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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
71

Desenvolvimento da metodologia física de produção de nanopartículas do tipo núcleo@casca / Development of gas aggregation source and radial magnetron sputtering for the production of core@shell metallic nanoparticles

Lima, Valquiria Fernanda Gonçalves de 12 February 2019 (has links)
Nos últimos anos novas propriedades magnéticas, eletrônicas e ópticas, têm sido observadas em sistemas de nanopartículas (NPs) feitas de diferentes tipos de materiais. Em nanoestruturas do tipo núcleo@casca, a composição de um núcleo magnético com uma casca plasmônica apresenta características que lhe conferem promissor potencial para aplicações em áreas como eletrônica, biomédica, farmacêutica, óptica e catálise. Este trabalho apresenta uma nova abordagem para a produção de nanopartículas metálicas do tipo núcleo@casca pela combinação de técnicas físicas, o método de agregação gasosa e fontes de magnetron sputtering planar/radial. As NPs produzidas foram analisadas magneticamente por VSM e SQUID, sua morfologia por HRTEM, a sua composição por RBS e EDS, a sua estrutura cristalina por XRD e as propriedades ópticas por espectrofotometria de UV-Visível. Os resultados experimentais serão apresentados para o sistema Co@Cu, mas a técnica pode ser utilizada para produzir NPs compostas de outros elementos químicos. Em paralelo a produção de nanopartículas, o gerador de NPs foi totalmente reestruturado. Foram testadas diferentes aberturas de saída das nanopartículas, viabilizando uma deposição do material de forma homogênea em áreas maiores. As novas aberturas possuem formato cônico, plano e de grades (600 furos com diâmetros entre 50 µm e 224 µm). Através destas grades foi possível obter uma distribuição espacial homogênea de nanopartículas. A entrada de gás no gerador também foi modificada, a fim de otimizar a deposição dos aglomerados e obter uma reprodutibilidade na operação do equipamento. Foram testados diversos modos de entrada do gás: na lateral do copo, no centro em diferentes distâncias do alvo e por último na região em torno do alvo, sendo a última a melhor configuração obtida. / In recent years new magnetic, electronic and optical properties have been observed in nanoparticles (NPs) made of different conjugation of materials. In magnetic nanostructures of the core@shell type, the compound of a magnetic core and a plasmonic shell, provides many features with potential for applications in areas such as electronics, biomedical, pharmaceutical, optical and catalysis. This work presents a new approach to the production of metallic core@shell nanoparticles by the combination of physical techniques, the gas aggregation method and planar/radial magnetron sputtering sources. The produced NPs were magnetically analyzed by VSM e SQUID, the morphology by SEM and HRTEM, the stoichiometry by RBS and EDS, the crystal structure by XRD and UV-Visible spectrophotometry. The experimental results will be presented for the system Co@Cu but the technique can be used to produce NPs composed of other chemical elements. In parallel to the production of nanoparticles, the NPs generator has been completely redesigned. Different apertures were tested enabling deposition of homogeneous material in large areas. The nanoparticles are now spread on the substrate using the frontal apertures shaped as conical, plane and grids (600 holes ranging from 50 µm to 224 µm diameters). Through these grids we have obtained a homogeneous spatial distribution of NPs. The gas inlet in the NP generator was modified, in order to optimize the deposition of NPs and to obtain reproducibility in the operation of the equipment. Several gas injection modes were explored, as p.e. lateral; frontal to the center of the target at different distances; and finally through the gap of the sputtering gun, in parallel to the target surface. The last option was the best configuration.
72

Nouvelles plateformes plasmoniques pour la spectroscopie Raman exaltée de surface / Novel plasmonic substrates for Surface Enhanced Raman Spectroscopy

