Secondary abnormal grain growth (SAGG) during sintering of barium titanate has been explained in terms of twin plane re-entrant edge (TPRE) growth mechanism by {111} double twin lamellae. But during sintering of Ti-excess barium titanate, {111} double twins lamellae are observed with out SAGG. In our group, Lin founded that when combine two different Ba/Ti ratio of powder to sintering above the eutectic temperature, the SAGG is observed in the interface between two different powders. Therefore, this thesis consists of three major researches: (a) {111} double twin, (b) Ba/Ti ratio, (c) liquid phase. In the experiment, we follow Lin¡¦s experiment to sinter the specimen contain with SAGG. And in this specimen, it can observe the specimen divided into three type of growth grain: (a) top surface with normal grain growth (NGG), (b) intermediate layer with abnormal grain growth (AGG), (c) bottom layer with secondary abnormal grain growth. It can all observed {111} double twin in these three different type of layer. This result confirmed that SAGG are not induced by TPRE growth mechanism. Then we used SEM/EDS to analysis the Ba/Ti ratio in the different type of grain growth layer. The Ba/Ti ratio in this analysis is not differing in NGG, AGG and SAGG. Therefore, we used OM, SEM, TEM to observe the grain boundary and triple grain junction in NGG, AGG and SAGG. It can observe that only the grain boundary and triple grain junction in SAGG are complete wetting. The experimental results shows that the grain growth behavior controlled by the liquid phase wetting degree.

Piezoceramics BaTiO3 doped with ZrO2 was studied in this thesis. Six different compositions were prepared from base powders of BaTiO3 and ZrO2. with 10, 20, 40, 60, 80 and 90 wt% ZrO2. These mixtures were sintered using convetional sintering method and by Spark Plasma Sintering. Resuting ceramic compacts were subjected to measuring of density, dielectric constant, permitivity, polarization P-E curves, piezoelekctric faktor, loss factor and dilatometric measurements. From these results can be said that i tis possible to create piezoceramic BaTiO3 doped by ZrO2 with relative density higher than 94 %t.d. and these ceramics can possess piezoelectric properties. Value of highest piezoelectrick factor 33=9 / was achieved with addition of 20 wt% ZrO2. Dilatometric measurements discovered effect of increasing ammount of ZrO2 in BaTiO3. Rising amount of ZrO2 had a lowering effect on initial sintering temperature and materials achieved higher relative densities. This was also true for samples sintered using SPS, where it was less obvious. Measuring of electrical properties discoverad electric conductivity for SPS sintered samples, which was most probably caused by carbon introduced into samples during SPS cycle.

The thesis deals with the study of the influences of selected groups of chemical agents on the stability of PTC ceramics based on BaTiO3. The experimental part includes elaboration of methodology for determination of these influences, their evaluation, including the hypotheses for their description, and evaluation of groups of chemical agents having these influences.

Dans un contexte où l’électronique est au centre de notre société, la productiond’appareils de plus en plus compacts et multifonctionnels concentre les efforts en rechercheet développement. Pour répondre à cette attente, une des options est d’augmenter lerendement volumique des composants passifs tels que les condensateurs, en se basant surl’utilisation de nanoparticules diélectriques du type BaTiO3. Dans un premier temps,l’objectif est d’optimiser la synthèse des nanoparticules de BaTiO3 et de comprendre leursmécanismes de formation en milieux fluides supercritiques. Pour ce faire nous avonscombiné des méthodes d’analyses ex situ telles que la microscopie électronique, ladiffraction des rayons X, et les spectroscopies Raman ou infra rouge à des mesures in situsynchrotron de diffraction des rayons X aux grands angles. L’étude a par la suite ététransposé à l’élaboration de la totalité des solutions solidesBa1-xSrxTiO3 (0 ≤ x ≤ 1) et BaTi1-yZryO3 (0 ≤ y ≤ 1). Une fois les synthèses optimisées, l’utilisation du spark plasma sintering(SPS) nous a permis de mettre en oeuvre des céramiques denses et nanostructurées,préservant la taille initiale des particules (20 nm), ceci afin d’étudier les propriétésintrinsèques des matériaux à l’échelle nanoscopique. Enfin, connaissant les propriétés debase de ces nanomatériaux, nous avons pu commencer à développer des matériauxhybrides diélectriques pour l’électronique flexible. / In a context where the electronic is at the center of our society, theproduction of more compact and multifunctional devices focuses the research efforts.To answer to the expectations, one option is to improve the volume efficiency ofpassive components such as capacitors using dielectric nanoparticles such asBaTiO3. First, the objective is to optimize the synthesis of BaTiO3 nanoparticles andunderstand their formation in supercritical fluids. To do this, we combinedconventional ex situ analyses such as X-ray diffraction, electronic microscopy,infrared and Raman spectroscopies with in situ synchrotron wide angle X-rayscattering analyses. This was then transferred to the development of Ba1-xSrxTiO3 (0≤ x ≤ 1) and BaTi1-yZryO3 (0 ≤ y ≤ 1) solid solutions. Once the syntheses wereoptimized, using spark plasma sintering (SPS), we processed the powders intodense and nanostructured ceramics keeping the starting particles size (20 nm), tostudy the materials intrinsic properties at the nanoscale. Finally, knowing thenanoparticles properties, we could start to develop hybrid dielectric materials forflexible electronics.

