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1
Garman, Christopher James. "Electrical characterization of thin film nanostructure templates." Morgantown, W. Va. : [West Virginia University Libraries], 2001. http://etd.wvu.edu/templates/showETD.cfm?recnum=2188.
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Thesis (M.S.)--West Virginia University, 2001.Title from document title page. Document formatted into pages; contains vi, 70 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 57-61).
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Saliba, Michael. "Plasmonic nanostructures and film crystallization in perovskite solar cells." Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:fdb36a9e-ddf5-4d27-a8dc-23fffe32a2c5.
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The aim of this thesis is to develop a deeper understanding and the technology in the nascent field of solid-state organic-inorganic perovskite solar cells. In recent years, perovskite materials have emerged as a low-cost, thin-film technology with efficiencies exceeding 16% challenging the quasi-paradigm that high efficiency photovoltaics must come at high costs. This thesis investigates perovskite solar cells in more detail with a focus on incorporating plasmonic nanostructures and perovskite film formation. Chapter 1 motivates the present work further followed by Chapter 2 which offers a brief background for solar cell fabrication and characterisation, perovskites in general, perovskite solar cells in specific, and plasmonics. Chapter 3 presents the field of plasmonics including simulation methods for various core-shell nanostructures such as gold-silica and silver-titania nanoparticles. The following Chapters 4 and 5 analyze plasmonic core-shell metal-dielectric nanoparticles embedded in perovskite solar cells. It is shown that using gold@silica or silver@titania NPs results in enhanced photocurrent and thus increased efficiency. After photoluminescence studies, this effect was attributed to an unexpected phenomenon in solar cells in which a lowered exciton binding energy generates a higher fraction of free charge. Embedding thermally unstable silver NPs required a low-temperature fabrication method which would not melt the Ag NPs. This work offers a new general direction for temperature sensitive elements. In Chapters 6 and 7, perovskite film formation is studied. Chapter 6 shows the existence of a previously unknown crystalline precursor state and an improved surface coverage by introducing a ramped annealing procedure. Based on this, Chapter 7 investigates different perovskite annealing protocols. The main finding was that an additional 130°C flash annealing step changed the film crystallinity dramatically and yielded a higher orientation of the perovskite crystals. The according solar cells showed an increased photocurrent attributed to a decrease in charge carrier recombination at the grain boundaries. Chapter 8 presents on-going work showing noteworthy first results for silica scaffolds, and layered, 2D perovskite structures for application in solar cells.
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Sun, Pei. "Ultrathin films of biomolecules with well-controlled nanostructures." Connect to this title online, 2005. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1109605487.
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Thesis (Ph. D.)--Ohio State University, 2005.Title from first page of PDF file. Document formatted into pages; contains xvi, 192 p.; also includes graphics Includes bibliographical references (p. 178-192). Available online via OhioLINK's ETD Center
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Zheng, Haimei. "Growth and characterization of multiferroic BaTiO3-CoFe2O4 thin film nanostructures." College Park, Md. : University of Maryland, 2004. http://hdl.handle.net/1903/2026.
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Thesis (Ph. D.) -- University of Maryland, College Park, 2004.Thesis research directed by: Material Science and Engineering. Title from t.p. of PDF. Includes bibliographical references. Published by UMI Dissertation Services, Ann Arbor, Mich. Also available in paper.
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Vempati, Sesha Pavan Kumar. "Thin film and nanostructures zinc oxide : characterisation and device applications." Thesis, Queen's University Belfast, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580108.
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This thesis reports the preparation and characterization of ZnO films and nanostructures and their incorporation in simple devices. The characterization includes imaging techniques - atomic force-, scanning electron- and transmission electron- microscopies (and accompanying analysis) - as well as X-ray diffraction (confirming wurzite structure in all the form of ZnO), photoluminescence (elucidating exciton and defect bands), Raman spectroscopy (dopent incorporation, including defects) and, importantly, optical absorption since it is crucial to confirm the various forms of ZnO as transparent conducting oxide. Also, electron scanning tunnelling microscopy reveals interesting bias- and polarity-dependent changes in 'topography' images originating with different density-of-states contributions from the conduction band, valence band and defect (surface) states. A new fabrication methodology, based on metal-salt decomposition, is introduced to prepare un doped and Co-doped thin films and nanowires on quartz where the doped ZnO exhibited Co2+ substitution of Zn2+ while retaining good optical transmission. Extending the wet-chemical approach synthesis a simple change in reaction temperature led to two quite different forms of ZnO-nanostructure:- nanocrystals and nanosheets. The potential of ZnO-nanosheets as a phosphor coating for producing (bluish-) white light from UV-LEDs is demonstrated. The nanocrystals were used in poly(3, 4- ethylenedioxythiophene)-poly(styrenesulfonate)(pEDOT:PSS) host matrix to form a nanocomposite exhibiting the fascinating property of negative photoconduction, explained in terms of decreased conductivity of the ZnO stemming from a charge transfer interaction with the PEDOT:PSS. The well-known difficulty in forming stable p-type 2nO films was confirmed by fabricating Li-doped 2nO/n-type 2nO homojunctions which failed to show rectifying behaviour, where the oxygen vacancies may indicate extinction of p-type behavior. However, a number of successful n-2nO (Ga- and In-doped 2nO films, honeycomb structured intrinsic .n-2nOIPEDOT:PSS and Ag-doped 2nO nanorods/p-Si heterojunctions were fabricated and their photoresponse examined in detail - these data, in particular polarity-dependent wavelength selectivity, are discussed and analysed in terms of basic band structure and carrier transport properties.
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Behler, Kristopher Gogotsi IU G. "Chemically modified carbon nanostructures for electrospun thin film polymer-nanocomposites /." Philadelphia, Pa. : Drexel University, 2008. http://hdl.handle.net/1860/2920.
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Jia, Roger (Roger Qingfeng). "Properties of thin film III-V/IV semiconductor alloys and nanostructures." Thesis, Massachusetts Institute of Technology, 2017. http://hdl.handle.net/1721.1/113928.
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Thesis: Ph. D., Massachusetts Institute of Technology, Department of Materials Science and Engineering, 2017.This electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.
Cataloged from student-submitted PDF version of thesis.
Includes bibliographical references (pages 116-121).
A large amount of research and development has been devoted to engineering materials for the next generation of semiconductor devices with high performance, energy efficiency, and economic viability. To this end, significant efforts have been made to grow semiconductor thin films with the desired properties onto lattice constants with viable, cost effective substrates. Comparatively less effort has been made to explore III-V/IV heterovalent nanostructures and alloys, which may exhibit properties not available in existing materials. The investigation of these structures, grown using MOCVD, is the goal of this thesis and is motivated by two factors: one, that III-V/IV nanostructures should be good thermoelectrics based on the "phonon glass electron crystal" concept, and two, that (GaAs)₁-x(Ge₂)x alloys were observed to exhibit near-infrared room temperature luminescence, a result that can have significant implications for low bandgap optical devices. A survey of various growth conditions was conducted for the growth of the model GaAs/Ge system using MOCVD to gain insight in the epitaxy involving heterovalent materials and to identify structures suitable for investigation for their thermoelectric and optical properties. A significant decrease in the thermal conductivities of GaAs/Ge nanostructures and alloys relative to bulk GaAs and bulk Ge was observed. This reduction can be attributed to the presence of the heterovalent interfaces. The electron mobilities of the structures were determined to be comparable to bulk Ge, indicating minimal disruption to electron transport by the interfaces. A further reduction in thermal conductivity was observed in an (In₀.₁Ga₀.₉As)₀.₈₄(Si0₀.₁Ge₀.₉)₀.₁₆ alloy; the alloy had a thermal conductivity of 4.3 W/m-K, comparable to some state-of-the-art thermoelectric materials. Room temperature photoluminescence measurements of various compositions of (GaAs)₁-x(Ge₂)x alloys revealed a maximum energy transition of 0.8 eV. This bandgap narrowing is the result of composition fluctuations; the fluctuations create regions of lower bandgap, resulting in a weak dependence on luminescence as a function of Ge composition as well as lower bandgap than the homogeneous alloy with the same composition. As silicon was added to the (GaAs)₁-x(Ge₂)x alloy, the bandgap increased despite the composition fluctuations. Based on the results from this work III-V/IV nanostructures show promise for thermoelectric and optical applications.
by Roger Jia.
Ph. D.
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Luk'yanov, A. Yu, P. V. Volkov, A. V. Goryunov, V. M. Daniltsev, D. A. Pryakhin, A. D. Tertyshnik, O. I. Khrykin, and V. I. Shashkin. "Optical monitoring of technological processes for fabrication of thin-film nanostructures." Thesis, Sumy State University, 2011. http://essuir.sumdu.edu.ua/handle/123456789/20681.
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Thisworkillustratesapplicationofthe uniquefiber-optic instrumentationforin situmonitoringofseveral
technologicalprocessescommonlyusedinfabricationof semiconducting
thin-film nanostructures. This instrumentation is basedonprinciplesoflowcoherenttandeminterferometry,
whichdetermineshighsensitivityandprecision in measuring
basic technological parameters, such as thickness of forming layers, temperature and
bending of the substrate.The probing wavelength = 1.55 m allows carrying out the
measurements on majority of substrates for semiconductor technology: Si, SOI, GaAs,
InP, GaP, Al2O3, diamond, ZrO2:Y. Monitoring of such processes as MOVPE,
MBEandplasmaetchingin various set-ups was realized. The absolute resolution achieved
in these experiments was limited only by calibration accuracy and corresponds to 1 at
sensitivity of 0.01 . The accuracy limit in estimating the thickness of layers during
their growth is 2 nm.
When you are citing the document, use the following link http://essuir.sumdu.edu.ua/handle/123456789/20681
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Syed, Abdul Samad. "Growth and Characterization of ZnO Nanostructures." Thesis, Linköpings universitet, Institutionen för fysik, kemi och biologi, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-72956.
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A close relation between structural and optical properties of any semiconductor material does exist. An adequate knowledge and understanding of this relationship is necessary for fabrication of devices with desired optical properties. The structural quality and hence the optical properties can be influenced by the growth method and the substrate used. The aim of this work was to investigate the change in optical properties caused by growth techniques and substrate modification. To study the influence of growth technique on optical properties, ZnO nanostructures were grown using atmospheric pressure metal organic chemical vapor deposition (APMOCVD) and chemical bath deposition (CBD) technique. The structural and optical investigations were performed using scanning electron microscopy (SEM) and micro photoluminescence (μ-PL), respectively. The results revealed that the grown structures were in the shape of nano-rods with slightly different shapes. Optical investigation revealed that low temperature PL spectrum for both the samples was dominated by neutral donor bound excitons emission and it tends to be replaced by free exciton (FX) emission in the temperature range of 60-140K. Both excitonic emissions show a typical red-shift with increase in temperature but with a different temperature dynamics for both the sample and this is due to difference in exciton-phonon interaction because of the different sizes of nano-rods. Defect level emission (DLE) is negligible in both the sample at low temperature but it increased linearly in intensity after 130 K up to the room temperature.Modification in substrate can also play a significant role on structural and optical properties of the material. Specially variation in the miscut angle of substrate can help to control the lateral sizes of the Nanostructures and thus can help to obtain better structural andoptical quality. Also optical quality is a key requirement for making blue and ultraviolet LEDs. Therefore, ZnO Nanostructures were grown on SiC on-axis and off-axis substrates having different off-cut angles. Morphological investigation revealed thatgrown structures are epitaxial for the case when substrate off-cut angle is higher and deposition rate is low. Low temperature PL spectrum of all the samples was dominated by neutral donor bound excitons and free exciton emission become dominant at 100 K for all the samples which completely eliminate the neutral donor bound excitonic emission at 160K. Two electron satellite of the neutral donor bound excitons and LO phonons of excitonic features are also present. A typical red-shift in excitonic features was evident in temperature dependence measurement. Red-shift behavior of free exciton for all the samples was treated by applying Varshni empirical expression and several important parameter, such as, the Debye temperature and the band gap energy value was extracted. Thermal quenching behavior was also observed and treated by thermal quenching expression and value of the activation energy for non-radiative channel was extracted. The results that are obtained demonstrate a significant contribution in the fields of ZnO based nano-optoelectronics and nano-electronics.
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Love, David Michael. "Functional design of magnetic nanostructures : a study of patterned elements, thin film interfaces & self-assembled systems." Thesis, University of Cambridge, 2015. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.709265.
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Степаненко, Андрій Олександрович, Андрей Александрович Степаненко, Andrii Oleksandrovych Stepanenko, А. О. Сітало, С. І. Шевченко, and О. А. Шулік. "Методика отримання плівкових наноструктур на основі Al та Cu." Thesis, Видавництво СумДУ, 2012. http://essuir.sumdu.edu.ua/handle/123456789/27665.
