Дисертації з теми "Conjugated organic polymers"
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Samuel, Ifor David William. "Femtosecond spectroscopy of conjugated polymers." Thesis, University of Cambridge, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.239657.
Повний текст джерелаBakbak, Selma. "Structural manipulation of conjugated polymers." Diss., Available online, Georgia Institute of Technology, 2006, 2006. http://etd.gatech.edu/theses/available/etd-01112006-211158/.
Повний текст джерелаDr. Uwe H. F. Bunz, Committee Chair ; Dr. Laren M. Tolbert, Committee Member ; Dr. Joseph Perry, Committee Member ; Dr. David M. Collard, Committee Member ; Dr. Anselm C. Griffin, Committee Member.
Wang, Chao. "Synthesis of Conjugated Polymers." University of Akron / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=akron1362783501.
Повний текст джерелаIsaksson, Joakim. "Organic Bioelectronics : Electrochemical Devices using Conjugated Polymers." Doctoral thesis, Linköpings universitet, Institutionen för teknik och naturvetenskap, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-9679.
Повний текст джерелаVokata, Tereza. "Synthetic Approaches to Flexible Fluorescent Conjugated Polymers." FIU Digital Commons, 2015. http://digitalcommons.fiu.edu/etd/1910.
Повний текст джерелаIsaksson, Joakim. "Organic bioelectronics : electrochemical devices based on conjugated polymers /." Norrköping : [Department of Science and Technology], Linköping University, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-9679.
Повний текст джерелаChen, Yi 1974. "Organic thin film transistors based on conjugated polymers." Thesis, McGill University, 2004. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=81533.
Повний текст джерелаThe characteristics of PTFTs fabricated using several polymers were studied. Among them, the ones based on regioregualr poly[3-hexylthiophene-2.5diy] (RR-P3HT) have the best performance with a field effect mobility (mueff) of about 0.01 cm2/V-s and ION/IOFF value of about 50 when doped with FeCl3. Results of measurement suggested that FeCl3 doping of P3HT could lead to a decrease of about 5 orders of magnitude in its contact resistance to Au electrodes, giving rise to two orders of magnitude increase of its apparent mobility. Therefore, it can be concluded that the contact resistances are the major limitation of performance of many PTFTs and need to be studied intensively in the future.
Murad, Ary. "Development of new conjugated polymers for organic photovoltaics." Thesis, University of Sheffield, 2017. http://etheses.whiterose.ac.uk/16317/.
Повний текст джерелаMask, Walker. "MODELING THE CONDENSED-PHASE BEHAVIOR OF Π-CONJUGATED POLYMERS". UKnowledge, 2019. https://uknowledge.uky.edu/chemistry_etds/120.
Повний текст джерелаHalls, Jonathan James Michael. "Photoconductive properties of conjugated polymers." Thesis, University of Cambridge, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.368812.
Повний текст джерелаPacios, Roberto. "Organic photovoltaic cells and photodiodes based on conjugated polymers." Thesis, Imperial College London, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.417853.
Повний текст джерелаMarshall, Jonathan. "Carborane containing conjugated polymers for use in organic electronics." Thesis, Imperial College London, 2014. http://hdl.handle.net/10044/1/24949.
Повний текст джерелаZhang, Xuan. "Dithienopyrrole-based conjugated materials for organic electronics." Diss., Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/37207.
Повний текст джерелаStedman, Troy C. "Thermal Fluctuations Tunneling in Doped Conjugated Polymers." Scholar Commons, 2015. https://scholarcommons.usf.edu/etd/5586.
Повний текст джерелаZhu, Yan. "New conjugated polymers for organic electronics : synthesis, properties, and applications /." Thesis, Connect to this title online; UW restricted, 2006. http://hdl.handle.net/1773/9856.
Повний текст джерелаTUNG, WEI-YAO. "FUNCTIONALIZED CONJUGATED POLYMERS PROMOTED HIGH PERFORMANCE MATERIALS FOR ORGANIC ELECTRONIC DEVICES." University of Akron / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=akron1624317157379185.
Повний текст джерелаRighi, Sara <1983>. "Charge transport properties of organic conjugated polymers for photovoltaic applications." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2014. http://amsdottorato.unibo.it/6460/.
Повний текст джерелаWright, Helen. "Fused ring conjugated polymers and small molecules for organic-semiconductors." Thesis, University of Manchester, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.542784.
Повний текст джерелаKymakis, Emmanouil. "Organic photovoltaic devices based on conjugated polymers and carbon nanotubes." Thesis, University of Cambridge, 2003. https://www.repository.cam.ac.uk/handle/1810/272018.
Повний текст джерелаCui, Chaohua. "Conjugated polymer and small-molecule donor materials for organic solar cells." HKBU Institutional Repository, 2014. https://repository.hkbu.edu.hk/etd_oa/37.
Повний текст джерелаApaydin, Dogukan Hazar. "Electrochromic And Photovoltaic Applications Of Conjugated Polymers." Master's thesis, METU, 2012. http://etd.lib.metu.edu.tr/upload/12614481/index.pdf.
