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Letteratura scientifica selezionata sul tema "Solar cells"

Autore: Grafiati

Pubblicato: 4 giugno 2021

Ultima modifica: 30 luglio 2024

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Articoli di riviste sul tema "Solar cells"

Rosana, N. T. Mary, e Joshua Amarnath . D. "Dye Sensitized Solar Cells for The Transformation of Solar Radiation into Electricity". Indian Journal of Applied Research 4, n. 6 (1 ottobre 2011): 169–70. http://dx.doi.org/10.15373/2249555x/june2014/53.

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Majidzade, Vusala A. "Sb2Se3-BASED SOLAR CELLS: OBTAINING AND PROPERTIES". Chemical Problems 18, n. 2 (2020): 181–98. http://dx.doi.org/10.32737/2221-8688-2020-2-181-198.

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Vlaskin, V. I. "Nanocrystalline silicon carbide films for solar cells". Semiconductor Physics Quantum Electronics and Optoelectronics 19, n. 3 (30 settembre 2016): 273–78. http://dx.doi.org/10.15407/spqeo19.03.273.

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Tsubomura, Hiroshi, e Hikaru Kobayashi. "Solar cells". Critical Reviews in Solid State and Materials Sciences 18, n. 3 (gennaio 1993): 261–326. http://dx.doi.org/10.1080/10408439308242562.

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Loferski, Joseph. "Solar cells". Solar Energy 42, n. 4 (1989): 355–56. http://dx.doi.org/10.1016/0038-092x(89)90040-6.

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Ma, Dongling. "Solar Energy and Solar Cells". Nanomaterials 11, n. 10 (12 ottobre 2021): 2682. http://dx.doi.org/10.3390/nano11102682.

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Thanks to the helpful discussions and strong support provided by the Publisher and Editorial Staff of Nanomaterials, I was appointed as a section Editor-in-Chief of the newly launched section “Solar Energy and Solar Cells” earlier this year (2021) [...]

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K Sengar, Saurabh. "CIGS based Solar Cells - A Scaps 1D Study". International Journal of Science and Research (IJSR) 13, n. 7 (5 luglio 2024): 969–71. http://dx.doi.org/10.21275/sr24719130851.

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Mohammad Bagher, Askari. "Comparison of Organic Solar Cells and Inorganic Solar Cells". International Journal of Renewable and Sustainable Energy 3, n. 3 (2014): 53. http://dx.doi.org/10.11648/j.ijrse.20140303.12.

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Mathew, Xavier. "Solar cells and solar energy materials". Solar Energy 80, n. 2 (febbraio 2006): 141. http://dx.doi.org/10.1016/j.solener.2005.06.001.

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Graetzel, Michael. "Editorial: Solar Cells and Solar Fuels". Current Opinion in Electrochemistry 2, n. 1 (aprile 2017): A4. http://dx.doi.org/10.1016/j.coelec.2017.05.005.

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Tesi sul tema "Solar cells"

Ehrler, Bruno. "Nanocrystalline solar cells". Thesis, University of Cambridge, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607785.

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Musselman, Kevin Philip Duncan. "Nanostructured solar cells". Thesis, University of Cambridge, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.609003.

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Subbaiyan, Navaneetha Krishnan. "Supramolecular Solar Cells". Thesis, University of North Texas, 2012. https://digital.library.unt.edu/ark:/67531/metadc149672/.

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Supramolecular chemistry - chemistry of non-covalent bonds including different type of intermolecular interactions viz., ion-pairing, ion-dipole, dipole-dipole, hydrogen bonding, cation-p and Van der Waals forces. Applications based on supramolecular concepts for developing catalysts, molecular wires, rectifiers, photochemical sensors have been evolved during recent years. Mimicking natural photosynthesis to build energy harvesting devices has become important for generating energy and solar fuels that could be stored for future use. In this dissertation, supramolecular chemistry is being explored for creating light energy harvesting devices. Photosensitization of semiconductor metal oxide nanoparticles, such as titanium dioxide (TiO2) and tin oxide (SnO2,), via host-guest binding approach has been explored. In the first part, self-assembly of different porphyrin macrocyclic compounds on TiO2 layer using axial coordination approach is explored. Supramolecular dye sensitized solar cells built based on this approach exhibited Incident Photon Conversion Efficiency (IPCE) of 36% for a porphyrin-ferrocene dyad. In the second part, surface modification of SnO2 with water soluble porphyrins and phthalocyanine resulted in successful self-assembly of dimers on SnO2 surface. IPCE more than 50% from 400 - 700 nm is achieved for the supramolecular self-assembled heterodimer photocells is achieved. In summary, the axial ligation and ion-pairing method used as supramolecular tools to build photocells, exhibited highest quantum efficiency of light energy conversion with panchromatic spectral coverage. The reported findings could be applied to create interacting molecular systems for next generation of efficient solar energy harvesting devices.

