This thesis describes the study of a variety of nanoscale materials and the development of novel synthetic strategies for their production. While the focus and bulk of this study have been directed specifically at subwavelength lithography, a significant portion of this thesis research involves nanoparticle synthesis, characterization, and functionalization. Put in very simple terms, optical lithography is a process where a beam of light, focused in a specific pattern, is used to generate a physical pattern on a solid substrate. This technology forms the basis for almost all microchip production in the world at the present time. As demand for faster and more powerful chips increases, the need to further miniaturize the patterns while minimizing cost has become very important. Multiple photochemical systems were developed in the search for non-reciprocal photochemistry at 193 nm to increase the resolution of lithographic processes at that wavelength. One approach, based on anthracene sensitization of sulfonium salts for acid generation, used photochemically reversible 4+4 aromatic cycloaddition reactions to introduce the non-linear photochemistry. A second approach took advantage of the photochemistry of N-methylphenothiazine and provided the first true example of a lithographically-relevant multi-photon acid generating process. Since all of the systems we studied used sulfonium salts as the acid generating species, we also looked at the photochemistry of the salts themselves. We evaluated the structural effects of the salts on their direct photochemistry and the implications for sensitized multi-photon photochemistry. We found that the identity of the anion plays a significant role in both processes and propose a new photochemical mechanism for acid generation that involves a charge transfer excitation process. We also describe the synthesis and characterization of novel fluorescent silver nanoparticles, both in solution and polymer films. We show that the fluorescent images can be patterned easily and preliminary results show that photolithography based on nanoparticle formation may be possible. This latter approach could provide a facile route to nanoparticle-embedded functional materials. This work with nanoparticles was inspired partly by earlier work, also presented herein, on semiconductor nanoparticles and their interactions with disulfide ligands.

This thesis describes the study of a variety of nanoscale materials and the development of novel synthetic strategies for their production. While the focus and bulk of this study have been directed specifically at subwavelength lithography, a significant portion of this thesis research involves nanoparticle synthesis, characterization, and functionalization. Put in very simple terms, optical lithography is a process where a beam of light, focused in a specific pattern, is used to generate a physical pattern on a solid substrate. This technology forms the basis for almost all microchip production in the world at the present time. As demand for faster and more powerful chips increases, the need to further miniaturize the patterns while minimizing cost has become very important. Multiple photochemical systems were developed in the search for non-reciprocal photochemistry at 193 nm to increase the resolution of lithographic processes at that wavelength. One approach, based on anthracene sensitization of sulfonium salts for acid generation, used photochemically reversible 4+4 aromatic cycloaddition reactions to introduce the non-linear photochemistry. A second approach took advantage of the photochemistry of N-methylphenothiazine and provided the first true example of a lithographically-relevant multi-photon acid generating process. Since all of the systems we studied used sulfonium salts as the acid generating species, we also looked at the photochemistry of the salts themselves. We evaluated the structural effects of the salts on their direct photochemistry and the implications for sensitized multi-photon photochemistry. We found that the identity of the anion plays a significant role in both processes and propose a new photochemical mechanism for acid generation that involves a charge transfer excitation process. We also describe the synthesis and characterization of novel fluorescent silver nanoparticles, both in solution and polymer films. We show that the fluorescent images can be patterned easily and preliminary results show that photolithography based on nanoparticle formation may be possible. This latter approach could provide a facile route to nanoparticle-embedded functional materials. This work with nanoparticles was inspired partly by earlier work, also presented herein, on semiconductor nanoparticles and their interactions with disulfide ligands.

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This thesis describes the study of a variety of nanoscale materials and the development of novel synthetic strategies for their production. While the focus and bulk of this study have been directed specifically at subwavelength lithography, a significant portion of this thesis research involves nanoparticle synthesis, characterization, and functionalization. Put in very simple terms, optical lithography is a process where a beam of light, focused in a specific pattern, is used to generate a physical pattern on a solid substrate. This technology forms the basis for almost all microchip production in the world at the present time. As demand for faster and more powerful chips increases, the need to further miniaturize the patterns while minimizing cost has become very important. Multiple photochemical systems were developed in the search for non-reciprocal photochemistry at 193 nm to increase the resolution of lithographic processes at that wavelength. One approach, based on anthracene sensitization of sulfonium salts for acid generation, used photochemically reversible 4+4 aromatic cycloaddition reactions to introduce the non-linear photochemistry. A second approach took advantage of the photochemistry of N-methylphenothiazine and provided the first true example of a lithographically-relevant multi-photon acid generating process. Since all of the systems we studied used sulfonium salts as the acid generating species, we also looked at the photochemistry of the salts themselves. We evaluated the structural effects of the salts on their direct photochemistry and the implications for sensitized multi-photon photochemistry. We found that the identity of the anion plays a significant role in both processes and propose a new photochemical mechanism for acid generation that involves a charge transfer excitation process. We also describe the synthesis and characterization of novel fluorescent silver nanoparticles, both in solution and polymer films. We show that the fluorescent images can be patterned easily and preliminary results show that photolithography based on nanoparticle formation may be possible. This latter approach could provide a facile route to nanoparticle-embedded functional materials. This work with nanoparticles was inspired partly by earlier work, also presented herein, on semiconductor nanoparticles and their interactions with disulfide ligands.