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Naseem, Abbasali. "Computation and Analysis of Effective Permittivity of Thin Film Nanostructures: An Effective Medium Perspective." University of Toledo / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1279298769.
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Forsberg, Mathias. "Study of GaN Based Nanostructures and Hybrids." Doctoral thesis, Linköpings universitet, Tunnfilmsfysik, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-132267.
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GaN and its alloys with Al and In belong to the group III nitride semiconductors and are today the materials of choice for efficient white light emitting diodes (LEDs) enabling energy saving solid state lighting. Currently, there is a great interest in the development of novel inexpensive techniques to fabricate hybrid LEDs combining high quality III-N quantum well (QW) structures with inexpensive colloidal nanoparticles or conjugated polymers. Such hybrid devices are promising for future micro-light sources in full-color displays, sensors and imaging systems. Organics can be engineered to emit at different wavelengths or even white light based on functional groups or by blend of several polymers. This is especially important for the green region, where there is still a lack of efficient LEDs. Besides optoelectronics, other applications such as biochemical sensors or systems for water splitting can be realized using GaN-based nanostructures. Despite a significant progress in the field, there is still a need in fundamental understanding of many problems and phenomena in III-nitride based nanostructures and hybrids to fully utilize material properties on demand of specific applications. In this thesis, hybrid structures based on AlGaN/GaN QWs and colloidal ZnO nano-crystals have been fabricated for down conversion of the QW emission utilizing non-radiative (Förster) resonant energy transfer. Time-resolved photoluminescence (TRPL) was used to investigate the QW exciton dynamics depending on the cap layer thickness in the bare QW and in the hybrid samples. Although the surface potential influences the exciton dynamics, the maximum pumping efficiency assuming a non-radiative energy transfer mechanism was estimated to be ~40 % at 60 K in the structure with thin cap layer of 3 nm. Since bulk GaN of large area is difficult to synthesize, there is a lack of native substrates. Thus, GaN-based structures are usually grown on SiC or sapphire, which results in high threading dislocation density in the active layer of the device and can be the reason of efficiency droop in GaN based LED structures. Fabricating GaN nanorods (NR) can be a way to produce GaN with lower defect density since threading dislocations can be annihilated toward the NR wall during growth. Here, GaN(0001) NRs grown on Si(111) substrates by magnetron sputtering using a liquid Ga target have been investigated. A high quality of NRs have been confirmed by transmission electron microscopy (TEM) and TRPL. Two strong near band gap emission lines at ~3.42 eV and ~3.47 eV related to basal plane stacking faults (SF) and donor-bound exciton (DBE), respectively, have been observed at low temperatures. TRPL properties of the SF PL line suggest that SFs form a regular structure similar to a multiple QWs, which was confirmed by TEM. The SF related PL measured at 5 K for a single NR has a significantly different polarization response compared to the GaN exciton line and is much stronger polarized (> 40 %) in the direction perpendicular to the NR growth axis. Hybrids fabricated using GaN NRs and the green emitting polyfluorene (F8BT) have been studied using micro-TRPL. In contrast to the DBE emission, the recombination time of the SF-related emission was observed to decrease, which might be due to the Förster resonance energy transfer mechanism. Compared to chemical vapor deposition, sputtering allows synthesis at much lower temperatures. Here, sputtering was employed to grow InAlN/GaN heterostructures with an indium content targeted to ~18 %, which is lattice matched to GaN. This means that near strain-free GaN films can be synthesized. It was found that using a lower temperature (~25 C) while depositing the top InAlN results in an improved interface quality compared to deposition at 700 C. In latter case, regions of quaternary alloy of InAlGaN forming structural micro-defects have been observed at the top InAlN/GaN interface in addition to optically active flower-like defect formations.
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Matanga, Jacques. "STUDY AND REALIZATION OF A MULTISPETRAL DETECTOR(FILTER) BY NON DESTRUCTIVE SPECTRAL DISPERSION THROUGH TE NANOSTRUCTURE FILM." Thesis, Bourgogne Franche-Comté, 2020. http://www.theses.fr/2020UBFCK019.
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Le développement des techniques d’imageries multispectral, d’holographie et de lithographie permet d’exploiter les propriétés des réseaux diffractant dans une grande variété de composants photoniques. Ils sont incorporés dans des diodes laser comme réflecteurs de Bragg distribués, dans différentes fonctions d’optique intégrée pour le multiplexage en longueur d’onde ou les interconnexions optiques, ou inscrits au sein même des fibres, conduisant à une grande variété de capteurs pour la détection d’éléments chimiques, la mesure des températures, des pressions, des accélérations d’acquisition et ou de restitution d’images multispectrales etc... [Lee et al. 2007] [Pagnoux et al. 2005].Parmi ces dispositifs, les réseaux résonnants suscitent un très vif intérêt car ils permettent d’obtenir des filtres ultra-sélectifs à partir d’une structure relativement simple. Cette structure est constituée par un guide diélectrique sur lequel est gravé un réseau sub-longueur d’onde de faible profondeur et ou épaisseur. Hors résonance, la structure réfléchit et transmet la lumière selon les propriétés de réflectivité et transmission très proches de celles du dioptre constitué par l’empilement de couches diélectriquesThe development of multispectral imaging, holography and lithography techniques exploits the properties of diffracting arrays in a wide variety of photonic components. They are incorporated in laser diodes as distributed Bragg reflectors, in various integrated optical functions for wavelength division multiplexing or optical interconnections, or inscribed within the fibers themselves, leading to a wide variety of sensors for detection of chemical elements, measurement of temperatures, pressures, accelerations of acquisition and or restitution of multispectral images, etc. [Lee et al. 2007] [Pagnoux et al. 2005].Among these devices, the resonant networks arouse a great interest because they allow to obtain ultra-selective filters from a relatively simple structure. This structure consists of a dielectric guide on which is etched a subwavelength network of shallow depth and thickness. Except resonance, the structure reflects and transmits the light according to the properties of reflectivity and transmission very close to those of the diopter constituted by the stack of dielectric layers.This work presents the experimental and theoretical studies carried out to overcome the technological obstacles inherent to the realization of thin-film multispectal optical filters.The aim of this thesis is to study and design ultra-selective optical filters based on nanoscale thin films, by exploiting a resonant network structure conceived by depositing multilayer nanowires of metamaterials to surpass the performances of the current filters. Particular in the field of their spectral characteristics and their sensitivity to polarization. An issue of the study is to develop the associated manufacturing process, to identify the technological limitations imposed by the state of the art, to propose a reproducible process and if possible compatible with a collective technological development and low cost.The second was to use the samples from the fabrication of the diffraction gratings to associate it with a tri-CCD transistor-based sensor in the LE2I laboratory, in order to design a sharp acquisition device in multispectral imaging and of vision.The analysis of experimental performances, confronted with theoretical predictions and technological limitations, must lead to a realistic estimate of the potentialities of the proposed filters. To do this we began our study with a literature review on all the key elements of the subject, Nanotechnology, nanoscience these advantages these disadvantages, these possibilities. A review of the literature on multispectral imaging and these ascendants
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Huotari, J. (Joni). "Vanadium oxide nanostructures and thin films for gas sensor applications." Doctoral thesis, Oulun yliopisto, 2018. http://urn.fi/urn:isbn:9789526219714.
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Abstract In this thesis work, crystal and phase structure, chemical composition and gas sensing properties of pulsed laser deposited vanadium oxide thin films were studied. Pulsed laser deposition was used to manufacture vanadium oxide thin films with various crystal structures, film morphologies and phase compositions. Both the well-known vanadium pentoxide V2O5, and a totally new stable phase in a solid-state thin-film form, V7O16, was produced. The existence of these phases was proven by several different characterization methods such as, X-ray diffraction, Raman spectroscopy, and X-ray photoelectron spectroscopy. The resistive gas sensing measurements of the films with pure V2O5 composition, and mixed phase compositions of V2O5 and V7O16, showed that behaviour of the electrical response to different gases at various measurement temperatures was dependent on the phase composition of the thin films. It was proved that in certain conditions the mixed phase films show p-type semiconducting gas sensing behaviour, instead of the pure n-type behaviour of V2O5. Both types of film compositions were shown to be highly sensitive to ammonia gas, down to 40 ppb-level. The mixed phase composition showed a higher response to ammonia compared to the pure V2O5 phase; however the pure V2O5 showed better long-term stability. Both sensing layer types also showed high selectivity to ammonia in comparison to NO and CO gases. Nanostructured pure V2O5 layers were successfully deposited on commercial microheater platforms and then used as a gas sensor. The V2O5 nanostructures were proven to be very promising candidates as gas sensor material to control the Selective Catalytic Reduction process used in the reduction of NOx gas emissions. The surface valence states of the thin film structures with various phase compositions were studied spectroscopically, and a clear connection between the valence states of the film surfaces and gas sensing properties was found. It was concluded that the pure V2O5 films also had some V4+ ions in the surface, and in the mixed phase thin films, the amount V4+ ions was already quite high, indicating a higher amount of oxygen vacancies in the thin film surface – another proof of the existence of V7O16 phase in the film composition. It is also suggested that the particular quantity of oxygen vacancies is one of the reasons for the high gas-sensing response of the thin filmsTiivistelmä Tässä työssä tutkittiin pulssilaserkasvatettujen vanadiinioksidiohutkalvojen kide- ja faasirakenteita sekä ominaisuuksia kaasuantureina. Vanadiinioksidiohutkalvoja, jotka omaavat erilaiset kide- ja faasirakenteet, sekä erilaiset morfologiat valmistettiin pulssilaserkasvatuksella. Tunnetun V2O5 -faasin lisäksi myös V7O16 -faasi onnistuttiin valmistamaan ensimmäistä kertaa kiinteän aineen epäorgaanisena faasina ohutkalvorakenteeseen. Näiden erilaisten faasirakenteiden olemassaolo todistettiin käyttämällä useita menetelmiä kuten röntgendiffraktiota, Raman spektroskopiaa ja röntgenfotoelektronispektroskopiaa. Sekä ainoastaan V2O5 -faasia sisältäviä ohutkalvoja, että V2O5 ja V7O16 sekafaasirakenteen omaavia ohutkalvoja tutkittiin kaasuanturina, ja mittaustulokset osoittivat erilaisten kalvojen sähköisten kaasuanturivasteiden ominaisuuksien voimakkaan riippuvuuden kalvojen faasirakenteesta. Havaittiin myös, että sekafaasirakenne omaa tietyissä olosuhteissa p-tyyppisen puolijohteen sähkönjohtavuusmekanismin, toisin kuin puhdas V2O5-rakenne, joka on täysin n-tyyppinen. Molemmat ohutkalvotyypit todennettiin olevan erityisen herkkiä ammoniakki (NH3) kaasulle, jopa 40 miljardisosatasolle. Kalvo, jossa oli sekafaasirakenne, omasi korkeamman sähköisen kaasuvasteen kuin puhtaasta V2O5 faasista koostuva ohutkalvo, joka taas toisaalta omasi paremman stabiiliuden pidemmällä aikavälillä. Molemmat kaasuanturimateriaalit havaittiin selektiiviseksi NH3 -kaasulle verrattuna NO- ja CO-kaasuihin. Puhdas V2O5 nanorakenne onnistuttiin myös kasvattamaan kaupalliselle anturialustalle, ja käyttämään menestyksekkäästi herkkänä NH3- kaasuanturina. Lisäksi puhtaan V2O5 nanorakenteen todennettiin olevan erittäin lupaava kaasuanturimateriaali hyödynnettäväksi NOx-kaasupäästöjen vähentämiseen käytettävän SCR-katalyysiprosessin (Selective Catalytic Reduction) ohjauksessa. Ohutkalvotyyppien pinnan sähköistä rakennetta tutkittiin röntgenspektroskopiamenetelmillä, ja selvä yhteys materiaalien pintojen valenssitilojen ja kaasuanturiominaisuuksien välillä havaittiin. Huomattiin, että myös puhdas V2O5 ohutkalvo omaa pinnallaan pienen määrän V4+ -ioneja, ja että ohutkalvossa, jossa on sekafaasirakenne, V4+ -ionien määrä on suuri, ollen yksi todiste lisää V7O16 faasin olemassaoloon kalvon rakenteessa. Tästä johtuva happivakanssien olemassaolo on yksi syy näiden ohutkalvojen korkeaan kaasuherkkyyteen
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Bangcuyo, Carlito Ganayo. "Synthesis of heterocyclic poly(aryleneetheynylene)s." Available online, Georgia Institute of Technology, 2006, 2004. http://etd.gatech.edu/theses/available/etd-01112005-182450/.
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Thesis (Ph. D.)--Chemistry and Biochemistry, Georgia Institute of Technology, 2007.Tolbert, Laren, Committee Member ; Weck, Marcus, Committee Member ; Bunz, Uwe, Committee Chair ; Srinivasarao, Mohan, Committee Member.
