Current Search: Atomism (x)
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Title
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Electronic properties and atomic scale microscopy of two dimensional materials: graphene and molybdenum disulfide.
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Creator
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Katoch, Jyoti, Ishigami, Marsahir, Mucciolo, Eduardo, Del Barco, Enrique, Coffey, Kevin, University of Central Florida
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Abstract / Description
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Novel two dimensional nanoscale materials like graphene and metal dichalcogenides (MX2) have attracted the attention of the scientific community, due to their rich physics and wide range of potential applications.It has been shown that novel graphene based transparent conductors and radiofrequency transistors are competitive with the existing technologies. Graphene's properties are influenced sensitively by adsorbates and substrates. As such not surprisingly, physical properties of graphene...
Show moreNovel two dimensional nanoscale materials like graphene and metal dichalcogenides (MX2) have attracted the attention of the scientific community, due to their rich physics and wide range of potential applications.It has been shown that novel graphene based transparent conductors and radiofrequency transistors are competitive with the existing technologies. Graphene's properties are influenced sensitively by adsorbates and substrates. As such not surprisingly, physical properties of graphene are found to have a large variability, which cannot be controlled at the synthesis level, reducing the utility of graphene. As a part of my doctorate dissertation, I have developed atomic hydrogen as a novel technique to count the scatterers responsible for limiting the carrier mobility of graphene field effect transistors on silicon oxide (SiO2) and identified that charged impurities to be the most dominant scatterer. This result enables systematic reduction of the detrimental variability in device performance of graphene. Such sensitivity to substrates also gives an opportunity for engineering device properties of graphene using substrate interaction and atomic scale vacancies. Stacking graphene on hexagonal boron-nitride (h-BN) gives rise to nanoscale periodic potential, which influences its electronic graphene. Using state-of-the-art atomic-resolution scanning probe microscope, I correlated the observed transport properties to the substrate induced extrinsic potentials. Finally in efforts to exploit graphene's sensitivity to discover new sensor technologies, I have explored noncovalentfunctionalization of graphene using peptides.Molybdenum disulfide (MoS2) exhibits thickness dependent bandgap. Transistors fabricated from single layer MoS2 have shown a high on/off ratio. It is expected that ad-atom engineering can be used to induce on demand a metal-semiconductor transition in MoS2. In this direction, I have explored controlled/reversible fluorination and hydrogenation of monolayer MoS2 to potentially derive a full range of integrated circuit technology. The in-depth characterization of the samples is carried out by Raman/photoluminescence spectroscopy and scanning tunneling microscopy.
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Date Issued
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2014
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Identifier
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CFE0005190, ucf:50614
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0005190
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Title
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Theoretical And Experimental Investigation Of The Cascading Nature Of Pressure-Swirl Atomization.
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Creator
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Choudhury, Pretam, Kumar, Ranganathan, Deng, Weiwei, Mansy, Hansen, University of Central Florida
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Abstract / Description
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Pressure swirl atomizers are commonly used in IC, aero-engines, and liquid propellant rocket combustion. Understanding the atomization process is important in order to enhance vaporization, mitigate soot formation, design of combustion chambers, and improve overall combustion efficiency. This work utilizes non-invasive techniques such as ultra -speed imaging, and Phase Doppler Particle Anemometry (PDPA) in order to investigate the cascade atomization process of pressure-swirl atomizers by...
