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- Title
- Development of enzyme-free hydrogen peroxide biosensor using cerium oxide and mechanistic study using in-situ spectro-electrochemistry.
- Creator
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Saraf, Shashank, Seal, Sudipta, Cho, Hyoung Jin, Zhai, Lei, Heinrich, Helge, Harper, James, University of Central Florida
- Abstract / Description
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During recent development, it has been demonstrated that cerium oxide nanoparticles (CNPs) have exhibited catalytic activity which mimics naturally existing enzymes such as superoxide dismutase (SOD) and catalase. The underlying mechanism is attributed to the modulation of oxygen vacancies on CNPs lattice by dynamic switching of the oxidation states between Ce3+ and Ce4+ due to the electron transfer resulting from the redox reaction between CNPs and reactive oxygen species such as hydrogen...
Show moreDuring recent development, it has been demonstrated that cerium oxide nanoparticles (CNPs) have exhibited catalytic activity which mimics naturally existing enzymes such as superoxide dismutase (SOD) and catalase. The underlying mechanism is attributed to the modulation of oxygen vacancies on CNPs lattice by dynamic switching of the oxidation states between Ce3+ and Ce4+ due to the electron transfer resulting from the redox reaction between CNPs and reactive oxygen species such as hydrogen peroxide (H2O2). Thereby the redox potential of CNPs is dependent on the surface chemistry i.e. the surface concentration of Ce3+ and Ce4+ Currently, the ratio of Ce3+/ Ce4+ in CNPs is characterized ex-situ using XPS or TEM which involves sample drying and exposure to high energy X-rays and electron beam, respectively. Sample drying and high energy beam exposure could lead to sample deterioration. The goal of the study is to explore a technique to characterize CNPs in-situ and identify the surface chemistry of CNPs. The in-situ investigation of CNPs was carried using spectroelectrochemistry wherein the electrochemical and optical measurements are carried out simultaneously. Detailed optical characterization of two different CNPs having different catalytic activity were carried under oxidation and reduction environments. Analysis of spectra revealed widely different redox potential for CNPs which was a function of pH and composition of buffer solution. In second part of dissertation a suitable surface chemistry of CNPs is investigated to replace the enzyme in biosensor assembly to allow amperometric detection of H2O2 in physiological conditions. Upon electrochemical investigation of the physio-chemical properties of CNPs, it was found that CNPs having higher surface concentration of Ce4+ as compared to Ce3+ oxidation states, demonstrated increased catalytic activity towards H2O2. The addition of CNPs resulted in 5 orders of increment in amperometric current with a response time of 400 msec towards detection of H2O2 and exhibited excellent selectivity in presence of interfering species. Additionally, cerium oxide was successfully integrated into the biosensor assembly through the anodic electrodeposition, which allowed the transfer of electron generated from the CNPs in the redox reaction to the electrode and demonstrated successful sensing of H2O2. Furthermore, to achieve detection of H2O2 in physiological conditions, CNPs were integrated with nanoporous gold (NPG) which exhibited anti-biofouling properties. The anti-biofouling property of NPG was investigated using electrochemical techniques and showed excellent signal retention in physiological concentration of albumin proteins. The novel study targets at developing robust enzyme free biosensor by integrating the detection ability of CNPs with the anti-biofouling activity of NPG based electrode.
Show less - Date Issued
- 2016
- Identifier
- CFE0006498, ucf:51404
- Format
- Document (PDF)
- PURL
- http://purl.flvc.org/ucf/fd/CFE0006498
- Title
- Interdiffusion, Crystallography and Mechanical Properties of Nickel Manganese Gallium Alloys.
- Creator
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Zhou, Le, Sohn, Yongho, Heinrich, Helge, Coffey, Kevin, An, Linan, Orlovskaya, Nina, University of Central Florida
- Abstract / Description
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NiMnGa Heusler alloys, functioning as either ferromagnetic shape memory alloys or mangetocaloric materials, have both practical applications and fundamental research value. The functional properties of NiMnGa alloys are closely related to the martensitic transformation from high temperature austenitic phase to low temperature martensitic phase. Alloys can be used for room temperature or high temperature applications, depending on the martensitic transformation temperature, which is...