Haidar, Israa 14 October 2016 (has links)
Depuis la démonstration de l’extrême sensibilité de la spectroscopie Raman exaltée de surface (acronyme SERS en anglais) à la fin des années 90, un des défis actuels consiste à élaborer des substrats SERS actifs composés de nanoparticules ayant des formes anisotropes avec des pointes prononcées ou des nanoparticules couplées de manière contrôlée et reproductible. De tels systèmes génèrent en effet une forte exaltation du champ électromagnétique, respectivement sur les régions à fort rayon de courbure et au sein de l’interstice. Ce fort confinement du champ, on parlera de point chaud, est essentiel dans le but de détecter de très faibles quantités de molécules. L’objectif principal de ma thèse est de développer et de caractériser finement de nouveaux substrats SERS obtenus par des méthodes d’élaboration chimiques (fonctionnalisation de surface) de substrats à points chauds contrôlés. La réalisation de tels substrats vise également une meilleure compréhension des mécanismes d’exaltation électromagnétique à l’origine de l’effet SERS. / The design of novel plasmonic platforms for Surface Enhanced Raman Spectroscopy (SERS) constitutes a very active field of research in nanosciences. Such platforms can be used for the detection and identification of various analytes at very low concentration, through a huge amplification of the Raman signal, resulting from the excitation of localized surface plasmon resonances. The main objective of my phd is to develop and to characterize new SERS substrates obtained by chemical assembly (surface functionalization) of nanoparticles with controlled hot spots. Design of such substrates contributes to a better understanding of the mechanisms of electromagnetic enhancement considered at the origin of the SERS effect.
73

Advanced transmission electron microscopy studies of semiconductor nanocrystals synthesized by colloidal methods / Etudes par microscopie électronique en transmission avancée de nanocristaux semiconducteur synthétisé par méthodes colloïdaux

Agnese, Fabio 16 October 2018 (has links)
Les recherches sur les nanocristaux semiconducteur (NCs) ont conduit à des résultats scientifiques fascinants, spécialement pour l'application en dispositifs optoelectroniques. Afin de répondre à certaines exigences comme des coûts mineurs, des gains d'efficacité, des composants respectueux de l'environnement, etc., des nouvelles méthodes sont explorées: dans les procédés en solution, dans l'ingénierie de bande et des niveaux d'énergie. En particulier, la méthode de synthèse peut influencer les propriétés optoélectroniques. Par conséquent, une meilleure compréhension des facteurs complexes pendant la synthèse entraînera une amélioration des performances.La microscopie électronique avancée fournit un moyen précis de recueillir des informations sur la morphologie, la structure cristalline et la composition chimique des matériaux avec une résolution spatiale au niveau atomique. La première partie de cette thèse traite de la synthèse et de la préparation des échantillons pour la microscopie électronique à transmission en haute résolution (HRTEM).La deuxième partie traite du mécanisme de croissance des NCs Cu2ZnSnS4 synthétisés par une méthode colloïdale. La morphologie et la stoechiométrie des intermédiaires de réaction extraits après différents intervalles de temps sont déterminés par HRTEM et analyse dispersive en énergie (EDS).Deux méthodes complémentaires, la diffraction par nanofaisceau d’électrons en précession (NPED) et la microscope électronique en transmission par balayage à haute résolution avec imagerie en champ sombre avec détecteur annulaire à grand angle (HRSTEM-HAADF) permettent une profonde caractérisation de la structure cristalline.En outre, la structure cristalline de NCs CsPbBr3 est résolue avec simulations de STEM-HAADF. Cet approche peut différencier entre structures cristallines cubiques et orthorhombiques, impossible avec techniques de diffraction traditionnelles. Enfin, l'influence des méthodes de synthèse sur la morphologie et sur la structure cristalline de NCs CuFeS2 pour applications dans le domaine de la thermoélectricité est analysée par HRTEM. / The investigations of semiconductor nanocrystals (NCs) led to fascinating scientific results in optoelectronic devices. In order to fulfill certain requirements, i.e. cheaper costs, higher efficiencies, environmental friendly components etc., new methods are explored in solution-processing, band gap and energy level engineering. Particularly, the method of synthesis can alter the optoelectronic properties. Therefore, a better understanding of the intricate factors during synthesis will lead to improved performances. Advanced electron microscopy provides a precise way to gather information about morphology, crystal structure and chemical composition of materials with a spatial resolution down to the atomic level. The first part of this thesis deals with the optimization of the synthesis and sample preparation for high resolution transmission electron microscopy (HRTEM).The second part deals with the growth mechanism of Cu2ZnSnS4 NCs synthesized by a colloidal method. The morphology and stoichiometry of the samples extracted after different time intervals are characterized by HRTEM and electron dispersion spectroscopy (EDS). Two complementary methods, Nanobeam Precession Electron Diffraction (NPED) and High Resolution Scanning Transmission Electron Microscopy by High Angle Annular Dark-Field Imaging (HRSTEM-HAADF), provide an in-depth crystal structure characterization.Moreover, the crystal structure of CsPbBr3 NCs is solved by probing STEM-HAADF simulations. This approach is able to differentiate cubic and orthorhombic crystal structures, which is otherwise impossible by diffraction techniques. Finally, the influence of synthesis methods on the morphology and crystal structure of CuFeS2 NCs is investigated by HRTEM for thermoelectric applications.
74