Durant ce travail de thèse, nous avons étudié l’effet d’un champ électrique intense (>3 kV.cm-1) sur des matériaux à structures pérovskites, le ferroélastique CaTiO3 et le ferroélectrique BaTiO3. Un tel champ agit comme une force extérieure dans la sélection, l’orientation et la distribution des domaines. Son application durant la croissance modifie la nucléation, le coefficient de partage des espèces et la possible modification du diagramme de phase du matériau considéré. En effet les ions dans un champ électrique voient leur énergie changer ce qui implique un nouvel équilibre thermodynamique. La première partie est dédiée à la croissance cristalline de CaTiO3 lorsque plusieurs paramètres de croissance sont modifiés (vitesse de croissance vG et potentiel électrique V). En faisant varier ces paramètres, nous montrons que nous pouvons contrôler la morphologie du cristal et ainsi altérer l’orientation cristalline des domaines. Des résultats similaires sont retrouvés avec BaTiO3.Plusieurs techniques expérimentales ont été employées dans le but d’étudier la microstructure des composés notamment la microscopie électronique miroir (MEM) et la microscopie électronique à faible énergie (LEEM) afin de caractériser les domaines et parois de domaines à la surface du titanate de calcium. La polarité de ces parois ayant été récemment prouvée, nous avons étudié et comparé le potentiel de surface entre les échantillons qui ont été élaborés sous et sans champ électrique. / In this work, we investigate electric field effect (>3 kV.cm-1) on perovskite compound, CaTiO3 (ferroelastic) and BaTiO3 (ferroelectric). This electric field acts like an external force in selection, orientation and distribution of piezoelectric/ferroelastic domains. The electric field can act on nucleation, the partition coefficient of species and the possible modification phases diagrams of a material during its growth. Indeed ions within an electric field see their energy changing which implies a new thermodynamic equilibrium.In the first part, we discuss about crystal growth of CaTiO3 with different growth parameters (velocity of cristal growth vG, electric potential V). By varying this parameters, we can control crystal shape and can alter the crystalline orientation of domains. Same results are found with BaTiO3.In a second step, we used Mirror Electron Micrsocopy (MEM) and Low Energy Electron Microscopy (LEEM) to caracterize domains walls at the surface of calcium titanate. Polarity of domains walls have been prooved recently, and so we have investigated surface potential between samples grown under or without electric field.

Non-stoichiometric barium titanate (BaTiO3) powder of TiO2-excess compositions has been investigated using both reducing sintering and acceptor-doping. Crystalline phases were analysed by XRD. Attention has been paid to the analysis of the corresponding sintered microstructure by adopting scanning and transmission electron microcopy. Reducing sintering was in the low oxygen partial pressure, so as to dominate the oxygen-deficient. According to the defect chemistry, the purpose of acceptor-doping was the same as reducing sintering. We look out for phenomena which may be indicative that oxygen vacancies generated by acceptor-doping and reducing sintering have resulted in the metastable retention of high temperature hexagonal-BaTiO3 to an ambient temperature. In the Mg-doped study investigated the possibility that Mg2+ substitutes on Ti4+ site rather than the Ba2+ site, as expected from the radii. According to the unknown phase was indexed a supercell of MgTiO3, that showed evidence of Mg2+ dissolves in BaTiO3 and occupies the Ba2+ site. To reduce in a hydrogen atmosphere was a high dark conductivity. The Ti3+ content was determined via colorimetry. Because of the defect chemistry led to oxygen-deficient h-BaTiO3, i.e.BaTi1-xTixO3-x/2. The observed volume expansion behavior under Ar-H2 atmosphere demonstrates the possibility of having various microstructures via control of oxygen partial pressure. The transformation matrix described the relation between the two reciprocal lattices of the twinning. Investigation of reciprocal lattices was shown that ordering oxygen deficient on the BaO3 layer in the twin boundary. There was evidence of XRD patterns and surface energy that explained more and more twins in the microstructure via control of the low oxygen partial pressure. According to this theory, lamellae twins were generated by oxygen-deficient. The hexagonal phase might be also expressed as the cubic BaTiO3 containing twin boundary at BaO3 planes every three layers. That demonstrates the possibility of hexagonal phase retention in BaTiO3 was oxygen vacancies.