Show moreNiMnGa Heusler alloys, functioning as either ferromagnetic shape memory alloys or mangetocaloric materials, have both practical applications and fundamental research value. The functional properties of NiMnGa alloys are closely related to the martensitic transformation from high temperature austenitic phase to low temperature martensitic phase. Alloys can be used for room temperature or high temperature applications, depending on the martensitic transformation temperature, which is compositional sensitive. The microstructure and crystallography of the martensites can be very complex but are crucial to the optimization of the material performance. In this study, for the first time, a combinatorial study by combining solid-to-solid diffusion couples and various characterization techniques was carried out to fundamentally investigate the NiMnGa ternary alloys. Phase equilibria, interdiffusion behavior, microstructural and crystallographic development, and mechanical properties in NiMnGa alloys were systematically examined. Selected diffusion couples between pure Ni, Ni25Mn75 and four ternary off-stoichiometric NiMnGa alloys (i.e., Ni52Mn18Ga30, Ni46Mn30Ga24, Ni52Mn30Ga18, Ni58Mn18Ga24 in atomic percent) were assembled and annealed at 800, 850 and 900 (&)deg;C for 480, 240 and 120 hours, respectively. The microstructure and concentration profiles of the interdiffusion zone were examined by scanning electron microscopy (SEM) equipped with energy dispersive spectroscopy (EDS). Concentration profiles across the interdiffusion zone were further quantified by electron probe micro analysis (EPMA). Detailed microstructure and crystallography of the austenite and martensite were investigated using transmission electron microscopy (TEM). TEM thin foils were prepared by using focused ion beam (FIB) in situ lift out (INLO) technique, which is able to select desired composition from diffusion couples. The mechanical properties, namely reduced elastic modulus and hardness, as a function of composition were assessed via nanoindentation. Solubility values obtained for various phases were mostly consistent with the existing isothermal phase diagrams, but the phase boundary of the ?(Mn) + ? two-phase region was slightly modified. In addition, equilibrium compositions for the ?(Ni) and ?' phases at 900 (&)deg;C were also determined for the respective two-phase regions. Both austenitic and martensitic phases were found at room temperature in each diffusion couple with a clear interphase boundary. The compositions at the interfaces corresponded close to valence electron concentration (e/a) of 7.6, but decreased to lower values when Mn concentration increased to more than 35 at. %. Average effective interdiffusion coefficients for the ? phase over various compositional ranges were determined and reported in the light of temperature-dependence. Ternary interdiffusion coefficients were also determined and examined to assess the ternary diffusional interactions among Ni, Mn and Ga. Ni was observed to interdiffuse the fastest, followed by Mn then Ga. Interdiffusion flux of Ni also has strong influences on the interdiffusion of Mn and Ga with large and negative cross interdiffusion coefficients. The main ternary interdiffusion coefficients exhibited minimum values near 52 at. % Ni concentration. Extensive TEM analyses have been performed for the study of microstructure and crystallography of austenite and martensite from all diffusion couples. Crystallographic variations in martensitic phase, including non-modulated (NM) martensite, modulated (5M or 7M) martensite, were found in the diffusion couples. The 5M and 7M martensites were only found near the interface between austenite and martensite, corresponding to compositions with lower e/a ratio. The NM martensites were found mostly away from the interface region, with high e/a ratios. The tetragonality ratio (c/a) for NM martensite generally increases with e/a ratio, but also depended on the composition. All martensitic microstructure consists of twinned variants with different orientations that were documented using electron diffraction. The twinning relationship along with the c/a ratio was correlated to martensitic transformation temperature. In addition, pre-martensitic state has been clearly observed in the cubic austenitic phase region, with distinctive tweed microstructure originating from the local lattice distortions. Mechanical properties including reduced elastic modulus (Er) and hardness (H) as a function of composition were measured and analyzed by nanoindentation. A decrease of Er and H was observed with Mn or Ni substituting Ga, and Ni substituting Mn for the austenitic phase. However, an opposite trend was found for the martensitic phase. The softening of the elastic constants near the vicinity of martensitic transformation contributed to the sharp decrease in Er and H near the interface region. The measured Er and H had larger scatter for the martensitic phase than those for the austenitic phase. The scatters observed were attributed to the martensitic variants with different orientations. Contribution from the variation in grain orientation or shape memory effect was determined to be small in this investigation.
