<p>The development of nanocomposite materials has had significant influence on modern material design. Novel properties can be achieved and controlled for a diverse range of applications. The work presented here focused on characterization of polyurethane based coatings with ITO nano-inclusions. The coatings displayed high transparency in the visible range, and UV/IR shielding properties when studied with UV-Vis spectroscopy. UV/IR shielding improved with greater ITO density, with minor affect on visible transmittance. The effective medium approximation was successfully applied to ellipsometry modeling. Coatings with varying fractions of nanoparticles were analyzed. The modeled volume percent of the nanoparticles followed a strong linear trend with the known weight percentages. SEM and TEM imaging determined that majority of the particles existed in clusters. The nanoparticles were oblong shaped, 10-20nm big, randomly distributed, with no segregation to interfaces. Agglomerates varied in size, with the largest observed agglomerate being 250nm.</p> <p>Thermal stability was studied by TGA and DSC. No degradation occurred until 238°C. DSC revealed that the matrix continued to undergo modifications with consecutive runs. It was inconclusive whether the changes were from the polyurethane or dispersive agents in the system. Electron micrographs showed that segregation did not occur post-annealing. Average surface roughness increased from 3.5nm to 5nm after annealing at 120°C for several weeks. Ellipsometry results showed that film thickness decreased 20nm and 50nm before equilibriating for the 80°C and 120°C anneals respectively. The optical and thermal measurements demonstrated that the coating has great potential for improving the PV performance.</p> / Master of Applied Science (MASc)

<p> New electrophoretic deposition methods for the fabrication of advanced organic-inorganic composite coatings on metallic substrates for biomedical applications have been developed. In the proposed methods, chitosan was used as a matrix for the fabrication of multilayer and functional graded chitosan- hydroxyapatite (HA) coatings. The HA particles showed preferred orientation of c-axis parallel to the layer surface, which is similar to the bone structure. Electrochemical studies showed that the obtained coatings provided corrosion protection of the metallic substrates, such as stainless steel and Nitinol.</p> <p> The feasibility of co-deposition of chitosan and heparin has been demonstrated. Composite chitosan-heparin layers were used for the surface modification of chitosan-HA coatings. Obtained results paved the way for the electrophoretic fabrication of novel coatings for biomedical implants with improved blood compatibility.</p> <p> The feasibility of co-deposition of hyaluronic acid and HA has also been demonstrated. The co-deposition of hyaluronic acid and HA resulted in the fabrication of novel nanocomposite films by electrodeposition. The chemical composition, microstructure, corrosion protection, and other functional properties of the nanocomposites have been investigated. Co-deposition of hyaluronic acid and multiwalled carbon nanotubes has been studied by TGA/DT A and SEM studies.</p> <p> The feasibility of deposition of novel composites based on alginic acid has been demonstrated. New electrochemical strategies were used for the fabrication of alginic acid-HA, alginic acid-heparin and alginic acid -hyaluronic acid nanocomposites. The composition of these nanocomposite coatings can be varied by variation in bath composition for EPD.</p> <p> The electrochemical mechanisms for the fabrication of all these advanced organic-inorganic composite coatings have been developed.</p> / Thesis / Master of Applied Science (MASc)

No description available.

