A wrinkling approach was used to study the mechanics of hybrid nanotube/nanocrystal coatings adhering to soft polymer (PDMS) substrates. We focused on three thicknesses: 10 nm, 30 nm, and 40 nm. The approach we used is the Strain-Induced Elastic Buckling Instability for Mechanical Measurements (SIEBIFMM) technique, which allows measurement of the SWCNT film mechanics by the buckling wavelength and the film thickness by inducing a compressive stress in the films at different strains; 2%, 4%, 6%, 8%, 10%, and 12%. In this thesis, dip-coating method with colloidal nanocrystals was used to enhance the rigidity of the carbon nanotube films by filling the pores of the nanotube network. Our results show an almost two-fold enhancement in the Young modulus of a thin SWCNT film related to the presence of a thin interpenetrating over-layer of the semiconductor nanocrystal.

Since the fortuitous discovery of the existence of quantum size effects on the band structure of colloidal semiconductor nanocrystals, the development of synthetic methods that can form nanoscale crystalline materials of controllable size, shape, and composition has blossomed as an empirical scientific achievement. The fact that the term “recipe” is commonly used within the context of describing these synthetic methods is indicative of the experimentally driven nature of the field. In this respect, the highly attractive photophysical properties of semiconductor nanocrystals—as cheap wavelength tunable and high quantum yield absorbers and emitters of light for various applications in lighting, biological imaging, solar cells, and photocatalysis—has driven much of the interest in these materials. Nevertheless, a more rigorously predictive first-principles-grounded understanding of how the basic processes of nanocrystal formation (nucleation and growth) lead to the formation of semiconductor nanocrystals of desired size and size dispersity remains an elusive practical and fundamental goal in materials chemistry. In this thesis, we describe efforts to directly study these dynamic nucleation and growth processes for lead chalcogenide nanoparticles, in many cases in-situ, using a mixture of X-ray scattering and UV-Vis/NIR spectroscopy. The lack of a rigorously predictive and verified mechanism for nanocrystal formation in solution for many material systems of practical interest is due both to the inherent kinetic complexity of these reactions, as well as the spectroscopic challenge of finding in-situ probes that can reliably monitor nanoscale crystal growth. In particular, required are direct time-resolved structural probes of metastable inorganic amorphous and crystalline intermediates formed under the high temperature inert conditions of nanocrystal synthesis. It is, at the very least, highly challenging to apply many of the standard spectroscopic tools of mechanistic inorganic and organic chemistry such as ¹H NMR spectroscopy, IR vibrational spectroscopy, and mass spectrometry to this task. A notable counterexample is, of course, UV-vis/NIR absorbance and emission spectroscopies, which are of great value to the studies described herein. Nevertheless, to address this relative dearth of conventional spectroscopic probes, here we explore the use of X-ray Total Scattering real space Pair Distribution Function (PDF) analysis and Small Angle X-ray Scattering (SAXS) techniques to directly probe the crystallization process in-situ. Time-resolved measurements of the small angle reciprocal space scattering data allow mapping of the time evolution of the colloidal size and concentration of the crystals during synthesis, while the Fourier transform of scattering data over a wide range of reciprocal space provides direct insight into the local structure. Through this approach, we compare direct observations of these nucleation and growth processes to the widely cited theoretical models of these processes (Classical Nucleation Theory and LaMer “Burst Nucleation”) and find a number of stark differences between these widely cited theories and our experiments. The first two chapters cover the results of these 𝘪𝘯-𝘴𝘪𝘵𝘶 diffraction studies. Chapter 1 focuses on small angle X-ray scattering data collection and modeling. Chapter 2 focuses upon lead sulfide and lead selenide real space PDF analysis of local structural evolution during synthesis. Finally, Chapter 3 discusses a project in which we examine the origins of emergent semiconducting electronic structure in an increasing size series of atomically precise oligomers of [Ru₆C(CO)₁₆]²⁻ bridged by Hg²⁺ and Cd²⁺ atoms. Using an atomically well-defined series of molecules that bridge the small molecule and nanoscale size regimes, we discuss the factors that give rise to controllable semiconductor electronic structure upon assembly into extended periodic structures in solution. In all these projects, we seek to highlight the value of applying concepts of molecular inorganic chemistry—ligand binding models, relative bond strengths, in addition to kinetics and thermodynamics—to explain our observations regarding nanocrystal nucleation and growth. Consideration of the chemistry of nanocrystal formation processes provides a valuable compliment to the physics-based classical models of nucleation and growth that do not explicitly consider the system specific molecular structure and bonding.