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Marchesini, Matteo. "Plasmon decay dynamics in hybrid metal/doped-semiconductor nanostructures." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2021. http://amslaurea.unibo.it/23223/.
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The study of interactions between plasmonic nanomaterials and dielectrics is a thriving field of research, which in recent years proved that such nanostructures can be applied in a wide range of applications, from sensing to catalysts. These are all based on the nanoscale surface interactions happening between the nanomaterials and their surrounding environment. In this thesis, the possible interaction between plasmonic nanoparticles and the V doping states in the Anatase (TiO_2) bandgap, rather than in their undoped counterpart, is studied. The aim is to better understand the dynamics of these phenomena, and obtaining insights on the V states position in the TiO_2 bandgap. The work done encompasses all the steps needed to achieve the experimental results: from the preparation and characterisation of the samples, to the simulations of the phenomena involved, until the actual measurements of their optical properties and the discussion of the results. The findings achieved are not decisive in explaining the dynamics involved, but preliminary interpretations could be formulated. Moreover, the specific investigations displayed in this thesis have never been done before in literature, and the work performed might be used in the future as a starting point for more thorough and deep studies of these phenomena.
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Vernon, Kristy C. "Strongly localised plasmons in metallic nanostructures." Queensland University of Technology, 2008. http://eprints.qut.edu.au/19318/.
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Strongly localised plasmons in metallic nano-structures offer exciting characteristics for guiding and focusing light on the nano-scale, opening the way for the development of new types of sensors, circuitry and improved resolution of optical microscopy. The work presented in this thesis focuses on two major areas of plasmonics research - nano-focusing structures and nano-sized waveguides. Nano-focusing structures focus light to an area smaller than the wavelength and will find applications in sensing, efficiently coupling light to nano-scale devices, as well as improving the resolution of near field microscopy. In the past the majority of nano-focusing structures have been nano-scale cones or tips, which are capable of focusing light to a spot of nano-scale area whilst enhancing the light field. The alternatives are triangular nano-focusing structures which have received far less attention, and only one type of triangular nano-focusing structure is known – a sharp V-groove in a metal substrate. This structure focuses light to a strip of nano-scale width, which may lead to new applications in microscopy and sensing. The difficulty with implementing the V-groove is that the structure is not robust and is quite difficult to fabricate. This thesis aims to develop new triangular nano-focusing devices which will overcome these difficulties, whilst still producing an intense light source on the nano-scale. The two proposed structures presented in this thesis are a metallic wedge submerged in uniform dielectric and a tapered metal film lying on a dielectric substrate, the latter being the easier to fabricate and the more structurally sound and robust. The investigation is performed using the approximation of continuous electrodynamics, the geometrical optics approximation and the zero-plane method. The second aim of this thesis is to investigate plasmonic waveguides and couplers for the development of nano-optical circuitry, more compact photonic devices and sensors. The research will attempt to fill the gaps in the current knowledge of the V-groove waveguide, which consists of a sharp triangular groove in a metal substrate, and the gap plasmon waveguide, which consists of a rectangular slot in a thin metal film. The majority of this work will be performed using the author’s in house finite-difference time-domain algorithm and FEMLAB as well as the effective medium method and geometric optics approximation. The V-groove may be used as either a nano-focusing or waveguiding device. As a waveguide the V-groove is one of the most promising plasmonic waveguides in the optical regime. However, there exist quite a number of gaps in the current knowledge of V-groove waveguides which this thesis will attempt to fill. In particular, the effect of rounded groove tip on plasmon propagation has been assessed for the V-groove. The investigation of rounded groove tip is important, as due to modern fabrication processes it’s not possibly to produce an infinitely sharp groove, and the existing literature has not considered the impact of this problem. The thesis will also investigate the impacts of the inclusion of dielectric filling in the groove on plasmon propagation parameters. This research will be important for optimising the propagation characteristics of the mode for certain applications, but it may also lead to easier methods of fabricating the V-groove device and prevent oxidation of the metal film. The gap plasmon waveguide is easier to fabricate than the V-groove, and is a new type of sub-wavelength waveguide which displays many advantages over other types of plasmon waveguides, including ease of fabrication, almost 100% transmission around sharp bends, sub-wavelength localisation and long propagation distances of the guided mode, etc. This waveguide may prove invaluable in the development of compact photonic devices. In the past the modes supported by this structure were not thoroughly analysed and the possibility of using this structure to develop sub-wavelength couplers for sensing and nano-optical circuits was not considered in detail. This thesis aims to resolve these issues. In conclusion, the results of this thesis will lead to a better understanding of Vgroove and gap plasmon waveguide devices for the development of nano-optical circuits, compact photonic devices and sensors. This thesis also proposes two new nano-focusing structures which are easier to fabricate than the V-groove structure and will lead to applications in sensing, coupling light efficiently into nano-scale devices and improving the resolution of near-field microscopy.
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Haber, Johann Friedrich Albert [Verfasser], and Ralf [Akademischer Betreuer] Röhlsberger. "Hard X-ray Quantum Optics in Thin-Film Nanostructures / Johann Friedrich Albert Haber ; Betreuer: Ralf Röhlsberger." Hamburg : Staats- und Universitätsbibliothek Hamburg, 2017. http://d-nb.info/1134866046/34.
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Farha, Rana. "Nanostructures organométalliques : croissance par photochimie de couches inorganiques sous films de Langmuir." Paris 6, 2007. http://www.theses.fr/2007PA066429.
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Notre but est de former des interfaces organo-minérales d’épaisseur nanométrique. Pour ce faire, nous déposons une monocouche organique (film de Langmuir) sur une solution contenant les ions métalliques. La croissance du film inorganique est obtenue par réaction photochimique au niveau des têtes amphiphiles de la monocouche organique qui sert donc de « moule » pour les ions adsorbés. Nous avons étudié deux systèmes par des mesures thermodynamiques, d’AFM et d’XPS. Dans le système platine/DODA, la monocouche organique est chargée positivement et on observe la formation de plaques métalliques d’épaisseur nanométrique à l’interface solution/air. Ces plaques, formées en deux étapes, ont une épaisseur de 3 à 4 nm. Nous les avons étudiés après 24 h et 96 h de réaction. Leur taille latérale et leur rigidité évoluent au cours du temps, ainsi que leur nature chimique qui se rapproche au cours du temps de celle du platine métallique. La réaction reste cependant inachevée au bout de 4 jours. Dans le cas du système Argent/acide béhénique, nous avons mis en évidence la formation de plaques d’argent sous la monocouche d’acide béhénique. Ces plaques de 3 à 5 nm d’épaisseur, semblent être formées par de l’argent métallique.
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Khoury, Rasha. "Nanometer scale point contacting techniques for silicon Photovoltaic devices." Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLX070/document.
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Au cours de cette thèse, j’ai étudié la possibilité et les avantages d’utiliser des contacts nanométriques au-dessous de 1 µm. Des simulations analytiques et numériques ont montré que ces contacts nanométriques sont avantageux pour les cellules en silicium cristallin comme ils peuvent entrainer une résistance ohmique négligeable. Mon travail expérimental était focalisé sur le développement de ces contacts en utilisant des nanoparticules de polystyrène comme un masque. En utilisant la technique de floating transfert pour déposer les nanosphères, une monocouche dense de nanoparticules s’est formée. Cela nécessite une gravure par plasma de O2 afin de réduire la zone de couverture des NPs. Cette gravure était faite et étudiée en utilisant la technique de plasmas matriciels distribués à résonance cyclotronique électronique (MD-ECR). Une variété de techniques de créations de trous nanométriques était développée et testée dans des structures de couches minces et silicium cristallin. Des trous nanométriques étaient formés dans la couche de passivation, de SiO2 thermique, du silicium cristallin pour former des contacts nanométriques dopés. Un dopage local de bore était fait, à travers ces trous nanométriques par diffusion thermique et implantation ionique. En faisant la diffusion, le dopage local était observé par CP-AFM en mesurant des courbes de courant-tension à l’intérieur et à l’extérieur des zones dopées et en détectant des cellules solaires nanométriques. Par contre le processus de dopage local par implantation ionique a besoin d’être améliorer afin d’obtenir un résultat similaire à celui de diffusionThe use of point contacts has made the Passivated Emitter and Rear Cell design one of the most efficient monocrystalline-silicon photovoltaic cell designs in production. The main feature of such solar cell is that the rear surface is partially contacted by periodic openings in a dielectric film that provides surface passivation. However, a trade-off between ohmic losses and surface recombination is found. Due to the technology used to locally open the contacts in the passivation layer, the distance between neighboring contacts is on the order of hundreds of microns, introducing a significant series resistance.In this work, I explore the possibility and potential advantages of using nanoscale contact openings with a pitch between 300 nm to 10 µm. Analytic and numerical simulations done during the course of this thesis have shown that such nanoscale contacts would result in negligible ohmic losses while still keeping the surface recombination velocity Seff,rear at an acceptable level, as long as the recombination velocity at the contact (Scont) is in the range from 103-105 cm/s. To achieve such contacts in a potentially cost-reducing way, my experimental work has focused on the use of polystyrene nanospheres as a sacrificial mask.The thesis is therefore divided into three sections. The first section develops and explores processes to enable the formation of such contacts using various nanosphere dispersion, thin-film deposition, and layer etching processes. The second section describes a test device using a thin-film amorphous silicon NIP diode to explore the electrical properties of the point contacts. Finally, the third section considers the application of such point contacts on crystalline silicon by exploring localized doping through the nanoholes formed.In the first section, I have explored using polystyrene nanoparticles (NPs) as a patterning mask. The first two tested NPs deposition techniques (spray-coating, spin-coating) give poorly controlled distributions of nanospheres on the surface, but with very low values of coverage. The third tested NPs deposition technique (floating transfer technique) provided a closely-packed monolayer of NPs on the surface; this process was more repeatable but necessitated an additional O2 plasma step to reduce the coverage area of the sphere. This was performed using matrix distributed electron cyclotron resonance (MD-ECR) in order to etch the NPs by performing a detailed study.The NPs have been used in two ways; by using them as a direct deposition mask or by depositing a secondary etching mask layer on top of them.In the second section of this thesis, I have tested the nanoholes as electrical point-contacts in thin-film a-Si:H devices. For low-diffusion length technologies such as thin-film silicon, the distance between contacts must be in the order of few hundred nanometers. Using spin coated 100 nm NPs of polystyrene as a sacrificial deposition mask, I could form randomly spaced contacts with an average spacing of a few hundred nanometers. A set of NIP a-Si:H solar cells, using RF-PECVD, have been deposited on the back reflector substrates formed with metallic layers covered with dielectrics having nanoholes. Their electrical characteristics were compared to the same cells done with and without a complete dielectric layer. These structures allowed me to verify that good electrical contact through the nanoholes was possible, but no enhanced performance was observed.In the third section of this thesis, I investigate the use of such nanoholes in crystalline silicon technology by the formation of passivated contacts through the nanoholes. Boron doping by both thermal diffusion and ion implantation techniques were investigated. A thermally grown oxide layer with holes was used as the doping barrier. These samples were characterized, after removing the oxide layer, by secondary electron microscopy (SEM) and conductive probe atomic force microscopy (CP-AFM)
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Hughes, William L. "Synthesis and characterization of zinc oxide nanostructures for piezoelectric applications." Diss., Available online, Georgia Institute of Technology, 2006, 2006. http://etd.gatech.edu/theses/available/etd-08232006-155547/.
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Thesis (Ph. D.)--Materials Science and Engineering, Georgia Institute of Technology, 2007.Wang, Zhong Lin, Committee Chair ; Wong, C.P., Committee Member ; Summers, Christopher J., Committee Member ; Degertekin, F. Levent, Committee Member ; Bottomley, Lawrence A., Committee Member.
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Le, Moal Eric. "Développement et organisation de nanostructures : applications à l'exaltation des processus optiques pour la Biologie." Phd thesis, Université Pierre et Marie Curie - Paris VI, 2007. http://tel.archives-ouvertes.fr/tel-00164549.
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La fluorescence d'une molécule est sensible à son environnement électromagnétique. La présence d'une structure métallique modifie l'excitation et l'émission des fluorophores, par le jeu d'interférences et de couplages avec les plasmons de surface. Nous avons élaboré et caractérisé des films métalliques de différentes morphologies (films de nanoparticules, percolés, continus, plans, rugueux. . .). Leur influence sur la réponse optiquedes fluorophores a été étudiée par la modélisation puis l'expérience, en fonction de la distance fluorophore-métal et de l'orientation moléculaire. Une amplification d'un à deux ordres de grandeur du signal détecté est observée, ainsi qu'une photostabilisation des fluorophores et une modification des transferts d'énergie intermoléculaires. Nous
démontrons l'intérêt de cette technologie pour améliorer la sensibilité dans les puces à ADN et pour l'imagerie des cellules et des tissus.