The process of TEMPO-mediated oxidation has gained broad usage towards the preparation of highly charged, carboxyl-functionalized polysaccharides. TEMPO-oxidized nanocelluloses (TONc) of high surface charge and measuring 3 to 5 nm in width have been recently prepared from TEMPO-oxidized pulp. This study examines as-produced and surface-hydrophobized TONc as reinforcing additives in cellulosic polymer matrices. In the first part of the work, covalent (amidation) and non-covalent (ionic complexation) coupling were compared as treatment techniques for the hydrophobization of TONc surfaces with octadecylamine (ODA). Subsequently, TONc and its covalently coupled derivative were evaluated as nanofiber reinforcements in a cellulose acetate butyrate (CAB) matrix. The properties of the resulting nanocomposites were compared with those of similarly prepared ones reinforced with conventional microfibrillated cellulose (MFC). It was found that both ionic complexation and amidation resulted in complete conversion of carboxylate groups on TONc surfaces. As a result of surface modification, the net crystallinity of TONc was lowered by 15 to 25% but its thermal decomposition properties were not significantly altered. With respect to nanocomposite performance, the maximum TONc reinforcement of 5 vol % produced negligible changes to the optical transmittance behavior and a 22-fold increase in tensile storage modulus in the glass transition region of CAB. In contrast, hydrophobized TONc and MFC deteriorated the optical transmittance of CAB by ca 20% and increased its tensile storage modulus in the glass transition region by only 3.5 and 7 times respectively. These differences in nanocomposite properties were attributed to homogeneous dispersion of TONc compared to aggregation of both the hydrophobized derivative and the MFC reference in CAB matrix. A related study comparing TONc with MFC and cellulose nanocrystals (CNC) as reinforcements in hydroxypropylcellulose (HPC), showed TONc reinforcements as producing the most significant changes to HPC properties. The results of dynamic mechanical analysis and creep compliance measurements could be interpreted based on similar arguments as those made for the CAB-based nanocomposites. Overall, this work revealed that the use of TONc (without the need for surface hydrophobization) as additives in cellulosic polymer matrices leads to superior reinforcing capacity and preservation of matrix transparency compared to the use of conventional nanocelluloses. / Ph. D.

All interfaces offer resistance to heat transport. As the size of a device or structure approaches nanometer lengthscales, the contribution of the interface thermal resistance often becomes comparable to the intrinsic thermal resistance offered by the device or structure itself. In many microelectronic devices, heat has to transfer across a metal-nonmetal interface, and a better understanding about the origins of this interface thermal conductance (inverse of the interface thermal resistance) is critical in improving the performance of these devices. In this dissertation, heat transport across different metal-nonmetal interfaces are investigated with the primary goal of gaining qualitative and quantitative insight into the heat transport mechanisms across such interfaces. A time-domain thermoreflectance (TDTR) system is used to measure the thermal properties at the nanoscale. TDTR is an optical pump-probe technique, and it is capable of measuring thermal conductivity, k, and interface thermal conductance, G, simultaneously. The first study examines k and G for amorphous and crystalline Zr47Cu31Al13Ni9 metallic alloys that are in contact with poly-crystalline Y2O3. The motivation behind this study is to determine the relative importance of energy coupling mechanisms such as electron-phonon or phonon-phonon coupling across the interface by changing the material structure (from amorphous to crystalline), but not the composition. From the TDTR measurements k=4.5 W m-1 K-1 for the amorphous metallic glass of Zr47Cu31Al13Ni9, and k=5.0 W m-1 K-1 for the crystalline Zr47Cu31Al13Ni9. TDTR also gives G=23 MW m-2 K-1 for the metallic glass/Y2O3 interface and G=26 MW m-2 K-1 for the interface between the crystalline Zr47Cu31Al13Ni9 and Y2O3. The thermal conductivity of the poly-crystalline Y2O3 layer is found to be k=5.0 W m-1 K-1. Despite the small difference between k and G for the two alloys, the results are repeatable and they indicate that the structure of the alloy plays a role in the electron-phonon coupling and interface conductance. The second experimental study examines the effect of nickel nanoparticle size on the thermal transport in multilayer nanocomposites. These nanocomposites consist of five alternating layers of nickel nanoparticles and yttria stabilized zirconia (YSZ) spacer layers that are grown with pulsed laser deposition. Using TDTR, thermal conductivities of k=1.8, 2.4, 2.3, and 3.0 W m-1 K-1 are found for nanocomposites with nickel nanoparticle diameters of 7, 21, 24, and 38 nm, respectively, and k=2.5 W m-1 K-1 for a single 80 nm thick layer of YSZ. The results indicate that the overall thermal conductivity of these nanocomposites is strongly influenced by the Ni nanoparticle size and the interface thermal conductance between the Ni particles and the YSZ matrix. An effective medium theory is used to estimate the lower limits for the interface thermal conductance between the nickel nanoparticles and the YSZ matrix (G>170 MW m-2 K-1), and the nickel nanoparticle thermal conductivity. / Ph. D.