The Development of an Integrated Simulation Model on Understandings on the Interaction between Electromagnetic Waves and Nanoparticles

Wang, Xiaojin 01 July 2019 (has links)
To investigate the interaction between nanoparticles and electromagnetic waves, a numerical simulation model based on FEM was built in this thesis. Numerical simulation is an important auxiliary research method besides experiments. The optical properties of nanoparticles consist of scattering, absorption, and extinction, and in the case of nanoparticle suspension, the transmission is also involved. This thesis addressed two typical applications based on the established model, one was regarding the nanofluids for solar energy harvesting, and the other was regarding the optical properties of atmospheric soot. In the case of the nanofluids solar energy harvesting, the established model provided a convenient and rapid screening of potential nanoparticles and nanofluids candidates for solar energy harvesting. A core-shell structure nanoparticle, using Cu as the core material in a diameter of 90 nm coated with 5 nm thickness graphene, exhibited a better photothermal property under the solar radiation. In the second case regarding atmospheric soot, the established model provided an efficient method for understandings on the optical properties and warming effects of realistic soot particles. It was found that the sizes and material characteristics of soot, would greatly affect their scattering and absorption of light. Moreover, two submodels were introduced and integrated, which can better predict behaviors of real atmospheric soot involving their core-shell structures (moisture or organic condensates) and their fractal agglomerate structures. In conclusion, the established model helps to understand the interaction between nanoparticles and electromagnetic waves, which shows great potentials of wide applications.
75

Etude des mécanismes à l’origine de la luminescence dans les polymères de coordination hétéro-lanthanides / Study of mechanisms at the origin of luminescence in hetero-lanthanide coordination polymers