This thesis describes the study of a variety of nanoscale materials and the development of novel synthetic strategies for their production. While the focus and bulk of this study have been directed specifically at subwavelength lithography, a significant portion of this thesis research involves nanoparticle synthesis, characterization, and functionalization. Put in very simple terms, optical lithography is a process where a beam of light, focused in a specific pattern, is used to generate a physical pattern on a solid substrate. This technology forms the basis for almost all microchip production in the world at the present time. As demand for faster and more powerful chips increases, the need to further miniaturize the patterns while minimizing cost has become very important. Multiple photochemical systems were developed in the search for non-reciprocal photochemistry at 193 nm to increase the resolution of lithographic processes at that wavelength. One approach, based on anthracene sensitization of sulfonium salts for acid generation, used photochemically reversible 4+4 aromatic cycloaddition reactions to introduce the non-linear photochemistry. A second approach took advantage of the photochemistry of N-methylphenothiazine and provided the first true example of a lithographically-relevant multi-photon acid generating process. Since all of the systems we studied used sulfonium salts as the acid generating species, we also looked at the photochemistry of the salts themselves. We evaluated the structural effects of the salts on their direct photochemistry and the implications for sensitized multi-photon photochemistry. We found that the identity of the anion plays a significant role in both processes and propose a new photochemical mechanism for acid generation that involves a charge transfer excitation process. We also describe the synthesis and characterization of novel fluorescent silver nanoparticles, both in solution and polymer films. We show that the fluorescent images can be patterned easily and preliminary results show that photolithography based on nanoparticle formation may be possible. This latter approach could provide a facile route to nanoparticle-embedded functional materials. This work with nanoparticles was inspired partly by earlier work, also presented herein, on semiconductor nanoparticles and their interactions with disulfide ligands.

No / Advanced Dental Biomaterials is an invaluable reference for researchers and clinicians within the biomedical industry and academia. The book can be used by both an experienced researcher/clinician learning about other biomaterials or applications that may be applicable to their current research or as a guide for a new entrant into the field who needs to gain an understanding of the primary challenges, opportunities, most relevant biomaterials, and key applications in dentistry.

Nanocomposite thin films with gold nanoparticles embedded in a host metal oxide prepared by spray pyrolysis deposition have been investigated. A single-step process has been developed using a one-pot solution containing precursors for both gold nanoparticles and host metal oxides. The films obtained display combined features of colouration, electrical conductivity and solar control. In this study two precursors for gold nanoparticles were used: preformed gold colloids and HAuCl₄. Three metal oxide host materials, TiO₂, SnO₂ and ZnO, were investigated. These films were deposited at a substrate temperature of 200-600 °C. Powder X-ray diffraction analysis reveals the presence of metallic gold. SEM inspection typically showed particulate gold of 5-20 nm in diameter, distributed at the surface or within the host matrix. Optical spectroscopy showed an intense absorption in the visible region due to the characteristic surface plasmon resonance (SPR) effects of gold nanoparticles. The wavelength of the SPR peaks varies depending on the refractive index of surrounding host material which is significantly influenced by the substrate deposition temperature. On the other hand, SnO₂ and ZnO, together with the introduction of dopants, were further investigated as suitable materials for transparent conducting oxides (TCO). SnO₂:F films were found to attain very low electrical resistivity, while ZnO films exhibit higher transparency in the visible. A double layered structure with a TCO layer of SnO₂:F on top of a layer embedded with gold nanoparticles has been employed to achieve the combined functionalities of conductivity and colouration. The electrical conductivity is significantly enhanced compared to a nanocomposite single layer film due to the introduction of the TCO top layer. In this thesis, spray pyrolysis deposition has demonstrated a simple and rapid approach to the production of a variety of thin films. It can be immediately integrated with current industrial coating equipment and scaled up for large-scale production process.

