File:Cnt diameter effect.jpg|150px|thumb| Figure 3. CNTs of various diameters separated within a centrifuge tube. Each distinct diameter results in a different color.]]
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| The preparation of CNT [[thin films]] for TCFs is composed of three steps: the CNT growth process, putting the CNTs in solution, and, finally, creation of the CNT thin film. Nanotubes can be grown using [[laser ablation]], electric-arc discharge, or different forms of [[chemical vapor deposition]] (such as PECVD). However, nanotubes are grown en-masse, with nanotubes of different chiralities stuck together due to [[Van der Waals force|van der Waals attraction]]. Density gradient ultracentrifugation (DGU) has recently been used to get rid of this problem.<ref name = "Green">{{cite journal|doi=10.1021/nl080302f|pmid=18393537|title=Colored Semitransparent Conductive Coatings Consisting of Monodisperse Metallic Single-Walled Carbon Nanotubes|year=2008|last1=Green|first1=Alexander A.|last2=Hersam|first2=Mark C.|journal=Nano Letters|volume=8|issue=5|pages=1417–22|bibcode = 2008NanoL...8.1417G }}</ref> Using DGU, transparent conductors were constructed using only metallic tubes. Because DGU allows for separation by density, tubes with similar optical properties (due to similar diameters) were selected and used to make CNT conductive films of different colors.
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| In order to separate the grown tubes, the CNTs are mixed with surfactant and water and sonicated until satisfactory separation occurs. This solution is then sprayed onto the desired substrate in order to create a CNT thin film. The film is then rinsed in water in order to get rid of excess surfactant.
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| ===Comparing CNTs to TCOs===
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| CNTs can also be used in addition to transparent conducting oxides (TCOs) in [[Thin-film photovoltaic cell|thin-film photovoltaic device]]s. Two TCOs which are often used are ZnO/Al and In<sub>2</sub>O<sub>3</sub>/Sn [[indium tin oxide]] (ITO). PV devices made with these TCOs attained energy-conversion efficiencies of 19.5% in CuIn<sub>1−x</sub>Ga<sub>x</sub>Se<sub>2</sub>-based ([[Copper indium gallium selenide|CIGS]]) solar cells and 16.5% in [[Cadmium telluride|CdTe]]-based solar cells. These photovoltaic devices had much higher efficiencies compared to the devices made with CNT thin films: Britz ''et al.'' report an efficiency of 8%, with an open circuit voltage (V<sub>oc</sub>) of 0.676 V, a short circuit flux (J<sub>sc</sub>) of 23.9 mA/cm<sup>2</sup>, and a fill factor of 45.48%.<ref>{{cite journal|doi=10.1021/jp075507b|title=Replacement of Transparent Conductive Oxides by Single-Wall Carbon Nanotubes in Cu(In,Ga)Se2-Based Solar Cells|year=2007|last1=Contreras|first1=M.A.|last2=Barnes|first2=T.|last3=Vandelagemaat|first3=J.|last4=Rumbles|first4=G.|last5=Coutts|first5=T.J.|last6=Weeks|first6=C.|last7=Glatkowski|first7=P.|last8=Levitsky|first8=I.|last9=Peltola|first9=J.|journal=Journal of Physical Chemistry C|volume=111|pages=14045|issue=38}}</ref> However, CNT thin films show many advantages over other transparent electrodes in the IR range. CNT thin films were reported to have a transmittance of over 90% in this range (400 nm – 22 µm). This paves the way for new applications, indicating that CNT thin films can be used as heat dissipaters in solar cells because of this high transmittance.
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| As stated previously, nanotube chirality is important in helping determine its potential aid to these devices. Before mass production can occur, more research is needed in exploring the significance of tube diameter and chirality for transparent conducting films in photovoltaic applications. It is expected that the conductivity of the SWNT thin films will increase with an increase in CNT length and purity. As stated previously, the CNT films are made using randomly oriented bundles of CNTs. Ordering these tubes should also increase conductivity, as it will minimize scattering losses and improve contact between the nanotubes.