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Béjaud, Romuald. "Formation et extension de macles de déformation dans des nanostructures cfc : simulations numériques." Thesis, Poitiers, 2017. http://www.theses.fr/2017POIT2318.
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Depuis quelques dizaines d'années, l'élaboration de matériaux nanostructurés tend de plus en plus à se développer. En effet, ces matériaux présentent souvent des propriétés intéressantes et en particulier des propriétés mécaniques surprenantes vis-à-vis de leurs homologues sous forme massive. Les métaux nano-maclés ou nano-lamellaires par exemple, sont connus pour avoir une bonne résistance mécanique, une bonne stabilité thermique et une excellente résistance aux radiations. Au fur et à mesure que l'espacement entre les interfaces diminue, leur densité augmente de manière significative et les propriétés macroscopiques du matériau sont de plus en plus dépendantes des interactions défaut-interface. Dans ce contexte, nous avons étudié, via des simulations atomistiques, la formation de macles de déformation et les mécanismes d'interaction d'une macle nouvellement formée avec une interface préexistante (un joint de macle ou une interface entre 2 métaux), pour une configuration modèle de film mince auto-supporté. Des premiers résultats montrent l'influence de marches de surface sur le maclage, pour un cas modèle sans interface. Puis nous avons identifié un mécanisme inédit aboutissant à la formation d'une dislocation de Lomer suite à l’interaction d'une macle en formation avec un joint de macle préexistant. En faisant varier la densité de défauts de surface, nous montrons l'influence particulière d'un joint de macle sur la taille et le nombre de macles formées. Enfin, pour les systèmes bimétalliques Cu/Ag, nos résultats mettent en évidence le rôle des dislocations d'épitaxie (à l'interface) dans la nucléation et l'extension des macles ainsi qu'une influence directe du type d'interface considéré sur la propagation de ces maclesFor several decades, the elaboration of nano-structured materials tends to develop more and more. Indeed, these materials often show interesting properties, and in particular surprising mechanical properties when compared to their bulk counterparts. For example, nano-twinned or nano-layered metals are known to have ultra-high mechanical strength, good thermal stability, and very good radiation resistance. As the interface spacing decreases to the nanometer-scale, the density of interfaces increases significantly and subsequently the macroscopic properties become largely governed by the interface-defect interactions. In that context, we have studied deformation twin formation and mechanisms of interaction between a new formed twin and a preexisting interface (a twin boundary or a bimetallic interface), using atomistic simulations and a thin film model configuration. First results show the influence of surface steps on mechanical twinning, for a model system without interface. Then we identify a new mechanism leading to the formation of a Lomer dislocation, following the interaction of a newly formed twin and a preexisting twin boundary. By varying the density of surface defects, we show the particular influence of a preexisting twin boundary on twin size and number. Finally, for the Cu/Ag bimetallic system, our results highlight the role of epitaxial dislocations (at the interface) in twin nucleation and extension as well as a direct influence of the interface type in twin propagation
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Mesguich, Frederic. "Stratégie innovante pour la mise en forme de nanostructures TiO2/Au à propriétés synergétiques pour le photovoltaïque." Phd thesis, Université Pierre et Marie Curie - Paris VI, 2014. http://tel.archives-ouvertes.fr/tel-00978847.
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Actuellement, le secteur des nanotechnologies est en développement intense. Les nanoparticules de dioxyde de titane et d¿or occupent une part importante de ce secteur, avec des applications utilisant principalement leurs propriétés optiques et catalytiques. Les synergies pouvant exister entre les nanoparticules d¿or et leur support, en particulier via l¿effet plasmon, permettent de modifier la réponse optique de dispositifs catalytiques ou photovoltaïques. Une nouvelle technique polyvalente de mise en forme de film mésoporeux à base de nanoparticules de dioxyde de titane et d¿or a été développée. L¿utilisation de différentes méthodes de synthèse des nanoparticules a permis le contrôle de la morphologie et des propriétés physiques des films déposés par centrifugation. Finalement, l¿adéquation de ces films à leur utilisation en tant qu¿anode de cellules solaires à colorant a été évaluée.
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Guillemin, Sophie. "Mécanismes de croissance de nanostructures de ZnO par voie chimie liquide et caractérisation avancée." Thesis, Lyon, INSA, 2014. http://www.theses.fr/2014ISAL0143/document.
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Les travaux présentés dans ce manuscrit traitent des mécanismes de croissance associés au dépôt de nanofils d’oxyde de zinc (ZnO) en bain chimique. Cette technique de croissance, attractive de par sa facilité de mise en œuvre et son coût limité, consiste à immerger un substrat dans une solution de précurseurs portée à basse température (typiquement 90°) pendant quelques heures. Le dépôt préalable d’une fine couche de ZnO fortement texturée est nécessaire à l’obtention de la morphologie nanofils et il est donc nécessaire de maîtriser le processus de croissance associé. Dans un souci de cohérence, la méthode sol-gel dite de trempage consistant à immerger le substrat dans une solution de précurseurs avant de recuire la couche ainsi déposée est ici adoptée. Le ZnO, sous sa morphologie nanofils, est actuellement fortement étudié du fait de son fort potentiel applicatif. Typiquement, il peut être utilisé en tant que brique de basse dans la réalisation de cellules solaires de types Grätzel ou à absorbeur extrêmement fin. Dans ce contexte, il est nécessaire que les nanostructures élaborées présentent des propriétés physiques attractives et ces dernières doivent donc être finement caractérisées. Dans un premier temps, l’influence des paramètres expérimentaux associés au processus de trempage sur les propriétés morphologiques et structurales de films minces de ZnO déposés via ce processus est quantifiée. Il est montré à cette occasion que dans des conditions extrêmes de recuits, les couches évoluent vers une morphologie de type fil. Fort des conclusions obtenues, les mécanismes régissant la croissance de nanofils de ZnO en bain chimique, et plus particulièrement l’influence de la surface de nucléation sur ces derniers, sont étudiés. La possibilité d’obtenir des nanofils localisés et parfaitement alignés à travers la réalisation de masques est démontrée. L’ensemble des nanostructures élaborées (couches et nanofils) sont caractérisées par photoluminescence afin de pouvoir estimer leur qualité structurelle et d’étudier les défauts en présence. Pour finir, une étude plus fondamentale consistant à suivre in situ l’évolution des nanofils au cours de la croissance par rayonnement synchrotron est proposée avec une attention toute particulière aux phénomènes de polaritéZnO nanowires are of strong interest in the realization of solar cells based on type-II band alignment. They can be grown by chemical bath deposition, a technique in which the substrate is seeded with ZnO nanoparticles by dip-coating and then placed in a precursor solution heated at 90°C for a couple of hours. In this document, we will discuss the nucleation and growth mechanisms associated with this low cost technique. In particular, we will see how the seed layer morphology can drive the one of the nanowires. Also, advanced characterization by photoluminescence and synchrotron radiation will be performed on the grown nanostructures
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Кузнецова, А. О., and О. Л. Волкова. "Тензо- і магніторезистивні властивості плівкових зразків на основі Pd/Fe." Thesis, Видавництво СумДУ, 2012. http://essuir.sumdu.edu.ua/handle/123456789/27668.
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Hrabec, Ales. "Etude de la dynamique de l'aimantation dans des nanostructures magnétiques à aimantation perpendiculaire : effet du champ magnétique et du courant électrique." Phd thesis, Université de Grenoble, 2011. http://tel.archives-ouvertes.fr/tel-00767418.
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Pendant les deux dernières décennies, la manipulation des parois de domaines est devenuel'une des parties inamovibles de la spintronique. L'interaction entre les électrons deconduction polarisés en spin et les moments magnétiques localisés en termes demagnétorésistance géante en 1988 et en termes de couple de transfert de spin en 1996, a lancéune avalanche de travaux expérimentaux sur la dynamique de l'aimantation induite par uncourant polarisé. Malgré les recherches très intensives dans ce domaine, de nombreusesquestions fondamentales restent sans réponse. Par exemple, l'origine des paramètresphénoménologiques alpha et bêta, étant au coeur de la description de la dynamique del'aimantation, n'est pas entièrement comprise. Habituellement, dans les systèmes étudiésexpérimentalement les paramètres micromagnétiques sont fixés, de sorte qu'il est impossiblede vérifier leur rôle dans la dynamique de l'aimantation. Par exemple, un changement d'unparamètres tel que l'aimantation ou le moment angulaire, la largeur de paroi de domaine, etc,pourrait éclaircir la compréhension de la dynamique de parois induite par du champ ou decourant. Dans la première partie de mon travail que je vais décrire un alliage de Gd1-xCoxavec un gradient de composition (et donc d'aimantation). La composition de l'alliage estchoisi de façon que une interface magnétique compensée est présente dans nos couchesminces. Une telle couche mince sert de système modèle idéal avec un changement continu d'aimantation à une température constante. Ce système fait l'objet d'une étude sur la dynamiquede l'aimantation induite par le courant electrique, le champ magnétique et la lumière. Dans laseconde partie de l'ouvrage des tricouches Pt/Co/AlOx, un système déjà montré être adapté àla manipulation des parois de domaines rapide et reproductible, est étudiée. J'ai testéexpérimentalement et prouvé l'hypothèse reliant le rendement du couple de transfert de spin àle présence d'un champ magnétique transverse ayant pour origine l'effet Rashba auxinterfaces du cobalt.
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Wang, Dong. "The Application of Thin Film Ionic Self-assembled Multilayer (ISAM) Nanostructures in Electromechanical Bending Actuators and Micro-fabricated Gas Chromatography (uGC) Devices." Diss., Virginia Tech, 2015. http://hdl.handle.net/10919/51186.
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Ionic self-assembled multilayer (ISAM) thin film nanostructures, including highly porous and conductive gold nanoparticles (GNP), and highly porous and thermally stable silica nanoparticles (SNP), were fabricated via the layer-by-layer (LbL) self-assembly technique. Their application in ionic polymer-metal composite (IPMC) electromechanical bending actuators and microfabricated gas chromatography (microGC) devices were investigated and significant performance improvements of these devices were achieved.
IPMC bending actuators, consisting of an ionic electroactive polymer (iEAP) membrane as backbone, ionic liquids (IL) as electrolyte, and ISAM GNP thin film as porous electrode, were fabricated and investigated. The influences of humidity, conductive network composite (CNC), and IL uptake on the bending performance were examined and discussed. An equivalent circuit model to simulate both the electrical and mechanical responses was also proposed and experimentally verified. Moreover, IPMC actuators made from other newly synthesized iEAP membranes were fabricated and tested. Some of them showed promising performance that was comparable or even better as compared to the ones made from Nafion.
LbL fabricated ISAM SNPs thin film coatings were also applied in the microGC devices including micro fabricated thermal preconcentrators (microTPC) and separation columns (microSC) as adsorbent and stationary phase materials, respectively. New fabrication approaches were developed to selectively coat uniform conformal ISAM SNP coatings in these devices with different 3D microstructures. Thus, functionalized microTPCs and microSCs showed good performance, which can be further improved by using the ISAM SNPs coating as a nanotemplate for modifying additional polymer adsorbents or as the anchor sites for incorporating functional molecules for targeting detection.Ph. D.
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Xiang, Shu. "Piezoelectric thin films and nanowires: synthesis and characterization." Thesis, Georgia Institute of Technology, 2011. http://hdl.handle.net/1853/41139.
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Piezoelectric materials are widely used for sensors, actuators and trasducers.
Traditionally, piezoelectric applications are dominated by multicomponent oxide
ferroelectrics such as lead zirconate titanate (PZT), which have the advantage of high piezoelectric coefficients. Recently, one-dimensional piezoelectric nanostructures such as nanowires of zinc oxide (ZnO) and gallium nitride (GaN) has gained a lot of attention due to their combined piezoelectric and semiconducting properties. The focus of this thesis is to study the processing and electric properties of such piezoelectric thin films and nanostructures for various applications.
There is an increasing interest to form thin films of multicomponent ferroelectric oxides such as PZT on three-dimensional structures for charge storage and MEMS applications. Traditional vapor phase deposition techniques of PZT offer poor conformality over threedimensional surfaces due to their reactant transport mechanisms. As an alternative, solgel synthesis may provide new process possibilities to overcome this hurdle but the film quality is usually inferior, and the yield data was usually reported for small device areas. The first part of this study is dedicated to the characterization of the electric properties and yield of PZT thin film derived from the sol-gel process. PZT thin films with good electric property and high yield over a large area have been fabricated. La doping was found to double the breakdown field due to donor doping effect. LaNiO3 thin films that can be coated on a three-dimensional surface have been synthesized by an all-nitrate based sol-gel route, and the feasibility to form a conformal coating over a three-dimensional surface by solution coating techniques has been demonstrated.
