À l'heure actuelle, il y a un intérêt croissant pour l’adaptation des propriétés physique des solides contenant des métaux de transition en modifiant leurs réseaux ioniques. Ces changements topologiques modifient non seulement le degré d’oxydation du métal de transition, mais peuvent également modifier sa sphère de coordinence, ainsi que les connectivités cation-anion-cation à longue distance, pouvant conduire à des changements radicaux de leurs propriétés physiques.Dans ce contexte, mon travail de thèse, réalisé au laboratoire UCCS à Lille (France), a consisté en une étude approfondie de deux différents exemples de transformations topotactiques. Premièrement, je présente l´échange anionique ainsi que l'exfoliation en nano-feuillets chargés positivement, de l'oxo-bromure de cobalt 14H-Ba7Co6BrO17. Le processus d'exfoliation a été caractérisé structuralement à l’aide de techniques telles que les microscopies, la diffraction ou l’absorption des rayons X.Dans la deuxième partie de mon travail, une étude complète du processus d’exsolution reversible du fer dans BaFe2(PO4)2 a été effectuée, en établissant une relation entre les évolutions structurales et la quantité de fer exsoluté. Une étude sur l'insertion éventuelle du lithium dans la structure de la phase la plus lacunaire en fer, BaFe1.33(PO4)2, ainsi que ses capacités en tant que cathode pour batteries au lithium, a également été réalisée. En outre, des études structurales et magnétiques des solutions solides BaFe2-YMY (PO4)2 par substitution du métal par Co2+ ou Ni2+a aussi été réalisée.Enfin, dans la dernière partie de ce manuscrit, je présente trois phases différentes à base de fer qui ont été découvertes lors de prospection pour trouver de nouvelles phases ayant des capacités de transformations topotactique. / At present, there is growing interest in tuning the physical behavior of solids containing transition metals by modifying their ionic lattices. These topological changes modify not only the electron count (through reduction or oxidation) but can also modify the local transition metal coordination sphere and the long-range cation-anion-cation connectivity, potentially leading to dramatic changes in their physical behavior. In this context, my PhD work developed in the UCCS laboratory at Lille (France), has consisted in a deep study of two different examples of topotactic transformations. Firstly I have performed anionic exchange as well as exfoliation into positively-charged nanoflakes, on the oxybromide cobaltites 15H-Ba7Co6BrO17. This exfoliation process has been structurally characterized by different techniques as microscopies, X-Rays diffractions and absorptions. For the last two, synchrotron radiation was used, the experiments being performed at SOLEIL.Secondely, a full study of the reversible iron exsolution process in BaFe2(PO4)2 has been carried out, establishing a relation between the structural features and the amount of iron exsoluted. A study about a possible lithium insertion in the lattice of the most exsoluted phase, BaFe1.33(PO4)2, as well as its capabilities determination as cathode in Li batteries was also performed. In addition, structural and magnetic studies has been realized in the substituted solid solutions of BaFe2-yMy(PO4)2 with M2+ = Co2+, Ni2+.Finally, the last part of the manuscript presents three different iron phases discovered during my prospecting work for new phases having abilities for topotactic transformation.

