Metal oxides are of interest not only because of their huge abundance but also for their many applications such as for electrocatalysts, gas sensors, diodes, solar cells and lithium ion batteries (LIBs). Nano-sized metal oxides are especially desirable since they have larger surface-to-volume ratios advantageous for catalytic properties, and can display size and shape confinement properties such as magnetism. Thus, it is very important to explore the synthetic methods for these materials. It is essential, therefore, to understand the reaction mechanisms to create these materials, both on the nanoscale, and in real-time, to have design control of materials with desired morphologies and functions. This dissertation covers both the design of new syntheses for nanomaterials, as well as real-time methods to understand their synthetic reaction mechanisms. It will focus on two parts: first, the synthesis of 1-dimension (1-D) featured nanomaterials, including manganese-containing spinel nanowires, and tin dioxide and zinc oxide-based negative nanowire arrays; and second, a mechanistic study of the synthetic reactions of nanomaterials using in situ transmission electron microscopy (TEM). The work presented here demonstrates unique synthetic routes to single crystalline “positive” and “negative” metal oxide nanowires, and introduces a new mechanism for the formation of single-crystalline hollow nanorods.

Cancer remains one of the world’s most devastating diseases, with more than 10 million new cases every year. However, traditional treatments have proven insufficient for successful medical management of cancer due to the chemotherapeutics’ difficulty in achieving therapeutic concentrations at the target site, non-specific cytotoxicity to normal tissues, and limited systemic circulation lifetime. Although, a concerted effort has been placed in developing and successfully employing nanoparticle(NP)-based drug delivery vehicles successfully mitigate the physiochemical and pharmacological limitations of chemotherapeutics, work towards controlling the subcellular fate of the carrier, and ultimately its payload, has been limited. Because efficient therapeutic action requires drug delivery to specific organelles, the subcellular barrier remains critical obstacle to maximize the full potential of NP-based delivery vehicles. The aim of my dissertation work is to better understand how NP-delivery vehicles’ structural, chemical, and physical properties affect the internalization method and subcellular localization of the nanocarrier. In this work we explored how side-chain and backbone modifications affect the conjugated polymer nanoparticle (CPN) toxicity and subcellular localization. We discovered how subtle chemical modifications had profound consequences on the polymer’s accumulation inside the cell and cellular retention. We also examined how complexation of CPN with polysaccharides affects uptake efficiency and subcellular localization. This work also presents how changes to CPN backbone biodegradability can significantly affect the subcellular localization of the material. A series of triphenyl phosphonium-containing CPNs were synthesized and the effect of backbone modifications have on the cellular toxicity and intracellular fate of the material. A mitochondrial-specific polymer exhibiting time-dependent release is reported. Finally, we present a novel polymerization technique which allows for the controlled incorporation of electron-accepting benzothiadiazole units onto the polymer chain. This facilitates tuning CPN emission towards red emission. The work presented here, specifically, the effect that side-chain and structure, polysaccharide formulation and CPN degradability have on material’s uptake behavior, can help maximize the full potential of NP-based delivery vehicles for improved chemotherapeutic drug delivery.

Tablets are the most common forms of drug administration. They are convenient to administer and easy to manufacture. However, problems associated with the adhesion of the powders to the tableting tools are common. This phenomenon is known as sticking and even though it has been well documented and studied, it remains poorly understood. The many factors that contribute to good performance of the powders make the sticking problem difficult to solve. The goal of this study is to establish a relationship between the properties measured at the nanoscale to the overall tablet mechanical properties, tablet performance and powder pre-processing induced modifications. By using atomic force microscopy (AFM) we aim to develop an analytical method to characterize the mechanical and adhesive properties of the pharmaceutical powders at the nanoscale. Other methodologies such as scanning electron microscopy (SEM), thermal analyses (DSC, TGA) and tablet strength test were also used. The materials used in this study are commonly used excipients, a sticky drug and magnesium stearate (MgSt). Two different approaches offered by AFM were employed: sharp tip imaging and colloidal probe force measurements. Nano-mechanical properties of the materials were evaluated with a sharp tip cantilever showing that higher adhesion correlates with higher tablet cohesion and that both are significantly affected by the presence of MgSt. AFM characterization of the particle surface mechanical properties at the nanoscale was also used to detect the crystallinity and amorphicity levels of the materials. New approaches to presenting such data considering the particle heterogeneity and to track the dynamics of surface recrystallization are revealed. Adhesive interactions between a steel sphere and sticky and non-sticky powders were performed with the colloidal probe technique. Sticky materials presented a higher adhesion against the steel surface, and reveal the mechanism of stickiness. This work thus contributes to the provision of predictability of the performance of formulations at an early stage of the development process. / <p>QC 20170315</p>