ZnO and GaN micro/nanowires are promising piezoelectric materials for energy harvesting and piezotronic device applications. The second part of this study is focused on the growth of ZnO and GaN micro/nanowires by physical vapor deposition techniques. The morphology and chemical compositions are revealed by electron microscopy. Utilizing the as-grown ZnO nanowires, single nanowire based photocell has been fabricated, and its performance was studied in terms of its response time, repeatability, excitation position and polarization dependence upon He-Cd UV-laser
illumination. The excitation position dependence was attributed to the competition of two opposite photo- and thermoelectric currents originated from the two junctions. The excitation polarization dependence was attributed to the difference in optical properties due to crystallographic anisotropy. Employing the as-grown GaN nanowires, single nanowire based strain sensor is demonstrated, and its behavior is discussed in terms of the effect of strain-induced piezopotential on the Schottky barrier height.
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Gunawidjaja, Ray. "Organic/inorganic nanostructured materials towards synergistic mechanical and optical properties /." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/29733.
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Thesis (Ph.D)--Industrial and Systems Engineering, Georgia Institute of Technology, 2010.Committee Chair: Tsukruk, Vladimir; Committee Member: Bucknall, David; Committee Member: Kalaitzidou, Kyriaki; Committee Member: Shofner, Meisha; Committee Member: Tannenbaum, Rina. Part of the SMARTech Electronic Thesis and Dissertation Collection.
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Mailhes, Romain. "Effets plasmoniques induits par des nanostructures d’argent sur des couches minces de silicium." Thesis, Lyon, 2016. http://www.theses.fr/2016LYSEI097/document.
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Le domaine du photovoltaïque en couches minces s’attache à réduire le coût de l’énergie photovoltaïque, en réduisant considérablement la quantité de matières premières utilisées. Dans le cas du silicium cristallin en couches minces, la réduction de l’épaisseur de la cellule s’accompagne d’une baisse drastique de l’absorption, notamment pour les plus fortes longueurs d’onde. Nombreuses sont les techniques aujourd’hui mises en œuvre pour lutter contre cette baisse de performance, dont l’utilisation des effets plasmoniques induits par des nanostructures métalliques qui permettent un piégeage de la lumière accru dans la couche absorbante. Dans ces travaux, nous étudions l’influence de nanostructures d’argent organisées suivant un réseau périodique sur l’absorption d’une couche de silicium. Ces travaux s’articulent autour de deux axes majeurs. L’influence de ces effets plasmoniques sur l’absorption est d’abord mise en évidence à travers différentes simulations numériques réalisées par la méthode FDTD. Nous étudions ainsi les cas de réseaux périodiques finis et infinis de nanostructures d’argent situés sur la face arrière d’une couche mince de silicium. En variant les paramètres du réseau, nous montrons que l’absorption au sein du silicium peut être améliorée dans le proche infrarouge, sur une large plage de longueurs d’onde. Le second volet de la thèse concerne la réalisation des structures modélisées. Pour cela, deux voies de fabrication ont été explorées et développées. Pour chacune d’entre elles, trois briques élémentaires ont été identifiées : (i) définition du futur motif du réseau grâce à un masque, (ii) réalisation de pores dans le silicium et (iii) remplissage des pores par de l’argent pour former le réseau métallique. La première voie de fabrication développée fait appel à un masque d’alumine, réalisé par l’anodisation électrochimique d’une couche d’aluminium, pour définir les dimensions du réseau métallique. Une gravure chimique assistée par un métal est ensuite utilisée pour former les pores, qui seront alors comblés grâce à des dépôts d’argent par voie humide. La seconde voie de fabrication utilise un masque réalisé par lithographie holographique, une gravure des pores par RIE et un remplissage des pores par dépôt d’argent electroless. Les substrats plasmoniques fabriqués sont caractérisés optiquement, au moyen d’une sphère intégrante, par des mesures de transmission, réflexion et absorption. Pour tous les substrats plasmoniques caractérisés, les mesures optiques montrent une baisse de la réflexion et de la transmission et une hausse de l’absorption pour les plus grandes longueurs d’ondeThin-film photovoltaics focus on lowering the cost reduction of photovoltaic energy through the significant reduction of raw materials used. In the case of thin-films crystalline silicon, the reduction of the thickness of the cell is linked to a drastic decrease of the absorption, particularly for the higher wavelengths. This decrease of the absorption can be fought through the use of several different light trapping methods, and the use of plasmonic effects induced by metallic nanostructures is one of them. In this work, we study the influence of a periodic array of silver nanostructures on the absorption of a silicon layer. This work is decomposed into two main axes. First, the influence of the plasmonic effects on the silicon absorption is highlighted through different numerical simulations performed by the FDTD method. Both finite and infinite arrays of silver nanostructures, located at the rear side of a thin silicon layer, are studied. By varying the parameters of the array, we show that the silicon absorption can be improved in the near infrared spectral region, over a wide range of wavelengths. The second part of the thesis is dedicated to the fabrication of such modeled structures. Two different approaches have been explored and developed inside the lab. For each of these two strategies, three major building blocks have been identified: (i) definition of the future array pattern through a mask, (ii) etching of the pattern in the silicon layer and (iii) filling of the pores with silver in order to form the metallic array of nanostructures. In the first fabrication method, an anodic alumina mask, produced by the electrochemical anodization of an aluminium layer, is used in order to define the dimensions of the metallic array. A metal assisted chemical etching is then performed to produce the pores inside the silicon, which will then be filled with silver through a wet chemical process. The second fabrication method developed involves the use of holographic lithography to produce the mask, the pores in silicon are formed by reactive ion etching and they are filled during an electroless silver deposition step. The fabricated plasmonic substrates are optically characterized using an integrating sphere, and transmission, reflection and absorption are measured. All the characterized plasmonic substrates shown a decrease of their reflection and transmission and an absorption enhancement at the largest wavelengths
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Wang, Weiliang. "Novel functional nano-coatings on glass by spray deposition." Thesis, University of Oxford, 2010. http://ora.ox.ac.uk/objects/uuid:45bd0d35-111e-4855-96f1-edf109e65b7b.
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Nanocomposite thin films with gold nanoparticles embedded in a host metal oxide prepared by spray pyrolysis deposition have been investigated. A single-step process has been developed using a one-pot solution containing precursors for both gold nanoparticles and host metal oxides. The films obtained display combined features of colouration, electrical conductivity and solar control. In this study two precursors for gold nanoparticles were used: preformed gold colloids and HAuCl4. Three metal oxide host materials, TiO2, SnO2 and ZnO, were investigated. These films were deposited at a substrate temperature of 200-600 °C. Powder X-ray diffraction analysis reveals the presence of metallic gold. SEM inspection typically showed particulate gold of 5-20 nm in diameter, distributed at the surface or within the host matrix. Optical spectroscopy showed an intense absorption in the visible region due to the characteristic surface plasmon resonance (SPR) effects of gold nanoparticles. The wavelength of the SPR peaks varies depending on the refractive index of surrounding host material which is significantly influenced by the substrate deposition temperature. On the other hand, SnO2 and ZnO, together with the introduction of dopants, were further investigated as suitable materials for transparent conducting oxides (TCO). SnO2:F films were found to attain very low electrical resistivity, while ZnO films exhibit higher transparency in the visible. A double layered structure with a TCO layer of SnO2:F on top of a layer embedded with gold nanoparticles has been employed to achieve the combined functionalities of conductivity and colouration. The electrical conductivity is significantly enhanced compared to a nanocomposite single layer film due to the introduction of the TCO top layer. In this thesis, spray pyrolysis deposition has demonstrated a simple and rapid approach to the production of a variety of thin films. It can be immediately integrated with current industrial coating equipment and scaled up for large-scale production process.
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Bock, Bradley D. "Surface influences on falling film boiling and pool boiling of saturated refrigerants : influences of nanostructures, roughness and material on heat transfer, dryout and critical heat flux of tubes." Thesis, University of Pretoria, 2020. http://hdl.handle.net/2263/78711.
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Falling film evaporators that operate in the nucleate boiling regime in the refrigeration industry offer a number of advantages over their flooded counterparts such as lower refrigerant charge and at times improved heat transfer. Existing literature has not characterised the influence of surface characteristics on the falling film boiling process, and they are poorly understood for the pool boiling process. The purpose of this study was therefore to experimentally measure the influence of roughness, material and nanostructures on the heat transfer of falling film boiling and pool boiling of saturated refrigerants on the outside of horizontal tubes. The critical heat flux point was measured if it occurred, and the falling film heat transfer enhancement ratio, critical dryout threshold and general dryout characteristics were investigated in the study.
The tubes tested consisted of plain copper, stainless steel and mild steel tubes that were polished and roughened with various grades of sandpaper. Furthermore, three types of nanostructured surfaces were applied to polished copper tubes, namely a layer-by-layer (LbL) coating of silica nanoparticles, a copper oxide (CuO) nanostructure coating and a commercial nanocoating process termed nanoFLUX.
The nanoFLUX tube had the highest heat transfer coefficients of tubes tested under both pool boiling and falling film conditions, with between 40 and 200% higher heat transfer coefficients than those of a polished copper tube. The nanoFLUX surface outperformed the other surfaces due to a combination of rougher microstructure and a unique heat transfer mechanism, possibly linked to capillary wicking of liquid inside the nanochannels of the porous coating.
The falling film heat transfer enhancement ratio was found to increases as surface roughness was increased on plain tubes, suggested to be as a result of enhanced microlayer evaporation from the trapped sliding bubbles in the thin flowing film.
The nanoFLUX and CuO surfaces experienced lower critical heat flux as a result of departure from nucleate boiling under pool boiling and falling film boiling conditions compared with plain surfaces.. However, the nanoFLUX and CuO tubes performed well in terms of critical dryout at lower heat fluxes. The wicking capabilities of the nanoFLUX and CuO surfaces were thought to be the cause of their improved dryout capabilities at lower heat fluxes, but increased heat fluxes possibly led to dryout of the nanostructures resulting in operation in the Cassie-Baxter state and subsequent reduced wettability.Thesis (PhD)--University of Pretoria, 2020.
Mechanical and Aeronautical Engineering
PhD (Mechanical Engineering)
Unrestricted
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Ben, Marai Achraf. "Etude et élaboration des nanoparticules Cu (In,Ga) (Se)₂ préparées par voie solvothermale et déposées en couches minces par rf-magnétron sputtering." Thesis, Perpignan, 2016. http://www.theses.fr/2016PERP0022.
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L’une des solutions proposées pour la diminution du coût par watt d'électricité produite par le photovoltaïque est de réduire la quantité des matériaux semiconducteurs entrants dans la fabrication de la cellule solaire. La 3ème génération des cellules solaires en couches minces nanostructurées vient pour répondre à cette exigence. Les matériaux CIGS sous leurs structures chalcopyrites, sont de nouveaux matériaux semiconducteurs fortement recommandés pour la fabrication des cellules solaires à base de couches minces. La synthèse par la méthode de pulvérisation cathodique et la caractérisation de ces derniers matériaux ont été l’objectif général de cette thèse. Toutes les couches ont été déposées grâce à une seule cible constituée par des grains nanométriques de CIGS, ces derniers ont été obtenus par la voie solvothermale. Dans la première partie de ce travail, nous avons étudié l’effet des différents paramètres de synthèse (température, durée de synthèse, le traitement thermique et l’effet du taux molaire de gallium et d’indium) sur les propriétés des nanoparticules CIGS, les mécanismes réactionnels mis en jeu ont été aussi étudié. Les conditions de synthèse optimales sont une température et une durée de synthèse égale à 220 °C et 24 heures. Après un traitement thermique, les nanoparticules de CIGS sont cristallisées suivant la structure chalcopyrite, avec l’absence des pics correspond aux phases secondaires, les diamètres des grains varie entre 15 et 30 nm. Dans la deuxième partie, Nous sommes intéressés à l’élaboration et la caractérisation des couches absorbantes ternaire et quaternaire de type CIS et CIGS (x = 0 et x = 0.3) obtenues par pulvérisation cathodique en variant la puissance de dépôt de 60 à 100 W. Toutes les couches élaborées présentent la phase chalcopyrite avec (112) comme axe d’orientation préférentiel de croissance. La taille moyenne des grains a le même ordre de grandeur que les poudres initiales. Les couches de CIGS sont généralement de type de conduction p avec des faibles valeurs de résistivités. Les caractérisations optiques des couches présentent une bonne absorption de l’ordre de 95 % dans la gamme de visible et le proche infra-rouge. La variation du coefficient d’absorption en fonction de l’énergie du photon, nous a permis de déterminer l’énergie du gap optique. Les valeurs obtenues pour les différentes couches sont cohérentes avec l’optimum pour la conversion photovoltaïqueOne of the proposed solutions for reducing the cost of electricity produced by the photovoltaic is to reduce the amount of incoming semiconductor materials in the manufacture of the solar cell. The 3rd generation solar cells based on nanostructured thin film come in response to this requirement. CIGS under their structures chalcopyrite are highly recommended for the manufacture of this solar cells type. The synthesis of these materials using sputtering method and their characterization were the overall goal of this thesis. All films were deposited onto glass substrates from single target composed trough nanoparticles of CIGS, which are obtained by the solvothermal route. In the first part of this work, we studied the effect of different synthesis parameters (temperature, synthesis time, the heat treatment and the effect of the molar ratio of gallium and indium) on the properties of CIGS nanoparticles. The reaction mechanisms were also studied. The optimum synthesis conditions are a temperature and a synthesis time equal to 220 ° C and 24 hours. After heat treatment, the nanoparticles are crystallized according CIGS chalcopyrite structure, with the absence of the peaks corresponding to the secondary phases, grain size between 15 and 30 nm. In the second part, we are interested in the deposition and characterization of ternary and quaternary absorbent thin film CIS and CIGS (x = 0 and x = 0.3) obtained by sputtering deposition by varying the power of pulverization from 60 to 100 W. All layers have crystallized in the chalcopyrite structure with the preferential orientation in the (112) plane were obtained. The average grain size has the same order of magnitude as the initial powders. All films are generally p-type conduction with low resistivity values. Optical characterizations of the layers exhibit a good absorption in the visible range and the near infrared. The variation of the absorption coefficient as a function of photon energy enabled us to determine the energy of the optical gap. The values obtained for the different layers are consistent with the optimum for the photovoltaic conversion
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Liu, Yanqing. "Thermal engineering in an epitaxial nanostructured germanium semiconductor." Thesis, Université Grenoble Alpes (ComUE), 2015. http://www.theses.fr/2015GREAY082/document.