No description available.

Neste trabalho, cerâmicas de BaTiO3 foram preparadas pelo método de Pechini com o propósito de estudar as suas propriedades dielétricas, incluindo as anomalias dielétricas de origem interfacial nestes ferroelétricos. Após calcinação das soluções precursoras a 600 oC por 2h, os pós compactados foram sinterizados a várias temperaturas entre 1150 e 1450 oC. Subseqüentemente, foram realizadas caracterizações (micro)estruturais aplicando as técnicas de microscopia eletrônica de varredura e difração de raios X, além de estudos dielétricos utilizando a técnica de espectroscopia de impedância. Destas caracterizações, verificou-se a obtenção de materiais cerâmicos com tamanhos de grãos variando entre 0,8 e 37 micrometros ao aumentar a temperatura de sinterização. Os resultados de dinâmica térmica de densificação indicam a contribuição de dois mecanismos independentes: (i) sinterização com participação de fase líquida, induzindo altas densidades dos materiais a partir de ~1300 oC (perto do ponto eutético), e (ii) sinterização via reação de estado sólido, implicando alta sinterabilidade mesmo abaixo dos 1300 oC, em se tratando de pós nanométricos, ou seja, com alta densidade de defeitos e, portanto, processos de difusão iônica intensificados. Por outro lado, a resposta dielétrica dos grãos evidenciou o cumprimento da lei de Curie-Weiss, típica de ferroelétricos, enquanto um fenômeno de anomalia dielétrica (não cumprimento desta lei) foi observado para as respostas totais destes materiais em altas temperaturas e baixas freqüências. A análise dos resultados de espectroscopia de impedância via circuito equivalente, sendo considerado o modelo de camadas (grãos e contornos de grãos) em série, revelou a predominância das propriedades dielétricas das interfaces intergranulares como a causa desta anomalia. Considerando a relação entre propriedades macroscópicas e microscópicas no modelo, a variação da intensidade da anomalia é discutida em função do tamanho dos grãos, sendo este parâmetro uma medida (função inversa) da densidade das interfaces intergranulares. Em geral, este trabalho revela uma excelente correlação entre microestruturas, circuito equivalente e propriedades dielétricas exibidas por estes materiais eletrocerâmicos. / BaTiO3 ceramics were prepared in this work, following the Pechinis method, with the purpose of studying their dielectric properties, including especially the occurrence and characteristics of dielectric anomalies associated to internal interfaces, as often found in ferroelectrics. After calcination of the precursor solutions at 600 oC for 2h, the synthesized green compacts were sintered at several temperatures from 1150 to 1450 oC. Subsequently, (micro)structural characterizations were carried out by applying scanning electron microscopy and X-ray diffraction techniques, followed by dielectric measurements using the impedance spectroscopy technique. From these characterizations, the production of ceramic bodies with average grain sizes varying from 0.8 to 37 micrometer was verified when increasing the sintering temperature. The results of thermal dynamics of densification indicate the contribution of two independent mechanisms, namely (i) liquid phase-assisted sintering, inducing high materials density from ~1300 oC (close to the eutectic point) above, and (ii) solid-state sintering, implying high sinterability even below 1300 oC, as dealing with nanoparticles-sized powders, meaning high density of surface defects and, thus, enhanced ionic diffusion processes. On the other hand, while the dielectric response of the grains satisfied the Curie-Weiss law, typical of ferroelectrics, a dielectric anomaly (departure from this law) phenomenon was observed for the total dielectric response of these materials towards higher temperatures and lower frequencies. The analysis of the results from impedance spectroscopy via equivalent circuit, involving consideration of the series layer (grains and grain boundaries) model, revealed that the predominance of the dielectric properties from the intergranular interfaces is responsible for occurrence of this anomaly. Considering the relation between macroscopic and microscopic properties holding in this model, the variation of the anomaly strength is here discussed in terms of the value of average grain size in these ceramics, a microstructural parameter that represents a measure (inverse function) of the density of the intergranular interfaces. In general, the present study reveals a really good correlation between microstructures, equivalent circuit and dielectric properties exhibited by these electroceramic materials.