Plasmonic polymer nanocomposites contain plasmonic nanoparticles that are dispersed within a polymer. The polymer matrix strongly influences the optical properties of plasmonic nanoparticles. It is imperative to understand the interaction between plasmonic nanoparticles and polymers so that one can develop functional devices using nanocomposites. The utilization of plasmonic nanoparticles as fillers has great potential to transform critical nanotechnologies where light management is crucial, such as refractive index based nanosensors, optical coatings, and light actuated devices. Despite the great potential, effective integration of plasmonic nanoparticles with polymers remains challenging. This dissertation presents i) the effects of dielectric media on the optical properties of plasmonic nanoparticles, ii) the sensing of polymer brush formation on nanoparticles, iii) the fabrication of plasmonic nanocomposite thin-films with controlled optical properties, and iv) the development of electrically conductive membranes for electrostatic speakers. The optical response of plasmonic nanoparticles (referred to as wavelength of localized surface plasmon resonance, λLSPR) is sensitive to changes in refractive index of the medium. The sensitivity (S) plays a critical role in determining the performance of nanoparticles in sensing applications. In this dissertation, I have conducted a systematic study on the sensitivity of plasmonic nanoparticles as a function of various parameters: shape, size, composition, initial plasmonic resonance wavelength, cross-sectional area, and aspect ratio. Among the parameters investigated, aspect ratio (R) is determined to be the key parameter that controls S, following an empirical equation, S = 46.87 R + 109.37. This relationship provides a guideline for selecting fillers in plasmonic polymer nanocomposites, and it predicts the final effect of plasmonic nanoparticles on the optical properties of polymer nanocomposites. Plasmonic nanoparticles are employed to probe polymer grafting on the surfaces of metal nanoparticles. Using ultraviolet-visible (UV-vis) spectroscopy, I have demonstrated the quantification of polymer grafting density on the surface of plasmonic nanoparticles. The λLSPR of plasmonic nanoparticles red-shifts as the polymer concentration near the nanoparticle surface increases. I have investigated the formation of polymer brush by grafting the nanoparticles with thiolated polyethylene glycol (PEG-SH) and revealed the three–regime kinetics in situ. Importantly, this study suggests that a latent regime arises due to fast polymer adsorption and prolonged chain rearrangement on nanoparticle surfaces. When the polymer chains rearrange and chemically tether to the surface, they contract and allow more polymer chains to graft onto the particle surface until saturation. This analytical method provides a new surface probing technique for polymer brush analysis, complementary to conventional methods such as quartz crystal microbalance, atomic force microscope, and microcantilivers. Commercial tinted glass employs expensive metalized films to reduce light transmittance but has limited spectral selectivity. To reduce the cost of metalized films and to improve the spectral selectivity, I have employed plasmonic nanoparticles in polymers to fabricate spectral-selective tinted films. First, I have synthesized two-dimensional (2D) plasmonic silver nanoparticles (AgNPs) using multi-step growth. The nanoparticles have a tunable plasmon resonance and provide spectral selectivity. The multi-step growth forgoes polymeric ligands such as poly(vinylpyrrolidone) (PVP) and solely relies on a small molecule sodium citrate. Briefly, small citrate-capped Ag seeds are first grown into small 2D AgNPs. The small 2D AgNPs are then used to grow large 2D AgNPs via multiple growth steps. The PVP-free method allows for fast synthesis of 2D AgNPs with large sizes and tunable plasmon resonance across the visible and NIR region. The 2D AgNPs are integrated with polymers to produce thin-film plasmonic nanocomposites. By controlling the planar orientation of the 2D AgNPs through layer-by-layer assembly, the polymer nancomposites have achieved reduced light transmittance and enhanced reflectance across the visible and NIR range. In contrast to conventional polymer nanocomposites where the AgNPs are randomly oriented, the thin-film polymer nanocomposites exhibit excellent control over nanoparticle density and hence the optical properties, that is, tunable light transmittance and reflectance across the visible and NIR. Lastly, graphene is used to prepare conductive free-standing polymer thin-films. Graphene, an ultralight weight 2D material with excellent electrical and mechanical properties, has potential for use in thin-film composites essential for photovoltaics, electrostatic speakers, sensors, and touch displays. Current graphene-based composite films contain graphene flakes randomly mixed in a polymer matrix and usually possess poor mechanical and electrical properties. In