Show morePressure swirl atomizers are commonly used in IC, aero-engines, and liquid propellant rocket combustion. Understanding the atomization process is important in order to enhance vaporization, mitigate soot formation, design of combustion chambers, and improve overall combustion efficiency. This work utilizes non-invasive techniques such as ultra -speed imaging, and Phase Doppler Particle Anemometry (PDPA) in order to investigate the cascade atomization process of pressure-swirl atomizers by examining swirling liquid film dynamics and the localized droplet characteristics of the resulting hollow cone spray. Specifically, experiments were conducted to examine these effects for three different nozzles with orifice diameters .3mm, .5mm, and .97mm. The ultra-speed imaging allowed for both visualization and interface tracking of the swirling conical film which emanated from each nozzle. Moreover, this allowed for the measurement of the radial fluctuations, film length, cone angle and maximum wavelength. Radial fluctuations are found to be maximum near the breakup or rupture of a swirling film. Film length decreases as Reynolds number increases. Cone angle increases until a critical Reynolds number is reached, beyond which it remains constant. A new approach to analyze the temporally unstable waves was developed and compared with the measured maximum wavelengths. The new approach incorporates the attenuation of a film thickness, as the radius of a conical film expands, with the classical dispersion relationship for an inviscid moving liquid film. This approach produces a new long wave solution which accurately matches the measured maximum wavelength swirling conical films generated from nozzles with the smallest orifice diameter. For the nozzle with the largest orifice diameter, the new long wave solution provides the upper bound limit, while the long wave solution for a constant film thickness provides the lower bound limit. These results indicate that temporal instability is the dominating mechanism which generates long Kelvin Helmholtz waves on the surface of a swirling liquid film. The PDPA was used to measure droplet size and velocity in both the near field and far field of the spray. For a constant Reynolds number, an increase in orifice diameter is shown to increase the overall diameter distribution of the spray. In addition, it was found that the probability of breakup, near the axis, decreases for the largest orifice diameter. This is in agreement with the cascading nature of atomization.
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Date Issued
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2015
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Identifier
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CFE0006030, ucf:51012
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0006030
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Title
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Direct measurement of thicknesses, volumes or compositions of nanomaterials by quantitative atomic number contrast in high-angle annular dark-field scanning transmission electron microscopy.
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Creator
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Yuan, Biao, Heinrich, Helge, Sohn, Yongho, Coffey, Kevin, Fang, Jiyu, Roldan Cuenya, Beatriz, University of Central Florida
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Abstract / Description
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The sizes, shapes, volumes and compositions of nanoparticles are very important parameters determining many of their properties. Efforts to measure these parameters for individual nanoparticles and to obtain reliable statistics for a large number of nanoparticles require a fast and reliable method for 3-D characterization. In this dissertation, a direct measurement method for thicknesses, volumes or compositions of nanomaterials by quantitative atomic number contrast in High-Angle Annular...
Show moreThe sizes, shapes, volumes and compositions of nanoparticles are very important parameters determining many of their properties. Efforts to measure these parameters for individual nanoparticles and to obtain reliable statistics for a large number of nanoparticles require a fast and reliable method for 3-D characterization. In this dissertation, a direct measurement method for thicknesses, volumes or compositions of nanomaterials by quantitative atomic number contrast in High-Angle Annular Dark-Field (HAADF) Scanning Transmission Electron Microscopy (STEM) is presented. A HAADF detector collects electrons scattered incoherently to high angles. The HAADF signal intensity is in first-order approximation proportional to the sample thickness and increases with atomic number. However, for larger sample thicknesses this approach fails. A simple description for the thickness dependence of the HAADF-STEM contrast has been developed in this dissertation. A new method for the calibration of the sensitivity of the HAADF detector for a FEI F30 transmission electron microscope (TEM) is developed in this dissertation. A nearly linear relationship of the HAADF signal with the electron current is confirmed. Cross sections of multilayered samples provided by TriQuint Semiconductors in Apopka, FL, for contrast calibration were obtained by focused ion-beam (FIB) preparation yielding data on the interaction cross section per atom.To obtain an absolute intensity calibration of the HAADF-STEM intensity, Convergent Beam Electron Diffraction (CBED) was performed on Si single crystals. However, for samples prepared by the focused ion beam technique, CBED often significantly underestimates the sample thickness. Multislice simulations from Dr. Kirkland's C codes are used for comparison with experimental results. TEM offers high lateral resolution, but contains little or no information on the thickness of samples. Thickness maps in energy-filtered TEM (EFTEM), CBED and tilt series are so far the only methods to determine thicknesses of particles in TEM. In this work I have introduced the use of wedge-shaped multilayer samples prepared by FIB for the calibration of HAADF-STEM contrasts. This method yields quantitative contrast data as a function of sample thickness. A database with several pure elements and compounds has been compiled, containing experimental data on the fraction of electrons scattered onto the HAADF detector for each nanometer of sample thickness. The use of thick samples reveals an increased signal at the interfaces of high- and low-density materials. This effect can be explained by the transfer of scattered electrons from the high density material across the interface into the less-absorbing low-density material. The calibrations were used to determine concentration gradients in nanoscale Fe-Pt multilayers as well as thicknesses and volumes of individual Au-Fe, Pt, and Ag nanoparticles. Volumes of nanoparticles with known composition can be determined with accuracy better than 15%. Porosity determination of materials becomes available with this method as shown in an example of porous Silicon.?