Abdallah, Ahmad 11 July 2019 (has links)
L’objectif de cette thèse était d’étudier les mécanismes responsables de la luminescence des ions lanthanides dans des polymères de coordination. Pour cela, des séries d’alliages moléculaires à base d’acide 4 carboxyphénylboronique ont été synthétisées, en faisant varier les proportions relatives des ions lanthanides. Les produits synthétisés ont été étudiés dans la perspective de leur application dans les domaines de la lutte anti-contrefaçon et des thermomètres moléculaires. D’autre part, de nouveaux systèmes utilisant d’autres dérivés d’acide boronique ont été synthétisés. Une nouvelle structure cristalline a été obtenue à base de l’acide 2-carboxyphénylboronique. La seconde partie de cette thèse a porté sur la synthèse et la caractérisation de poudres microcristallines de type coeur-coquille. Il s’agit de la première micro-structuration de polymères de coordination réalisée à l’échelle micrométrique. Les poudres synthétisées ont été caractérisées par microscopies électroniques à balayage, à transmission et par analyses EDS. Leurs propriétés optiques ont été comparées avec celles des alliages moléculaires. Les résultats obtenus ont mis en évidence l'intérêt de la micro-structuration de ces poudres concernant les transferts d'énergie intermétalliques. Cette technique de synthèse basée sur la croissance épitaxiale, est rendue possible par les propriétés chimiques similaires des terres rares. Nos travaux ont montré que lorsque les constantes thermodynamiques et\ou cinétiques le permettent, la phase cristalline de la coquille présente la structure cristalline du cœur même lorsque le composé constituant la coquille cristallise dans une autre phase lorsqu'il est synthétisé seul. / The aim of this thesis was to study the luminescence mechanisms of lanthanide ions in coordination polymers. Series of molecular alloys (hetero-lanthanide compounds in which lanthanide ions are randomly distributed) based on 4-carboxyphenylboronic acid were synthesized, by varying the relative contents of the lanthanide ions. The synthesized products have been studied from the perspective of their application in the fields of anti-counterfeiting and molecular thermometers. On the other hand, new systems using other boronic acid derivatives have been synthesized. A new crystal structure was obtained based on 2-carboxyphenylboronic acid. The second part of this thesis focused on the synthesis and characterization of core-shell microcrystalline powders. This is the first time that micro-structuration of a coordination polymer is achieved at the micrometric scale. The synthesized powders were characterized by scanning electron microscopy, transmission electron microscopy and EDS analyses. Their optical properties have been compared with those of the corresponding molecular alloys. The obtained results highlighted the interest of the micro-structuration concerning intermetallic energy transfers. This strategy of synthesis based on epitaxial growth, is possible because of lanthanide similar chemical properties. This work demonstrates that in the case where the thermodynamic and\or kinetic constants allow it, the shell crystallizes according to the same crystal structure than the core even if its crystal structure is different when it is synthesized alone.
76

Interaction Between Microgels and Oppositely Charged Proteins

Johansson, Christian January 2009 (has links)
This thesis reports on interactions between microgels and oppositely charged proteins. Two types of negatively charged microgels are investigated: poly(acrylic acid) microgels of 60-80 µm in diameter, and colloidal poly(NIPAM-co-acrylic acid) microgels of around 1 µm in diameter. The proteins used are lysozyme and cytochrome c, which both have positive net charge. The experimental techniques used in the studies of the larger microgels are mainly micromanipulator-assisted microscopy and confocal microscopy, while the smaller microgels are studied mainly with dynamic light scattering. It is observed that large amounts of protein are absorbed by the microgels, and that the uptake involves a substantial deswelling of the microgel. The uptake generally decreases as the ionic strength is increased, which is characteristic of electrostatic interactions. An ionic strength optimum is however observed in the case of lysozyme and poly(acrylic acid) microgels, where the highest uptake (10 gram lysozyme / gram microgel) is observed at ionic strength 40 mM. Cytochrome c uptake in poly(acrylic acid) microgels results in homogenous cytochrome c distribution throughout the microgel, whereas lysozyme uptake results in core-shell formation; the lysozyme concentration becomes much higher in the shell (outer part of the microgel) than in the core (inner part of the microgel). The shell constitutes a stress-bearing network which is sufficiently porous to allow protein diffusion through the shell. The different protein distributions are associated with different protein-protein interactions; strong protein-protein attraction promotes shell formation. In the case of colloidal microgels, lysozyme uptake decreases the electrophoretic mobility and the colloidal stability of the microgels. The microgels flocculate as the uptake reaches charge ratio 0.6-0.7 (positive lysozyme charges/negative microgel charges), largely independent of ionic strength. Initial experiments on the combination of cytochrome c and colloidal microgels show that colloidal stability is maintained at a range of conditions (ionic strength, protein concentration) where flocculation occurred in the case of lysozyme.
77

Energy Transfer Dynamics and Dopant Luminescence in Mn-Doped CdS/ZnS Core/Shell Nanocrystals