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Orientador: Prof. Dr. Daniel Zanetti de Florio / Dissertação (mestrado) - Universidade Federal do ABC, Programa de Pós-Graduação em Nanociências e Materiais Avançados, 2017. / A obtencao de nanoparticulas por exsolucao e uma tecnica que tem sido extensivamente pesquisada e aprimorada recentemente. As particulas exsolvidas apresentam propriedades superiores quando comparadas as depositadas. O metodo de exsolucao consiste na reducao de ions previamente solubilizados em uma matriz, dando origem a particulas fortemente ligadas ao substrato. Materiais com composicoes (La1-xSrx)z(Cr1-yNiy)O3-¿Â (x e y = 0%, 5%, 10%, 15% e 20%; z = 100% e 80%) foram sintetizados, utilizando o metodo de polimerizacao de complexos. A resina produzida no processo de sintese foi analisada utilizando tecnicas de analise termica, tal que a temperatura de calcinacao foi determinada sendo igual a 900 ¿C. Foi utilizada a tecnica de difracao de raios X para caracterizacao estruturas e identificacao das fases presentes. Todas as amostras foram reduzidas com objetivo de criar, atraves de exsolucao, nanoparticulas de niquel metalico. Analises magneticas foram conduzidas para determinar o comportamento magnetico dos materiais produzidos. Materiais nao estequiometricos foram sintetizados para verificar a influencia de diferentes estequiometrias no processo de exsolucao. O sitio A nao estequiometrico prejudicou a solubilizacao do Ni e Sr na estrutura da cromita de lantanio. Todas as amostras com dopantes apresentaram uma diminuicao da temperatura de Neel da cromita de lantanio. Entretanto, o tratamento de reducao provocou um aumento da temperatura de Neel, se comparado com as amostras oxidadas. Esse e um indicativo da diminuicao de concentracao de niquel em solucao solida, um resultado condizente com o mecanismo de exsolucao. Utilizando as medidas de magnetismo foi possivel verificar o mecanismo de exsolucao e fracao massica de niquel metalico para cada amostra. Utilizando tecnicas de microscopia eletronica foi possivel detectar a presenca de nanoparticulas apos o tratamento de reducao com diametro de aproximadamente 20 nm. Ao realizar uma analise quimica local utilizando um microscopio eletronico de transmissao, foi possivel verificar que as particulas em questao sao de niquel metalico. / The production of nanoparticles by exsolution is a technique that has been extensively researched and improved recently. Exsolved particles have superior properties when compared to deposited particles. The method of exsolution consists in the reduction of previously solubilized ions in a matrix, giving rise to particles strongly attached to the substrate. Materials with compositions (La1-xSrx)z(Cr1-yNiy)O3-ä (x and y = 0%, 5%, 10%, 15% and 20%, z = 100% and 80%) were synthesized using the polymerization of complexes technique. The resin produced in the synthesis process was analysed using thermal analysis and the calcination temperature was determined to be 900 ° C. The X-ray diffraction technique was used to characterize structures and identify the present phases. All samples were reduced in order to create nanoparticles of metallic nickel by exsolution. Magnetic analysis was conducted to determine the magnetic behaviour of the produced materials. Non-stoichiometric materials were synthesized to verify the influence of different stoichiometry in the exsolution process. Non-stoichiometric A site impaired the solubilisation of Ni and Sr in the lanthanum chromite structure. All samples with dopants showed a decrease in the temperature of Neel of the lanthanum chromite. However, the reduction treatment caused an increase in the Neel temperature when compared to the oxidized samples. This is indicative of the decrease in nickel concentration in solid solution, a result consistent with the exsolution mechanism. Using the measurements of magnetism it was possible to verify the mechanism of exsolution and mass fraction of metallic nickel for each sample. Using electron microscopy techniques it was possible to detect the presence of nanoparticles after the reduction treatment with a diameter of approximately 20 nm. When performing a local chemical analysis using a transmission electron microscope, it was possible to verify that the particles in question are of metallic nickel.