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Date Issued
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2012
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Identifier
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CFE0004464, ucf:49355
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0004464
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Title
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STRUCTURAL, ELECTRONIC, VIBRATIONAL AND THERMODYNAMICAL PROPERTIES OF SURFACES AND NANOPARTICLES.
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Creator
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Yildirim, Handan, Rahman, Talat S., University of Central Florida
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Abstract / Description
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The main focus of the thesis is to have better understanding of the atomic and electronic structures, vibrational dynamics and thermodynamics of metallic surfaces and bi-metallic nanoparticles (NPs) via a multi-scale simulational approach. The research presented here involves the study of the physical and chemical properties of metallic surfaces and NPs that are useful to determine their functionality in building novel materials. The study follows the ÃÂ"bottom-upÃ&...
Show moreThe main focus of the thesis is to have better understanding of the atomic and electronic structures, vibrational dynamics and thermodynamics of metallic surfaces and bi-metallic nanoparticles (NPs) via a multi-scale simulational approach. The research presented here involves the study of the physical and chemical properties of metallic surfaces and NPs that are useful to determine their functionality in building novel materials. The study follows the ÃÂ"bottom-upÃÂ" approach for which the knowledge gathered at the scale of atoms and NPs serves as a base to build, at the macroscopic scale, materials with desired physical and chemical properties. We use a variety of theoretical and computational tools with different degrees of accuracy to study problems in different time and length scales. Interactions between the atoms are derived using both Density Functional Theory (DFT) and Embedded Atom Method (EAM), depending on the scale of the problem at hand. For some cases, both methods are used for the purpose of comparison. For revealing the local contributions to the vibrational dynamics and thermodynamics for the systems possessing site-specific environments, a local approach in real-space is used, namely Real Space GreenÃÂ's Function method (RSGF). For simulating diffusion of atoms/clusters and growth on metal surfaces, Molecular Statics (MS) and Molecular Dynamics (MD) methods are employed.
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Date Issued
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2010
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Identifier
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CFE0003064, ucf:48300
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0003064
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Title
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Redox-Active Solid State Materials and its Biomedical and Biosensing Applications.
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Creator
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Gupta, Ankur, Seal, Sudipta, Dong, Yajie, Cho, Hyoung Jin, Zhai, Lei, Schulte, Alfons, University of Central Florida
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Abstract / Description
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Reactive oxygen species (ROS) are byproducts of physiological processes in human body, and strengthened production of ROS is known to cause acute conditions such as inflammation, aging, Alzheimer's disease, melanoma and ovarian cancer, fibrosis and multiple sclerosis. Therefore, early detection of ROS at nanomolar concentration (at cellular level) and developing more potent antioxidants is essential for regular health monitoring. As an example, ROS are also responsible for inflammation...
Show moreReactive oxygen species (ROS) are byproducts of physiological processes in human body, and strengthened production of ROS is known to cause acute conditions such as inflammation, aging, Alzheimer's disease, melanoma and ovarian cancer, fibrosis and multiple sclerosis. Therefore, early detection of ROS at nanomolar concentration (at cellular level) and developing more potent antioxidants is essential for regular health monitoring. As an example, ROS are also responsible for inflammation reactions at orthopedic implants-tissue interface triggered by wear debris. Inflammation induced by ROS results in revision surgery. Coatings of redox-active materials exhibiting antioxidant properties on implants have potential to mitigate the inflammation and delay the need of revision surgery. This dissertation focus on developing advanced functional nanomaterials