Les développements récents en électronique de puissance visent à augmenter la densité de puissance totale dans les systèmes de conversion d'énergie. Cela contraint alors de plus en plus les matériaux isolants, tels que l'encapsulation dans les modules de puissance. Si les renforcements de champ électrique au sein des polymères isolants atteignent des valeurs critiques, cela peut entraîner une activité de décharges partielles, des arborescences voire la rupture totale de l'isolation. L'objectif de cette thèse est d'étudier l'adaptation des propriétés diélectriques d'un polymère composite isolant afin de réduire les contraintes autour des zones de renforcements de champ électrique. Nous proposons une nouvelle approche de gradation de potentiel pour minimiser les renforcements de champ à travers une structuration locale du matériau composite sous forme d'un gradient de permittivité auto-adaptatif localisé là où les contraintes sont les plus intenses. Cette structuration est réalisée via l'application d'un champ électrique DC lors du procédé d'élaboration du matériau composite, permettant le déplacement par électrophorèse des particules. Le composite à gradient de permittivité est composé d'une matrice époxy chargée en particules à forte permittivité (titanate de strontium SrTiO3 ou titanate de baryum BaTiO3). L'action d'un champ électrique DC sur la résine liquide chargée en particules engendre leur accumulation vers l'électrode de plus fort potentiel, formant ainsi une couche fortement chargée, qui confère à cette région une permittivité plus élevée. Chaque région du composite structuré (zone de la couche accumulée et zone faiblement chargée en particules) a été caractérisée en termes de propriétés diélectriques (permittivité et pertes). Alors que la région des composites faiblement chargée en particules conserve une permittivité voisine de celle des composites homogènes, la couche accumulée présente une augmentation importante liée à l'augmentation de la densité de particules. Les concentrations en particules de chaque région du matériau structuré ont été déterminées précisément, et les valeurs de permittivités associées se corrèlent bien avec les valeurs de permittivité des matériaux composites homogènes de taux de chargement équivalent. Cela montre que la couche accumulée ne s'est pas organisée d'une façon particulière. Concernant la rigidité diélectrique de la couche accumulée, elle présente des valeurs suffisantes pour tenir les contraintes rencontrées et ses valeurs suivent la loi de puissance classique en fonction de l'épaisseur. Des simulations par éléments finis confirment l'intérêt de ces matériaux pour la minimisation des renforcements de champ électrique au niveau du point triple dans les modules de puissance. Ces résultats montrent tout le potentiel applicatif de ces nouveaux matériaux à gradient de champ. Ils pourraient permettre l'amélioration de la fiabilité et de la robustesse des modules de puissance et autres systèmes électriques travaillant sous fort champ. / New developments in power electronics allow increasing the power density of the conversion systems. This means that the insulating materials, such as the encapsulation in power modules, are more are more stressed. If the electric field reinforcements in insulating polymers reach critical values, this can lead to a partial discharge activity, electrical treeing and eventually a complete breakdown of the insulation. The objective of this thesis is to study the appropriate matching of the dielectric properties of insulating polymer composites in order to reduce the electrical stress in the regions of field reinforcement. A new approach to minimize the reinforcements is proposed through a local structuration of the composite material allowing an auto-adaptive permittivity gradient where the largest stresses are present. This structuration is achieved thanks to the application of a DC electric field during the elaboration process of the composite material, leading to the displacement of the particles by electrophoresis. The field grading material is an epoxy matrix filled with high permittivity particles (strontium titanate SrTiO3 or barium titanate BaTiO3). Applying a DC electric field on the liquid resin containing the particles induces their accumulation on the high voltage electrode, building an accumulated layer highly concentrated in particles, conferring to this region a higher permittivity. Each region of the structured composite (accumulated layer and low concentrated region) was characterized in terms of dielectric properties (permittivity and losses). While the low concentrated region of particles keeps a permittivity close to that of homogeneous composites one, the accumulated layer exhibits a significant increase due to the increase in the local particle content. The particle concentration in each region of the structured material were precisely determined, and the related permittivity values are in good agreement with the permittivity values of the homogeneous composite materials of the same filler content. This shows that the accumulated layer was not organized in a particular way. Regarding the dielectric strength of the accumulated layer, its values are large enough for the applications and these values follow the typical power law versus thickness. Finite element methods prove that these materials are appropriate for minimizing the electric field reinforcements at the triple point, between the metal, the ceramic and the encapsulation. These results highlight the interests of these new kind of field grading materials. They could allow improving the reliability and the robustness of power modules or other electrical systems working at high field.