Following the discovery of graphene, 2D nanostructures have been noted for their potential in a range of high-impact applications, such as sensing, catalysis, and composite reinforcement. Liquid-phase exfoliation and chemical vapour deposition have been demonstrated and indicate the feasibility of mass-scale production. With the advent of mass-produced 2D nanostructures a key focus of research is to characterise these materials. This thesis is concerned with imaging and structural properties of the 2D nanomaterials, hexagonal boron nitride (h-BN), molybdenum disulfide (MoS₂), tungsten disulfide (WS₂), titanium disulfide (TiS₂) and hexabenzocoronene (HBC), produced via liquid phase exfoliation. HBC strictly speaking is not 2D nanomaterial, however, it can be viewed as transition molecule from benzene to graphene. The data used for characterisation is based primarily on electron diffraction and, in particular, aberration corrected annular dark field (ADF) scanning transmission electron microscopy (STEM). The incoherent nature of ADF STEM provides direct atomic imaging without the contrast reversals upon focus changes seen in conventional high-resolution transmission electron microscopy (HRTEM). The main structural feature investigated in this thesis was the stacking sequences in few-layers h-BN, MoS₂, WS₂ and TiS₂. Simple stacking (AAA) can be distinguished from Bernal (ABA) and rhombohedral (ABC) on the basis of intensity ratio, I_{10̅10}/I_{11̅20} , in diffraction patterns and indirectly in HRTEM images. Nonetheless acquisition of the diffraction patterns suitable for analysis can be challenging due to the sample issues. Non-bulk stacking sequences were reliably confirmed for all above 2D nanomaterials on the basis of atomically resolved ADF STEM. 20 h-BN, 28 MoS₂, 5 WS₂ and 6 TiS₂ nanoflakes were imaged and analysed. Amongst them 2 h-BN, 9 MoS2, 4 WS2 and 1 TiS2 nanoflakes displayed non-bulk stacking. Hence, it appears that 2D WS2 has the greatest affinity for non-bulk stacking. Finally, an interesting structural transformation was observed in HBC molecules. Under the influence of electron beam HBC agglomerates were transformed into crystalline phase with 90^o symmetry.

Composite materials have become viable alternatives to traditional engineering materials for many different product categories. Liquid transfer moulding (LTM) processes, specifically resin transfer moulding (RTM), is a cost-effective manufacturing technique for creating high performance composite parts. These parts can be tailor-made to their specific application by optimizing the properties of the textile preform. Preforms which require little or no further assembly work and are close to the shape of the final part are critical to obtaining high quality parts while simultaneously reducing labour and costs associated with other composite manufacturing techniques. One type of fabric which is well suited for near-net- shape preforms is stitched non-crimp fabrics. These fabrics offer very high in-plane strength and stiffness while also having increased resistance to delamination. Manufacturing parts from these dry preforms typically involves long-scale fluid flow through both open channels and porous fibre bundles. This thesis documents and analyzes the flow of fluid through preforms manufactured from non-crimp fabrics featuring through-thickness stitches. The objective of this research is to determine the effect of this type of stitch on the RTM injection process. All of the tests used preforms with fibre volume fractions representative of primary and secondary structural parts. A series of trials was conducted using different fibre materials, flow rates, fibre volumes fractions, and degrees of fibre consolidation. All of the trials were conducted for cases similar to RTM. Consolidation of the fibres showed improvements to both the thoroughness of the filling and to the fibre volume fraction. Experimentally determined permeability data was shown to trend well with simple models and precision of the permeability data was comparable to values presented by other authors who studied fabrics which did not feature the through-thickness stitches.

Composite materials have become viable alternatives to traditional engineering materials for many different product categories. Liquid transfer moulding (LTM) processes, specifically resin transfer moulding (RTM), is a cost-effective manufacturing technique for creating high performance composite parts. These parts can be tailor-made to their specific application by optimizing the properties of the textile preform. Preforms which require little or no further assembly work and are close to the shape of the final part are critical to obtaining high quality parts while simultaneously reducing labour and costs associated with other composite manufacturing techniques. One type of fabric which is well suited for near-net- shape preforms is stitched non-crimp fabrics. These fabrics offer very high in-plane strength and stiffness while also having increased resistance to delamination. Manufacturing parts from these dry preforms typically involves long-scale fluid flow through both open channels and porous fibre bundles. This thesis documents and analyzes the flow of fluid through preforms manufactured from non-crimp fabrics featuring through-thickness stitches. The objective of this research is to determine the effect of this type of stitch on the RTM injection process. All of the tests used preforms with fibre volume fractions representative of primary and secondary structural parts. A series of trials was conducted using different fibre materials, flow rates, fibre volumes fractions, and degrees of fibre consolidation. All of the trials were conducted for cases similar to RTM. Consolidation of the fibres showed improvements to both the thoroughness of the filling and to the fibre volume fraction. Experimentally determined permeability data was shown to trend well with simple models and precision of the permeability data was comparable to values presented by other authors who studied fabrics which did not feature the through-thickness stitches.