Les nanostructures métalliques permettent de confiner la lumière à des échelles sub-longueur d’onde grâce à l'excitation de plasmons de surface. Elles ouvrent la voie à de nombreuses applications que ce soit en imagerie, en élaboration de composants photoniques ou en information quantique. Cette thèse porte sur l’étude de nanostructures métalliques, semi-continues ou constituées par des réseaux de trous au désordre contrôlé, et à leur interaction avec des nanocristaux semi-conducteurs colloïdaux particulièrement photostables. En associant plusieurs approches expérimentales complémentaires (spectroscopie en champ lointain, microscopie de champ proche optique, microscopie avec une sonde active de champ proche, caractérisation par microscopie confocale de l’émission de nanocristaux couplés aux surfaces métalliques), nous avons pu mettre en évidence les caractéristiques spécifiques des modes plasmons de ces différentes structures. Pour les réseaux au désordre contrôlé, nous avons en particulier analysé l’apparition progressive de modes localisés intenses et déterminé l’influence de paramètres tels que l’épaisseur de la couche d’or, le diamètre des trous ou la périodicité initiale du réseau. Les résultats expérimentaux obtenus se sont révélés en très bon accord avec les simulations numériques réalisées par FDTD. / Metallic nanostructures allow to confine light at subwavelength scales by the excitation of surface plasmon. They open the way for many applications in imaging, photonic components development and quantum information. This thesis deals with the study of metallic nanostructures, semi-continuous or based on holes gratings with a controlled disorder, and their interaction with colloidal semiconductor nanocrystals that are very photostable. Combining several complementary experimental approaches (far-field spectroscopy, near-field optical microscopy, near-field active probe microscopy, characterization by confocal microscopy of the emission of nanocrystals coupled to the metallic surfaces), we were able to highlight specific characteristics of the plasmon modes of these different structures. For the gratings with a controlled disorder, we have in particular analyzed the emergence of intense localized modes and determined the influence of parameters such as the thickness of the gold layer, the diameter of the holes or the initial periodicity of the grating. The experimental results are in very good agreement with the numerical simulations carried out by FDTD.

Photon avalanching (PA), one of the more unique nonlinear optical processes due to its combination of efficiency and extreme response, first attracted attention from the optics community more than four decades ago. But interest waned as researchers found that it did not provide immediately useful features observed in other nonlinear optical systems, such as amplified coherent light generation from lasing or optoelectronic amplification and transduction afforded by light-stimulated electron avalanching. The material systems supporting PA were also found to be rather limited, with reports concentrating on fragile, bulk lanthanide-doped crystals. However, the inter-ionic energy transfer mechanisms responsible for PA and its extreme nonlinearity are, in principle, realizable in objects with dimensions at the nanoscale. Further, new applications for PA in nanomaterials including simple super-resolution microscopy have recently been proposed. These factors motivated my research on the development of the first-ever lanthanide-doped nanoparticles capable of supporting PA behavior. In this thesis, the optical properties of Tm³⁺-doped NaYF₄ nanocrystals are investigated with photoluminescence microscopy, spectroscopy and differential rate equation model simulations. First, the photon avalanching behavior of Tm³⁺-doped NaYF₄ nanocrystals is studied. Specifically, the excitation-power-dependent luminescence of 1%, 4%, 8%, 20%, and 100% Tm³⁺-doped NaYF₄ is measured. The slopes of log-log excitation intensity versus emission intensity plots show that photon avalanche is realized in the nanocrystals when Tm³⁺ content is 8% and above. Time-resolved luminescence and rate equation model fitting to the experimental data validate the existence of photon avalanche, showing luminescence rise times > 600 ms, and the ratio of the ³F₄-to-³F₃ excited state absorption to the ³H₆-to-³F₄ ground state absorption is > 10⁴, which are signatures of photon avalanche. The design-dependent shift of the photon avalanching threshold also shows that photon avalanche is the main excitation scheme for the nanocrystals and implies potential applications for ultra-sensitive nano-sensing with the help of extreme nonlinearity. Additionally, the steep nonlinearity leads to super-resolution microscopy of single 8% Tm³⁺-doped nanocrystals with resolution down to <70 nm using conventional confocal microscopy without sophisticated techniques. In the second part of the thesis, the photodarkening effect of Tm³⁺-doped NaYF₄ nanocrystals is studied. We have found that photodarkening behavior is observed in Tm³⁺-doped nanocrystals that exhibit the photon avalanche effect. Power-dependent luminescence of a single 8% Tm3+-doped nanocrystal reveals that photodarkened nanocrystals still support photon avalanche behavior, but the avalanching threshold is shifted to a higher value. A photodarkening mechanism is proposed based on the concentration-dependent and power-dependent luminescence properties, and optical spectroscopic data. Notably, photodarkened nanocrystals are found to recover their original brightness and behavior under Vis-NIR optical illumination. This so-called “photobrightening” allows novel photoswitching of the inorganic nanocrystals, which has never before been achieved. We observe robust single nanocrystal photoswitching over 1000 cycles without permanent photodegradation. In addition, rewritable photolithography of multiple patterns using NIR lasers at 700 nm and 1064 nm is demonstrated.