Chen, Hsiang-Yun 14 March 2013 (has links)
Mn-doped II-VI semiconductor nanocrystals exhibit bright dopant photoluminescence that has potential usefulness for light emitting devices, temperature sensing, and biological imaging. The bright luminescence comes from the 4T1→6A1 transition of the Mn2+ d electrons after the exciton-dopant energy transfer, which reroutes the exciton relaxation through trapping processes. The driving force of the energy transfer is the strong exchange coupling between the exciton and Mn2+ due to the confinement of exciton in the nanocrystal. The exciton-Mn spatial overlap affecting the exchange coupling strength is an important parameter that varies the energy transfer rate and the quantum yield of Mn luminescence. In this dissertation, this correlation is studied in radial doping location-controlled Mn-doped CdS/ZnS nanocrystals. Energy transfer rate was found decreasing when increasing the doping radius in the nanocrystals at the same core size and shell thickness and when increasing the size of the nanocrystals at a fixed doping radius. In addition to the exciton-Mn energy transfer discussed above, two consecutive exciton-Mn energy transfers can also occur if multiple excitons are generated before the relaxation of Mn (lifetime ~10^-4 - 10^-2 s). The consecutive exciton-Mn energy transfer can further excite the Mn2+ d electrons high in conduction band and results in the quenching of Mn luminescence. The highly excited electrons show higher photocatalytic efficiency than the electrons in undoped nanocrystals. Finally, the effect of local lattice strain on the local vibrational frequency and local thermal expansion was observed via the temperature-dependent Mn luminescence spectral linewidth and peak position in Mn-doped CdS/ZnS nanocrystals. The local lattice strain on the Mn2+ ions is varied using the large core/shell lattice mismatch (~7%) that creates a gradient of lattice strain at various radial locations. When doping the Mn2+ closer to the core/shell interface, the stronger lattice strain softens the vibrational frequency coupled to the 4T1→6A1 transition of Mn2+ (Mn luminescence) by ~50%. In addition, the lattice strain also increases the anharmonicity, resulting in larger local thermal expansion observed from the nearly an order larger thermal shift of the Mn luminescence compared to the Mn-doped ZnS nanocrystals without the core/shell lattice mismatch.
78

Synthesis of bi-magnetic core|shell and onion- like nanoparticles based on iron and manganese oxides