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Stenberg, Jonas. "Perovskite solar cells". Thesis, Umeå universitet, Institutionen för tillämpad fysik och elektronik, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-137302.

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Perovskite solar cells (PSC) performance has risen rapidly the last few years with the current record having power conversion efficiency (PCE) of 22.1 %. This has attracted a lot of attention towards this alternative solar cell that can be manufactured with less energy and toxic material than traditional silicon solar cells. The purpose of this thesis is to reproduce high performance PSC from known recipe by Zhang et al. with potential of PCE reaching above 18 %. The thesis covers the theory regarding how a PSC operates, how they are measured and which parameters are important for a high performance PSC. The thesis includes a detailed manuscript on how to manufacture high performance PSC layer by layer and how to characterize the performance of the cells by IV-measurements. Furthermore, it includes scanning electron microscopy (SEM), by which the cells surface layers and cross-section could be evaluated. The result shows that it is possible to reproduce the PSC from literature and achieve a PCE of 18.8 %. However, the cells PCE decrease by 15 % during 2 hours of constant illumination, due to lack of stability. The manufactured PSC was used to power two catalysts that splits water into O2 and H2 and managed to reach a solar to hydrogen conversion efficiency (STHCE) of 13 %.

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Bett, Alexander Jürgen [Verfasser], e Stefan [Akademischer Betreuer] Glunz. "Perovskite silicon tandem solar cells : : two-terminal perovskite silicon tandem solar cells using optimized n-i-p perovskite solar cells". Freiburg : Universität, 2020. http://d-nb.info/1214179703/34.

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Noel, Nakita K. "Advances in hybrid solar cells : from dye-sensitised to perovskite solar cells". Thesis, University of Oxford, 2014. https://ora.ox.ac.uk/objects/uuid:e0f54943-546a-49cd-8fd9-5ff07ec7bf0a.

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This thesis presents a study of hybrid solar cells, specifically looking at various methods which can be employed in order to increase the power conversion efficiency of these devices. The experiments and results contained herein also present a very accurate picture of how rapidly the field of hybrid solar cells has progressed within the past three years. Chapters 1 and 2 present the background and motivation for the investigations undertaken, as well as the relevant theory underpinning solar cell operation. Chapter 2 also gives a brief review of the literature pertinent to the main types of devices investigated in this thesis; dye-sensitised solar cells, semiconductor sensitized solar cells and perovskite solar cells. Descriptions of the synthetic procedures, as well as the details of device fabrication and any measurement techniques used are outlined in Chapter 3. The first set of experimental results is presented in Chapter 4. This chapter outlines the synthesis of mesoporous single crystals (MSCs) of anatase TiO₂ as well as an investigation of its electronic properties. Having shown that this material has superior electronic properties to the conventionally used nanoparticle films, they were then integrated into low temperature processed dye-sensitised solar cells and achieved power conversion efficiencies of > 3%, exhibiting electron transport rates which were orders of magnitude higher than those obtained for the high temperature processed control films. Chapter 5 further investigates the use of MSCs in photovoltaic devices, this time utilising a more strongly absorbing inorganic sensitiser, Sb₂S₃. Utilising the readily tunable pore size of MSCs, these Sb₂S₃ devices showed an increase in voltage and fill factor which can be attributed to a decrease in recombination within these devices. This chapter also presents the use of Sb₂S₃ in the meso-superstructured configuration. This device architecture showed consistently higher voltages suggesting that in this architecture, charge transport occurs through the absorber and not the mesoporous scaffold. Chapters 6 and 7 focus on the use of hybrid organic-inorganic perovskites in photovoltaic devices. In Chapter 6 the mixed halide, lead-based perovskite, CH₃NH₃PbI_3-xCl_x is employed in a planar heterojunction device architecture. The effects of Lewis base passivation on this material are investigated by determining the photoluminescence (PL) lifetimes and quantum efficiencies of treated and untreated films. It is found that passivating films of this material using Lewis bases causes an increase in the PLQE at low fluences as well as increasing the PL lifetime. By globally fitting these results to a model the trap densities are extracted and it is found that using these surface treatments decreases the trap density of the perovskite films. Finally, these treatments are used in complete solar cells resulting in increased power conversion efficiencies and an improvement in the stabilised power output of the devices. Chapter 7 describes the materials synthesis and characterisation of the tin-based perovskite CH₃NH₃SnI₃ and presents the first operational, lead-free perovskite solar cell. The work presented in this thesis describes significant advances in the field of hybrid solar cells, specifically with regards to improvements made to the nanostructured electrode, and the development and implementation of more highly absorbing sensitizers. The improvements discussed here will prove to be quite important in the drive towards exploiting solar power as a clean, affordable source of energy.

