Au cours de ce travail, nous avons décrit et mis en œuvre la fabrication de surfaces nanostructurées d’alumine par anodisation de feuilles d’aluminium de très grande pureté. Les paramètres morphologiques caractérisant la membrane d’oxyde que sont le diamètre des pores, leur profondeur et leur espacement sont finement contrôlés par les paramètres expérimentaux. Ces surfaces nanotexturées ont permis l’étude approfondie de l’interaction solide-liquide au sein des pores et de la physique de la ligne de contact devant composer avec les nano-aspérités de surface. Ces deux éléments ont pu être appréhendés par des mesures d’angles de contact à l’équilibre et d’hystérésis de mouillage. La modélisation des résultats a montré l’inadéquation des modèles classiques de CASSIE, WENZEL ou de capillarité à cette situation. L’adjonction du terme controversé de tension de ligne permet de bonnes prévisions. Nous montrons que cette interprétation n’est pas unique ; une diminution de l’énergie de surface due à la forte courbure des pores conduit à des résultats identiques. Une investigation théorique a été menée par l’intégration des forces de VAN DER WAALS. La baisse de l’énergie de surface est prévue mais dans des proportions insuffisantes. Le modèle peut être amélioré. Les mesures d’hystérésis ont dévoilé le pouvoir adhésif des surfaces nanoporeuses. À cause des forces de capillarité dans les pores, la ligne de contact ne peut jamais reculer. Les angles d’avancée ont montré que la ligne de contact a une épaisseur négligeable devant la dizaine de nanomètre. Elle peut en outre parfaitement contourner les pores, imprimant de fortes courbures à l’interface liquide-gaz à la base de la goutte. Sa forme tridimensionnelle a été abordée au travers d’un modèle numérique restant à perfectionner. / In this work, we have described and carried out the fabrication of nanostructured alumina surfaces by anodizing highly pure aluminum foils. The pore diameter, depth and spacing are finely controled through experimental parameters. These nanotextured surfaces allowed a thorough study of the solid-liquid interactions within the pores and of the contact-line constrained by the surface nanoasperities. Equilibrium contact-angle and wetting hysteresis measurements were helpful to apprehend them. Modeling the results has revealed the inability of classical CASSIE, WENZEL and capillarity models to properly match the situation. Adding the controversial line-tension term solves the problem and provides good predictions. Anyway, this interpretation is not unique. A lower surface energy within the pores due to their strong curvature yields the same modeling quality. This case has been theoretically investigated through the integration of VAN DER WAALS’ forces. A surface-energy decrease has been calculated but it is not as strong as required. The model still can be improved. Hysteresis measurements have highlighted the nanoporous surfaces are strongly adhesive. Because of the pore size, the capillarity is very marked and keeps the contact line from receding. The advancing contact angles have shown that the contact-line thickness is negligible with respect of ten nanometres. In addition, it can circumvent the pore openings which involves strong liquid–gas interface curvatures at the drop base. The three-dimensional liquid–gas interface shape has been studied with a numerical model that still has to be enhanced.

Nanoporous GaN films are prepared by UV assisted electrochemical etching using HF solution as an electrolyte. To assess the optical quality and morphology of these nanoporous films, micro-photoluminescence (PL), micro-Raman scattering, scanning electron microscopy (SEM), and atomic force microscopy (AFM) techniques have been employed. SEM and AFM measurements revealed an average pore size of about 85-90 nm with a transverse dimension of 70-75 nm. As compared to the as-grown GaN film, the porous layer exhibits a substantial photoluminescence intensity enhancement with a partial relaxation of compressive stress. Such a stress relaxation is further confirmed by the red shifted E₂(TO) phonon peak in the Raman spectrum of porous GaN. / Singapore-MIT Alliance (SMA)

Exploring and understanding how the smallest scale features of a cell affect biochemical reactions has always been a challenge. Nanoscale fabrication advancements have allowed scientists to create small volume reaction containers that resemble the physical scale of cell membranes. Engineers seek to use biological design principles to manipulate information and import new functionality to such synthetic devices, which in turn, play a crucial role in allowing them to explore the effects of physical transport and extreme conditions of temperature and pH on reaction systems. Engineered reaction containers can be physically and chemically defined to control the flux of molecules of different sizes and charge. The design and testing of such a container is described here. It has a volume of 19 pL and has defined slits of 10-200 nm. The device successfully contains DNA and protein molecules and has been used to conduct and analyze enzyme reactions under different substrate concentrations and a continuous cell-free protein synthesis. The effect of DNA concentration and slit size on protein yield is also discussed. Glucose oxidase and horseradish peroxidase were loaded in the small volume container and fed with a solution containing glucose and Amplex Red™ to produce Resorufin. Fluorescent microscopy was used to monitor the reaction, which was carried out under microfluidic control. Enzyme kinetics were characterized and compared with conventional scale results. Continuous cell free protein synthesis in arrays of nanoporous, picoliter volume containers has also been achieved. A multiscale fabrication process allows for the monolithic integration of the containers and an addressable microfluidic network. Synthesis of enhanced green fluorescent protein (eGFP) in the nanoporous containers continues beyond 24 hours and yields more than twice the amount of protein, on a per volume basis, than conventional scale batch reactions. These picoliter, nanoporous containers provide new ways for quick determination of enzyme kinetics and continuous protein synthesis in microfluidic systems. They can be used in a wide variety of applications such as drug discovery, clinical diagnostics and high-throughput screening.