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Ce travail de thèse porte sur les propriétés de transport thermique liées aux phonons dans un nouveau matériau nanostructuré constituée de couches minces de Ge:Mn de type "electron crystal - phonon glass". Ce matériau est élaboré par épitaxie par jets moléculaire au CEA/INAC à Grenoble sur des substrats spécifiques « Germanium-on-insulator (GOI) ». Il consiste en une matrice de germanium possédant une qualité cristalline parfaite dans laquelle sont inclues une importante concentration de nano-inclusions de Ge3Mn5 de forme quasi-sphérique. Révélé par les caractérisations de TEM, les nano-inclusions ont une distribution de diamètre variant de 5 à 50 nm. Il est par ailleurs possible de jouer sur les paramètres de croissance afin de modifier la dispersion de taille des inclusions ainsi que leur concentration. Cette possibilité nous a donc permit d'étudier l'influence des nano-inclusions sur le transport de chaleur de façon exhaustive autour de la température ambiante.Pour ce faire, une expérience de mesure de conductivité thermique « 3 omega » dédiée à ces échantillons et extrêmement sensible, a été fabriquée à l'institut Néel. Cette expérience nous a permis de mesurer les variations de conductivité thermique induites par la modification de la distribution en taille des nano-inclusions de Ge:Mn dans des couches minces d'une centaine de nanomètre d'épaisseur avec une erreur réduite d'environ 12%. Il a été montré que le transport thermique dans ces couches minces pouvait être réduit d'un facteur 20 comparé au germanium massif puisque des valeurs de conductivité thermique de l'ordre de 3 W.m-1.K-1 ont été mesurées. Ces valeurs ont été confirmées par des expériences SThM au CETHIL de Lyon. Les valeurs obtenues sont mêmes en dessous de la limite d'alliage pour le SiGe, ce qui n'est pas explicable par les théories actuelles. Ces faibles conductivités thermiques ainsi que la grande mobilité des porteurs dans le germanium font de ces matériaux à base de GeMn de bons candidats pour la thermoélectricité. Des simulations numériques ont été utilisées afin de mieux comprendre cette diminution spectaculaire de la conductivité thermique et d'interpréter les données expérimentalesThis PhD project is an exhaustive study on the characterization of the thermal properties of a new type semiconducting materials based on germanium. It is a germanium matrix containing nano-inclusions with the objective of creating a perfect "electron crystal - phonon glass" material. The materials are thin films of an epitaxial germanium matrix embedded with Ge:Mn nano-inclusions, grown on a Germanium-on-insulator (GOI) substrate in CEA/INAC in Grenoble. From TEM images of the thin films it has been demonstrated that both the matrix and inclusions are monocrystalline, and the nano-inclusions have generally a spherical form with a diameter distribution ranging from 5 to 50 nm. Depending on the growth parameters in molecular beam epitaxy, i.e. the Mn concentration and the annealing temperature, the geometries, mean diameters and diameter distributions of nano-inclusions in Ge:Mn can be varied. With these unique structural features, these Ge:Mn thin films are one of the most interesting models for the study of the influence of nano-inclusions on thermal transport in a crystalline matrix.The characterization of the thermal properties of the material have been done using two advanced techniques: the 3-omega method in Institut Néel, and the Scanning Thermal Microscopy (SThM) in CETHIL (Centre d'Energétique et de Thermique de Lyon) in Lyon. A highly sensitive differential 3-omega measurement setup has been developed in the work, which permits precise (error~12%) measurements of electrical conductive thin films having low thermal conductivities. Dramatically reduced thermal conductivities have been revealed for Ge:Mn thin films containing different Mn% and having different inclusion geometries at room temperature, compared to crystalline bulk Ge. A minimum value of 3.3 Wm-1K-1 was found for Ge:Mn thin film containing 10% Mn, beating the “alloy limit” of thermal conductivity set by SiGe alloys at room temperature (6-12 Wm-1K-1). The measurement results of SThM confirmed the low thermal conductivities for all Ge:Mn/GOI samples at room temperature. Numerical simulations using different models have been performed to try to interpret the experimental results and to understand the mechanisms of the influence of the nano-inclusions on the phonon transport in semiconductor materials
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Porto, Ledilege Cucco. "Etude de films minces et de nanoparticules obtenus par auto-assemblage de copolymères à blocs et leurs interactions avec un oligo/polysaccharide." Thesis, Grenoble, 2011. http://www.theses.fr/2011GRENU011/document.
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Ce travail décrit la séparation de microphase à l'état solide d'un copolymère dibloc comprenant un bloc hautement biocompatible poly [2 - (méthacryloyloxy) éthyl phosphorylcholine] et un bloc pH-sensible poly [2 - (diisopropylamino) méthacrylate d'éthyle] (PMPC-b-PDPA). L'auto-assemblage d'un copolymère dibloc amphiphiles à base de polystyrène (PS) et le poly (acide acrylique) (PAA), a été étudié en suspension aqueuse, et leur décoration par du chitosane, afin de vérifier leur capacité à encapsuler et à libérer par voie transdermique la finastéride, une molécule stéroïdiens inhibiteur de la enzyme 5-alpha-réductase, qui a été recommandée pour le traitement de l'alopécie androgénétique. La morphologie des films PMPC30-b-PDPA60 a été analysée par SAXS et (S) TEM. Films du PMPC30-b-PDPA60 préparés dans une solution de l'éthanol à température ambiante présentent une morphologie cylindrique, qui subit une transition ordre-ordre sur un recuit thermique à 170 ° C: la structure lamellaire résultant coexiste avec une proportion de cylindres organisée dans une phase hexagonale compacte. En revanche, les films du copolymère préparé à partir de méthanol ne subissent pas la même transition morphologique, résultant dans des structures mal organisées, indépendante de traitement thermique. Enfin, les structures lamellaires sont obtenues directement à partir d'une solution aqueuse à pH 4, sans traitement thermique. Ces systèmes offrent une nouvelle alternative pour la fabrication de structures lamellaires constituées d'un matériau biomimétique et anti-fouling, élargissant l'éventail des possibilités dans le domaine de l'ingénierie macromoléculaire.Une autre stratégie adoptée dans ce travail a été basé sur le développement de nanoparticules bien organisé avec des propriétés de surface nature bioinspirés, formé entre polymersomes chargés négativement à base des copolymères à blocs de polystyrène (PS) et le poly (acide acrylique) (PAA) décorés avec du chitosane, un polysaccharide de charge opposée. Le rôle de l'adsorption du chitosane avec deux poids moléculaires distincts (chitosane oligosaccharides et du chitosane avec un faible poids moléculaire) sur la surface des nanoparticules PS139-b-PAA17 et des nanoparticules PS404-b-PAA63 ont été démontrés par diffusion dynamique de la lumière, potentiel zêta et caractérisation morphologiques. En présence du chitosane, le potentiel zêta de polymersomes devient positif. Ce résultat a été interprété en termes d'interactions électrostatiques, qui induisent une adsorption du chitosane sur la surface des polymersomes. Ce résultat a été confirmé par une observation comparative par microscopie entre des polymersomes et des polymersomes décorées. Polymersomes avec un diamètre <200 nm et une distribution granulométrique relativement étroite ont été obtenus pour les deux systèmes. L'effet de la décoration des nanoparticules par du chitosane sur la perméation cutanée in vitro du finastéride, incorporé dans la paroi hydrophobe de polymersomes, a également été évaluée. La pénétration cutanée du finastéride a été estimée par les paramètres de perméabilité tels que le flux, temps de latence et du coefficient de perméabilité de la finastéride. Une amélioration de la perméation du finastéride à partir des nanoparticules a été observée, en particulier à partir de nanoparticules décorées avec du chitosane. Le polymersome PS404-b-PAA63 décorées avec du chitosane semble être le système le plus approprié car il favorisé une meilleure rétention du médicament dans la peau et les faibles valeurs de flux de perméation, suggérant que le système fournit un véhicule de remplacement pour l'administration transdermique de finastérideThis work describes the microphase separation in bulk of an diblock copolymer comprising a highly biocompatible poly[2-(methacryloyloxy)ethyl phosphorylcholine] block and a pH-sensitive poly[2-(diisopropylamino) ethyl methacrylate] block (PMPC-b-PDPA). The self-assembly of an amphiphilic diblock copolymer based on polystyrene (PS) and poly(acrylic acid) (PAA) was studied in terms of their decoration with the chitosan, verifying their ability to incorporate and transdermally release the drug finasteride, a steroidal molecule 5-alpha-reductase inhibitor that has been recommended for the treatment of androgenetic alopecia. The morphology of PMPC30-b-PDPA60 films was analyzed using SAXS and (S)TEM. PMPC30-b-PDPA60 films cast from ethanol solution at room temperature exhibit a thermodynamically quasi-stable cylindrical morphology, which undergoes an order-order transition upon thermal annealing at 170 oC: the resulting lamellar structure coexists with a minor proportion of cylinders organized into a hexagonal compact phase. In contrast, copolymer films cast from methanol do not undergo the same morphological transition. Instead, short-range liquid-like structures are obtained regardless of the annealing processes. Finally, direct self-assembly to form a lamellar morphology at room temperature can be achieved by solvent-casting from aqueous solution at pH 4. These systems offer a new alternative for the fabrication of lamellar structures in which one layer is biomimetic and non-fouling, expanding the range of possibilities in the macromolecular engineering field. Another strategy adopted in this work was based on the development of well-organized nanoparticles with nature-bioinspired surface properties, formed between negatively charged polymersomes based on polystyrene (PS) and poly(acrylic acid) (PAA) block copolymers decorated with chitosan, an oppositely charged polysaccharide. The role of chitosan with two distinct molecular weights (chitosan oligosaccharide and low molecular weight chitosan) adsorption on the surface of oppositely charged PS139-b-PAA17 and PS404-b-PAA63 nanoparticles were demonstrated by dynamic light scattering measurements, zeta potential and morphological characterization. In the presence of chitosan, the zeta potential of polymersomes becomes positive. This result was interpreted in terms of electrostatic interactions, which induce a flat adsorption of the chitosan on the surface of the polymersomes. This result was further confirmed by a comparative observation by microscopy of bare and chitosan-decorated polymersomes. Polymersomes with a diameter < 200 nm and a relatively narrow size distribution were obtained for both systems. The effect of chitosan decoration of self-assembled nanoparticles on skin penetration in vitro of finasteride was also evaluated, once incorporated in the wall hydrophobic of polymersomes. The skin permeation through pig ear skin of finasteride was estimated by the permeability parameters such as flux, lag time and permeability coefficient of finasteride. An improved permeation of finasteride from the nanoparticle system was observed, especially from nanoparticles decorated with chitosan. The PS404-b-PAA63 polymersome decorated with chitosan seems to be the most appropriate system since it provided higher drug retention in skin and low permeation flux values, suggesting that the PS-b-PAA/chitosan system provides an alternative for transdermal drug delivery system of finasteride
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Zhang, Yuelan. "Synthesis and Characterization of Nanostructured Electrodes for Solid State Ionic Devices." Diss., Georgia Institute of Technology, 2006. http://hdl.handle.net/1853/14000.