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Søiland, Anne Karin. "Silicon for Solar Cells". Doctoral thesis, Norwegian University of Science and Technology, Department of Materials Technology, 2005. http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-565.

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This thesis work consists of two parts, each with a different motivation. Part II is the main part and was partly conducted in industry, at ScanWafer ASA’s plant no.2 in Glomfjord.

The large growth in the Photo Voltaic industry necessitates a dedicated feedstock for this industry, a socalled Solar Grade (SoG) feedstock, since the currently used feedstock rejects from the electronic industry can not cover the demand. Part I of this work was motivated by this urge for a SoG- feedstock. It was a cooperation with the Sintef Materials and Chemistry group, where the aim was to study the kinetics of the removal reactions for dissolved carbon and boron in a silicon melt by oxidative gas treatment. The main focus was on carbon, since boron may be removed by other means. A plasma arc was employed in combination with inductive heating. The project was, however, closed after only two experiments. The main observations from these two experiments were a significant boron removal, and the formation of a silica layer on the melt surface when the oxygen content in the gas was increased from 2 to 4 vol%. This silica layer inhibited further reactions.

Multi-crystalline (mc) silicon produced by directional solidification constitutes a large part of the solar cell market today. Other techniques are emerging/developing and to keep its position in the market it is important to stay competitive. Therefore increasing the knowledge on the material produced is necessary. Gaining knowledge also on phenomenas occurring during the crystallisation process can give a better process control.

Part II of this work was motivated by the industry reporting high inclusion contents in certain areas of the material. The aim of the work was to increase the knowledge of inclusion formation in this system. The experimental work was divided into three different parts;

1) Inclusion study

2) Extraction of melt samples during crystallisation, these were to be analysed for carbon- and nitrogen. Giving thus information of the contents in the liquid phase during soldification.

3) Fourier Transform Infrared Spectroscopy (FTIR)-measurements of the substitutional carbon contents in wafers taken from similar height positions as the melt samples. Giving thus information of the dissolved carbon content in the solid phase.

The inclusion study showed that the large inclusions found in this material are β-SiC and β-Si3N4. They appear in particularly high quantities in the top-cuts. The nitrides grow into larger networks, while the carbide particles tend to grow on the nitrides. The latter seem to act as nucleating centers for carbide precipitation. The main part of inclusions in the topcuts lie in the size range from 100- 1000 µm in diameter when measured by the Coulter laser diffraction method.

A method for sampling of the melt during crystallisation under reduced pressure was developed, giving thus the possibility of indicating the bulk concentration in the melt of carbon and nitrogen. The initial carbon concentration was measured to ~30 and 40 ppm mass when recycled material was employed in the charge and ~ 20 ppm mass when no recycled material was added. Since the melt temperature at this initial stage is ~1500 °C these carbon levels are below the solubility limit. The carbon profiles increase with increasing fraction solidified. For two profiles there is a tendency of decreasing contents at high fraction solidified.

