Thesis advisor: Chia-Kuang Tsung / Incorporating shape and size controlled metal nanoparticles (NPs) into metal-organic-frameworks (MOFs) shows great potential in heterogeneous catalysis. The combination of ordered nanoporous structure of MOFs and the well-defined surfaces of metal NPs provides a new tool to modulate the catalysis on the metal surface. Due to the large pore size, framework flexibility and selective interaction with gas molecules, MOFs have been widely used for gas storage with high selectivity. Among which have been developed to date, Zeolitic Imidazolate Frameworks-8 (ZIF-8) and UiO-66 show advantageous properties. The solvent resistivity and high thermal stability makes them stand out to be good candidates as shell materials in core shell catalysts. In our work, we developed an efficient way to create a yolk-shell structure of Pd nanoparticles in ZIF-8 and, at the same time, a method to incorporate the shape/size controlled Pt nanoparticles into well-defined octahedral UiO-66 nanocrystals with the control of concentration and dispersion. The formation mechanisms of both yolk-shell and core-shell structures were also studied in the work. / Thesis (MS) — Boston College, 2012. / Submitted to: Boston College. Graduate School of Arts and Sciences. / Discipline: Chemistry.

In this thesis numerical methods are used to understand the individual and collective optical response of metal nanoparticles (MNPs). In particular, finite 1D assemblies of MNPs are characterized by analytical solutions to Maxwell's equations. Small particle solutions such as the well-established plasmon hybridization scheme as well as a novel circuit model explaining the intrinsic mechanisms of free electron dynamics help to characterize the optical response of single and coupled MNPs. Complex systems of closely spaced MNPs with small interparticle gaps are studied with the help of full scattering solutions to Maxwell's equations. It is shown that higher order plasmon modes facilitate strong near-fields between MNPs, and in linear chains foster specific optical attributes which are present in more complex systems, playing a key role in energy propagation along practical MNP waveguides.

Histopathology studies of metal nanoparticles (NPs) compared to traditional forms of metal in fish are scarce. Additionally, it is unclear whether metal nanoparticles cause greater or different pathologies compared to other forms of metal. The current study aimed to assess the pathological effects of Cu-NPs and TiO2 NPs on rainbow trout via various routes of exposure and, where appropriate, to compare them to either the equivalent dissolved metal salts or bulk powder forms. The first experiment showed that waterborne exposure to Cu-NPs and CuSO4 caused similar types of organ pathologies and alteration in the spleen content, however there were some material-type effects in the incidence injuries; with Cu-NPs in some organs by causing more injury in the intestine, liver, and brain when compared to effects caused by the equivalent concentration of CuSO4. Lowering water pH did have an effect on the toxicity of Cu-NPs and dissolved Cu in trout, and the results illustrated that both Cu treatments are more toxic at pH 5 than pH 7 by causing more physiological and pathological changes, although both CuSO4 and Cu-NP treatments showed similar types of organ lesions. Waterborne exposure to TiO2 NPs and bulk forms of TiO2 showed similar types of organ pathologies and alteration in the spleen contents, but there was a material-type effect in some organs (more injury with the bulk treatment than the NP form). After 96 h following intravenous injections of bulk or TiO2 NPs in trout, organs showed similar types of pathologies; except the spleen and kidney which showed a material-type effects (more injury with NPs than the bulk forms). This could be attributed to the highest Ti accumulation from the TiO2 NP treatment in the kidney and spleens, or to the role of these organs in filtrating the circulating blood. Overall, this thesis demonstrates that metal-NPs produced similar types of organ pathologies to traditional forms of metals through different routes of exposure, but there were some material-type effects on the incidence of injuries in some organs. The results have also added some understanding on the fate, and effects of NPs by identifying the target organs involved. Some of the nano-specific effects may need to be given extra consideration in environmental and human health risk assessments.

Thesis advisor: Chia-Kuang (Frank) Tsung / The core-shell hybrid structure is the simplest motif of two-component systems which consists of an inner core coated by an outer shell. Core-shell composite materials are attractive for their biomedical, electronic and catalytic applications in which interface between core and shell is critical for various functionalities. However, it is still challenging to study the exact role that interface plays during the formation of the core-shell structures and in the properties of the resulted materials. By studying the formation mechanism of a well interface controlled one-to-one metal nanoparticle (NP)@zeolite imidazolate framework-8 (ZIF-8) core-shell material, we found that the dissociation of capping agents on the NP surface results in direct contact between NP and ZIF-8, which is essential for the formation of core-shell structure. And the amount of capping agents on the NP surface has a significant effect to the crystallinity and stability of ZIF-8 coating shell. Guided by our understanding to the interface, one-to-one NP@UiO-66 core-shell structure has also been achieved for the first time. We believe that our research will help the development of rational design and synthesis of core-shell structures, particularly in those requiring good interface controls. / Thesis (MS) — Boston College, 2017. / Submitted to: Boston College. Graduate School of Arts and Sciences. / Discipline: Chemistry.