Повний текст джерелаJagtap, Subodh Prakash. "Design and synthesis of and π-stacked conjugated oligomers and polymers". Diss., Georgia Institute of Technology, 2012. http://hdl.handle.net/1853/47574.
Повний текст джерелаMitchell, William John. "Polymer-electrode interactions in light emitting diodes." Thesis, University of Oxford, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.289406.
Повний текст джерелаGiraud, Lauriane. "Bis-vanillin substrates as source of π-conjugated polymers for organic electronic". Thesis, Bordeaux, 2019. http://www.theses.fr/2019BORD0404.
Повний текст джерелаThe objective of this PhD is to synthesize π-conjugated bio-based polymers from vanillin, with potential applications in the field of organic electronic (photovoltaic, Organic Light Emitting Diode, OLED). Polyazomethines with high molar masses were obtained via the copolymerization of divanillin with various diamines. This polycondensation was performed in 5 minutes under microwave irradiation, followed by solvent removal using a rotary evaporator. Divanillin-based polyazomethines absorb in the near-UV range but have a short conjugation pathway, as revealed investigations on model compounds. To improve this conjugated pathway, a divanillin-based molecule bearing aldehyde functions in para positions with respect to the link between the rings, was designed. This so-called para-divanillin, never reported before, was copolymerized to yield polyazomethines. These latter polymers also have a short conjugation pathway due to steric hindrance between the two aromatic rings of the para-divanillin skeleton. A last family of divanillin-based polymers was thus investigated: polythiazolothiazoles. The latter exhibit specific emission properties as they emit in the blue range in solution and in the yellow range in films. Benzothiazole-based model compounds were also synthesized and exhibited a fluorescence quantum yield of 20% and “herringbone-like” π-stacking, giving them a strong potential for various organic electronic applications
Huang, Wei [Verfasser]. "Conjugated porous polymers for visible light-induced organic transformations / Wei Huang." Mainz : Universitätsbibliothek Mainz, 2017. http://d-nb.info/1143985516/34.
Повний текст джерелаShaw, Paul E. "Measurements of exciton diffusion in conjugated polymers." Thesis, University of St Andrews, 2009. http://hdl.handle.net/10023/831.
Повний текст джерелаZhan, Hongmei. "Synthesis, characterization and optoelectronic applications of new conjugated organic and organometallic polymers." HKBU Institutional Repository, 2011. http://repository.hkbu.edu.hk/etd_ra/1240.
Повний текст джерелаDaoud, Walid. "Synthesis of conjugated polymers and their use in photovoltaic cells." Thesis, University of Sheffield, 2002. http://etheses.whiterose.ac.uk/14469/.
Повний текст джерелаMori, Daisuke. "Development of Polymer Blend Solar Cells Composed of Conjugated Donor and Acceptor Polymers." 京都大学 (Kyoto University), 2015. http://hdl.handle.net/2433/199331.
Повний текст джерелаLuo, Yanqi. "Interfacial Interactions between Carbon Nanoparticles and Conjugated Polymers." DigitalCommons@CalPoly, 2014. https://digitalcommons.calpoly.edu/theses/1291.
Повний текст джерелаThomsen, Elizabeth Alice. "Characterisation of materials for organic photovoltaics." Thesis, St Andrews, 2008. http://hdl.handle.net/10023/462.
Повний текст джерелаWatt, Shannon L. "Synthesis and Characterization of Regioregular, Amphiphilic Semifluoroalkyl-Substituted Polythiophenes and Cofacial Bis(oligothienyl)naphthalenes." Diss., Georgia Institute of Technology, 2007. http://hdl.handle.net/1853/19787.
Повний текст джерелаSkrypnychuk, Vasyl. "Vertical charge transport in conjugated polymers." Doctoral thesis, Umeå universitet, Institutionen för fysik, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-133180.
Повний текст джерелаCheung, Wai-kei, and 張偉基. "Low band-gap donor-acceptor polymers and heterolyptic ruthenium complex containing polymers for photovoltaic applications." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2012. http://hub.hku.hk/bib/B47753006.
Повний текст джерелаpublished_or_final_version
Chemistry
Master
Master of Philosophy
Goossens, Mark. "Ultrafast organic lasers and solid-state amplifiers." Thesis, St Andrews, 2007. http://hdl.handle.net/10023/315.
Повний текст джерелаHaylett, Nick. "Investigations into the synthesis, characterisation and properties of some conjugated organic polymers." Thesis, Durham University, 1995. http://etheses.dur.ac.uk/5406/.
Повний текст джерелаKerszulis, Justin Adam. "Reading the rainbow: tailoring the properties of electrochromic polymers." Diss., Georgia Institute of Technology, 2014. http://hdl.handle.net/1853/53071.
Повний текст джерелаHo, Cheuk Lam. "Conjugated metal-organic phosphorescent materials and polymers containing fluorene and carbazole units." HKBU Institutional Repository, 2007. http://repository.hkbu.edu.hk/etd_ra/808.