by tailoring the surface chemistry of existing materials. Surface chemistry of materials can be altered by introducing surface and edge defects in the lattice structure Three materials system doped cerium oxide nanoparticles (d-CNPs), cerium oxide thin films (CeOx) and molybdenum disulfide (MoS2) nanoparticles, have been studied for its surface and edge contributions in potential biomedical and biosensing applications. Surface (d-CNPs and CeOx thin films) and edge chemistry (MoS2) have been tailored to understand its role and specific response.Surface Ce3+/Ce4+ oxidation state in CNPs controls the bio-catalytic activity. Higher superoxide dismutase (SOD) is demonstrated by high Ce3+/Ce4+ oxidation state. On the other hand, improved catalase mimetic activity is observed for low Ce3+/Ce4+ CNPs. Different CNPs preparation results in different Ce3+ to Ce4+ ratio, particle size, surface coating, and agglomeration, thus significantly varying the antioxidant properties of CNPs. In the first section of the dissertation, sustainable one-step room temperature synthesis of rare earth element (La, Sm, and Er) d-CNPs have been developed to effectively control the Ce3+ to Ce4+ ratio for specific biological application. Substitution of Ce4+ ions by trivalent dopants from ceria lattice increases the oxygen vacancies and density of catalytic sites. Uniform distribution of trivalent dopant in ceria lattice confirmed by EFTEM is attributed to enhanced SOD mimetic activity, ROS scavenging and tuning surface Ce3+/Ce4+ oxidation state in CNPs. Surface chemistry of redox-active cerium oxide coating on orthopedic implants also plays a vital role in scavenging ROS and mitigating inflammation. Thus, surface chemistry of CeOx thin films deposited by atomic layer deposited (ALD), have also been tailored by controlling the film thickness. CeOx film of 2 nm thickness has high Ce3+/Ce4+ (ratio 1) whereas higher thickness films (6-33 nm) have lower Ce3+/Ce4+ (ratio 0.30-0.37). These films have been further tested for catalase mimetic activity and hydrogen peroxide (H2O2) detection. Sensor selectivity is always a key issue. Most often, ascorbic acid found in the biological system, interfere in the electrochemical detection of H2O2 resulting in selectivity issue, thus protective Nafion layer is required to prevent cerium oxide-ascorbic acid interaction.To improve the selectivity of electrochemical sensors, Sulfur-deficient redox-active MoS2 have been utilized for electrochemical detection of pharmaceutically relevant chemical species. S-deficient MoS2 nanoparticles have been prepared by liquid exfoliation method to increase Mo-edge density and tested as sensing materials for detection of pharmaceutically relevant H2O2, hypochlorous acid (HOCl) and reactive nitrogen (NO*) species. The addition of ascorbic acid and uric acid have shown no interference during H2O2 detection. Change in S to Mo ratio have been studied using x-ray photoelectron spectroscopy. Density functional theory (DFT) have been employed to understand the detection mechanism and size-dependent sensitivity of MoS2. DFT study further reveals the role of S-deficiency and Mo- and S-edges in the higher catalytic activity of 5-7 nm MoS2 particles.Through these studies, the importance of defects in nanomaterials and their exotic properties at the nanoscale have been demonstrated. Understanding developed from these studies have provided the framework to develop more advanced functional nanomaterials for biomedical and biosensing applications.
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Date Issued
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2017
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Identifier
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CFE0006944, ucf:51655
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0006944
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Title
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QUANTITATIVE SCANNING TRANSMISSION ELECTRON MICROSCOPY OF THICK SAMPLES AND OF GOLD AND SILVER NANOPARTICLES ON POLYMERIC SURFACES.
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Creator
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Dutta, Aniruddha, Heinrich, Helge, Del Barco, Enrique, Chow, Lee, Chen, Bo, Kuebler, Stephen, University of Central Florida
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Abstract / Description
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Transmission Electron Microscopy (TEM) is a reliable tool for chemical and structural studies of nanostructured systems. The shape, size and volumes of nanoparticles on surfaces play an important role in surface chemistry. As nanostructured surfaces become increasingly important for catalysis, protective coatings, optical properties, detection of specific molecules, and many other applications, different techniques of TEM can be used to characterize the properties of nanoparticles on surfaces...