López Ortega, Alberto 27 September 2012 (has links)
Aquesta tesi engloba la síntesi i la caracterització estructural i magnètica de dos tipus de nanopartícules polymagnètiques: estructures nucli-escorça (core|shell, CS) i tipus ceba (onion-like). El primer sistema està format per un nucli-MnO|escorça-Mn 3O4 ( -Mn2O3) amb doble inversió, on el nucli i l'escorça mostren un comportament AFM i FiM, respectivament . Es de neix com estructuralment inversa ja que l'AFM es localitza al nucli i el FiM a l'escorça; a més, també es troba magnèticament invertida, és a dir, la temperatura de Néel de l'AFM presenta valors més elevats que la temperatura de Curie del FiM. Les nanopartícules nucli-escorça de MnO|Mn3O4 ( -Mn2O3) s'han obtingut a través de la passivació controlada de l'escorça de nanopartícules de MnO prèviament sintetitzades. Aquest procés permet controlar tant la grandària del nucli com el gruix de l'escorça. Es va con rmar que la composició de l'escorça un cop passivada depèn de la grandària inicial de les nanopartícules; conseqüentment, les nanopartícules més grans estan formades principalment per Mn3O4. No obstant, a mesura que es disminueix la grandària, la densitat de defectes augmenta obtenint, d'aquesta manera, una escorça més estable formada per la fase -Mn2O3. D'altra banda, nuclis AFM de MnO relativament petits poden induir un efecte magnètic de proximitat (magnetic proximity e ects) a l'escorça de FiM -Mn2O3 tot mantenint el seu ordre magnètic molt per sobre de la seva temperatura de Curie, TC; a més, aquest sistema presenta un augment de la temperatura de Néel de l'AFM. El segon sistema es basa en la síntesi de nanopartícules d'òxid de manganès i ferro del tipus nucli-escorça i ceba. Nanopartícules de dos òxids de ferro diferents (FeO|Fe3O4 CS i Fe3O4 monofàsica) s'han utilitzat com a llavors per a la posterior deposició d'òxid de manganès. A partir de les llavors nucli-escorça d'òxid de ferro s'han sintetitzat dos tipus de nanopartícules ceba (tres-components FeO|Fe 3O4|Mn3O4 i quatre-components FeO|Fe3O4|MnO|Mn3O4). D'altra banda, nanopartícules d'òxid de ferro monofàsiques han estat utilitzades com a llavors per a dipositar una capa na de manganès al seu voltant amb l'objectiu d'incentivar l'interdifusió del manganès-ferro i formar nanopartícules nucli-escorça de MnxFe3 ��xO4|FexMn3 ��xO4 amb una interfase graduada. S'ha observat que l'òxid de manganès creix epitaxialment en els plans (111) sobre les cares truncades del llavors cúbiques d'oxid de ferro. Finalment, nanopartícules nucli-escorça de MnxFe3 ��xO4|FexMn3 ��xO4 formades per una estructura tou-FiM/dur- FiM amb una composició gradual a l'interfase demostren un bon l'acoblament magnètic entre ambdues, tova i dura, fases FiM. / This thesis deals with the synthesis and magnetic and structural characterization of two di erent systems based in polymagnetic nanoparticles with core|shell (CS) and onion-like architectures. The rst system is formed by a double inverted core-MnO|shell- Mn3O4 ( -Mn2O3) where core and shell display an antiferromagnetic (AFM) and ferrimagnetic (FiM) behavior, respectively. It is de ned as structurally inverted since the AFM is placed in the core and the FiM in the shell (in contrast to conventional ferromagnetic( FM)/AFM CS systems); in addition, it is, also, magnetically inverted because the Néel temperature of the AFM is larger than the Curie temperature of the FiM (contrarily to standard exchange bias systems). MnO|Mn3O4 ( -Mn2O3) CS nanoparticles have been synthesized through the controlled shell passivation of pre-made MnO nanoparticles. This procedure allows reaching a good control over the nal core size and shell thickness. It was con rmed that the passivated shell composition depends on the nanoparticle size, where the larger nanoparticles presenting mainly Mn3O4. However, when the size diminishes, the density of defects in the MnO core increases and consequently -Mn2O3 is the more stable shell phase. Besides, small AFM MnO cores can induce a magnetic proximity e ect to the FiM -Mn2O3 shell, maintaining its magnetic order well above its Curie temperature, TC. Moreover, surface e ects in the MnO core can also lead an increase of the Néel temperature of the AFM. Further, given the AFM/FiM exchange coupling the system exhibits large coercivities and loop shifts along the eld axis, i.e., exchange bias. The second type of system comprises the synthesis of CS and onion-like nanoparticles based in manganese and iron oxides. Two di erent iron oxide nanoparticles (FeO|Fe3O4, AFM|FiM, CS and single phase FiM Fe3O4) have been used as seeds for the posterior manganese oxide deposition. From iron oxide CS seeds two di erent onion-like nanoparticles (three-components FeO|Fe3O4|Mn3O4 and four-components FeO|Fe3O4|MnO|Mn3O4) have been synthesized. The temperature dependence of the magnetization of these onion nanoparticles exhibits several magnetic transitions, in concordance with the presence of diverse magnetic phases. In addition, single phase iron oxide seeds were employed to deposit a manganese thin shells at high temperatures forcing a manganese-iron interdi usion to form the nal MnxFe3 �xO4|FexMn3 �xO4 CS nanoparticles with a graded interphase. The structural results show that the (111) planes of the manganese oxide grow epitaxially onto the (111) planes of the truncated faces of the initial cubic iron oxide seeds. Finally, the CS MnxFe3 �xO4|FexMn3 �xO4 nanoparticle, formed by soft-FiM|hard-FiM structure with a graded interphase composition, shows a strong exchange coupling between the hard and soft FiM phases.
79

Silver nanostructures: chemical synthesis of colloids and composites nanoparticles, plamon resonance properties and silver nanoparticles monolayer films prepared by spin-coating

