Over the past few decades there has been great interest in exploring alternatives to conventional separation methods due to their high cost and energy requirements. Membranes offer a potentially attractive alternative as they potentially address both of these points. The overarching theme of this dissertation is to design nanocomposite membranes for processes where existing separation schemes are inadequate. This dissertation focuses on three challenges: 1) designing organic-inorganic hybrid membranes for reverse-selective removal of alkanes from light gases, 2) defect-free inorganic nanocomposite membranes that have uniform pores, and 3) nanocomposite membranes for minimizing protein fouling in microfiltration applications. Reverse-selective gas separations that preferentially permeate larger/heavier molecular species based on their greater solubility have attracted considerable recent attention due to both economic and environmental concerns. In this study, dendrimer-ceramic hybrid membranes showed exceptionally high propane/nitrogen selectivities. This result was ascribed to the presence of stable residual solvent that affects the solubility of hydrocarbon species. Mesoporous silica-ceramic nanocomposite membranes have been fabricated to provide defectless mesoporous membranes. As mesoporous silica is iteratively synthesized in the ceramic macropores, the coating method and the surfactant removal step significantly affected permeance and selectivity. It was also shown that support layers can cause a lower selectivity than Knudsen limit. Membrane fouling which results from deposition and nonspecific adsorption of proteins on the membrane surface is irreversible in nature, and results in a significant decrease in the membrane performance. To address this problem, two approaches were explored: 1) control of the surface chemistry tethering alumina membranes with organic components and 2) development of a novel photocatalytic membrane that exhibits hydrophilicity and can be easily regenerated. Both approaches can offer a viable route to the synthesis of attractive membranes, in that 1) the density of protein-resistant organic groups such as PEG is controllable by changing scaffolds or synthesis conditions and 2) the photocatalytic nanocomposite membranes can open the way for a new regeneration method that is environmentally benign.

The development and design of efficient catalysts are essential for catalytic energy technologies, accompanied with the fundamental understanding of structure-property relationships of these catalysts. Metal-organic frameworks (MOFs), as the new class of promising catalysts, have been intensively investigated primarily in their fundamental electrochemistry and the broad spectrum of catalytic applications due to their structural flexibility, tailorable crystalline, and multi-functionality. In this work, we combine experiments and mechanism investigation to gain a fundamental understanding of how the surface property and the structure of MOFs affect their catalytic performance. With the aim of material design for MOFs catalysts, we developed two novel superhydrophilic and aerophobic metal-organic frameworks (AlFFIVE-1-Ni MOFs and FeFFIVE-1-Ni MOFs) used as electrocatalysts for the first time during oxygen evolution reactions (OER). Under the facilitation of hydrophilicity and aerophobicity, developed FeFFIVE-1-Ni MOFs electrocatalysts deliver optimal OER performance, better than that of the state-of-art RuO2 and referred NiFe-BDC MOFs electrocatalysts. Most importantly, the practical strategy demonstrated that the hydrophilic and aerophobic structure of MOFs does indeed deliver the optimal electrocatalytic performance. With the aim of investigating the structural transformation process of metal-organic framework, we used a series of advanced characterization techniques to monitor the structure evolution and defects presence for post-heating treated UiO-66 MOFs. The structural and electronic features of UiO-66 MOFs were intensely studied in their hydroxylated, dehydroxylated, defected, and pyrolytic forms. Meanwhile, one concept about the framework situation, quasi-MOF (like a transition state, defined high activation along the structure evolution corresponding to the presence of many defects), was presented and demonstrated. Compared with pristine UiO-66 MOF, the Quasi-MOF with the presence of active defects showed enhanced catalytic activity on the Meerwein-Ponndorf-Verley reduction reaction, which offers an opportunity to understand the structure-property relationship along with the structure evolution process of UiO-66 MOFs.