For nitrogen the initial contents were 10, 12 and 44 ppm mass. The nitrogen contents tend to decrease with increasing fraction solidified. The surface temperature also decreases with increasing fraction solidified. Indicating that the melt is saturated with nitrogen already at the initial stage. The proposed mechanism of formation is by dissolution of coating particles, giving a saturated melt, where β-Si3N4 precipitates when cooling. Supporting this mechanism are the findings of smaller nitride particles at low fraction solidified, that the precipitated phase are β-particles, and the decreasing nitrogen contents with increasing fraction solidified.

The carbon profile for the solid phase goes through a maximum value appearing at a fraction solidified from 0.4 to 0.7. The profiles flatten out after the peak and attains a value of ~ 8 ppma. This drop in carbon content is associated with a precipitation of silicon carbide. It is suggested that the precipitation of silicon carbide occurs after a build-up of carbon in the solute boundary layer.

FTIR-measurements for substitutional carbon and interstitial oxygen were initiated at the institute as a part of the work. A round robin test was conducted, with the Energy Research Centre of the Netherlands (ECN) and the University of Milano-Bicocci (UniMiB) as the participants. The measurements were controlled against Secondary Ion Mass Spectrometer analyses. For oxygen the results showed a good correspondence between the FTIR-measurements and the SIMS. For carbon the SIMS-measurements were significantly lower than the FTIR-measurements. This is probably due to the low resistivity of the samples (~1 Ω cm), giving free carrier absorption and an overestimation of the carbon content.

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Falkenberg, Christiane. "Optimizing Organic Solar Cells". Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2012. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-89214.