[EN] Several major problems have to be solved before Solid Oxide Fuel Cells (SOFC) can operate continuously using hydrocarbon fuels such as natural gas. The risk of low catalytic behavior for fuel reforming, the carbon formation/deposition on the anode material at high operating temperatures and the presence of impurities in the fuel (in particular sulfides) can dramatically reduce the performance and durability of the cells. Taking all this into account, new anode materials with adequate (electro)catalytic properties are required. Recently, manganite compounds with Ruddlesden-Popper (RP) structure have been studied as potential new anode materials in INTERFASE group at Universidad Industrial de Santander (UIS). Their electrochemical performance have been described in previous works with promising results, but a fundamental knowledge was missing concerning the catalytic properties of such materials and the way to improve them by the addition of nickel metallic particles on the electrode surface. The current Ph.D. thesis was focused on the synthesis, characterization and catalytic study for steam reforming in SOFC anode conditions (low steam content) of a new RP manganite (La1.5Sr1.5Mn1.5Ni0.5O7±δ), which, in reducing atmosphere at high operating temperatures promotes via an exsolution mechanism the formation of two phases, i.e. an RP manganite of composition LaSrMnO4±δ decorated with metallic active Ni nanoparticles embedded in the surface; such strategy can be viewed as an original way to improve the (electro)catalytic properties of the anode materials and then a promising option for future SOFC systems operating with Colombian natural gas. The first chapter deals with the synthesis and characterization of the RP n= 2 phase La1.5Sr1.5Mn1.5Ni0.5O7±δ using the Pechini method. In agreement with SOFC operating temperature, Ni exsolution has been studied in diluted H2 at different temperatures (750, 800 and 850 °C) and reduction times. Ni nanoparticles decorating an RP n= 1 manganite is confirmed by XRD, TEM-EDS analysis and the size of the metallic particles on the oxide surface, below 100 nm, is characterized as a function of the exsolution conditions. The second chapter presents the catalytic behavior for the methane steam reforming reaction of the exsolved material applying the Gradual Internal Reforming concept adapted to SOFC operation (i.e. low water content, steam to carbon ratio equal to 0.15) at different reaction temperatures (750, 800 and 850 °C). The catalytic properties of Ni impregnated samples using a similar (La,Sr)2MnO4±δ ceramic support are also presented for comparison. The exsolved material exhibits better performance than the impregnated manganite for the reaction, especially at 850 °C, with higher conversion, conversion rate, and H2 production rate. Concerning the steam reforming of light alkane gas mixtures (CH4-C2H6, and CH4-C3H8), the behavior is affected due to the competition between the molecules and low available metallic active sites, but without affecting the H2 production. In addition, at long reaction times, the activity over the exsolved material is stable even with 100 h of reaction, without formation of carbonaceous species on the Ni particles, as confirmed by TEM and TGA/MS analysis. In the third and last chapter, the possible coke formation and sulfide poisoning are presented. Despite the high and stable catalytic behavior for methane steam reforming reaction with considerable carbon formation resistance, the exsolved material exhibits a high level of sensitivity to H2S poisoning, similar to the case of state-of-the-art Ni/YSZ anodic cermet and or Ni impregnated catalyst, with a drop of the activity to almost zero. Nevertheless, the exceptional overall results obtained for the exsolution-based material are promising for a possible use as SOFC anode operating with sulfur-free Colombian natural gas. / [ES] Muchos son los problemas que deben resolverse antes de que las celdas de combustible de óxido sólido (SOFC por sus siglas en inglés) puedan operar continuamente usando combustibles hidrocarbonados como por ejemplo el gas natural. El riesgo de una baja actividad catalítica para el reformado del combustible, la formación y depósito en el material de ánodo a elevadas temperaturas de operación y la presencia de impurezas en el combustible empleado (en particular de sulfuros) pueden reducir dramáticamente el desempeño y la durabilidad de las celdas. Teniendo todo esto en cuenta, nuevos materiales de ánodo con adecuadas propiedades (electro)catalíticas son necesarios. Recientemente, en el grupo INTERFASE de la Universidad Industrial de Santander (UIS), compuestos de tipo manganita con