Show moreTransmission Electron Microscopy (TEM) is a reliable tool for chemical and structural studies of nanostructured systems. The shape, size and volumes of nanoparticles on surfaces play an important role in surface chemistry. As nanostructured surfaces become increasingly important for catalysis, protective coatings, optical properties, detection of specific molecules, and many other applications, different techniques of TEM can be used to characterize the properties of nanoparticles on surfaces to provide a path for predictability and control of these systems.This dissertation aims to provide fundamental understanding of the surface chemistry of Electroless Metallization onto Polymeric Surfaces (EMPS) through characterization with TEM. The research focuses on a single EMPS system: deposition of Ag onto the cross-linked epoxide (")SU8("), where Au nanoparticles act as nucleation sites for the growth of Ag nanoparticles on the polymer surface. TEM cross sections were analyzed to investigate the morphology of the Au nanoparticles and to determine the thicknesses of the Ag nanoparticles and of the Ag layers. A method for the direct measurement of the volume and thickness of nanomaterials has been developed in the project using High-Angle Annular Dark-Field (HAADF) Scanning Transmission Electron Microscopy (STEM). The morphology of Au and Ag NPs has been studied to provide reliable statistics for 3-D characterization. Deposition rates have been obtained as a function of metallization conditions by measuring the composition and thickness of the metal for EMPS. In the present work a calibration method was used to quantify the sensitivity of the HAADF detector. For thin samples a linear relationship of the HAADF signal with the thickness of a material is found. Cross-sections of multilayered samples provided by Triquint Semiconductors, FL, were analyzed as calibration standards with known composition in a TECNAI F30 transmission electron microscope to study the dependence of the HAADF detector signal on sample thickness and temperature.Dynamical diffraction processes play an important role in electron scattering for larger sample thicknesses. The HAADF detector intensity is not linearly dependent on sample thicknesses for thick samples. This phenomenon involves several excitation processes including Thermal Diffuse Scattering (TDS) which depends on temperature-dependent absorption coefficients. Multislice simulations have been carried out by Python programming using the scattering parameters available in the literature. These simulations were compared with experimental results. Wedge-shaped Focused Ion Beam (FIB) samples were prepared for quantitative HAADF-STEM intensity measurements for several samples and compared with these simulations. The discrepancies between the simulated and experimental results were explained and new sets of absorptive parameters were calculated which correctly account for the HAADF-STEM contrasts. A database of several pure elements is compiled to illustrate the absorption coefficients and fractions of scattered electrons per nanometer of the sample.In addition, the wedge-shaped FIB samples were used for studying the HAADF-STEM contrasts at an interface of a high- and a low-density material. The use of thick samples reveals an increased signal at the interfaces of high- and low-density materials. This effect can be explained by the transfer of scattered electrons from the high density material across the interface into the less-absorbing low-density material. A ballistic scattering model is proposed here for the HAADF-STEM contrasts at interfaces of thick materials using Python. The simulated HAADF-STEM signal is compared with experimental data to showcase the above phenomenon. A detailed understanding of the atomic number contrast in thick samples is developed based on the combination of experimental quantitative HAADF-STEM and simulated scattering. This approach is used to describe the observed features for Ag deposition on SU-8 polymers.
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Date Issued
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2014
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Identifier
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CFE0005485, ucf:50333
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0005485
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Title
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Optically Induced Forces in Scanning Probe Microscopy.
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Creator
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Kohlgraf-Owens, Dana, Dogariu, Aristide, Christodoulides, Demetrios, Kik, Pieter, DeWilde, Yannick, University of Central Florida
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Abstract / Description
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The focus of this dissertation is the study of measuring light not by energy transfer as is done with a standard photodetector such as a photographic film or charged coupled device, but rather by the forces which the light exerts on matter. In this manner we are able to replace or complement standard photodetector-based light detection techniques. One key attribute of force detection is that it permits the measurement of light over a very large range of frequencies including those which are...