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This thesis deals with the characterization and implementation of transparent electron transport materials (ETM) in vacuum deposited p-i-n type organic solar cells (OSC) for substituting the parasitically absorbing standard ETM composed of n-doped C60. In addition to transparency in the visible range of the sun spectrum, the desired material properties include high electron mobility and conductivity, thermal and morphological stability, as well as good energy level alignment relative to the adjacent acceptor layer which is commonly composed of intrinsic C60. In this work, representatives of three different material classes are evaluated with regard to the above mentioned criteria. HATCN (hexaazatriphenylene hexacarbonitrile) is a small discoid molecule with six electron withdrawing nitrile groups at its periphery. It forms smooth thin films with an optical energy gap of 3.3eV, thus being transparent in the visible range of the sun spectrum. Doping with either 5wt% of the cationic n-dopant AOB or 7wt% of the proprietary material NDN1 effectively increases the conductivity to 7.6*10^-6 S/cm or 2.2*10^-4 S/cm, respectively. However, the fabrication of efficient OSC is impeded by the exceptionally high electron affinity (EA ) of approximately 4.8eV that causes the formation of an electron injection barrier between n-HATCN and intrinsic C60 (EA=4.0eV). This work presents a strategy to remove the barrier by introducing doped and undoped C60 intermediate layers, thus demonstrating the importance of energy level matching in a multi-layer structure and the advantages of Fermi level control by doping. Next, a series of six Bis-Fl-NTCDI (N,N-bis(fluorene-2-yl)-naphthalenetetracarboxylic diimide) compounds, which only differ by the length of the alkyl chains attached to the C9 positions of the fluorene side groups, is examined. When increasing the chain length from 0 to 6 carbon atoms, the energy levels remain nearly unchanged: We find EA=3.5eV as estimated from cyclic voltammetry, an ionization potential (IP ) in the range between 6.45eV and 6.63eV, and Eg,opt=3.1eV which means that all compounds form transparent thin films. Concerning thin film morphology, the addition of side chains results in the formation of amorphous layers with a surface roughness <1nm on room temperature glass substrates, and (1.5+/-0.5)nm for deposition onto glass substrates heated to 100°C. In contrast, films composed of the side chain free compound Bis-HFl-NTCDI exhibit a larger surface roughness of (2.5+/-0.5)nm and 9nm, respectively, and are nanocrystalline already at room temperature. Moreover, the conductivity achievable by n-doping is very sensitive to the side chain length: Whereas doping of Bis-HFl-NTCDI with 7wt% NDN1 results in a conductivity in the range of 10^-4 S/cm, the attachment of alkyl chains causes a conductivity which is more than three orders of magnitude smaller despite equal or slightly higher doping concentrations. The insufficient transport properties of the alkylated derivatives lead to the formation of pronounced s-kinks in the jV -characteristics of p-i-n type OSC while the use of n-Bis-HFl-NTCDI results in well performing devices. The last material, HATNA-Cl6 (2,3,8,9,14,15- hexachloro-5,6,11,12,17,18-hexaazatrinaphthylene), exhibits Eg,opt=2.7eV and is therefore not completely transparent in the visible range of the sun spectrum. However, its energy level positions of EA=4.1eV and IP=7.3eV are well suited for the application as ETM in combination with i-C60 as acceptor. The compound is dopable with all available n-dopants, resulting in maximum conductivities of sigma=1.6*10^-6, 3.5*10^-3, and 7.5*10^-3 S/cm at 7.5wt% AOB, Cr2(hpp)4, and NDN1, respectively. Applying n-HATNA-Cl6 instead of the reference ETM n-C60 results in a comparable or improved photocurrent density at an ETM thickness d(ETM)=40nm or 120nm, respectively. At d(ETM)=120nm, the efficiency eta is more than doubled as it increases from eta(n-C60)=0.4% to eta(n-HATNA-Cl6)=0.9% . Optical simulations show that the replacement of n-C60 by n-Bis-HFl-NTCDI, n-HATNA-Cl6, or the previously studied n-NTCDA (naphthalenetretracarboxylic dianhydride) in p-i-n or n-i-p type device architectures is expected to result in an increased photocurrent due to reduced parasitic absorption. For quantifying the gain, the performance of p-i-n type OSC with varying ETM type and thickness is evaluated. Special care has to be taken when analyzing devices comprising the reference ETM n-C60 as its conductivity is sufficiently large to extend the area of the aluminum cathode and thus the effective device area which may lead to distorted results. Overall, the experiment is able to confirm the trends predicted by the optical simulation. At large ETM thickness in the range between 60 and 120nm, the window layer effect of the ETM is most pronounced. For instance, at d(ETM)=120nm, eta(C60) is more than doubled using n-HATNA-Cl6 and even more than tripled using n-Bis-HFl-NTCDI or n-NTCDA. At optimized device geometry the photocurrent gain is slightly less than expected but nonetheless, the efficiency is improved from eta(max)=2.1% for n-C60 and n-HATNA-Cl6 solar cells to eta(max)=2.3, and 2.4% for n-Bis-HFl-NTCDI and n-NTCDA devices, respectively. This development is supported by generally higher Voc and FF in solar cells with transparent ETM. Finally, p-i-n type solar cells with varying ETM are aged at a temperature of 50°C and an illumination intensity of approximately 2 suns. Having extrapolated lifetimes t(80) of 36, 500, and 14000h and nearly unchanged jV-characteristics after 2000h, n-C60 and n-Bis-HFl-NTCDI devices exhibit the best stability. In contrast, n-NTCDA devices suffer from a constant decrease in Isc while n-HATNA-Cl6 solar cells show a rapid dscegradation of both Isc and FF associated with a decomposition of the material or a complete de-doping of the ETM. Here, lifetimes of only 4500h and 445hare achieved.

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Hadipour, Afshin. "Polymer tandem solar cells". [S.l. : Groningen : s.n. ; University Library of Groningen] [Host], 2007. http://irs.ub.rug.nl/ppn/305349066.

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Vaynzof, Yana. "Inverted hybrid solar cells". Thesis, University of Cambridge, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.609823.

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Più fonti

Libri sul tema "Solar cells"

Sharma, S. K., e Khuram Ali, a cura di. Solar Cells. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-36354-3.

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Arya, Sandeep, e Prerna Mahajan. Solar Cells. Singapore: Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-7333-0.

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Travino, Michael R. Dye-sensitized solar cells and solar cell performance. Hauppauge, N.Y: Nova Science Publisher, 2011.

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Moddel, Garret, e Sachit Grover, a cura di. Rectenna Solar Cells. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-3716-1.

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Hiramoto, Masahiro, e Seiichiro Izawa, a cura di. Organic Solar Cells. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-9113-6.