estructura Ruddlesden-Popper (RP) han sido estudiados como potenciales materiales de ánodo. Su desempeño electrocatalítico ha sido descrito en trabajos previos con promisorios resultados, pero el conocimiento fundamental sobre las propiedades catalíticas de dichos materiales y la forma de mejorarlos mediante la adición de partículas metálicas de níquel en la superficie del electrodo aún faltaba. La presente tesis doctoral se enfocó en la síntesis, caracterización y estudio catalítico en el reformado con vapor en condiciones de ánodo de celdas SOFC (bajo contenido de vapor) de una nueva manganita de tipo RP (La1.5Sr1.5Mn1.5Ni0.5O7±δ), la cual, en atmósfera reductora y a elevadas temperaturas de operación, promueven a través del mecanismo de exsolución la formación de dos fases: una manganita tipo RP de composición LaSrMnO4±δ decorada con nanopartículas metálicas y activas de Ni incrustadas en la superficie; dicha estrategia puede ser vista como una manera muy original de mejorar las propiedades (electro)catalíticas de los materiales de ánodo y por lo tanto ser consideradas como una opción prometedora para sistemas SOFC operados con gas natural colombiano. El primer capítulo trata sobre la síntesis de la fase RP n= 2 La1.5Sr1.5Mn1.5Ni0.5O7±δ usando el método de Pechini y su caracterización. De acuerdo con la temperatura de operación de las celdas SOFC, la exsolución del Ni en atmósfera de H2 diluido a diferentes temperaturas (750, 800 y 850 °C) y tiempos de reducción fue estudiada. Las nanopartículas de Ni decorando la manganita de estructura RP n= 1 es confirmada a través de análisis de DRX, MET-EDS y el tamaño de las partículas metálicas en la superficie del óxido, inferiores a 100 nm, es caracterizado en función de las condiciones de exsolución. El segundo capítulo presenta el comportamiento catalítico del material exsuelto en la reacción de reformado de metano aplicando el concepto de reformado interno gradual (GIR por sus siglas en inglés) adaptado a celdas SOFC (en otras palabras, bajo contenido de agua, relación vapor carbono igual a 0.15) a diferentes temperaturas de reacción (750, 800 y 850 °C). Las propiedades catalíticas de las muestras impregnadas con Ni utilizando como soporte un material cerámico similar (La,Sr)2MnO4±δ, son también presentados como comparación. El material exsuelto exhibe un mejor desempeño catalítico en la reacción de reformado que la manganita impregnada, especialmente a 850 °C, mostrando una más alta conversión, velocidad de conversión y de producción de H2. Con respecto al reformado de la mezcla de alcanos ligeros (CH4 -C2H6, y CH4 -C3H8), el comportamiento catalítico es afectado debido a la competición entre moléculas y la baja disponibilidad de sitios activos metálicos, sin afectar la producción de H2. Adicionalmente, a tiempos de reacción prolongados, la actividad en el material exsuelto es estable incluso con 100 h de reacción, sin formación de especies carbonáceas sobre las partículas de Ni como lo confirman las imágenes MET y el ATG/MS. En el tercer y último capítulo, la posible formación y depósito de carbón y el envenenamiento con sulfuros son presentados. Sin embargo, a pesar de la elevada y estable actividad catalítica en la reacción de reformado de metano con vapor con una considerable resistencia a la formación de carbón, el material exsuelto tiene un alto nivel de sensibilidad al envenenamiento con H2S, similar al Ni/YSZ (material de referencia de la literatura) o al material impregnado con Ni, con una disminución de la actividad catalítica a prácticamente cero No obstante, el excepcional resultado global obtenido en el material exsuelto es prometedor para un posible uso como material de ánodo en sistemas SOFC alimentados con gas natural colombiano libre de H2S. / [CA] Molts són els problemes que han de ser resolts abans que les cel·les de combustible d'òxid sòlid (SOFC per les seues sigles en anglès) puguen operar contínuament usant combustibles hidrocarbonats com per exemple el gas natural. El risc d'una baixa activitat catalítica per al reformat del combustible, la formació i depòsit en el material d'ànode a elevades temperatures d'operació i la presència d'impureses en el combustible emprat (en particular de sulfurs) poden reduir dramàticament l'acompliment i la durabilitat de les cel·les. Tenint tot això en compte, nous materials d'ànode amb propietats (electro)catalítiques adequades són necessaris. Recentment, en el grup d'investigació INTERFASE de la Universitat Industrial de Santander (UIS), compostos de tipus manganita amb estructura Ruddlesden-Popper (RP) han sigut estudiats com a potencials materials anòdics. El seu acompliment electroquímiques ha sigut tractades