Torres Heredia, Victor Elias 08 November 2011 (has links)
El presente trabajo tiene como objetivo desarrollar en solución acuosa y a tem-peratura ambiente, rutas de síntesis química coloidal de nanopartículas de plata y nano-partículas compuestas estables. Se obtienen nanopartículas de plata reproducibles, con un control morfológico de tamaño y forma durante el proceso de síntesis. Llevamos a cabo el estudio de las propiedades ópticas (espectros de absorción de las resonancias de plasmones superficiales (SPR)) que caracterizan a una determinada forma y tamaño. El análisis incluye estructuras nanométricas de plata de diferentes tamaños, en ambientes diversos y formas diferentes, como esferas, prolates, y prismas de diferente sección transversal, etc Se ha demostrado que la síntesis química produce coloides de nanopartículas de plata esféricas y anisotrópicas estables. La morfología y estabilidad de las nanopartícu-las coloidales son estudiadas mediante técnicas de espectroscopia y microscopía elec-trónica. El rol y concentración necesaria de cada uno de los reactivos para producir co-loides estables mediante síntesis química son determinadas. Se ha demostrado que, con-trariamente a las opiniones actualmente expresadas en la literatura, es posible controlar el tamaño de las nanopartículas de plata y obtener coloides de nanopartículas de plata esféricas y anisotrópicas estables por largo tiempo, utilizando una ruta de síntesis quí-mica sencilla y una baja concentración de reactivos estabilizadores (PVP). Recubrimientos de nanopartículas esféricas de plata estabilizadas con polivinilpirroli-dona (PVP) sobre substratos de vidrio óptico son preparados mediante el proceso de spin-coating y un posterior tratamiento térmico. Diferentes morfologías tipo core-shell de Ag@SiO2 son preparados mediante un método químico simple y rápido, sin necesidad de adicionar reactivos de acoplamiento o modificadores superficiales de la sílice. Proponemos mecanismos de reacción para la preparación de diferentes nano-estructuras tipo core-shell de plata-sílice. Las nanopartí-culas compuestas de sílice-plata muestran unas propiedades de absorción de resonancia plasmónica muy evidentes. El trabajo de éste capítulo ha sido realizado en colaboración con Juan C. Flores, quien desarrolló la ruta de síntesis como parte de sus estudios de doctorado. Por último, una modificación del método sol-gel es empleada para la prepara-ción de nanopartículas de TiO2, y partículas compuestas de Ag@TiO2, SiO2@TiO2-Ag y SiO2@Ag@TiO2. Diferentes morfologías tipo core-shell son preparadas mediante un método químico simple y rápido sobre un substrato óxido, sin necesidad de adicionar agentes de acoplamiento o modificaciones superficiales. Las evidentes propiedades de absorción plasmónica de las nanopartículas de plata mostradas por las partículas com-puestas han demostrado la presencia de plata metálica sobre la titania, sin la posterior oxidación de la capa de plata por el contacto directo con la titania (TiO2). Esta evidencia es confirmada por la técnica de microscopía electrónica de alta resolución. Las propie-dades de absorción plasmónica de las partículas compuestas hacen a estos materiales muy prometedores para aplicaciones foto-catalíticas. / The present work aims to develop chemical synthesis routes of stable colloidal silver nanoparticles and composites nanoparticles in aqueous solution at room tempera-ture. We obtain reproducible morphological control of silver nanoparticles size and shape during synthesis solely by solution chemistry and carry out the study of the opti-cal properties (surface plasmon resonances (RPS) absorption spectra) which character-ize a specific shape and size. The analysis includes silver nanosized bodies of different size, in diverse environments and of various shapes, as spheres, prolates, and prisms of different transversal section, etc. Synthetic wet chemistry routes yielding stable colloids of spherical and aniso-tropic silver nanoparticles are demonstrated, and the morphology and stability of the colloidal nanoparticles studied extensively through spectroscopy and electron micros-copy techniques. The role of each reagent and the concentrations required to obtain sta-ble colloid via these wet chemical routes is determined. It was shown that, contrary to commonly expressed opinions in the literature, it is possible to control the particle size of silver nanoparticles and obtain long-term sable colloids of both spherical and aniso-tropic silver nanoparticles using simple chemical routes and low concentration of stabi-lizing agent (PVP). Films of polyvinylpyrrolidone (PVP) stabilized spherical silver nanoparticles are also prepared, by using spin coating on standard optical glass plates and subsequent thermal processing. Different core-shell type morphologies of Ag@SiO2 are also produced using a simple and rapid chemical method, without using added coupling agents or surface modifications of silica. We propose reaction mechanisms for the formation of the dif-ferent silica-silver core-shell nanostructures. The silica-silver composite nanoparticle display clear plasmonic resonance absorption properties. This chapter work has been done in collaboration with PhD student Juan C. Flores who developed the synthesis route as part of his doctoral studies. Finally, a sol-gel chemistry approach was used to fabricate nanoparticles in the systems TiO2, Ag@TiO2, Ag@TiO2-SiO2 and TiO2@Ag@SiO2. Different core-shell morphologies are produced using a simple and rapid chemical method. without using added coupling agents or surface modifications of the oxide substrate. Clear silver na-noparticle plasmonic absorption properties shown by the composite nanoparticles demonstrate the formation of metallic Ag, without the oxidation of Ag nanoshell in di-rect contact with TiO2, evidence confirmed also by high resolution electron microscopy. The plasmonic absorption properties of the composites nanoparticles make them a promising material for photocatalytic applications.
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Graft Polymers: From Dendrimer Hybrids to Latex Particles