Show less - Date Issued
- 2016
- Identifier
- CFE0006204, ucf:51108
- Format
- Document (PDF)
- PURL
- http://purl.flvc.org/ucf/fd/CFE0006204
- Title
- X-ray Scattering Investigations of Metallic Thin Films.
- Creator
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Warren, Andrew, Coffey, Kevin, Sohn, Yongho, Suryanarayana, Challapalli, Heinrich, Helge, Barmak, Katayun, Toney, Michael, University of Central Florida
- Abstract / Description
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Nanometric thin films are used widely throughout various industries and for various applications. Metallic thin films, specifically, are relied upon extensively in the microelectronics industry, among others. For example, alloy thin films are being investigated for CMOS applications, tungsten films find uses as contacts and diffusion barriers, and copper is used often as interconnect material. Appropriate metrology methods must therefore be used to characterize the physical properties of...
Show moreNanometric thin films are used widely throughout various industries and for various applications. Metallic thin films, specifically, are relied upon extensively in the microelectronics industry, among others. For example, alloy thin films are being investigated for CMOS applications, tungsten films find uses as contacts and diffusion barriers, and copper is used often as interconnect material. Appropriate metrology methods must therefore be used to characterize the physical properties of these films. X-ray scattering experiments are well suited for the investigation of nano-scaled systems, and are the focus of this doctoral dissertation. Emphasis is placed on (1) phase identification of polycrystalline thin films, (2) the evaluation of the grain size and microstrain of metallic thin films by line profile analysis, and (3) the study of morphological evolution in solid/solid interfaces.To illustrate the continued relevance of x-ray diffraction for phase identification of simple binary alloy systems, Pt-Ru thin films, spanning the compositional range from pure Pt to pure Ru were investigated. In these experiments, a meta-stable extension of the HCP phase is observed in which the steepest change in the electronic work function coincides with a rapid change in the c/a ratio of the HCP phase.For grain size and microstrain analysis, established line profile methods are discussed in terms of Cu and W thin film analysis. Grain sizes obtained by x-ray diffraction are compared to transmission electron microscopy based analyses. Significant discrepancies between x-ray and electron microscopy are attributed to sub-grain misorientations arising from dislocation core spreading at the film/substrate interface. A novel "residual" full width half max parameter is introduced for examining the contribution of strain to x-ray peak broadening. The residual width is subsequently used to propose an empirical method of line profile analysis for thin films on substrates.X-ray reflectivity was used to study the evolution of interface roughness with annealing for a series of Cu thin films that were encapsulated in both SiO2 and Ta/SiO2. While all samples follow similar growth dynamics, notable differences in the roughness evolution with high temperature ex-situ annealing were observed. The annealing resulted in a smoothing of only one interface for the SiO2 encapsulated films, while neither interface of the Ta/SiO2 encapsulated films evolved significantly. The fact that only the upper Cu/SiO2 interface evolves is attributed to mechanical pinning of the lower interface to the rigid substrate. The lack of evolution of the Cu/Ta/SiO2 interface is consistent with the lower diffusivity expected of Cu in a Cu/Ta interface as compared to that in a Cu/SiO2 interface. The smoothing of the upper Cu/SiO2 interface qualitatively follows that expected for capillarity driven surface diffusion but with notable quantitative deviation.