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The demands for advanced power sources with high energy efficiency, minimum environmental impact, and low cost have been the impetus for the development of a new generation of batteries and fuel cells. One of the key challenges in this effort is to develop and fabricate effective electrodes with desirable composition, microstructure and performance. This work focused on the design, fabrication, and characterization of nanostructured electrodes in an effort to minimize electrode polarization losses.
Solid-state diffusion often limits the utilization and rate capability of electrode materials in a lithium-ion battery, especially at high charge/discharge rates. When the fluxes of Li+ insertion or extraction exceed the diffusion-limited rate of Li+ transport within the bulk phase of an electrode, concentration polarization occurs. Further, large volume changes associated with Li+ insertion or extraction could induce stresses in bulk electrodes, potentially leading to mechanical failure. Interconnected porous materials with high surface-to-volume ratio were designed to suppress the stress and promote mass transport. In this work, electrodes with these unique architectures for lithium ion batteries have been fabricated to improve the cycleability, rate capability and capacity retention.
Cathodic interfacial polarization represents the predominant voltage loss in a low-temperature SOFC. For the first time, regular, homogeneous and bimodal porous MIEC electrodes were successfully fabricated using breath figure templating, which is self-assembly of the water droplets in polymer solution. The homogeneous macropores promoted rapid mass transport by decreasing the tortuosity. And mesoporous microstructure provided more surface areas for gas adsorption and more TPBs for the electrochemical reactions. Moreover, composite electrodes were developed with a modified sol-gel process for honeycomb SOFCs. The sol gel derived cathodes with fine grain size and large specific surface area, showed much lower interfacial polarization resistances than those prepared by other existing processing methods.
Nanopetals of cerium hydroxycarbonate have been synthesized via a controlled hydrothermal process in a mixed water-ethanol medium. The formation of the cerium compound depends strongly on the composition of the precursors, and is attributed to the favored ethanol oxidation by Ce(IV) ions over Ce(IV) hydrolysis process. Raman studies showed that microflower CeO2 preferentially stabilizes O2 as a peroxide species on its surface for CO oxidation.
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Tian, Yayang. "Elaboration of New Layer by Layer (LbL) Fluorescent thin films and their functionalization for the sensitive detection of bacteria." Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLN029/document.
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Les antibiotiques ont été utilisés pour le traitement des infections bactériennes depuis plus de 70 ans, sauvant des millions de vies. Cependant, leur mauvaise et sur-utilisation ont conduit à l’émergence de la résistance bactérienne. Outre le développement de nouvelles familles d'antibiotiques, la détection rapide et sensible de bactéries est très importante pour le diagnostic médical. Les polymères fluorescents représentent un grand potentiel, car ils sont faciles à fonctionnaliser, synthétiser et greffer. Les films sont plus pratiques, faciles à manipuler et peuvent être réutilisés, ce qui n'est pas le cas des méthodes de détection en solution. L’objectif de ce travail est de développer un film de polymère nanostructuré fluorescent et sensible sur des surfaces de verre pour la détection bactérienne. Sur la base de la méthode de polymérisation radicalaire par transfert de chaîne réversible par addition-fragmentation (RAFT), trois types de polyélectrolytes fluorescents à base de BODIPY (FPC) ont été synthétisés : des chaînes relativement courtes à caractère polyélectrolyte faible (SW FPC), des chaînes courtes à caractère polyélectrolyte fort (SS FPC) et enfin des chaînes longues à caractère polyélectrolyte faible (FPC LW). Les films FPC LbL ont été élaborés sur des lames en verre par interaction électrostatique. Les propriétés photophysiques et de surface des FPC LbL ont été contrôlées en ajustant les conditions de dépôt. Les films FPC LbL à base de BODIPY ont été utilisés comme dispositif de première génération pour la détection de E. coli. Dans l'étape suivante, la sensibilité des films a été augmentée en utilisant le principe de fluorescence exaltée par plasmon (Metal Enhanced Fluorescence MEF). Un film LbL -MEF a été préparé et testé pour la détection de bactéries. Des nanoparticules d'or sphériques (Au NPs) ont été synthétisées et recouvertes de poly(chlorhydrate d'allylamine) (PAH). Le FPC LW a été sélectionné comme couche fluorescente. Différents films contenant des Au NPs et LW FPC- ont été fabriqués. La distance entre les NPs Au et LW FPC- a été ajustée par l'ajout de deux polymères de charge opposée (PC + et PC-). Les deux surfaces de AuNP / 4 couches PC / LWFPC- et Au NPs / 8 couches PC / LWFPC- ont montré que E. coli peut être ciblée par LW FPC-.La sélectivité des films LbL a été ajoutée en introduisant un anticorps comme site de reconnaissance spécifique. Le polyanion et le polycation avec le groupe fonctionnel 4-dibenzocyclooctynol (DIBO) ont été assemblés sur des lames de verre activées. L'anticorps anti-E. coli a ensuite été introduit sur la surface en une seule étape via la réaction de cycloaddition azide-alcyne (SPAAC). Le nombre d'E. coli capturées dépend de la concentration d’anticorps sur la surface. La surface a montré une sélectivité significative pour E. coli, comparée à B. subtilis.La croissance bactérienne peut être détectée sur un film mince LbL en introduisant un fluorophore sensible au pH (fluorescéine). En effet, la croissance des bactéries est souvent associée à une diminution du pH du milieu due à une libération de métabolites acides. Nous avons préparé avec succès différents types de films LbL sensibles au pH. Dans un premier temps, la synthèse de différents polyanions fonctionnalisés (chaîne courte et longue de DIBO-PC et polymère fluorescent rouge) a été achevée. Ensuite, trois types de surfaces sensibles au pH contenant de la fluorescéine (DIBO-SWPC- / fluorescéine, DIBO-LW PC- / fluorescéine et ratiométrique RFPC- / fluorescéine) ont été préparés sur la base d'assemblage LbL et de chimie click. Enfin, trois surfaces sensibles au pH ont été étudiées pour la détection de la croissance des bactéries. Toutes les surfaces étaient biocompatibles, le nombre de E. coli augmentait même après plusieurs heures d'incubation sur chaque surface. La détection par le changement de fluorescence est en cours de développementAntibiotics have been used for the treatment of bacterial infections for over 70 years, saving millions of lives. The current antibiotic resistance crisis has been attributed to the overuse and misuse of these medications. Therefore, the prevention of infection transmission by the rapid and sensitive detection of antibiotic resistant strains is needed in managing this crisis. Fluorescent polymers show great potential for bacteria detection, because they are easy to functionalize, reproduce and graft. Compared with the methods used for bacterial detection in liquid, bacterial detection on a film surface is more convenient, easier to handle and is applied in devices that can be easily reused. The goal of my PhD work is to develop fluorescent and sensitive nanostructured polymer films on surfaces for bacterial detection. Three types of BODIPY-based fluorescent polyelectrolytes (FPC) with different features were synthetized based on reversible addition-fragmentation transfer (RAFT) polymerization: relatively Short chains and Weak polyelectrolytes (SW FPC), Short chains and Strong polyelectrolytes (SS FPCs) and Long chains and Weak polyelectrolytes (LW FPCs). FPC LbL films were fabricated on activated glass slides by means of electrostatic attraction. The photophysical and surface properties of FPC LbL fims were easily controlled by adjusting the deposition conditions.The following step aimed at increasing the films’ sensitivity by using the metal-enhanced fluorescence (MEF) principle. A MEF based LbL film was prepared and tested for bacteria detection. Spherical gold nanoparticles (Au NPs) were synthesized and coated with poly(allylamine hydrochloride) (PAH). The LW FPC- was selected as the fluorescent layer. Different films containing Au NPs and LW FPC- were fabricated and the distance between the Au NPs and LW FPC- was adjusted by changing the numbers of layers with two oppositely charged polymers (PC+ and PC-). Both Au NPs/4 layers PCs/LWFPC- and Au NPs/8 layers PCs/LWFPC- surfaces indicated that E. coli can be detected by LW FPC-.The selectivity of LbL films was added by introducing an antibody on the surface of the film to provide specific recognition of a chosen bacterial strain. This LbL surface achieved a rapid, effective and specific detection of E. coli bacteria. The polyanion and polycation with a 4-dibenzocyclooctynol (DIBO) functional group were assembled on the activated glass slides and an anti-E. coli antibody containing an azide group was efficiently introduced on the surface in a single step based on the azide-alkyne cycloadditions (SPAAC) reaction. The number of E. coli captured on the surface was shown to be dependent on the amount of antibody on the surface. The anti-E. coli antibody surface showed significant selectivity for E. coli, compared with B. subtilis. An alternative approach is to detect bacterial growth on thin LbL film by introducing pH sensitive fluorophore (fluorescein). The growth of bacteria is often associated with a decrease in pH of the growth medium due to a release of acidic metabolites. Different types of pH sensitive LbL film were prepared and tested for the detection of bacterial growth. Firstly, the synthesis of different functionalized polyanions (short and long chain of DIBO-PC- and red fluorescent polymer) was carried out. Three types of pH sensitive surfaces containing fluorescein (DIBO-SWPC-/fluorescein, DIBO-LW PC-/fluorescein and ratiometric RFPC-/fluorescein surfaces) were prepared based on the combination of LbL assembly and copper-free click chemistry. Finally, three pH sensitive surfaces were studied for bacteria growth detection. All the surfaces were shown to be biocompatible, the number of E. coli increased after several hours of incubation on each surface, as detected by brightfield microscopy imaging. The application for the fluorophore-dependent detection of bacterial growth remains to be developed
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Schulze, Carsten. "Magnetization Reversal in Film-Nanostructure Architectures ." Doctoral thesis, Universitätsbibliothek Chemnitz, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-142720.
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The concept of percolated perpendicular media (PPM) for magnetic data storage is expected to surpass the areal storage density of 1 Tbit in -², which is regarded as the fundamental limit of conventional granular CoCrPt:oxide based recording media. PPM consist of a continuous ferromagnetic thin film with densely distributed defects acting as pinning sites for magnetic domain walls.
In this study, practical realizations of PPM were fabricated by the deposition of [Co/Pt]8 multilayers with perpendicular magnetic anisotropy onto nanoperforated templates with various perforation diameters and periods. The structural defects given by the templates serve as pinning sites for the magnetic domain walls within the [Co/Pt]8 multilayers. Magnetometry at both the integral and the local level was employed to investigate the influence of the template on the magnetization reversal and the domain wall pinning.
It was found, that magnetic domains can be pinned at the ultimate limit, between three adjacent pinning sites. The coercivity and the depinning field, which both are a measure for the strength of the magnetic domain wall pinning, were found to increase with increasing perforation diameter. The size of magnetic domains within the magnetic film appeared not to depend solely on the diameter of the nanoperforations or on the period of the template, but on the ration between diameter and period. By means of micromagnetic simulations it was found, that the presence of ferromagnetic material within the pinning site given supports the pinning of magnetic domain walls, compared to a pinning site that is solely given by a hole in the magnetic thin film.
Investigation of the evolution of the magnetization in magnetic fields smaller than the coercive field revealed, that the energy barrier against thermally induced magnetization reversal is sufficiently large to provide long-term (> 10 years) stability of an arbitrary magnetization state. This could also be qualitatively supported by micromagnetic simulations.
Static read/write tests with conventional hard disk recording heads revealed the possibility of imprinting bit patterns into the PPM under study. The minimum bit pitch that could be read back thereby depended on the period of the nanoperforated template.
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Ramos, Chagas Gabriela. "Polymères électrodéposés nanostructurés : design et propriétés de films dérivés de monomères du thienothiophène et du pyrène." Thesis, Université Côte d'Azur (ComUE), 2017. http://www.theses.fr/2017AZUR4108/document.