en treballs previs amb resultats promissoris, però el coneixement fonamental sobre les característiques catalítiques d'aquests materials i la manera de millorar-los mitjançant l'addició de partícules metàl·liques de níquel en la superfície de l'elèctrode encara faltava. La present tesi de doctorat es va enfocar en la síntesi, caracterització i estudi d'activitat catalítica en el reformat amb vapor en condicions d'ànode de cel·les SOFC (sota contingut de vapor) d'una nova manganita de d'estructura RP (La1.5Sr1.5Mn1.5Ni0.5O7±δ), la qual, en atmosfera reductora i a elevades temperatures d'operació, promouen, a través del mecanisme de exsolució; la formació de dues fases: una manganita de composició LaSrMnO4±δ decorada amb nanopartícules metàl·liques i actives de Ni incrustades en la superfície; aquesta estratègia pot ser vista com una manera molt original de millorar les propietats (electro)catalítiques dels materials d'ànode i per tant, ser considerades com una prometedora opció per a futurs usos en sistemes SOFC alimentats amb gas natural colombià. El primer capítol tracta sobre la síntesi de la fase RP n= 2 La1.5Sr1.5Mn1.5Ni0.5O7±δ usant el mètode de Pechini i la seua caracterització. D'acord amb la temperatura d'operació de les cel·les SOFC, la exsolució del Ni en atmosfera d'H2 diluït a diferents temperatures (750, 800 i 850 °C) i temps de reducció va ser estudiada. Les nanopartícules de Ni decorant la manganita d'estructura RP n= 1 és confirmada a través d'anàlisi de DRX, MET-EDS i la grandària de les partícules metàl·liques en la superfície de l'òxid, inferiors a 100 nm, és caracteritzat en funció de les condicions de exsolució. El segon capítol presenta el comportament catalític del material d’exsolució en la reacció de reformat de metà amb vapor aplicant el concepte de reformat gradual intern (GIR per les seues sigles en anglès) adaptat a cel·les SOFC (en altres paraules, sota contingut de vapor, relació vapor-carboni de 0.15) a diferents temperatures de reacció (750, 800 i 850 °C). Les propietats catalítiques de les mostres impregnades amb Ni utilitzant com a suport un material ceràmic similar (La,Sr)2MnO4±δ, són també presentats com a comparació. El material d’exsolució exhibeix un millor resultat catalític en la reacció de reformat que la manganita impregnada, especialment a 850 °C, mostrant una més alta conversió, velocitat de conversió i de producció d'H2. En el reformat de la mescla d'alcans lleugers (CH4 -C2H6, i CH4 -C3H8), el comportament catalític és afectat per la competició entre molècules i la baixa disponibilitat de llocs actius metàl·lics, sense afectar la producció d'H2. Addicionalment, a temps de reacció llargs, l'activitat en el material d’exsolució és estable fins i tot desprès de 100 h de reacció, sense formació d'espècies carbòniques sobre les partícules de Ni, com ho confirmen les imatges MET i el ATG/MS. En el tercer i últim capítol, la possible formació i depòsit de carbó i l'enverinament amb sulfurs són presentats. No obstant això, malgrat l'elevada i estable activitat catalítica en la reacció de reformat de metà amb vapor amb una considerable resistència a la formació de carbó, el material d’exsolució té un alt nivell de sensibilitat a l'enverinament amb H2S, similar al Ni/YSZ (material de referència de la literatura) o el material impregnat amb Ni, amb una disminució de l'activitat catalítica a pràcticament zero No obstant això, l'excepcional resultat global obtingut aquest nou material és prometedor per a un possible ús futur com a material d'ànode en sistemes SOFC alimentats amb gas natural colombià lliure d'H2S. / Al Departamento Administrativo de Ciencia, Tecnología e Innovación (COLCIENCIAS) por la beca de estudios de Doctorados Nacionales Conv. 647 y el proyecto # 110265842833 “Symmetrical high temperature Fuel Cell operating with Colombian natural gas”. Al Consejo Superior de Investigaciones Científicas por el apoyo con la ayuda económica para la estancia mediante la convocatoria I-coop Project # COOPA20112. / Vecino Mantilla, JS. (2020). Nickel exsolution effect on the catalytic behavior of ruddlesden-popper manganites in sofc conditions using colombian natural gas [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/149474