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| ==References==
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| {{Reflist|2}}
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| <references />
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| {{DEFAULTSORT:Transparent Conducting Film}}
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| [[Category:Solar cells]]
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Phhhhzzz. A fuzzy yellow ball flys earlier you - you happen to be not confident when it passed you, but irrespective, you by some means know the male throughout the web won the level. You glance all over, and locate yourself hitting along with a overseas searching female - in fact, there are quite a few, probably fifty, children who are hitting below that look...diverse. They all hit the ball with a fluid, compact movement, whipping the ball around the courtroom like a engage in toy. Which it technically is. The manicured eco-friendly courts are surrounded by fences with windbreakers more than them, an occasional Babolat ad poster on the fence. There are South American young ones, Danish kids, Russian youngsters...there are Us citizens there, too. They all communicate the exact same language: tennis.
Glimpse at the dude across the internet. Even though you might not know it, he is Ryan Harrison, a indigenous of Shreveport, Louisiana, who happens to educate right here. His image may well not be acquainted to you, but it before long will. His deep blue eyes and filthy blond hair are not almost as piercing as his groundstrokes, but however, he stands out from the other children - typically simply because of his compact and impressive forehand, his consistant and driving backhand, and his in general courtroom sense. He has no immediate toughness that would make him stand out, but that's mainly because his entire match is very good.
Your switch is in excess of with him now, and as you stroll absent, you enjoy a Chinese child feed the ball to Ryan with some speed. Ryan smiles. He sets up almost flawlessly, his feet and coiling approximately fantastic, and unleashes a forehand winner to the corner.
"Feed it more difficult," Ryan says.
If you have a great ample creativity, you might have been able to see what I observed when I strike with him. And I know I'm not the only just one observing the expertise in Ryan. Chatting to the tennis professionals at John Newcombe's, who are, by the way, from many different nations (mainly Australia) and are ex-ATP players, I found out that Ryan had overwhelmed most of them six-, 6-. "Yeah, he is really very good," I recall Sal, a Mexican tennis pro, say. "Unquestionably likely to be top fifty a person working day." Ryan has trained for decades at Newk's, but he is originally from Shreveport, Louisiana. His father, Pat, was earlier a Head Tennis Pro and Tennis Director in Shreveport, LA, but immediately after 15 several years, he bought a position coaching at Newcombe's. Ryan was around 8 several years old, a promising junior and not particularly rooted to Louisiana, so they made the soar to Texas. Ryan has explained he had a very long discussion with his mothers and fathers about his job soon after their shift, and "he knew that he was heading to convert pro. University was not an challenge, but he didn't like it." mentioned the straight A pupil. At any time due to the fact then, Pat Harrison has been getting ready his two sons for the huge time.
Ryan is very gifted, but his very little brother, Christian, is just as excellent. He is fourth in the country for 14's, and thirty second for 16's boys singles, and has traveled internationally and gone deep in situations.
Useless to say, Pat and Phil Hendrie, the Academy Director, operate a good academy. Here's their routine (or at least the just one I was informed they had).
Physical fitness - 5:00 A.M.
Morning Hitting Session (Drills) - seven:00 A.M.-10:00 A.M.
Lunch - ten:30 A.M.-Noon
Absolutely free TIme - Midday -1:forty five P.M.
Evening Hitting Session (Drills/Match Engage in) - two:00 P.M.-five:00 P.M.
Dinner - 6:thirty P.M.
Totally free Time - 7:00-8:00 P.M.
Bedtime - Around 9:30 P.M.
At to start with look, not that hard, but have confidence in me, it kills you. Rather brief posting, hope you loved it.
Racquet: Babolat Pure Storm
Sponsor: Babolat, Nike
Born in: Shreveport, Louisiana
Birthdate: five/seven/92
Current Residence: New Braunfels, Texas
Performs: Right-handed, Two-handed backhand
Vocation Prize Funds: $1,796
Best Slam Outcomes: None (however)
Currently Ranked: 1277
Top: 6'0"
Pounds: one hundred sixty lbs.
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