Des revêtements sol-gel nanocomposites TiO2-SiO2 ont été réalisés à partir de mélanges d'une suspension nanocristalline de TiO2 anatase et de sols polymériques de silice. Ces revêtements présentent une superhydrophilie naturelle, persistante et photo-régénérable. La présence de charges localisées aux interfaces granulaires TiO2-SiO2 est une des hypothèses permettant d'expliquer cette superhydrophilie naturelle. Toutefois des effets de morphologie (rugosité, porosité de surface) sont également connus pour influencer le mouillage. Des études ont été menées pour mettre directement en évidence l'effet intrinsèque des interfaces granulaires. Les études se sont recentrées sur l'effet extrinsèque de paramètres morphologiques susceptibles d'influencer la mouillabilité des revêtements nanocomposites selon des modèles thermodynamiques des surfaces connus. De nouveaux protocoles de synthèse par voie sol-gel ont été mis au point afin d'analyser i/ en quoi la superhydrophilie naturelle et photo-induite des revêtements TiO2-SiO2 pouvait être influencée par des effets de morphologie et de composition, et ii/ en quoi une exacerbation de ces effets via des structurations artificielles pouvaient encore accroître la superhydrophile de surface. Une extrapolation de ces protocoles a également permis d'étudier des revêtements superhydrophobes. / Sol-gel TiO2-SiO2 nanocomposites coatings have been deposited from a suspension of anatase TiO2 nanocristallites mixed with different polymeric silica sols. These coatings show a natural and persistent superhydrophilicity, which can also be photo-regenerated. This outstanding property can probably be explained by electrical charges localized at TiO2-SiO2 granular interfaces. Yet, some morphological features (roughness, surface porosity) may also influence wetting properties. Studies have firstly been carried out to directly evidence the intrinsic effect of those electrical charges. The studies have then been focused on the extrinsic effect of morphological parameters than can influence the composite wettability, according to thermodynamic models. New sol-gel protocols were carried out to better understand in which extent i/ the natural and photo-induced wetting properties of composite coatings may be influenced by composition and morphological features, and ii/ artificial structuration of the coating surface may enhance their superhydrophilicity. Those structuration protocols have been extrapolated to the study of superhydrophobic coatings.

Les matériaux à base de polydopamine (PDA) s’inspirent de la forte adhésion du byssus de la moule sous l’eau. L’oligomérisation de la dopamine dans un milieu basique permet la formation de revêtement de PDA sur n’importe quel matériau. En plus de la simplicité du procédé celui-ci est vert et versatile. La PDA a des propriétés similaires aux mélanines, d’où son utilisation dans le domaine des phénomènes de conversion d’énergie, de l’environnement et du biomédical. Cependant la structure de la PDA étant inconnue, l’élaboration de matériaux basés sur la relation structure propriétés est difficile. L’un des buts de cette thèse a été de comprendre cette relation pour élaborer de nouveaux matériaux de PDA. En choisissant l’oxydant adéquat nous avons déposé un film épais, superhydrophile et biocompatible sur n’importe quels substrats. De plus nous avons découverts la possibilité de former des films de PDA à l’interface air/eau. L’étude de ce phénomène a permis de former des membranes autosupportées et stimuli responsives. / Polydopamine (PDA) materials are inspired from mussels’ byssus strong adhesion underwater. The oligomerization of dopamine in a basic medium allows forming a PDA coating on virtually any materials. In addition to the simplicity, ecofriendly and versatility of the deposition method, PDA has properties similar to those of melanin pigments and displays many outstanding properties. Thus PDAis widely used in energy, environmental and biomedical sciences. However design of PDA based new materials with tailored properties is a challenge since its structure is still unknown. In that sense one of the aims of this thesis is to gain knowledge in PDA structure-property relationship in order to design PDA materials with new properties. By choosing the appropriate oxidant we deposited thick and superhydrophylic films on any materials for the elaboration of low fouling and biocompatible surfaces. Additionally we discovered the possibility to form PDA films at the air/water interface. The investigation of this phenomenon led to the formation of stimuli responsive free standing membranes.

In this work, the mechanism of the corrosion behavior of laser-treated aluminum is studied. Two different laser techniques are used to fabricate the samples, direct laser interference patterning (DLIP) and direct laser writing (DLW), using nanosecond laser sources. The DLIP treatment uses a two-beam optical configuration producing line-like periodic structures. The DLW technique is employed to produce non-periodic structures on the Al-surface with the same cumulated fluences as in DLIP. The surface topography is analyzed by confocal microscopy, and the formation of oxide layers is investigated by scanning electron microscopy of cross-sections produced using a focused ion beam. Wetting measurements performed on the laser-treated samples exhibit a contrasting behavior, leading to either superhydrophobic or superhydrophilic states. In the case of the DLIP treatment, the static water contact angle is increased from 81° up to 158°, while for DLW, it decreases to 3°. Electrochemical tests demonstrate a decreased corrosion rate after laser treatment. Additionally, findings indicate no correlation between wettability and corrosion reduction. Therefore, the improvement in corrosion resistance is mainly attributed to the oxide layer formed by laser treatment. Although similar corrosion rates are achieved for both treatments, surfaces produced with DLIP can be beneficial when additional surface properties are required.