In recent years, ionic liquids have emerged as one of the most promising alternatives to traditional volatile organic solvents when it comes to catalytic reactions. Stable metal nanoparticles suspended in ionic liquids, are catalytic systems that mimic aspects of nanoparticles on solid supports, as well as traditional metal-ligand complexes used in organometallic catalysis. While alkylimidazolium ionic liquids, with or without appended functionalities, have been earmarked as the media of choice for the dispersal of nanoparticles, the tetraalkylphosphonium family of ionic liquids has largely been overlooked, despite their facile synthesis, commercial availability, chemical resemblance to surfactants traditionally used for nanoparticle stabilization, stability under basic conditions, and wide thermal as well as electrochemical windows. It is only recently that a number of research groups have given this family of novel alternative solvents the recognition it deserves, and used metal NPs dispersed in these ILs as catalysts in reactions such as hydrogenations, oxidations, C-C cross-couplings, hydrodeoxygenations, aminations, etc. This thesis investigates the synthesis, characterization, and catalytic applications of transition metal nanoparticles in tetraalkylphosphonium ionic liquids. The ionic liquids described in this thesis functioned as the reaction media as well as intrinsic nanoparticle stabilizers during the course of the catalytic processes. Metallic nanoparticles synthesized in these ionic liquids proved to be stable, efficient and recyclable catalytic systems for reactions of industrial significance, such as hydrodeoxygenations, hydrogenations, and oxidations. It was demonstrated that stability and catalytic activity of these systems were profoundly dependent on the properties of the ionic liquids, such as the nature of the alkyl chains attached to the phosphonium cation, and the coordination ability of the anion. Since heat-induced nanoparticle sintering was a problem, a procedure was devised to redisperse the aggregated and/or sintered nanoparticles so as to restore their initial sizes and catalytic activities. The presence of halides as counter-ions in tetraalkylphosphonium ionic liquids was seen to facilitate the oxidative degradation of agglomerated metal nanoparticles, which was a key step in our redispersion protocol. It was demonstrated that this redispersion protocol, when applied to heat-sintered nanoparticles, produces nanostructures that resemble the freshly made nanoparticles not only in size but also in catalytic activities. The presence of by-products from the borohydride reduction step used to generate the nanoparticles in the ionic liquids actually facilitated multistep reactions such as hydrodeoxygenation of phenol, where a Lewis Acid was necessary for a dehydration step. Finally, an attempt was made to utilize nanoparticles of an earth-abundant metal (iron) as a hydrogenation catalyst in a variety of alternative solvents (including tetraalkylphosphonium ionic liquids) in order to enhance the “green”ness of the catalyst systems. X-ray absorption spectroscopy (XAS) of the iron- nanoparticles/ionic liquid systems at the Canadian Light Source revealed significant details about the chemical interaction between iron and the ionic liquid matrices, which added to our understanding of this neoteric family of catalysts.

Yes / Colloidal nanoparticles, such as gold nanoparticles (AuNPs), are promising materials for the delivery of hydrophilic drugs via the pulmonary route. The inhaled nanoparticle drug carriers primarily deposit in lung alveoli and interact with the alveolar surface known as lung surfactants. Therefore, it is vital to understand the interactions of nanocarriers with the surfactant layer. To understand the interactions at the molecular level, here we simulated model lung surfactant monolayers with phospholipid (PL)-wrapped AuNPs at the vacuum-water interface using coarse-grained molecular dynamics simulations. The PL-wrapped AuNPs quickly adsorbed into the surfactant layer, altered the structural properties of the monolayer, and at high concentrations initiated the compressed monolayer to collapse/buckle. Among the surfactant monolayer lipid components, cholesterol adsorbed to the AuNPs preferentially over PL species. The position of the adsorbed PL-AuNPs within the monolayer, and subsequent monolayer perturbation, vary depending on the monolayer phase, monolayer composition, and species of PL used as a ligand. Information provided by these molecular dynamic simulations helps to rationalize why some colloidal nanoparticles work better as nanocarriers than others and aid the design of new ones, to avoid biological toxicity and improve efficacy for pulmonary drug delivery.

In recent years, research has focused on reducing the cost of catalysts in a variety of ways including using less expensive materials, improving the synthetic method, and increasing the catalytic activity, recovery, and recyclability. Typically with nanoparticles, the size, shape, composition, and surface coating have an effect on catalytic activity.1-2 In this work, we focused on reducing the cost of precious metal based catalysts by altering the synthetic methods. One way to lower the cost of synthesizing precious metal nanoparticles is by debasing the precious metal with a second cheaper more abundant metal. CuPd nanoparticles were synthesized in oleylamine and displayed catalytic activity in several cross-coupling reactions. Due to copper being present in the nanoparticle, a copper halide co-catalyst was not needed for Sonogashira cross coupling to be successful.3 While this method produced reactive catalysts, low product yield hinders its application for industry. Solution based synthesis of metallic nanoparticles typically require long reaction times and high temperatures, which make large scale production of nanoparticles on an industrial scale difficult.4-5 The use of continuous flow microreactors provides greater control of synthetic parameters, leading to lower batch-to-batch variability and increasing the efficient of heat and mass transfer and have been applied to the synthesis of metals, semiconductors, zeolites, organic compounds, and semiconductors.5-7 To compare continuous flow methods to benchtop reactions, a well-characterized benchtop reaction synthesizing Cu@Ni core/shell nanoparticles was successfully transferred to a flow reactor set-up. Cu@Ni nanoparticles were synthesized using a capillary microreactor in under 1 minute compared to the 1 hour reaction on benchtop with similar properties in a green solvent.2 The Cu@Ni nanocomposites were active towards the Fischer Tropsch reaction.8 2 nm platinum nanoparticles and platinum bimetallic alloys were synthesized in water using a capillary microwave flow reactor. Investigations showed the nanoparticles were activity toward hydrogenation of octene. With further development, continuous flow synthesis of metallic nanoparticles can be applied to the synthesis of a wide variety of catalysts on an industrial scale. Continuous flow methods provide greater control of reaction parameters, increased safety by reacting smaller volumes of chemicals at a given time, and decreasing the batch-to-batch variability.