Neste trabalho, cerâmicas de BaTiO3 foram preparadas pelo método de Pechini com o propósito de estudar as suas propriedades dielétricas, incluindo as anomalias dielétricas de origem interfacial nestes ferroelétricos. Após calcinação das soluções precursoras a 600 oC por 2h, os pós compactados foram sinterizados a várias temperaturas entre 1150 e 1450 oC. Subseqüentemente, foram realizadas caracterizações (micro)estruturais aplicando as técnicas de microscopia eletrônica de varredura e difração de raios X, além de estudos dielétricos utilizando a técnica de espectroscopia de impedância. Destas caracterizações, verificou-se a obtenção de materiais cerâmicos com tamanhos de grãos variando entre 0,8 e 37 micrometros ao aumentar a temperatura de sinterização. Os resultados de dinâmica térmica de densificação indicam a contribuição de dois mecanismos independentes: (i) sinterização com participação de fase líquida, induzindo altas densidades dos materiais a partir de ~1300 oC (perto do ponto eutético), e (ii) sinterização via reação de estado sólido, implicando alta sinterabilidade mesmo abaixo dos 1300 oC, em se tratando de pós nanométricos, ou seja, com alta densidade de defeitos e, portanto, processos de difusão iônica intensificados. Por outro lado, a resposta dielétrica dos grãos evidenciou o cumprimento da lei de Curie-Weiss, típica de ferroelétricos, enquanto um fenômeno de anomalia dielétrica (não cumprimento desta lei) foi observado para as respostas totais destes materiais em altas temperaturas e baixas freqüências. A análise dos resultados de espectroscopia de impedância via circuito equivalente, sendo considerado o modelo de camadas (grãos e contornos de grãos) em série, revelou a predominância das propriedades dielétricas das interfaces intergranulares como a causa desta anomalia. Considerando a relação entre propriedades macroscópicas e microscópicas no modelo, a variação da intensidade da anomalia é discutida em função do tamanho dos grãos, sendo este parâmetro uma medida (função inversa) da densidade das interfaces intergranulares. Em geral, este trabalho revela uma excelente correlação entre microestruturas, circuito equivalente e propriedades dielétricas exibidas por estes materiais eletrocerâmicos. / BaTiO3 ceramics were prepared in this work, following the Pechinis method, with the purpose of studying their dielectric properties, including especially the occurrence and characteristics of dielectric anomalies associated to internal interfaces, as often found in ferroelectrics. After calcination of the precursor solutions at 600 oC for 2h, the synthesized green compacts were sintered at several temperatures from 1150 to 1450 oC. Subsequently, (micro)structural characterizations were carried out by applying scanning electron microscopy and X-ray diffraction techniques, followed by dielectric measurements using the impedance spectroscopy technique. From these characterizations, the production of ceramic bodies with average grain sizes varying from 0.8 to 37 micrometer was verified when increasing the sintering temperature. The results of thermal dynamics of densification indicate the contribution of two independent mechanisms, namely (i) liquid phase-assisted sintering, inducing high materials density from ~1300 oC (close to the eutectic point) above, and (ii) solid-state sintering, implying high sinterability even below 1300 oC, as dealing with nanoparticles-sized powders, meaning high density of surface defects and, thus, enhanced ionic diffusion processes. On the other hand, while the dielectric response of the grains satisfied the Curie-Weiss law, typical of ferroelectrics, a dielectric anomaly (departure from this law) phenomenon was observed for the total dielectric response of these materials towards higher temperatures and lower frequencies. The analysis of the results from impedance spectroscopy via equivalent circuit, involving consideration of the series layer (grains and grain boundaries) model, revealed that the predominance of the dielectric properties from the intergranular interfaces is responsible for occurrence of this anomaly. Considering the relation between macroscopic and microscopic properties holding in this model, the variation of the anomaly strength is here discussed in terms of the value of average grain size in these ceramics, a microstructural parameter that represents a measure (inverse function) of the density of the intergranular interfaces. In general, the present study reveals a really good correlation between microstructures, equivalent circuit and dielectric properties exhibited by these electroceramic materials.