Biologically inspired materials are being developed with the aim of improving the integration of medical implants and minimizing non-desirable host reactions. A promising strategy is the design of topographically patterned surfaces that resemble those found in the extracellular environment. Nanoporous alumina has been recognized as a potential biomaterial and as an important template for the fabrication of nanostructures. In this thesis in vitro studies were done to elucidate the role of alumina nanoporosity on the inflammatory response. Specifically, by comparing alumina membranes with two pore sizes (20 and 200 nm in diameter). Complement and platelet activation were evaluated as well as monocyte/macrophage behaviour. Whole blood was incubated with the alumina membranes and thereafter the biomaterial surfaces were evaluated in terms of protein and platelet adhesion as well as procoagulant properties. The fluid phase was analyzed for complement activation products and platelet activation markers. Besides, human mononuclear cells were cultured on the alumina membranes and cell adhesion, viability, morphology and release of pro-inflammatory cytokines were evaluated. The results indicated that nanoporous alumina with 200 nm pores promotes higher complement activation than alumina with 20 nm pores. In addition, platelet response to nanoporous alumina was found to be highly dependent on the material porosity, as reflected by differences in adhesion, PMP generation and procoagulant characteristics. A clear difference in monocyte/macrophage adhesion and activation was found between the two pore size alumina membranes. Few but highly activated cells adhered to the 200 nm membrane in contrast to many but less activated monocytes/macrophages on the 20 nm surface. The outcome of this work emphasizes that nanotopography plays an important role in the host response to biomaterials. Better understanding of molecular interactions on nano-level will undoubtedly play a significant role in biomaterial implant development and will contribute to design strategies for controlling specific biological events.

The very large number of distinct structures that are known for metal-organic frameworks (MOFs) and zeolites presents both an opportunity and a challenge for identifying materials with useful properties for targeted separations. In this thesis we propose a three-stage computational methodology for addressing this issue and comprehensively screening all available nanoporous materials. We introduce efficient pore size calculations as a way of discarding large number of materials, which are unsuitable for a specific separation. Materials identified as having desired geometric characteristics can be further analyzed for their infinite dilution adsorption and diffusion properties by calculating the Henry's constants and activation energy barriers for diffusion. This enables us to calculate membrane selectivity in an unprecedented scale and use these values to generate a small set of materials for which the membrane selectivity can be calculated in detail and at finite loading using well-established computational tools. We display the results of using these methods for >500 MOFs and >160 silica zeolites for spherical adsorbates at first and for small linear molecules such as CO₂ later on. In addition we also demonstrate the size of the group of materials this procedure can be applied to, by performing these calculations, for simple adsorbate molecules, for an existing library of >250,000 hypothetical silica zeolites. Finally, efficient methods are introduced for assessing the role of framework flexibility on molecular diffusion in MOFs that do not require defining a classical forcefield for the MOF. These methods combine ab initio MD of the MOF with classical transition state theory and molecular dynamics simulations of the diffusing molecules. The effects of flexibility are shown to be large for CH₄, but not for CO₂ and other small spherical adsorbates, in ZIF-8.

Acrylonitrile were copolymerized with 2-ethylhexyl acrylate and hexyl acrylate via one step emulsion polymerization using ammonium persulfate (initiator), 1-dodecanthiol (chain transfer agent) and DOWFAX 8390 (surfactant) in the presence of water at about 68 0C. Poly (acrylonitrile-2ethylhexyl acrylate) and poly (acrylonitrile-hexyl acrylate) copolymers with three different comonomer composition (8, 12 and 16 molar percent) were prepared. FTIR and 1H-NMR were used in order to clarify the chemical structure of copolymers. The comonomer amount incorporated into copolymers was determined by using 1H-NMR spectra. The thermal behavior of copolymers was determined by DSC and TGA. Molecular weights of copolymers were determined by intrinsic viscosity (IV) measurements. IV measurements revealed that both poly (acrylonitrile-2ethylhexyl acrylate) and poly (acrylonitrile-hexyl acrylate) have sufficient molecular weight to form nanoporous filtration membranes. Nanoporous filtration membranes were prepared and tested for chromium (IV) removal. It was observed that chromium (VI) rejections of nanoporous filtration membrane were highly dependent on the concentration and the pH of the solutions. Almost complete removal (99, 9 percent Cr (VI)) rejection was achieved at pHs 2, 5 and 7 for solution containing 50 ppm, chromium (VI) with permeate flux within a range from 177 to 150 L/m2h at 689.5 kPa. Also, chemical structure, swelling ratios, sheet resistivity and fracture morphologies of the nanoporous filtration membrane were studied. It should be noted that the nanoporous filtration membranes were fouling resistant.