DNA nanotechnology represents a powerful medium for manipulating the nanoscale arrangement of functional components. The first 15 years of DNA explorations has fast reached into every area of science and technology. Our group has focused attention on the utility of DNA as a structural material by folding DNA into rigid DNA objects such as tetrahedron or octahedron. These objects form the basis for engineered self-assembly by activating vertices of the nano-objects to interact with each other allowing for DNA mediated interaction which can achieve long range ordered cellular structures. Application of DNA nanotechnology can be likened to generating a flexible platform leveraging the precision afforded by the DNA sequences of A,G,T,C, and mostly are limited to experiments that could be accomplished within a 1μm3 volume. To scale emergent properties on the nanoscale, DNA origami techniques need profound improvements in synthesis and tools for characterization. The roadmap to transition DNA origami from a test tube to practical applications required a number of developments undertaken in this body of work. Critical milestones included: 1. Knowledge of nucleation and growth of DNA crystals (Chapters 1-3) 2. Transitioning DNA origami structures to the solid state (Chapters 4-7) 3. Characterization techniques to evaluate hierarchically engineered objects (Chapters 8-9) In the first thrust we performed investigative studies into the growth and nucleation of DNA origami crystals investigating thermodynamics and kinetics via in-situ experiments, these results iteratively improved synthesis conditions of DNA origami superlattices to grow from ~1um to over 250um single crystals up to 10x faster compared to previous synthesis conditions. These developments worked in tandem to explore methods to transition DNA constructs to the solid state via sol-gel synthesis of silica. The conversion process was reduced from by a factor of 12 from 24 hours to 2hours for rapid evaluation of crystals leveraged by a number of projects. The silication of structures allowed for further expanding the library of chemical structures available through the integration of liquid infiltration, atomic layer deposition and direct metallization of structures. The rapid development of DNA superlattices into larger and more complex motifs required the development of characterization techniques which could evaluate hierarchically designed materials spanning from 3-4nm to over 100 um. We characterize bulk mechanical properties of silica nanolattices leveraging in-situ indenters to examine nanoscale failure mechanisms. To characterize superlattices real-space artifacts we developed tomographic techniques to explore the spatial and elemental distribution of engineered constructs along with adopting biological serial sectioning approaches to evaluate defects in the assemblies.

京都大学 / 0048 / 新制・課程博士 / 博士(理学) / 甲第18641号 / 理博第4020号 / 新制||理||1579(附属図書館) / 31555 / 京都大学大学院理学研究科化学専攻 / (主査)教授 北川 宏, 教授 吉村 一良, 准教授 前里 光彦 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DGAM

The continued size reduction in electronic integrated circuits has lead to a demand for on-chip high-bandwidth and low loss communication channels. Optical interconnects are considered an essential addition to the silicon electronics platform. A major challenge in the field of integrated Si photonics is the development of cost effective silicon compatible light sources. This thesis investigates the sensitization of group IV doped silica films emitting at 1.535μm for applications as silicon compatible light sources. Thin erbium-doped silica films containing excess silicon and germanium were deposited using a multi-gun sputter system. The composition of the deposited materials was verified by Rutherford Backscattering Spectrometry. Samples from each deposition were annealed in a controlled atmosphere tube furnace at temperatures between 500ºC and 1100ºC for 30 minutes. The photoluminescence spectra from the visible to the near-infrared region were acquired while pumping either near or far from the Er3+ absorption lines. Under both excitation conditions all samples annealed at temperatures below 1000ºC show clear emission at 1.535μm from Er3+ ions in the host material. In the current literature this is attributed to exciton mediated excitation of the Er3+. By contrast, in these studies indirect excitation was observed for samples annealed at temperatures well below the onset of nanocrystal nucleation and growth (between 500ºC and 1000ºC), suggesting excitation via small clusters or lattice defects. These findings could have significant implications in the further development of group IV sensitized silicon compatible gain media.