Show less - Date Issued
- 2013
- Identifier
- CFE0004770, ucf:49784
- Format
- Document (PDF)
- PURL
- http://purl.flvc.org/ucf/fd/CFE0004770
- Title
- Structure, stability, vibrational, thermodynamic, and catalytic properties of metal nanostructures: size, shape, support, and adsorbate effects.
- Creator
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Behafarid, Farzad, Roldan Cuenya, Beatriz, Chow, Lee, Heinrich, Helge, Kara, Abdelkader, Schoenfeld, Winston, University of Central Florida
- Abstract / Description
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Recent advances in nanoscience and nanotechnology have provided the scientific community with exciting new opportunities to rationally design and fabricate materials at the nanometer scale with drastically different properties as compared to their bulk counterparts. In this dissertation, several challenges have been tackled in aspects related to nanoparticle (NP) synthesis and characterization, allowing us to make homogenous, size- and shape-selected NPs via the use of colloidal chemistry,...
Show moreRecent advances in nanoscience and nanotechnology have provided the scientific community with exciting new opportunities to rationally design and fabricate materials at the nanometer scale with drastically different properties as compared to their bulk counterparts. In this dissertation, several challenges have been tackled in aspects related to nanoparticle (NP) synthesis and characterization, allowing us to make homogenous, size- and shape-selected NPs via the use of colloidal chemistry, and to gain in depth understanding of their distinct physical and chemical properties via the synergistic use of a variety of ex situ, in situ, and operando experimental tools. A variety of phenomena relevant to nanosized materials were investigated, including the role of the NP size and shape in the thermodynamic and electronic properties of NPs, their thermal stability, NP-support interactions, coarsening phenomena, and the evolution of the NP structure and chemical state under different environments and reaction conditions.
Show less - Date Issued
- 2012
- Identifier
- CFE0004779, ucf:49796
- Format
- Document (PDF)
- PURL
- http://purl.flvc.org/ucf/fd/CFE0004779
- Title
- QUANTITATIVE SCANNING TRANSMISSION ELECTRON MICROSCOPY OF THICK SAMPLES AND OF GOLD AND SILVER NANOPARTICLES ON POLYMERIC SURFACES.
- Creator
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Dutta, Aniruddha, Heinrich, Helge, Del Barco, Enrique, Chow, Lee, Chen, Bo, Kuebler, Stephen, University of Central Florida
- 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.
Show less - Date Issued
- 2014
- Identifier
- CFE0005485, ucf:50333
- Format
- Document (PDF)
- PURL
- http://purl.flvc.org/ucf/fd/CFE0005485
- Title
- Photophysical and photochemical factors affecting multi-photon direct laser writing using the cross-linkable epoxide SU-8.
- Creator
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Williams Jr., Henry, Kuebler, Stephen, Elsheimer, Seth, Zhai, Lei, Liao, Yi, Heinrich, Helge, University of Central Florida
- Abstract / Description
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For the past decade, the epoxy based photoresist SU-8 has been used commercially and in the lab for fabricating micro- and nano-structures. Investigators have studied how processing parameters such as pre- and post-exposure bake temperatures affect the resolution and quality of SU-8 structures patterned using ultraviolet or x-ray lithography. Despite the advances in understanding the phenomena, not all of them have been explored, especially those that are specific to multi-photon direct laser...