Повний текст джерелаLiyanage, Arawwawala Don T. "FLUORINATED ARENE, IMIDE AND UNSATURATED PYRROLIDINONE BASED DONOR ACCEPTOR CONJUGATED POLYMERS: SYNTHESIS, STRUCTURE-PROPERTY AND DEVICE STUDIES." UKnowledge, 2013. http://uknowledge.uky.edu/chemistry_etds/23.
Повний текст джерелаTwomey, Megan. "Conjugated Polymer-Based Biomaterials Through Controlled Self-Assembly." FIU Digital Commons, 2016. http://digitalcommons.fiu.edu/etd/2452.
Повний текст джерелаWoody, Kathy Beckner. "Design, synthesis and characterization of self-assembling conjugated polymers for use in organic electronic applications." Diss., Georgia Institute of Technology, 2011. http://hdl.handle.net/1853/43627.
Повний текст джерелаYang, Kun. "CONJUGATED POLYMERS AND SMALL MOLECULES WITH LATENT HYDROGEN-BONDING FOR ORGANIC ELECTRONIC APPLICATIONS." University of Akron / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=akron149083508357808.
Повний текст джерелаYau, Chin Pang. "Design, synthesis and characterisation of conjugated polymers containing reactive functionality for organic photovoltaics." Thesis, Imperial College London, 2014. http://hdl.handle.net/10044/1/33159.
Повний текст джерелаLarsson, Oscar. "Empirical parameterization of organic electrochemical transistors." Thesis, Linköping University, Department of Science and Technology, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-1503.
Повний текст джерелаIn this diploma work, organic electrochemical transistors based on PEDOT:PSS have been studied, focusing on the influence of the geometry and physical dimensions on the transistor characteristics. The geometrical parameters studied are the area ratio between the gate and channel, the channel width and the channel length. Each parameter has been varied in five steps with each step containing three identical transistors. Results concerning the geometrical influence of the linear region resistance, the saturation current (density) and the on/off ratio are presented and discussed. Also, empirical curve-fits of the geometrical influence on the linear region resistance and the saturation current have been performed. In addition, tentative results of the locus of the saturation current versus saturation voltage for specific transistors have been obtained.
Manuelli, Alessandro. "Influences of Printing Techniques on the Electrical Performances of Conjugated Polymers for Organic Transistors." Doctoral thesis, Universitätsbibliothek Chemnitz, 2007. http://nbn-resolving.de/urn:nbn:de:swb:ch1-200700044.
Повний текст джерелаSaid, Elias. "Electrolyte-Based Organic Electronic Devices." Licentiate thesis, Linköping : Department of Science and Technology, Linköping University, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-9955.
Повний текст джерелаLiang, Zhiming. "MORPHOLOGICAL AND ENERGETIC EFFECTS ON CHARGE TRANSPORT IN CONJUGATED POLYMERS AND POLYMER-NANOWIRE COMPOSITES." UKnowledge, 2018. https://uknowledge.uky.edu/chemistry_etds/99.
Повний текст джерелаGuo, Xugang. "IMIDE-FUNCTIONALIZED CONJUGATED POLYMERS: SYNTHESIS, STRUCTURE-PROPERTY AND DEVICE STUDIES." Lexington, Ky. : [University of Kentucky Libraries], 2009. http://hdl.handle.net/10225/1100.
Повний текст джерелаTitle from document title page (viewed on October 29, 2009). Document formatted into pages; contains: xvi, 227 p. : ill. (some col.). Includes abstract and vita. Includes bibliographical references (p. 207-224).
Bheemireddy, Sambasiva Reddy. "SYNTHESIS OF CONJUGATED SMALL MOLECULES AND POLYMERS BY A PALLADIUM CATALYZED CYCLOPENTANNULATION STRATEGY – TOWARDS NEW ORGANIC SEMICONDUCTORS." OpenSIUC, 2017. https://opensiuc.lib.siu.edu/dissertations/1338.
Повний текст джерелаSobczak, Quentin. "Synthesis of new amino-containing π-conjugated polymers via dimerization of acyclic aminoarylcarbenes". Thesis, Bordeaux, 2019. http://www.theses.fr/2019BORD0208.
Повний текст джерелаIn this thesis, the study focuses on the synthesis of semi-conducting polymers by an original pathway free from metals, in order to integrate them into organic electronic devices such as OLEDs (Organic light emitting diodes). The aim is to develop and optimize a new methodology using acyclic bis-aminoarylcarbenes as building blocks to synthesize new PPV-like polymers. First, the dimerization reaction is studied at a molecular level with the synthesis and characterization of diaminoalkenes obtained from monofunctional acyclic aminoarylcarbenes. The mechanism and the selectivity of this dimerization reaction is also investigated experimentally and theoretically. In a second step, the dimerization reaction was extended at a macromolecular level with the synthesis and characterization of new PPV-like polymers containing amino functions in α of the double bond. Subsequently, the influence of these chemically modified amino groups on the optoelectronic properties of these N-PPVs has been studied. Finally, the specific characteristics of the diaminoalkenes synthesized during this thesis has allowed a preliminary study on their potential applications as organocatalysts in the atom transfer radical polymerization reaction