Carbon dots (CDs) have attracted much attention as an excellent gene/drug delivery and biological imaging agent for early cancer theranostics. In this study, we prepared two series of nanoparticles (NPs), which are composed of (CDs) with a targeting agent, folic acid (FA), and a chemotherapeutic agent Doxorubicin (Dox). All the NPs and their intermediates were characterized using ultraviolet-visible spectroscopy (UV-vis), fluorescence spectroscopy, and Fourier transform-infrared spectroscopy (FT-IR). The drug loading capacity (DLC) and drug loading efficiency (DLE) of two series of FA-CDs-Dox were assessed using UV-vis absorption spectroscopy at the wavelength of 485 nm. Both showed good DLE and DLC results when compared to literature data. In addition, the cumulative release property of Dox from the FA-CDs-Dox complexes were investigated in a pH solution of 7.4.

Nanoparticles (NPs) have been used widely in various fields ranging from biomedical applications to life science due to their highly tunable properties. It is essential to understanding how NPs interact with biological systems of interest, therefore, analytical platforms to efficiently track NPs from cell to animal level are essential. In this thesis, laser desorption ionization mass spectrometry (LDI-MS) and inductively-coupled plasma mass spectrometry (ICP-MS) has been developed and applied to quantify NP/cell and NP/biological surface interactions. These two methods provide fast, label-free and quantitative analysis. New capability of LDI-MS to differentiate cell surface-bound and internalized NPs were established and ICP-MS coupled with a library of surface- functionalized AuNPs were used to probe the affinity between NPs and human hair surface. NPs interacting with biological surfaces and plasma membrane were quantified and the interactions were controlled by the chemical properties of the interface between NP and biological systems.

Adhesives are widespread. They hold together the furniture, cars and electronics that we use on a daily basis. The majority of commercially available glues are sourced from petroleum-based monomers and are not degradable in any practical way. The permanent nature of these adhesive materials makes disassembly for recycling difficult. Current bio-based glues such as hide and starch glue are not strong enough to compete with commercial glues. Inspiration from nature is helping us to tackle this problem. Marine mussels achieve strong bonding to underwater surfaces through the use of adhesive plaques containing the uncommon amino acid 3,4-dihydroxyphenylalanine. Incorporating this chemistry into a degradable polylactic acid backbone allows for the development of strong bonding biodegradable glue. Throughout this work, the synthesis of these materials is discussed as well as methods to improve the bonding of these materials to compete with commercial glues. The degradation of these materials as well as their cytocompatibility is discussed.

My research goals are to synthesize new zwitterionic perfluorosulfonimide (PFSI) monomer/polymers. They are expected to replace traditionally used perfluorosulfonic acid (PFSA) polymers as the electrolyte in PEM fuel cells. For the PFSI monomer preparation, we designed a nine-step synthesis route. Thus far, I have successfully completed the synthesis of 4- (2-bromotetrafluoroethoxy)-benzenesulfonyl amide, 4-acetoxybenzenesulfonic acid sodium salt, and 4-chlorosulfonyl phenyl acetate. The coupling reaction of 4-(2-bromotetrafluoroethoxy)- benzenesulfonyl amide with 4-chlorosulfonyl phenyl acetate, was troublesome due to slow reaction kinetics and byproducts. Additionally, I did a methodology study for the homopolymerziation of the perfluoro 3(oxapent-4-ene) sulfonyl fluoride monomer. We compared the weight average molecular weight (Mw) of different reaction conditions. The best Mw was achieved when the polymerization was carried out for five days at 100 °C and150 psi with 2 wt % initiator and 5 g of monomer. All the compounds were characterized by melting point, GC-MS, GPC, FT-IR, and 13C/1H/19F NMR.