Show moreThe focus of this dissertation is the study of measuring light not by energy transfer as is done with a standard photodetector such as a photographic film or charged coupled device, but rather by the forces which the light exerts on matter. In this manner we are able to replace or complement standard photodetector-based light detection techniques. One key attribute of force detection is that it permits the measurement of light over a very large range of frequencies including those which are difficult to access with standard photodetectors, such as the far IR and THz. The dissertation addresses the specific phenomena associated with optically induced force (OIF) detection in the near-field where light can be detected with high spatial resolution close to material interfaces. This is accomplished using a scanning probe microscope (SPM), which has the advantage of already having a sensitive force detector integrated into the system. The two microscopies we focus on here are atomic force microscopy (AFM) and near-field scanning optical microscopy (NSOM). By detecting surface-induced forces or force gradients applied to a very small size probe ( diameter), AFM measures the force acting on the probe as a function of the tip-sample separation or extracts topography information. Typical NSOM utilizes either a small aperture ( diameter) to collect and/or radiate light in a small volume or a small scatterer ( diameter) in order to scatter light in a very small volume. This light is then measured with an avalanche photodiode or a photomultiplier tube.These two modalities may be combined in order to simultaneously map the local intensity distribution and topography of a sample of interest. A critical assumption made when performing such a measurement is that the distance regulation, which is based on surface induced forces, and the intensity distribution are independent. In other words, it is assumed that the presence of optical fields does not influence the AFM operation. However, it is well known that light exerts forces on the matter with which it interacts. This light-induced force may affect the atomic force microscope tip-sample distance regulation mechanism or, by modifying the tip, it may also indirectly influence the distance between the probe and the surface. This dissertation will present evidence that the effect of optically induced forces is strong enough to be observed when performing typical NSOM measurements. This effect is first studied on common experimental situations to show where and how these forces manifest themselves. Afterward, several new measurement approaches are demonstrated, which take advantage of this additional information to either complement or replace standard NSOM detection. For example, the force acting on the probe can be detected while simultaneously extracting the tip-sample separation, a measurement characteristic which is typically difficult to obtain. Moreover, the standard field collection with an aperture NSOM and the measurement of optically induced forces can be operated simultaneously. Thus, complementary information about the field intensity and its gradient can be, for the first time, collected with a single probe. Finally, a new scanning probe modality, multi-frequency NSOM (MF-NSOM), will be demonstrated. In this approach, the tuning fork is driven electrically at one frequency to perform a standard tip-sample distance regulation to follow the sample topography and optically driven at another frequency to measure the optically induced force. This novel technique provides a viable alternative to standard NSOM scanning and should be of particular interest in the long wavelength regime, e.g. far IR and THz.
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Date Issued
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2013
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Identifier
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CFE0004705, ucf:49829
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0004705
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Title
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SELF-ASSEMBLED LIPID TUBULES: STRUCTURES, MECHANICAL PROPERTIES, AND APPLICATIONS.
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Creator
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Zhao, Yue, Fang, Jiyu, University of Central Florida
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Abstract / Description
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Self-assembled lipid tubules are particularly attractive for inorganic synthesis and drug delivery because they have hollow cylindrical shapes and relatively rigid mechanical properties. In this thesis work, we have synthesized lipid tubules of 1,2-bis(tricosa-10,12-dinoyl)-sn-glycero-3-phosphocholine (DC8,9PC) by self-assembly and polymerization in solutions. We demonstrate for the first time that both uniform and modulated molecular tilt orderings exist in the tubule walls, which have been...
Show moreSelf-assembled lipid tubules are particularly attractive for inorganic synthesis and drug delivery because they have hollow cylindrical shapes and relatively rigid mechanical properties. In this thesis work, we have synthesized lipid tubules of 1,2-bis(tricosa-10,12-dinoyl)-sn-glycero-3-phosphocholine (DC8,9PC) by self-assembly and polymerization in solutions. We demonstrate for the first time that both uniform and modulated molecular tilt orderings exist in the tubule walls, which have been predicted by current theories, and therefore provide valuable supporting evidences for self-assembly mechanisms of chiral molecules. Two novel methods are developed for studying the axial and radial deformations of DC8,9PC lipid tubules. Mechanical properties of DC8,9PC tubules are systematically studied in terms of persistence length, bending rigidity, strain energy, axial and radial elastic moduli, and critical force for collapse. Mechanisms of recovery and surface stiffening are discussed. Due to the high aspect ratio of lipid tubules, the hierarchical assembly of lipid tubules into ordered arrays and desired architectures is critical in developing their applications. Two efficient methods for fabricating ordered arrays of lipid tubules on solid substrates have been developed. Ordered arrays of hybrid silica-lipid tubes are synthesized by tubule array-templated sol-gel reactions. Ordered arrays of optical anisotropic fibers with tunable shapes and refractive indexes are fabricated. This thesis work provides a paradigm for molecularly engineered structures.
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Date Issued
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2007
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Identifier
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CFE0001918, ucf:47486
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0001918
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Title
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PROBING THE NANOSCALE INTERACTION FORCES AND ELASTIC PROPERTIES OF ORGANIC AND INORGANIC MATERIALS USING FORCE-DISTANCE (F-D) SPECTROSCOPY.