this dissertation, I have developed thin-film nanocomposites comprised of chemical vapor deposited (CVD) graphene and high-performance polyetherimide (PI). The CVD-grown graphene is polycrystalline, and it cannot be used as a free-standing film. By enforcing the polycrystalline graphene with a thin layer of PI, I have prepared free-standing thin-film composites with a high aspect ratio of 105. Mechanical and electrical property characterization reveals a Young's modulus of 3.33 GPa and a resistance of 200 - 500 Ω across the membrane. A typical spring constant of the membrane is ~387 N/m. Dynamic electromechanical actuation shows that the membrane vibrates at various input frequencies. The polymer/graphene film has excellent acoustic properties, and when used as a speaker membrane, it reduces the electrical power consumption by a factor of 10-100 over the frequency range of 600–10,000 Hz. / Doctor of Philosophy / Nanomaterials such as plasmonic nanoparticles and graphene have optical, electrical, and mechanical properties that are important for light filters, sensors, printing, photovoltaics, touch screens, speakers, and biomedical devices. To fully employ the nanomaterials, a support such as polymer is often required. However, when the nanomaterials and polymers are combined, their optical, electrical, and mechanical properties drastically change. Therefore, it is imperative to understand the interactions between nanomaterials and polymers, as well as the resulting properties. Towards this goal, I have studied the sensitivity of plasmonic nanoparticles in a dielectric media and then utilized the sensitivity to investigate polymer brush formation on nanoparticle surfaces. In addition, I have investigated the integration of plasmonic nanoparticles and graphene with polymers to develop thin-film nanocomposites for window coatings and audio speakers, respectively. Plasmonic nanoparticles can detect trace amounts of chemicals, biomolecules, toxics, warfare agents, and environmental pollutants. Sensitivity is the key criterion that determines the performance of nanoparticles for such applications. Firstly, I have conducted a detailed and comprehensive study of the plasmonic sensitivity as a function of various nanoparticle parameters including shape, size, composition, cross-sectional area, initial plasmonic resonance wavelength, and aspect ratio. I have found that the sensitivity scaled linearly with aspect ratio. The strong dependence of sensitivity on aspect ratio provides insight into designing effective plasmonic sensors. Based on the sensitivity study, I have used plasmonic nanoparticles as sensors to probe and understand the mechanism of polymer brush formation in situ. When the concentration of polymer increases on the nanoparticle surfaces, the optical response of the nanoparticle changes. Through functionalizing the plasmonic nanoparticles with polymers, I have confirmed the three different regimes of polymer brush formation. Plasmonic nanoparticles resonating in the visible and near infrared have a great potential in designing polymer nanocomposites for window coatings. Among different exotic shapes, two-dimensional nanoplates are the most important as their optical properties can be easily tuned across a wide range of wavelengths. However, most of the current methods require polymers, long hours of reaction time, and multiple purification steps. I have developed a new multi-step strategy to synthesize Ag nanoplates which absorb in the range of 500–1660 nm. Utilizing the plasmonic nanoparticles, the spectral-selective plasmonic nanocomposites comprised of polymers and planarly oriented Ag nanoparticles of judiciously selected sizes and compositions were prepared. The plasmonic polymer nanocomposites spectral-selectively reflect, scatter, and filter light of any desired wavelength. The nanocomposites will impact on the tinted glass in modern energy-efficient buildings. The outstanding electrical and mechanical properties of graphene have stirred a large volume of research in the last 15 years. Most graphene-based technologies focus on graphene at the nano or micro scale. To further the practicality of graphene in large devices like audio speakers, large areas and thin films are needed to reduce energy consumption. Graphene on its own cannot be used over large areas due to the inherent defects arising during the growth. Here I present results on combining suspended sheets of single layer graphene with a mechanically strong polymer thin film. The acoustic properties of speakers made of polymer/graphene thin films are similar to those of conventional electrodynamic speakers in modern cellphones. The energy consumption, however, reduces sharply by a factor of 10-100 for the polymer/graphene based speakers. This sharp decrease in energy is attributed to the lightweight, flexibility, and excellent electrical conductivity. Apart from speakers, the membrane designed here also has huge potential in other devices like touch panels, capacitive sensors, and photovoltaics.