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Choy, Wallace C. H., a cura di. Organic Solar Cells. London: Springer London, 2013. http://dx.doi.org/10.1007/978-1-4471-4823-4.

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Tress, Wolfgang. Organic Solar Cells. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-10097-5.

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Sankir, Nurdan Demirci, e Mehmet Sankir, a cura di. Photoelectrochemical Solar Cells. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2018. http://dx.doi.org/10.1002/9781119460008.

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Hou, Shaocong. Fiber Solar Cells. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-2864-9.

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Giovanni, Palmisano, e Ciriminna Rosaria, a cura di. Flexible solar cells. Weinheim [Germany]: Wiley-VCH, 2008.

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Capitoli di libri sul tema "Solar cells"

Buecheler, Stephan, Lukas Kranz, Julian Perrenoud e Ayodhya Nath Tiwari. "CdTe Solar Cells solar cell". In Encyclopedia of Sustainability Science and Technology, 1976–2004. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-0851-3_463.

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Grätzel, Michael. "Mesoscopic Solar Cells Mesoscopic Solar Cells". In Solar Energy, 79–96. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-5806-7_465.

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Grätzel, Michael. "Mesoscopic Solar Cells Mesoscopic Solar Cells". In Encyclopedia of Sustainability Science and Technology, 6566–83. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-0851-3_465.

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Głowacki, Eric Daniel, Niyazi Serdar Sariciftci e Ching W. Tang. "Organic Solar Cells organic solar cell". In Solar Energy, 97–128. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-5806-7_466.

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Głowacki, Eric Daniel, Niyazi Serdar Sariciftci e Ching W. Tang. "Organic Solar Cells organic solar cell". In Encyclopedia of Sustainability Science and Technology, 7553–84. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-0851-3_466.

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Gregory, Peter. "Solar Cells". In High-Technology Applications of Organic Colorants, 45–52. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3822-6_6.

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Lin, Ching-Fuh. "Solar Cells". In Topics in Applied Physics, 237–59. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9392-6_9.

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Böer, Karl W. "Solar Cells". In Survey of Semiconductor Physics, 1119–70. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2912-1_34.

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Zhu, Yimei, Hiromi Inada, Achim Hartschuh, Li Shi, Ada Della Pia, Giovanni Costantini, Amadeo L. Vázquez de Parga et al. "Solar Cells". In Encyclopedia of Nanotechnology, 2459. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-90-481-9751-4_100783.

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Goodnick, Stephen M., e Christiana Honsberg. "Solar Cells". In Springer Handbook of Semiconductor Devices, 699–745. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-79827-7_19.

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Atti di convegni sul tema "Solar cells"

McGehee, Michael. "Nanostructured Solar Cells". In Solar Energy: New Materials and Nanostructured Devices for High Efficiency. Washington, D.C.: OSA, 2008. http://dx.doi.org/10.1364/solar.2008.swa1.

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Ruby, Douglas S., Saleem Zaidi, S. Narayanan, Satoshi Yamanaka e Ruben Balanga. "RIE-Texturing of Industrial Multicrystalline Silicon Solar Cells". In ASME 2003 International Solar Energy Conference. ASMEDC, 2003. http://dx.doi.org/10.1115/isec2003-44003.

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We developed a maskless plasma texturing technique for multicrystalline Si (mc-Si) cells using Reactive Ion Etching (RIE) that results in higher cell performance than that of standard untextured cells. Elimination of plasma damage has been achieved while keeping front reflectance to low levels. Internal quantum efficiencies higher than those on planar and wet-textured cells have been obtained, boosting cell currents and efficiencies by up to 6% on tricrystalline Si cells.

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Bhat, P. K., D. S. Shen e R. E. Hollingsworth. "Stability of amorphous silicon solar cells". In Amorphous silicon materials and solar cells. AIP, 1991. http://dx.doi.org/10.1063/1.41008.

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Wang, Renze, e Zhiping Zhou. "Nanowire tandem solar cells". In SPIE Solar Energy + Technology, a cura di Loucas Tsakalakos. SPIE, 2012. http://dx.doi.org/10.1117/12.929104.