Surfactants and Thickeners are both additives used in fully-formulated waterborne coatings to provide colloidal stability, thickening, and other functionality. The behavior of each ingredient in a coating must be understood and controlled to maintain colloidal stability as well as balance other desired properties of the liquid coating and the dry paint film. In this work, quaternary systems of Water-Latex-Thickener-Surfactant were investigated to further the understanding of their behavior in coatings. The thickener used was a well characterized, hydrophobically-modified, ethoxylated urethane (HEUR) with two C18 terminal hydrophobes and 795 average repeat units of ethylene oxide as the hydrophilic spacer. Two latexes, a hydrophobic butyl acrylate/styrene and a hydrophilic butyl acrylate/methyl methacrylate, each containing a small amount of methacrylic acid monomer were used. Six different surfactants, three non-ionic and three-anionic, were used. By maintaining the concentrations of latex and HEUR thickener as constants and varying the surfactant concentration, effects of the surfactant loading on rheology were determined. As concentration of surfactant increases, a characteristic shear-thickening maximum associated with bridging of latex particles by the HEUR thickener was seen to shift to higher shear rates; surfactants at all concentrations studied, except SDS, lowered the viscosities within the low shear rate region. Dynamic viscoelastic measurements shed further light into the behavior of the mixtures. The results will be explained based on surfactant and latex surface polarities and the competitive adsorption between the v surfactant and HEUR hydrophobes, and other interactions between surfactants and thickeners.

The goal of this work was to evaluate the electrochemical properties of TiZrNbTa thin films deposited by magnetron sputtering using an industrial physical vapor deposition system. Samples were deposited on both Si(001) and 316L stainless steel. The samples deposited on Si(001) were either crystalline (bcc reflections) or amorphous, depending on the sputtering parameters. The crystalline films were composed of thin films with two different layers. The upper layer was nanocolumnar composed of elongated nanocolumns, while the lower was dense. The amorphous films had only one nanocolumnar layer and higher porosity. Polarization curves revealed that all samples had low corrosion current densities, in the order of 10-8 A/cm2. The samples showed an extended passive region up to 3.0 V vs Ag/AgCl due to the growth of a passivating oxide. The surface of the samples consisted of Nb2O5, ZrO2, TiO2 and Ta2O5. The chronoamperometry tests showed current oscillations, related to a break-down and reformation of the passive film. Electrochemical impedance spectroscopy revealed that all samples behaved similarly in all three electrolytes, and the simulated electrical circuits were indicating no corrosion reactions. A decrease in capacitance values after polarization was observed and was related to the formed surface oxide. Samples deposited on 316L stainless steel showed a passive regime for a shorter potential window, probably related to surface defects of the films. Heat treatments at 400 and 800 Celsius for 20 hours could not trigger the phase transformation from single bcc to hcp or dual bcc, as predicted by the Thermo-Calc software.

The near future will put a lot of demand on the increasing need for energy production and storage. Issues regarding the modern-day battery technology’s environmental benignity, safety and cost to sustain such demands thus serve as a huge bottleneck, necessitating the research into alternative electrochemical energy storage solutions. Conducting redox polymers are a class of materials which combines the concepts of conducting polymers and redox active molecules to work as fully organic electrode materials. In this work three conducting redox polymers based on 3,4-ethylenedioxythiopene and 3,4-propylenedioxythiopene (EPE) with hydroquinone, catechol and quinizarin pendant groups were investigated. The polymers were electrochemically characterized with regards to their ability to cycle protons (aqueous electrolyte) and cations (non-aqueous electrolyte), their kinetics and charge transport and as cathodes in a battery. In non-aqueous electrolyte, hydroquinone and catechol did not exhibit redox activity in a potential region where the backbone was conducting as they were not redoxmatched. Quinizarin showed redox-matching as concluded by in situ conductance and UV-vis measurements when cycling Na+, Li+, Ca2+ and Mg2+-ions in acetonitrile. Comparison of the kinetics revealed that the rate constant for Ca2+-ion cycling was several magnitudes larger than the rest, and galvanostatic charge/discharge showed that 90% of the polymer capacity was attainable at 5C. An EPE-Quinizarin cathode and metallic calcium anode coin cell assembly displayed output voltages of 2.4 V, and the presented material thus shows promising and exciting properties for future sustainable battery chemistries.