Metal-organic frameworks (MOFs) or porous coordination polymers (PCPs) have become the focus of intense study over the past decade due to their potential for advancing a variety of applications including air purification, gas storage, adsorption separations, catalysis, gas sensing, drug delivery, and so on. These materials have some distinct advantages over traditional porous materials such as the well-defined structures, uniform pore sizes, chemically functionalized sorption sites, and potential for post-synthetic modification, etc. Thus, synthesis and adsorption studies of porous MOFs have increased substantially in recent years. Among various prospective applications, air purification is one of the most immediate concerns, which has urgent requirements to improve current nuclear, biological, and chemical (NBC) filters involving commercial and military purposes. Thus, the major goal of this funded project is to search, synthesize, and test these novel hybrid porous materials for adsorptive removal of toxic industrial chemicals (TICs) and chemical warfare agents (CWAs), and to install the benchmark for new-generation NBC filters. The objective of this study is three-fold: (i) Advance our understanding of coordination chemistry by synthesizing novel MOFs and characterizing these porous coordination polymers; (ii) Evaluate porous MOF materials for gas-adsorption applications including CO2 capture, CH4 storage, other light gas adsorption and separations, and examine the chemical and physical properties of these solid adsorbents including thermal stability and heat capacity of MOFs; (iii) Evaluate porous MOF materials for next-generation NBC filter media by adsorption breakthrough measurements of TICs on MOFs, and advance our understanding about structure-property relationships of these novel adsorbents.

Nanoporous (NP) metal foams combine desirable characteristics of metals with unique nanoarchitectural features to yield weight normalized properties far superior than either dense metals or bulk metal foams. Due to their high surface to volume ratios these structures show great promise as components of fuel cells, as sensors and have been suggested for use in biological applications, for example as antimicrobial scaffolds or as platforms on which to explore biological material behavior. While most NP metal foams are isotropic, structures with anisotropic features spanning different length scales can further extend applications. This work examines the parameters controlling the synthesis of transversely isotropic NP Platinum foam by dealloying an amorphous Pt-Si alloy. The structure that is examined in this work is hierarchical with Voronoi polyhedra that form on the free surface and under each polyhedral hyper-structure, nanocrystalline NP Pt foam forms with radial struts of length ~60 nm and grain size of 5 nm. The size of the polyhedra can be tailored by changing the dealloying potential. In turn, the mechanical properties of these structures as assessed by nanoindentation can range from 1 to 3GPa depending on the geometric arrangement of the struts. Finally, the initiation location of these structures and the relationship between electrochemical parameters and dealloying front evolution is examined.

Nanoporous (np) materials with pore size below 100 nano-meters exist naturally in biological and mineral structures, and synthetic np materials have been used industrially for centuries. Np materials have attracted significant research interest in recent decades, as the development of new characterization techniques and nanotechnology allow the observation and design of np materials at a new level. This study focuses on two np materials: nanoporous silicon (np-Si) and nanoporous palladium (np-Pd). Silicon (Si), because of its high capacity to store lithium (Li), is increasingly becoming an attractive candidate as anode material for Li ion batteries (LIB). One significant problem with using Si as an anode is the large strain that accompanies charge-discharge cycling, due to swelling of the Si during Li insertion and deinsertion. Np-Si offers a large amount of free volume for Li absorption, which could allow the anode material to swell without cracking. A new method to fabricate thin films of high-purity (100% Si content) np-Si, which is promising as an anode material for LIB, is demonstrated and discussed in this study. Microstructural characterization, chemical analysis, battery performance testing and mechanical behavior of thin film np-Si are discussed here. Palladium (Pd) is considered an ideal and reliable hydrogen sensor and storage material, due to its fast response and selectivity for hydrogen gas. This research not only demonstrates a method to fabricate np-Pd thin films, but also proposes a method to fabricate bulk np-Pd. The uniformly crack-free and sponge-like np-Pd thin film provides high sensitivity to low concentrations of H2, showing promise as a hydrogen sensor material. Stress changes during hydrogenation/dehydrogenation were measured using wafer curvature. For bulk np-Pd, ultra-fine pore sizes were achieved by electrochemically dealloying bulk PdNi alloy. Mechanical behavior of bulk np-Pd was studied using in-situ transmission electron microscopy (TEM). Scanning electron microscopy (SEM) and x-ray diffraction were also used to characterize the structure and morphology of np-Pd. This doctoral research has involved the optimization of fabrication conditions and investigations of microstructural evolution during processing, yielding an improved understanding of the properties, mechanical behavior and potential applications of np-Si and np-Pd.