In situ thermal treatment (ISTT) applications require successful gas capture for the effective remediation of chlorinated solvent dense non-aqueous phase liquid (DNAPL) source zones. Gas production and transport mechanisms during bench-scale electrical resistance heating (ERH) experiments were examined in this study using a quantitative light transmission visualization method. Processed images during water boiling indicated that gas bubble nucleation, growth and coalescence into a connected steam phase occurred at critical gas saturations of Sgc = 0.233 ± 0.017, which allowed for continuous gas transport out of the heated zone. Critical gas saturations were lower than air-water emergence gas saturations of Sgm = 0.285 ± 0.025, derived from the inflection point of ambient temperature capillary pressure-saturation curves. Coupled electrical current and temperature measurements were identified as a metric to assess gas phase development. Processed images during co-boiling of pooled trichloroethene (TCE) DNAPL and water indicated that discontinuous gas transport occurred above the DNAPL pool. When colder zones were introduced, condensation prevented the development of continuous steam channels and caused redistribution of DNAPL along the vapour front. These results suggest that water boiling temperatures should be targeted throughout the subsurface (i.e., from specific locations of DNAPL to extraction points) during ERH applications. Because convective heat loss and non-uniform power distributions have the potential to prevent the achievement of boiling temperatures, a thermal enhancement was developed where dissolved gas delivered to the target heated zone liberates from solution at elevated temperatures and increases gas production. Processed images of ERH-activated carbon dioxide (CO2) exsolution indicated that discontinuous gas transport occurred above saturations of Sg = 0.070 ± 0.022. Maximum exsolved gas saturations of Sg = 0.118 ± 0.005 were sustained during continuous injection of the saturated CO2 solution into the heated zone. Estimated groundwater relative permeabilities of krw = 0.642 ± 0.009 at these saturations are expected to decrease convective heat loss. Discontinuous transport of exsolved gas at sub-boiling temperatures also demonstrated the potential of the enhancement to bridge vertical gas transport through colder zones. In conclusion, sustained gas saturations and transport mechanisms were dependent on the mechanism of gas production and effects of condensation. / Thesis (Master, Civil Engineering) -- Queen's University, 2014-03-27 15:26:30.683

Oxygen Transport Membranes (OTMs) can drastically reduce the energy and cost demands of processes that require pure oxygen, as they offer the possibility to combine a separation unit with a chemical reactor. One of the most commercially viable applications of OTMs is the partial oxidation of hydrocarbons for syngas production. A typical OTM configuration is a sequential arrangement of layers, i.e. an inactive support, a fuel oxidation layer, a dense layer and an oxygen reduction layer. However, one of the limitations of the OTM system is the low catalytic activity and stability of the materials currently used for the fuel oxidation layer. Moreover, the traditional deposition techniques that are used for the catalysts preparation are difficult to perform, as the fuel oxidation layer is buried deeply in the structure of the OTM. To simplify the OTM fabrication and improve the catalysts activity and stability, this thesis explores the exsolution of Ni nanoparticles from two different host lattice compositions, as potential materials for the fuel oxidation layer of OTMs. The (La₀.₇₅Sr₀.₂₅)(Cr₀.₅Mn₀.₄₅Ni₀.₅)O₃ (LSCMNi5) perovskite was selected, as the first candidate material for the OTMs. During reduction, the exsolution of Ni nanoparticles from the perovskite lattice took place and enhanced significantly the catalytic activity of the material regarding methane conversion. However, these nanoparticles were oxidised during the first hours of the testing and slowly reincorporated into the perovskite structure, leading to drop in the performance. Thereafter, the (La₀.₇₅Sr₀.₂₅)(Cr₀.₅Mn₀.₄₅Ni₀.₅)O₃ (LSCMNi5) perovskite was selected as an alternative composition. When the oxide lattice was sufficiently reduced, the exsolution of Fe-Ni alloy nanoparticles occurred. The catalytic testing suggested that the Fe-Ni alloy nanoparticles on LSCFNi5 presented lower activity for methane conversion comparing to the Ni nanoparticles on LSCMNi5, but higher stability in oxidising conditions. By increasing the Ni doping on the B-site of LSCF to 15 mol%, the catalytic activity of the material regarding methane conversion was increased and exceeded that of LSCMNi5. A CH₄ conversion of 70% was achieved, which was 20 times higher than that of the initial LSCF perovskite. Therefore, by tailoring the perovskite composition and the exsolution of the Fe-Ni alloy nanoparticles, it was possible to synthesize a material for the fuel oxidation layer of OTMs, which combined the high catalytic activity of Ni and the good redox stability of Fe.