Polymeric membranes for gas separation are limited in their performance by a trade-off between permeability and selectivity. New methods of design are necessary in making membranes, which can show both high permeability and selectivity. A mixed matrix membrane is one such particular design, which brings in the superior gas separation performance of inorganic membranes together with the easy processability and price of the polymers. In a mixed matrix membrane, the inorganic phase is dispersed in the polymeric continuous phase. Nanocomposite membranes have a more sophisticated design with a thin separation layer on top of a porous support. The objective of this research was to fabricate thin SWNT nanocomposite membranes for gas separation, which have both high permeability and selectivity. SWNT/polyacrylic nanocomposite membranes were fabricated by orienting the SWNTs by high vacuum filtration. The orientation of SWNTs on top of the porous support was sealed by UV polymerization. For making these membranes, the CNTs were purified and cut into small open tubes simultaneously functionalizing them with COOH groups. Gas sorption of CO2 in COOH functionalized SWNTs was lower than in purified SWNTs. Permeabilities in etched membrane were higher than Knudsen permeabilities by a factor of 8, and selectivities were similar to Knudsen selectivities. In order to increase the selectivities, SWNTs were functionalized with zwitterionic functional groups. Gas sorption in zwitterion functionalized SWNTs was very low compared to in COOH functionalized SWNTs. This result showed that the zwitterionic functional groups are kinetically blocking the gas molecules from entering the pore of the CNT. SWNT/polyamide nanocomposite membranes were fabricated using the zwitterion functionalized SWNTs by interfacial polymerization. The thickness of the separation layer was around 500nm. Gas permeabilities in the CNT membranes increased with increasing weight percentage of the SWNTs. Gas permeabilities were higher in COOH SWNT membrane than in zwitterion SWNT membrane. Gas selectivities were similar to the Knudsen selectivities, and also to the intrinsic selectivities in the pure polyamide membrane. The water flux in SWNT-polyamide membranes increased with increasing weight percentage of zwitterion functionalized SWNTs, along with a slight increase in the salt rejection. Membranes exhibited less than 1% variability in its performance over three days. / Ph. D.