We have discovered that the current protocols to assemble Au nanoparticles based on DNA hybridization do not work well with the small metal nanoparticles (e.g. 5 nm Au, 3.6 nm Pt and 3.2 nm Ru particles). Further investigations revealed the presence of strong interaction between the oligonucleotide backbone and the surface of the small metal nanoparticles. The oligonucleotides in this case are recumbent on the particle surface and are therefore not optimally oriented for hybridization. The nonspecific adsorption of oligonucleotides on small metal nanoparticles must be overcome before DNA hybridization can be accepted as a general assembly method. Two methods have been suggested as possible solutions to this problem. One is based on the use of stabilizer molecules which compete with the oligonucleotides for adsorption on the metal nanoparticle surface. Unfortunately, the reported success of this approach in small Au nanoparticles (using K₂BSPP) and Au films (using 6-mercapto-1-hexanol) could not be extended to the assembly of Pt and Ru nanoparticles by DNA hybridization. The second approach is to simply use larger metal particles. Indeed most reports on the DNA hybridization induced assembly of Au nanoparticles have made use of relatively large particles (>10 nm), hinting at a weaker non-specific interaction between the oligonucleotides and large Au nanoparticles. However, most current methods of nanoparticle synthesis are optimized to produce metal nanoparticles only within a narrow size range. We find that core-shell nanoparticles formed by the seeded growth method may be used to artificially enlarge the size of the metal particles to reduce the nonspecific binding of oligonucleotides. We demonstrate herein a core-shell assisted growth method to assemble Pt and Ru nanoparticles by DNA hybridization. This method involves firstly synthesizing approximately 16 nm core-shell Ag-Pt and 21 nm core-shell Au-Ru nanoparticles from 9.6 nm Ag seeds and 17.2 nm Au seeds respectively by the seed-mediated growth method. The core-shell nanoparticles were then functionalized by complementary thiolated oligonucleotides followed by aging in 0.2 M PBS buffer for 6 hours. The DNA hybridization induced bimetallic assembly of Pt and Ru nanoparticles could then be carried out in 0.3 M PBS buffer for 10 hours. / Singapore-MIT Alliance (SMA)

In this work, the structural and optical properties of metal nanoparticles fabricated on various substrates have been investigated. The particles were fabricated by electron beam lithography (EBL) and dewetting of a thin metal film. The advantages and disadvantages of these two fabrication techniques are discussed by considering the properties of the nanoparticles and the applicability to large area substrates. Being a practical fabrication method, dewetting can be applied to any substrate with either small or large surfaces. For comparison between different sample types, some process parameters such as film thickness, annealing temperature and duration were fixed during the whole study. Gold (Au) and silver (Ag) were preferred for nanoparticle formation because of their superior optical properties for solar cell applications. We used silicon (Si), silicon nitride (Si3N4), silicon dioxide (SiO2) and indium tin oxide (ITO) on glass, and textured Si as the substrate for the particle formation. These substrates are commonly used in solar cell technology for different purposes. The formation of the metal nanoparticles, their size and size distribution were monitored by Scanning Electron Microscope (SEM). We performed a dimension analysis on the SEM images using a program called Gwyddion. We observed that the substrate type greatly affects particle mean size, suggesting a dependence of the dewetting process on the interface properties. Moreover, the effect of the annealing temperature was found to be a function of the substrate type. Scattering measurements have been carried out in order to observe the localized surface plasmon resonance (LSPR) conditions. The effect of the particle size and the dielectric environment was observed as a shift in the plasmon resonance peak position along the wavelength axis. As expected from the theory, the resonance peaks shift to longer wavelengths with increasing particle size and dielectric constant. In order to compare the experimental results with the theory, Mie theory was applied to calculate the plasmon resonance peaks. We obtained fairly well agreement between the experimental and theoretical results. In this study, nanoparticles were assumed to be in contact with more than one medium, namely air and the underlying substrate. Finally, we have reached a successful methodology and knowledge accumulation for the metal particle formation on variety of substrates by the dewetting technique. It is clear that this knowledge can form basis for the photovoltaic applications.

Thesis (Ph.D.)--University of Wisconsin--Madison, 2006. / Includes bibliographical references. Also available on the Internet.