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Creator
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Vincent, Abhilash, Seal, Sudipta, University of Central Florida
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Abstract / Description
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Due to their therapeutic applications such as radical scavenging, MRI contrast imaging, Photoluminescence imaging, drug delivery, etc., nanoparticles (NPs) have a significant importance in bio-nanotechnology. The reason that prevents the utilizing NPs for drug delivery in medical field is mostly due to their biocompatibility issues (incompatibility can lead to toxicity and cell death). Changes in the surface conditions of NPs often lead to NP cytotoxicity. Investigating the role of NP surface...
Show moreDue to their therapeutic applications such as radical scavenging, MRI contrast imaging, Photoluminescence imaging, drug delivery, etc., nanoparticles (NPs) have a significant importance in bio-nanotechnology. The reason that prevents the utilizing NPs for drug delivery in medical field is mostly due to their biocompatibility issues (incompatibility can lead to toxicity and cell death). Changes in the surface conditions of NPs often lead to NP cytotoxicity. Investigating the role of NP surface properties (surface charges and surface chemistry) on their interactions with biomolecules (Cells, protein and DNA) could enhance the current understanding of NP cytotoxicity. Hence, it is highly beneficial to the nanotechnology community to bring more attention towards the enhancement of surface properties of NPs to make them more biocompatible and less toxic to biological systems. Surface functionalization of NPs using specific ligand biomolecules have shown to enhance the protein adsorption and cellular uptake through more favorable interaction pathways. Cerium oxide NPs (CNPs also known as nanoceria) are potential antioxidants in cell culture models and understanding the nature of interaction between cerium oxide NPs and biological proteins and cells are important due to their therapeutic application (especially in site specific drug delivery systems). The surface charges and surface chemistry of CNPs play a major role in protein adsorption and cellular uptake. Hence, by tuning the surface charges and by selecting proper functional molecules on the surface, CNPs exhibiting strong adhesion to biological materials can be prepared. By probing the nanoscale interaction forces acting between CNPs and protein molecules using Atomic Force Microscopy (AFM) based force-distance (F-D) spectroscopy, the mechanism of CNP-protein adsorption and CNP cellular uptake can be understood more quantitatively. The work presented in this dissertation is based on the application of AFM in studying the interaction forces as well as the mechanical properties of nanobiomaterials. The research protocol employed in the earlier part of the dissertation is specifically aimed to understand the operation of F-D spectroscopy technique. The elastic properties of thin films of silicon dioxide NPs were investigated using F-D spectroscopy in the high force regime of few 100 nN to 1 õN. Here, sol-gel derived porous nanosilica thin films of varying surface morphology, particle size and porosity were prepared through acid and base catalyzed process. AFM nanoindentation experiments were conducted on these films using the F-D spectroscopy mode and the nanoscale elastic properties of these films were evaluated. The major contribution of this dissertation is a study exploring the interaction forces acting between CNPs and transferrin proteins in picoNewton scale regime using the force-distance spectroscopy technique. This study projects the importance of obtaining appropriate surface charges and surface chemistry so that the NP can exhibit enhanced protein adsorption and NP cellular uptake.
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Date Issued
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2010
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Identifier
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CFE0003079, ucf:48305
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0003079
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Title
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STRUCTURAL CHARACTERIZATION OF SPUTTER-DEPOSITED SS304+XAL (X = 0, 4, 7 AND 10 WT.%) COATINGS AND MECHANICALLY MILLED TI, ZR AND HF POWDERS.
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Creator
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Seelam, Uma Maheswara, Suryanarayana, Challapalli, University of Central Florida
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Abstract / Description
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Study of the metastable phases obtained by non-equilibrium processing techniques has come a long way during the past five decades. New metastable phases have often given new perspectives to the research on synthesis of novel materials systems. Metastable materials produced by two non-equilibrium processing methods were studied for this dissertation- 304-type austenitic stainless steel (SS304 or Fe-18Cr-8Ni)+aluminum coatings produced by plasma enhanced magnetron sputter-deposition (PEMS) and...