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Le contrôle de l'hydrophobie de surface et de l'adhésion à l'eau est un outil fondamental pour diverses applications. L'électropolymérisation est une méthode très polyvalente qui peut être utilisée pour contrôler ces paramètres et pour la production de matériaux nanostructurés à façon. Ici, nous montrons qu'en différentiant le noyau polymérisable (thienothiophène ou pyrène), des morphologies et des mouillabilités de surface variées sont produites par un procédé direct d'électropolymérisation. Des nanotubes et des structures en forme d'arbre sont obtenus en utilisant des dérivés de thienothiophène sans utiliser de membrane structurante. En fonction de la méthode d'électrodéposition et des paramètres, différents types de nanotubes sont obtenus. La méthode électrochimique et le substituant greffé jouent un rôle important dans la structuration de surface. Les surfaces affichent différents angles de contact, mais toujours une forte adhésion à l'eau. D'autre part, des pyrènes avec divers substituants sont utilisés pour conduire à des propriétés hydrophobes/superhydrophobes, fluorescentes et, pour la première fois, à des applications en anti-bioadhesion et anti-biofilm. Des copolymères de pyrène ont été électrodéposés pour donner des surfaces avec une sensibilité au pH et une adhérence contrôlable à l'eau. Une nouvelle méthode utilisant un système de catapult a été mise en œuvre pour mesurer le comportement adhésif de surfaces collantes et non collantes. Ainsi, il a été montré le rôle important du noyau de monomère sur les propriétés finales des surfaces ouvrant de nouvelles portes pour explorer ce domaine dans le domaine des sciences de surface et de leurs applicationsControlling surface hydrophobicity and water adhesion is a fundamental tool for various applications. Electropolymerization is a very versatile method that can be used to control these parameters and for the production of tunable nanostructured materials. Here, we show that by differentiating the polymerizable core (thienothiophene or pyrene), varied surface morphologies and wettabilities are produced by a direct electropolymerization process. Nanotubes and tree-like structures are obtained starting from thienothiophene derivatives without using any template. Depending on the electrodeposition method and parameters, different kinds of nanotubes are obtained. The electrochemical method and the grafted substituent play an important role on the surface structuration. The surfaces display different contact angles, but always with high water adhesion. On the other hand, pyrenes with various substituents are employed to produce hydrophobic/ superhydrophobic and fluorescent surfaces and, for the first time, with anti-bioadhesion and anti-biofilm properties. Copolymers of pyrenes were electrodeposited to yield surfaces with pH-responsivity and controllable water adhesion. A new method using a catapult system was implemented to measure the adhesive behavior of sticky and non-sticky surfaces. Thus, it has been shown the important role of the monomer core on the final properties of the surfaces opening new doors to explore this domain in the surface science field and applications
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Giroud-Garampon, Cedric. "Réalisation et étude des propriétés thermoélectriques de couches minces et nanofils de types Bi2-XSbxTe3 et Bi2Te3-xSex." Phd thesis, Université de Grenoble, 2011. http://tel.archives-ouvertes.fr/tel-00576282.
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De récentes études montrent que les films minces présentent des performances thermoélectriques nettement plus importantes (jusqu'à un facteur 3) que celles obtenues dans les matériaux massifs. Nous avons choisi de développer des couches minces thermoélectriques Bi0,5Sb1,5Te3 de type p et Bi2Te2,7Se0,3 de type n présentant les performances thermoélectriques les plus intéressantes à des températures proches de l'ambiante. La technique de dépôt utilisé est la PVD magnétron. L'optimisation des conditions de dépôt (pression Ar, puissance plasma, distance cible-substrat et temps de dépôt) ainsi que du traitement thermique de recuit a permis obtenir des figures de mérite ZT les plus élevées possibles. De plus, les phénomènes physiques mis en jeu dans les films minces étant différents de ceux des massifs, il a été nécessaire des les étudier pour améliorer les performances thermoélectriques des couches minces. De petits dispositifs thermoélectriques en couche minces ont pu être réalisé et caractérisé. En parallèle nous avons exploré la possibilité de faire croître des filaments thermoélectriques de compositions semblables aux couches et de dimensions manométriques au sein d'une matrice d'alumine nanoporeuse. En effet la réduction des dimensions géométriques permet d'augmenter les performances thermoélectriques des matériaux. Nous avons pu réaliser les premiers fils n et p ainsi que les premières caractérisations thermoélectriques.
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Douglas, C. D. "Nanostructured media on thin film porous alumina." Thesis, Queen's University Belfast, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.419568.
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Carlier, Thomas. "Croissance de couches minces et de nanostructures piézoélectriques A2WO6 (A=lanthanide) par ablation laser et caractérisation nanométrique par microscopie à force atomique." Thesis, Artois, 2016. http://www.theses.fr/2016ARTO0407/document.
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Afin de répondre à l’essor des nanotechnologies dans le domaine des capteurs et du stockage de l’information, la recherche de nouveaux matériaux éco-acceptables, sous forme de films minces et possédant de hautes performances s’inscrit dans une politique environnementale toujours plus présente.Le but de ce travail est donc double : (i) synthétiser des films minces d’oxydes de A2WO6 (A = lanthanide) et d’en démontrer le caractère piézo-/ferroélectrique à l’échelle locale ; (ii) nanostructurer ce type de matériau par une approche « bottom-up ».Cette thèse a débuté par l’étude de ces oxydes sous forme massive et notamment de leur comportement en température. À la suite de cette étude, des films minces de La2WO6 ont été synthétisés par ablation laser pulsé sur des substrats de SrTiO3 et de LaAlO3 orientés (100). La caractérisation structurale par diffraction de rayons X haute résolution et par microscopie électronique en transmission a permis de déterminer les paramètres de maille ainsi que les relations d’épitaxie de ces films. Par la suite, le caractère piézo-/ferroélectrique des films de α-La2WO6 haute température a été confirmé à l’échelle locale par microscopie à force piézoélectrique ainsi que par TEM-STM in situ. Le composé Nd2WO6 présente également toutes les caractéristiques d’un matériau piézoélectrique. Enfin, la nanostructuration via un masque en nitrure de silicium et l’ablation laser pulsé a permis la fabrication d’îlots piézoélectriques de La2WO6 de diamètres de 1,2 μm et 450 nm. Ces résultats prometteurs font des oxydes A2WO6 des candidats de choix pour la conception de nano-dispositifs piézo-/ferroélectriquesWith the development of nanotechnology in the field of sensors and information storage, the research for new eco-friendly materials in the form of thin films with high performances is part of an ever present environmental policy. The purpose of this work is twofold. It is (i) to synthesize oxide thin films of A2WO6 (A = lanthanide) and to demonstrate the local piezo / ferroelectric behavior; (ii) to nanostructure this type of material by using a "bottom-up" approach. Thus this thesis has began by studying the behavior of these oxides in bulk form, considering particularly the temperature and pressure effects. As a result, La2WO6 thin films were grown by pulsed laser deposition on (100)-oriented SrTiO3 and LaAlO3 substrates. The structural characterization by X-ray diffraction high resolution and transmission electron microscopy was used to determine the lattice parameters and the epitaxial relationships of these films. Thereafter, the piezo / ferroelectric behavior of high temperature α-La2WO6 film was locally confirmed by piezoelectric force microscopy and transmission electronic microscopy combined with the scanning tunneling microscopy. The Nd2WO6 compound has also the characteristics of a piezoelectric material. Finally, the nanostructuration by combining a silicon nitride mask and the pulsed laser deposition technique has enabled the fabrication of La2WO6 piezoelectric islands with diameters of 1.2 μm and 450 nm. These promising results make A2WO6 oxides ideal candidates for the design of piezo / ferroelectric nanodevices
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Cotier, Bradley Neville. "Fullerene nanostructures, monolayers and thin films." Thesis, University of Nottingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.342471.
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Chung, Tien-Kan. "Magnetoelectric coupling in layered thin film and nanostructure." Diss., Restricted to subscribing institutions, 2009. http://proquest.umi.com/pqdweb?did=1835573651&sid=1&Fmt=2&clientId=1564&RQT=309&VName=PQD.
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Vandamme, Nicolas. "Nanostructured ultrathin GaAs solar cells." Thesis, Paris 11, 2015. http://www.theses.fr/2015PA112111/document.
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L’amincissement des cellules solaires semi-conductrices est motivé par la réduction des coûts de production et l’augmentation des rendements de conversion. Mais en deçà de quelques centaines de nanomètres, il requiert de nouvelles stratégies de piégeage optique. Nous proposons d’utiliser des concepts de la nanophotonique et de la plasmonique pour absorber la lumière sur une large bande spectrale dans des couches ultrafines de GaAs. Nous concevons et fabriquons pour ce faire des structures multi-résonantes formées de réseaux de nanostructures métalliques. Dans un premier temps, nous montrons qu’il est possible de confiner la lumière dans une couche de 25 nm de GaAs à l’aide d’une nanogrille bidimensionnelle pouvant servir de contact électrique en face avant. Nous analysons numériquement les modes résonants qui conduisent à une absorption moyenne de 80% de la lumière incidente entre 450 nm et 850 nm. Ces résultats sont validés par la fabrication et la caractérisation de super-absorbeurs ultrafins multi-résonants. Dans un second temps, nous appliquons une approche similaire dans le but d’obtenir des cellules photovoltaïques dix fois plus fines que les cellules GaAs records, avec des absorbeurs de 120 nm et 220 nm seulement. Un miroir arrière nanostructuré en argent, associé à des contacts ohmiques localisés, permet d’améliorer l’absorption tout en garantissant une collecte optimale des porteurs photo-générés. Nos calculs montrent que les densités de courant de court-circuit (Jsc) dans ces structures optimisées peuvent atteindre 22.4 mA/cm2 et 26.0 mA/cm2 pour les absorbeurs d’épaisseurs respectives t=120 nm et t=220 nm. Ces performances sont obtenues grâce à l’excitation d’une grande variété de modes résonants (Fabry-Pérot, modes guidés,…). En parallèle, nous avons développé un procédé de fabrication complet de ces cellules utilisant la nano-impression et le transfert des couches actives. Les mesures montrent des Jsc records de 17.5 mA/cm2 (t=120 nm) et 22.8 mA/cm2 (t=220 nm). Ces résultats ouvrent la voie à l’obtention de rendements supérieurs à 20% avec des cellules solaires simple jonction d’épaisseur inférieure à 200 nmThe thickness reduction of solar cells is motivated by the reduction of production costs and the enhancement of conversion efficiencies. However, for thicknesses below a few hundreds of nanometers, new light trapping strategies are required. We propose to introduce nanophotonics and plasmonics concepts to absorb light on a wide spectral range in ultrathin GaAs layers. We conceive and fabricate multi-resonant structures made of arrays of metal nanostructures. First, we design a super-absorber made of a 25 nm-thick GaAs slab transferred on a back metallic mirror with a top metal nanogrid that can serve as an alternative front electrode. We analyze numerically the resonance mechanisms that result in an average light absorption of 80% over the 450nm-850nm spectral range. The results are validated by the fabrication and characterization of these multi-resonant super-absorbers made of ultrathin GaAs. Second, we use a similar strategy for GaAs solar cells with thicknesses 10 times thinner than record single-junction photovoltaic devices. A silver nanostructured back mirror is used to enhance the absorption efficiency by the excitation of various resonant modes (Fabry-Perot, guided modes,…). It is combined with localized ohmic contacts in order to enhance the absorption efficiency and to optimize the collection of photogenerated carriers. According to numerical calculations, the short-circuit current densities (Jsc) can reach 22.4 mA/cm2 and 26.0 mA/cm2 for absorber thicknesses of t=120 nm and t=220 nm, respectively. We have developed a fabrication process based on nano-imprint lithography and on the transfer of the active layers. Measurements exhibit record short-circuit currents up to 17.5 mA/cm2 (t=120 nm) and 22.8 mA/cm2 (t=220 nm). These results pave the way toward conversion efficiencies above 20% with single junction solar cells made of absorbers thinner than 200 nm
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Schulze, Carsten [Verfasser], Manfred [Akademischer Betreuer] Albrecht, Manfred [Gutachter] Albrecht, and Sibylle [Gutachter] Gemming. "Magnetization Reversal in Film-Nanostructure Architectures : Magnetization Reversal in Film-Nanostructure Architectures / Carsten Schulze ; Gutachter: Manfred Albrecht, Sibylle Gemming ; Betreuer: Manfred Albrecht." Chemnitz : Universitätsbibliothek Chemnitz, 2014. http://d-nb.info/1214302173/34.
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Ulianova, V. O., A. T. Orlov, and O. V. Bogdan. "Formation of ZnO Nanostructured Thin Film by Hydrothermal Method." Thesis, Sumy State University, 2013. http://essuir.sumdu.edu.ua/handle/123456789/35191.
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Formation of zinc oxide nanostructured thin films at different temperatures on Al-coated silicon and
lithium niobate substrates by hydrothermal method was presented. The comparison of morphology of
nanostructured thin films formed by hydrothermal and electrodeposition method was carried out. The opportunity
to use the hydrothermal method instead electrodeposition to obtain nanostructured films on a
conductive layer was shown. The dependence of morphology and crystallinity from growth temperature
was established using scanning electron microscopy and X-ray diffractometry. The application of synthesized
films as sensing layer of acoustic wave based and electrochemical sensors could enhance its sensitivity
to pollutants in gas or liquid phases by an active area increasing.
When you are citing the document, use the following link http://essuir.sumdu.edu.ua/handle/123456789/35191
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Sines, Paul B. "Fabrication of thin film nanoscale alumina templates." Morgantown, W. Va. : [West Virginia University Libraries], 2001. http://etd.wvu.edu/templates/showETD.cfm?recnum=2183.
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Thesis (M.S.)--West Virginia University, 2001.Title from document title page. Document formatted into pages; contains vii, 44 p. : ill. (some col.). Vita. Includes abstract. Includes bibliographical references (p. 35-37).