Show moreFor the past decade, the epoxy based photoresist SU-8 has been used commercially and in the lab for fabricating micro- and nano-structures. Investigators have studied how processing parameters such as pre- and post-exposure bake temperatures affect the resolution and quality of SU-8 structures patterned using ultraviolet or x-ray lithography. Despite the advances in understanding the phenomena, not all of them have been explored, especially those that are specific to multi-photon direct laser writing (mpDLW). Unlike conventional exposure techniques, mpDLW is an inherently three-dimensional (3D) process that is activated by nonlinear absorption of light.This dissertation reports how several key processing parameters affect mpDLW using SU-8 including pre-exposure bake duration, focal depth, incident laser power, focal-point scan speed, and excitation wavelength. An examination of solvent content of films at various stages in the mpDLW by 1H-NMR shows that even moderate solvent content (over 1 wt-%) affects film viscosity and photoacid diffusion lengths, and can greatly affect the overall fidelity of small features. A study of micro-fabricated feature size versus writing depth in the material shows that even slight refractive index mismatch between SU-8 and the medium between it and the focusing objective introduces spherical aberration that distorts the focus, causing feature size to decrease or even increase in size with writing depth, depending on the average exposure power used. Proper adjustment of the average exposure power was demonstrated as a means to fabricate more uniform features with writing depth. Third, when varying the power and scan speed, it was observed that the feature-size scales with these two parameters in a manner that is consistent with a three-photon absorption mechanism at an excitation wavelength of 800 nm. When aniiiexcitation wavelength of 725 nm is used, the feature-size scaling becomes consistent with that of two photon absorption. This shows that the photoinitiators in the SU-8 can be activated by either two- or three-photon absorption over this wavelength range. Using an irradiance of ~2 TW cm-2 and elongated femtosecond pulses resulted in an observed fourth order power dependence. This observation is in agreement with the literature and suggests that the effective absorptive nonlinearity is also sensitive to pulse duration. These findings will be useful for creating accurate models of the process of mpDLW in SU-8. These models could be used to optimize the processing parameters and develop new processing methods and materials for high-resolution fabrication of robust 3D microstructures. Some of the findings were used to develop a method for fabricating functional microlenses on the tip of optical fibers. This approach opens a new route to functional integrated photonic devices.
Show less - Date Issued
- 2013
- Identifier
- CFE0005441, ucf:50403
- Format
- Document (PDF)
- PURL
- http://purl.flvc.org/ucf/fd/CFE0005441
- Title
- TAILORING THE PROPERTIES OF POLYELECTROLYTE COATED CERIUM OXIDE NANOPARTICLES AS A FUNCTION OF MOLECULAR WEIGHT.
- Creator
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Saraf, Shashank, Seal, Sudipta, Cho, Hyoung, Zhai, Lei, Heinrich, Helge, Harper, James, University of Central Florida
- Abstract / Description
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The application of Cerium oxide nanoparticles (CNPs) for therapeutic purposes requires a stable dispersion of nanoparticles in biological environment. The objective of this study is to tailor the properties of polyelectrolyte coated CNPs as a function of molecular weight to achieve a stable and catalytic active dispersion. This was achieved by coating CNPs with polyacrylic acid (PAA)which increased the dispersion stability of CNPs and enhanced the catalytic ability. The stability of PAA...
Show moreThe application of Cerium oxide nanoparticles (CNPs) for therapeutic purposes requires a stable dispersion of nanoparticles in biological environment. The objective of this study is to tailor the properties of polyelectrolyte coated CNPs as a function of molecular weight to achieve a stable and catalytic active dispersion. This was achieved by coating CNPs with polyacrylic acid (PAA)which increased the dispersion stability of CNPs and enhanced the catalytic ability. The stability of PAA coating was analysed using the change in the Gibbs free energy computed by Langmuir adsorption model. The adsorption isotherms were determined using soft particle electrokinetics which overcomes the challenges presented by other techniques. The Gibbs free energy was highest for PAA coated CNPs by 250 kg/mole indicating the most stable coating. The free energy for PAA 100 kg/mole coated CNPs is 85% lower than the PAA250 coated CNPs. This significant difference is caused by the strong adsorption of PAA100 on CNPs. Catalytic activity of PAA-CNPs is accessed by the catalase enzymatic activity of nanoparticles. The catalase activity was higher for PAA coated CNPs as compared to bare CNPs which indicated preferential adsorption of hydrogen peroxide induced by coating. Apart from PAA coating the catalase activity is also affected by the structure of the coating layer.
Show less - Date Issued
- 2013
- Identifier
- CFE0005410, ucf:50410
- Format
- Document (PDF)
- PURL
- http://purl.flvc.org/ucf/fd/CFE0005410