Show moreStudy of the metastable phases obtained by non-equilibrium processing techniques has come a long way during the past five decades. New metastable phases have often given new perspectives to the research on synthesis of novel materials systems. Metastable materials produced by two non-equilibrium processing methods were studied for this dissertation- 304-type austenitic stainless steel (SS304 or Fe-18Cr-8Ni)+aluminum coatings produced by plasma enhanced magnetron sputter-deposition (PEMS) and nanocrystalline Ti, Zr and Hf powders processed by mechanical milling (MM). The objective of the study was to understand the crystallographic and microstructural aspects of these materials. Four SS304+Al coatings with a nominal Al percentages of 0, 4, 7 and 10 wt.% in the coatings were deposited on an SS304 substrate by PEMS using SS304 and Al targets. The as-deposited coatings were characterized by x-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and three-dimensional atom probe microscopy (3DAP). Surface morphology and chemical analysis were studied by SEM. Phase identification was carried out by XRD and TEM. The microstructural features of all the coatings, as observed in the TEM, consisted of columnar grains with the columnar grain width (a measure of grain size) increasing with an increase in the Al content. The coatings had grains with average grain sizes of about 100, 290, 320 and 980 nm, respectively for 0, 4, 7 and 10 wt.% Al. The observed grain structures and increase in grain size were related to substrate temperature during deposition. XRD results indicated that the Al-free coating consisted of the non-equilibrium ferrite and sigma phases. In the 4Al, 7Al and 10Al coatings, equilibrium ferrite and B2 phases were observed but no sigma phase was found. In 10Al coating, we were able to demonstrate experimentally using 3DAP studies that NiAl phase formation is preferred over the FeAl phase at nano scale. During mechanical milling of the hexagonal close packed (HCP) metals Hf, Ti and Zr powders, unknown nanocrystalline phases with face centered cubic (FCC) structure were found. The FCC phases could be either allotropes of the respective metals or impurity stabilized phases. However, upon MM under high purity conditions, it was revealed that the FCC phases were impurity stabilized. The decrease in crystallite size down to nanometer levels, an increase in atomic volume, lattice strain, and possible contamination were the factors responsible for the transformation.
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Date Issued
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2010
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Identifier
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CFE0003161, ucf:48595
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0003161
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Title
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Advanced Nanoscale Characterization of Plants and Plant-derived Materials for Sustainable Agriculture and Renewable Energy.
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Creator
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Soliman, Mikhael, Tetard, Laurene, Vaidyanathan, Raj, Kang, Hyeran, Santra, Swadeshmukul, Zhai, Lei, Chumbimuni Torres, Karin, University of Central Florida
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Abstract / Description
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The need for nanoscale, non-invasive functional characterization has become more significant with advances in nano-biotechnology and related fields. Exploring the ultrastructure of plant cell walls and plant-derived materials is necessary to access a more profound understanding of the molecular interactions in the systems, in view of a rational design for sustainable applications. This, in turn, relates to the pressing requirements for food, energy and water sustainability experienced...
Show moreThe need for nanoscale, non-invasive functional characterization has become more significant with advances in nano-biotechnology and related fields. Exploring the ultrastructure of plant cell walls and plant-derived materials is necessary to access a more profound understanding of the molecular interactions in the systems, in view of a rational design for sustainable applications. This, in turn, relates to the pressing requirements for food, energy and water sustainability experienced worldwide.Here we will present our advanced characterization approach to study the effects of external stresses on plants, and resulting opportunities for biomass valorization with an impact on the food-energy-water nexus.First, the adaption of plants to the pressure imposed by gravity in poplar reaction wood will be discussed. We will show that a multiscale characterization approach is necessary to reach a better understanding of the chemical and physical properties of cell walls across a transverse section of poplar stem. Our Raman spectroscopy and statistical analysis reveals intricate variations in the cellulose and lignin properties. Further, we will present evidence that advanced atomic force microscopy can reveal nanoscale variations within the individual cell wall layers, not attainable with common analytical tools. Next, chemical stresses, in particular the effect of Zinc-based pesticides on citrus plants, will be considered. We will show how multiscale characterization can support the development of new disease management methods for systemic bacterial diseases, such as citrus greening, of great importance for sustainable agriculture. In particular, we will focus on the study of new formulations, their uptake and translocation in the plants following different application methods. Lastly, we will consider how plant reactions to mechanical and chemical stresses can be controlled to engineer biomass for valorization applications. We will present our characterization of two examples: the production of carbon films derived from woody lignocellulosic biomass and the development of nanoscale growth promoters for food crop. A perspective of the work and discussion of the broader impact will conclude the presentation.
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Date Issued
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2018
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Identifier
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CFE0007415, ucf:52717
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0007415
Pages