Munam, Abdul January 2007 (has links)
The research presented focused on the synthesis and the characterization of graft polymers, of interest either as model systems or for large-scale applications. The materials selected as substrates for grafting reactions were carbosilane dendrimers, linear and branched polystyrenes, and cross-linked polystyrene latex particles. The synthesis of dendrimer-arborescent polymer hybrids was thus achieved by derivatization of the carbosilane dendrimers with dichlorosilane moieties and coupling with 1,4-polybutadiene side chains with Mn ≈ 1000. A second derivatization and coupling reaction with Mn ≈ 1500, 5000, or 30000 side chains yielded hybrid polymers with narrow molecular weight distributions (Mw/Mn ≤ 1.16). In the second part of the thesis, a procedure for the large-scale (100-g) synthesis of arborescent styrene homopolymers and copolymers incorporating poly(2-vinylpyridine) segments is presented. End-capping of the polystyryllithium chains with 1,1-diphenylethylene in the presence of LiCl, followed by the addition of 3 – 6 equivalents of 2-vinylpyridine per side chain, eliminated side reactions and led to grafting yields of up to 95 %. A systematic investigation of the solution properties of polyelectrolytes obtained by protonation of the poly(2-vinylpyridine) arborescent copolymers with a strong acid (trifluoroacetic acid) is also presented. The relative importance of the electrostatic repulsion and the elastic deformation forces on molecular expansion was investigated by examining the solution properties of the copolymers as a function of structure, protonation level, and the presence of salts in polar solvents (methanol, DMF, H2O). The viscosity of the arborescent copolymer solutions was also found to be much lower than for linear P2VP samples under the same conditions. In the last part of the thesis, the synthesis of model filler particles was achieved by grafting polyisoprene chains onto cross-linked polystyrene latex particles derivatized with acetyl coupling sites. These substrates, which can be viewed as an extreme case of a dense (hard-sphere) arborescent polymer structure, were used to investigate the influence of filler-matrix polymer interactions on the rheological behavior of filled polyisoprene samples. The influence of the filler structure on the rheological behavior of the blends was examined by dynamic mechanical analysis in terms of frequency-dependent complex viscosity, storage modulus, and damping factor. All the blends exhibited enhanced complex viscosity, storage modulus, and decreased damping factor values relative to the matrix polymer.

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