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Franklin, Evan, Andrew Blakers, Vernie Everett e Klaus Weber. "Sliver solar cells". In Microelectronics, MEMS, and Nanotechnology, a cura di Hark Hoe Tan, Jung-Chih Chiao, Lorenzo Faraone, Chennupati Jagadish, Jim Williams e Alan R. Wilson. SPIE, 2007. http://dx.doi.org/10.1117/12.759594.

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Chambouleyron, I. "MULTIJUNCTION SOLAR CELLS". In Proceedings of the International School on Crystal Growth and Characterization of Advanced Materials. WORLD SCIENTIFIC, 1988. http://dx.doi.org/10.1142/9789814541589_0022.

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Ho-Baillie, Anita. "Perovskite Solar Cells". In Organic, Hybrid, and Perovskite Photovoltaics XXII, a cura di Zakya H. Kafafi, Paul A. Lane, Gang Li, Ana Flávia Nogueira e Ellen Moons. SPIE, 2021. http://dx.doi.org/10.1117/12.2602805.

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Enriquez, Christian, Deidra Hodges, Angel De La Rosa, Luis Valerio Frias, Yves Ramirez, Victor Rodriguez, Daniel Rivera e Alberto Telles. "Perovskite Solar Cells". In 2019 IEEE 46th Photovoltaic Specialists Conference (PVSC). IEEE, 2019. http://dx.doi.org/10.1109/pvsc40753.2019.8980712.

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Polman, Albert. "Plasmonic Solar Cells". In Optical Nanostructures for Photovoltaics. Washington, D.C.: OSA, 2010. http://dx.doi.org/10.1364/pv.2010.pwa2.

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Brandt, Martin S., e Martin Stutzmann. "Investigation of the Staebler-Wronski effect in a-Si:H by spin-dependent photoconductivity". In Amorphous silicon materials and solar cells. AIP, 1991. http://dx.doi.org/10.1063/1.41015.

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Rapporti di organizzazioni sul tema "Solar cells"

Gur, Ilan. Nanocrystal Solar Cells. Office of Scientific and Technical Information (OSTI), gennaio 2006. http://dx.doi.org/10.2172/922721.

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Hall, R. B., C. Bacon, V. DiReda, D. H. Ford, A. E. Ingram, J. Cotter, T. Hughes-Lampros, J. A. Rand, T. R. Ruffins e A. M. Barnett. Thin silicon solar cells. Office of Scientific and Technical Information (OSTI), dicembre 1992. http://dx.doi.org/10.2172/10121623.

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Matson, Rick. National solar technology roadmap: Sensitized solar cells. Office of Scientific and Technical Information (OSTI), giugno 2007. http://dx.doi.org/10.2172/1217460.

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Huo, Jiayan. Vapor deposited perovskites solar cells. Ames (Iowa): Iowa State University, gennaio 2019. http://dx.doi.org/10.31274/cc-20240624-1581.

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McNeely, James B., Gerald H. Negley e Allen M. Barnett. GaAsP Top Solar Cells for Increased Solar Conversion Efficiency. Fort Belvoir, VA: Defense Technical Information Center, gennaio 1989. http://dx.doi.org/10.21236/ada206808.

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Sinton, R. A., A. Cuevas, R. R. King e R. M. Swanson. High-efficiency concentrator silicon solar cells. Office of Scientific and Technical Information (OSTI), novembre 1990. http://dx.doi.org/10.2172/6343818.

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Mitzi, David, e Yanfa Yan. High Performance Perovskite-Based Solar Cells. Office of Scientific and Technical Information (OSTI), gennaio 2020. http://dx.doi.org/10.2172/1582433.

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Ager III, J. W., e W. Walukiewicz. High efficiency, radiation-hard solar cells. Office of Scientific and Technical Information (OSTI), ottobre 2004. http://dx.doi.org/10.2172/840450.

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Speck, James S., Steven P. DenBaars, Umesh K. Mishra e Shuji Nakamura. High Performance InGaN-Based Solar Cells. Fort Belvoir, VA: Defense Technical Information Center, maggio 2012. http://dx.doi.org/10.21236/ada562115.

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Prasad, Paras N. Novel Flexible Plastic-Based Solar Cells. Fort Belvoir, VA: Defense Technical Information Center, marzo 2011. http://dx.doi.org/10.21236/ada566134.

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