Nanotechnology is emerging to be one of the most important scientific disciplines that physics, chemistry and biology truly overlap with each other. Over the last two decades science and technology have witnessed tremendous improvement in the hope of unveiling the true secrets of the nature in molecular or atomic level. Today, the regime of nanometer is truly reached. ZnO is a promising material due to the wide direct band gap (3.37 eV) and the room temperature large exciton binding energy (60 meV). Recent studies have shown considerable attraction towards ZnO nanostructures, particularly on one-dimensional ZnO nanorods, nanowires, and nanotubes due to the fact that, for a large number of applications, shape and size of the ZnO nanostructures play a vital role for the performance of the devices. The noncentrosymmetric property of ZnO makes it an ideal piezoelectric material for nanomechanical devices. Thus, mechanical characterization of one dimensional ZnO nanostructures including strength, toughness, stiffness, hardness, and adhesion to the substrate is very important for the reliability and efficient operation of piezoelectric ZnO nanodevices. Moreover, owing to the large effective surface area with high surface-to-volume ratio, the surface of one dimensional ZnO nanowires, nanorods, and nanotubes is very sensitive to the changes in surface chemistry and hence can be utilized to fabricate highly sensitive ZnO electrochemical sensors. This thesis studies mechanical properties and electrochemical sensor applications of ZnO nanostructures. The first part of the thesis deals with mechanical characterization of vertically grown ZnO nanorods and nanotubes including buckling, mechanical instability, and bending flexibility. In paper I, we have investigated mechanical instability and buckling characterization of vertically aligned single-crystal ZnO nanorods grown on Si, SiC, and sapphire substrates by vapor-liquid-solid (VLS) method. The critical loads for the ZnO nanorods grown on Si, SiC, and sapphire were measured and the corresponding buckling and adhesion energies were calculated. It was found that the nanorods grown on SiC substrate have less residual stresses and are more stable than the nanorods grown on Si and sapphire substrates. Paper II investigates nanomechanical tests of bending flexibility, kinking, and buckling failure characterization of vertically aligned single crystal ZnO nanorods/nanowires grown by VLS and aqueous chemical growth (ACG) methods. We observed that the loading and unloading behaviors during the bending test of the as-grown samples were highly symmetrical and the highest point on the bending curves and the first inflection and critical point were very close. The results also show that the elasticity of the ZnO single crystal is approximately linear up to the first inflection point and is independent of the growth method. In Paper III, we quantitatively investigated the buckling and the elastic stability of vertically well aligned ZnO nanorods and ZnO nanotubes grown on Si substrate by nanoindentation technique. We found that the critical load for the nanorods was five times larger than the critical load for nanotubes. On the contrary, the flexibility for nanotubes was five times larger than nanorods. The discovery of high flexibility for nanotubes and high elasticity for nanorods can be utilized for designing efficient piezoelectric nanodevices. The second part of this thesis investigates electrochemical sensor applications of ZnO nanorods, nanotubes , and nanoporous material. In paper IV, we utilized functionalized ZnO nanorods on the tip of a borosilicate glass capillary coated with ionophore-membrane to construct intracellular Ca2+ selective sensor. The sensor exhibited a Ca2+-dependent electrochemical potential difference and the response was linear over a large dynamic concentration range, which enabled this sensor to measure Ca2+ concentrations in human adipocytes or in frog oocytes. The results were consistent with the values of Ca2+ concentrations reported in the literature. In paper V, ZnO nanotubes and nanorods were used to create pH sensor devices. The developed ZnO pH sensors display good reproducibility, repeatability, and long-term stability. The ZnO pH sensors exhibited a pH-dependent electrochemical potential difference over a large dynamic pH range. We found that the ZnO nanotubes provide sensitivity as high as twice that of the ZnO nanorods. The possible reasons of enhanced sensitivity were explained. Paper VI investigates an improved potentiometric intracellular glucose biosensor based on the immobilization of glucose oxidase on the ZnO nanoporous material. We demonstrated that using ZnO nanoporous material as a matrix material for enzyme immobilization improves the sensitivity of the biosensor as compared to using ZnO nanorods. In addition, the fabrication method of the intracellular biosensor was simple and excellent performance in sensitivity, stability, selectivity, reproducibility, and anti-interference was achieved.