A diploma thesis was objected to a figure analyzing and a figure interpretation of ingot processing. The described figures were obtained from samples which were taking from feeder-heads of ingot of lower ram, produced in Vitkovice Machinery Group. The thesis was focused on ingot solidification and segregation processes which were associated with this procedure. The figures obtained from numeric simulation of ingot solidification in defined places were analyzed using statistic method – linear regression, as well as linear regression was used for evaluation of explored samples, their chemical compositions and mechanical properties. In conclusion all acquired results were summarized.

京都大学 / 0048 / 新制・課程博士 / 博士(理学) / 甲第18087号 / 理博第3965号 / 新制||理||1572(附属図書館) / 30945 / 京都大学大学院理学研究科地球惑星科学専攻 / (主査)准教授 三宅 亮, 教授 土`山 明, 准教授 河上 哲生 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DGAM

The development of technologies that enable efficient and reliable energy inter-conversion and storage is of key importance for tempering the intermittent availability of renewable energy sources, and thus for developing an energy economy based on sustainable, clean energy production. Solid oxide electrolysis cells (SOECs) may be used to store excess electrical energy as hydrogen, while solid oxide fuel cells (SOFCs) could convert back hydrogen into electricity, thus balancing energy availability and demand. However, the current state-of-the-art hydrogen electrode used in both SOECs and SOFCs, the Ni-yttria-stabilised zirconia cermet (Ni-YSZ), is unreliable in conjunction with intermittent energy sources, in particular due to its innate redox instability. This thesis explores the fundamental properties of various inherently redox stable A-site deficient titanate perovskite systems (A1-αBO3, B = Ti), seeking to uncover the principles that enhance their properties so that they may be used to replace Ni-YSZ. In particular, this work demonstrates that the versatility of perovskites with respect to the introduction of lattice defects such as vacancies and cation substitutions enables considerable improvements in the extent of reduction, electronic conductivity and overall electrochemical activity. Most importantly, the defect chemistry context set by the presence of A-site vacancies was found to trigger the exsolution of electrocatalytically active nanoparticles from the parent perovskite, upon reduction. This is an entirely new phenomenon which was explored and exploited throughout this study to produce perovskite surfaces decorated with uniformly distributed catalytically active nanoparticles. As demonstrated in this study, the exsolution phenomenon excels in terms of producing nanoparticles with uniform size, distribution, diverse composition and ‘unconventional' surface anchorage. The resulting enhanced properties, and especially the exsolution phenomenon, contributed coherently towards improving the suitability of the perovskites developed here towards their application as hydrogen electrode materials. Consequently, when integrated into SOEC button cells as hydrogen electrodes, they exhibited a step-change increase in performance compared to other perovskites considered to date. Many of the principles and perovskite defect chemistry explored and exemplified in this study on perovskite titanates may be extended to other perovskites as well. In particular the advanced control and understanding achieved in this work over the exsolution phenomenon may inspire the formulation of new and sophisticated oxide materials with advanced functionality.

No description available.