No description available.

No description available.

The objective of this thesis is to incorporate cellulose nanocrystals (CNCs) into polymer latexes prepared using various emulsion polymerization methods. CNCs are a promising new class of renewable materials with unique properties including nanoscale dimensions, a high aspect ratio, low density, and high strength. They show significant promise to enhance the properties of existing materials, but challenges often arise due to incompatibility and processing difficulties. This work investigates novel surface modification routes to improve the compatibility of CNCs with emulsion polymerization components, and aims to control the location and function of CNCs in latex systems in order to modify latex properties. Three approaches to incorporate CNCs into polymer latexes are presented: (1) exploiting CNC-surfactant interactions in order to promote CNCs as Pickering stabilizers or as “passive” additives in the water phase, (2) enhancing the surface activity of CNCs by adsorbing the surface active biopolymer methyl cellulose (MC) to act as Pickering co-stabilizers, or (3) hydrophobic modification of CNCs through polymer grafting in order to provide improved compatibility between CNCs and the monomer/polymer phase to incorporate CNCs into the latex core. First, the interactions between CNCs and surfactants were studied in suspension and at surfaces and the CNC-surfactant combinations were used to stabilize miniemulsion polymerization of methyl methacrylate (MMA), a model system used in this work. Oppositely charged CNCs and surfactants showed improved stability as Pickering stabilizers and the ability to co-stabilize the monomer/polymer-water interface. When like-charged CNCs and surfactants were used, the poly(methyl methacrylate) (PMMA) polymer particles were stabilized by surfactant only, while the CNCs remained in the water phase. Next, in order to avoid the use of surfactants, CNCs were coated with MC to provide improved surface activity. MC-coated CNCs were effectively used as Pickering stabilizers in the microsuspension polymerization of MMA, where a double morphology of PMMA particles was observed, and the morphology could be tuned based on the ratio of CNC to MC used. Finally, CNCs were modified with hydrophobic polymer via two different “grafting from” methods: free radical polymerization and atom transfer radical polymerization (ATRP). Free radical polymer grafting from CNCs resulted in polymer-grafted CNCs but the method lacked control over polymer graft length and graft density. To overcome this, CNCs were modified via surface initiated ATRP where considerably higher amounts of polymer were grafted from the CNCs in short reaction times and with simple purification steps. Furthermore, polymer-grafted CNCs were added to the monomer phase of the miniemulsion polymerization of MMA and latexes with CNCs inside the hydrophobic polymer particle core were prepared. Given the difficulties in characterizing polymer grafted CNCs, a novel solution state NMR method was used, whereby the modified CNCs were dissolved in ionic liquids and the polymer grafts were cleaved and collected to determine graft length and graft density. Overall, this work provides three approaches for the preparation of nanocomposite latexes with CNCs using PMMA as a model system. The results presented here may expand the use of CNCs in latex products such as adhesives, paints, coatings, and cosmetics. / Thesis / Doctor of Philosophy (PhD) / This research aims to prepare polymer latexes with tailorable properties using renewably-sourced particles and nanotechnology. Latexes are polymer particles dispersed in water, typically on the order of a few hundred to thousand nanometers (where a “nanometer” is one billionth of a meter), and are used in products such as adhesives, paints, and coatings. The field of nanotechnology takes advantage of nanomaterials where unique properties stem from the small size and high surface-area-to-volume ratio. In this work, we use cellulose, the most abundant natural polymer on earth, in the form of cellulose nanocrystals (CNCs). These nanoparticles are extracted from pulp, cotton, and other natural resources to yield nanometer-sized rigid rod-like particles. CNCs have recently gained attention in research and the media because of their new industrial production and “safe nanomaterial” designation in Canada. In this work, CNCs were chemically modified by the attachment of new molecules or by coating them with polymers and were subsequently added during the synthesis of the polymer latex. Incorporating CNCs imparted new properties and the ability to control latex size, shape, and surface topography. CNCs are also expected to improve the overall mechanical strength of the latex, and may enhance the stickiness of adhesive latexes in particular, leading to products that are more environmentally friendly and that show improved performance.