Supercritical carbon dioxide (scCO2) was used as a processing aid to improve the level of exfoliation achievable in a PET-layered silicate nanocomposite produced from melt compounding. Layered silicate and scCO2 were allowed to mix for a period of time before being released into the second stage of a single screw extruder. The rapid expansion forced silicate particles into a modified hopper containing neat PET pellets. The mixture of layered silicate and PET was immediately melt mixed in a single screw extruder, cooled in a water bath and pelletized. Two sets of samples each containing layered silicate with different surface chemistries were produced with this method at 1, 3 and 5 wt% silicate. For comparison, samples of the same weight fraction and type of silicate were produced from a traditional melt compounding method. Wide angle x-ray diffraction (WAXD), mechanical testing and rheological analysis were used in order to characterize the silicate morphology, the composite mechanical properties and the relative amount of degradation between the various samples. Results show that scCO2 processed samples contain a higher degree of layered silicate exfoliation than samples produced with traditional melt compounding. Mechanical property improvements are shown to be dependent on the type of silicate surface modification employed. Finally, degradation of the PET matrix appears to be far less extensive in the scCO2 processed samples as shown from rheological data. / Master of Science

Multiferroics have attracted lots of research interest due to their potential in numerous multifunctional applications. The multiferroic materials could simultaneously exhibit two or more ferroic order parameters, and the coupling effects between ferroelectricity and ferromagnetism are named as magnetoelectric (ME) effect. Recently, with the development of thin film growth techniques, the multiferroics magnetoelectric composite heterostructures exhibit a very promising future prospects. This dissertation focused on the design, fabrication and characterization of new multiferroics magnetoelectric composite heterostructures. First, based on the specific phase architectures in BFO-CFO self-assembled thin films grown on variously oriented STO substrates and the epitaxial film growth knowledge, I designed two kinds of new film heterostructures: (i) I utilized self-assembled BFO nanopillars in a BFO-CFO two phase layer on (111) STO as a seed layer on which to deposit a secondary top BiFeO3 layer. The growth mechanism and multiferroic properties of these new heterostructures were investigated. (ii) I demonstrated the formation of a new quasi-(0-3) heterostructure by alternately growing (2-2) and (1-3) layers within the film. I proposed a new concept to overcome limitations of both the (2-2) and (1-3) phase connectivities and identified an indirect ME effect by the switching the characteristics of the piezoresponse for the new heterostructure. Second, for the option for candidates thin film materials with a high piezoelectric coefficient, which is a critical factor for ME composite films, I utilized the simple compositional BaSn0.11Ti0.89O3 bulk ceramic material as a target to grow films with the large piezoelectric properties. The grown high qualify lead-free epitaxial thin films had a chemical constituent similar to the reported giant piezoelectric ceramics near the MPB and with the QP. Both coherent and incoherent regions were observed in the interface and a larger piezoelectric coefficient d33 was achieved in this film. Finally, with respect to their characteristics and potential, I redirected from two-dimensional thin film materials to one-dimensional nanowire materials. By utilizing vertically aligned templates, I fabricated a new type of coaxial two-phase composite nanowires. Multiferroic properties of these new one-dimensional materials have been investigated. All these multiferroics magnetoelectric composite herterostructures would provide lots of potential in applications. / PHD

This thesis presents the study of nanocomposites based on immiscible polymer blend of polycarbonate and acrylonitrile-butadiene-styrene (PC/ABS) filled with multi-walled carbon nanotubes (MWCNT). The aim is to achieve an improvement of mechanical properties and electrical conductivity of the nanocomposites. In an initial stage, a twin-screw extruder was used to obtain nanocomposites by melt compounding. Three methods of carbon nanotubes addition were studied: direct addition, dilution from a masterbatch and feeding of MWCNT suspension in ethanol. For each method, the influence of nanofiller content and processing parameters on morphology and final properties of the nanocomposite was analyzed. Furthermore, the influence of two types of carbon nanotubes modifications was studied: covalent modification by surface-oxidation (MWCNT-COOH) and non-covalent modification by an addition of surfactant promoting the nanofiller-matrix interactions. A good dispersion of the MWCNT was obtained for masterbatch dilution and suspension feeding. Both methods showed preferential localization of carbon nanotubes in polycarbonate phase (PC). Samples processed by masterbatch dilution showed the 30 % increase of rigidity and a decrease of ductility of PC/ABS for 0.5 wt. % MWCNT. Electrical conductivity was influenced by processing temperature and carbon nanotubes type. The percolation threshold value was 2.0 wt. % for pristine MWCNT and 1.5 wt. % for modified MWCNT-COOH. Better balance of mechanical properties and electrical conductivity was achieved in the samples obtained by the masterbatch route. These properties were studied in a subsequent phase, when the extruded nanocomposite was injection molded in order to obtain a defined geometry. / Wegrzyn, M. (2014). Nanocomposites of Multiphase Polymer Blend Reinforced with Carbon Nanotubes: Processing and Characterization [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/36869