Miniaturization of electronic devices for enhancing their performance is associated with higher heat fluxes and cooling requirements. Surface modifi cation by texturing or coating is the most cost-effective approach to enhance the cooling of electronic devices. Experiments on carbon nanotube coated heater surfaces have shown heat transfer enhancement of 60 percent. In addition, silicon nanotubes etched on the silicon substrates have shown heat flux enhancement by as much as 120 percent. The heat flux augmentation is attributed to the combined effects of increase in the surface area due to the protruding nanotubes (nano- n eff ect), disruption of vapor lms and modi fication of the thermal/mass di ffusion boundary layers. Since the e ffects of disruption of vapor lms and modifi cation of the thermal/mass di ffusion boundary layers are similar in the above experiments, the difference in enhancement in heat transfer is the consequence of dissimilar nano- n eff ect. The thermal conductivity of carbon nanotubes is of the order of 6000 W/mK while that of silicon is 150 W/mK. However, in the experiments, carbon nanotubes have shown poor performance compared to silicon. This is the consequence of interfacial thermal resistance between the carbon nanotubes and the surrounding fluid since earlier studies have shown that there is comparatively smaller interface resistance to the heat flow from the silicon surface to the surrounding liquids. At the molecular level, atomic interactions of the coolant molecules with the solid substrate as well as their thermal-physical-chemical properties can play a vital role in the heat transfer from the nanotubes. Characterization of the e ffect of the molecular scale chemistry and structure can help to simulate the performance of a nano fin in diff erent kinds of coolants. So in this work to elucidate the eff ect of the molecular composition and structures on the interfacial thermal resistance, water, ethyl alcohol, 1-hexene, n-heptane and its isomers and chains are considered. Non equilibrium molecular dynamic simulations have been performed to compute the interfacial thermal resistance between the carbon nanotube and different coolants as well as to study the diff erent modes of heat transfer. The approach used in these simulations is based on the lumped capacitance method. This method is applicable due to the very high thermal conductivity of the carbon nanotubes, leading to orders of magnitude smaller temperature gradients within the nanotube than between the nanotube and the coolants. To perform the simulations, a single wall carbon nanotube (nano-fin) is placed at the center of the simulation domain surrounded by fluid molecules. The system is minimized and equilibrated to a certain reference temperature. Subsequently, the temperature of the nanotube is raised and the system is allowed to relax under constant energy. The heat transfer from the nano- fin to the surrounding fluid molecules is calculated as a function of time. The temperature decay rate of the nanotube is used to estimate the relaxation time constant and hence the e ffective thermal interfacial resistance between the nano-fi n and the fluid molecules. From the results it can be concluded that the interfacial thermal resistance depends upon the chemical composition, molecular structure, size of the polymer chains and the composition of their mixtures. By calculating the vibration spectra of the molecules of the fluids, it was observed that the heat transfer from the nanotube to the surrounding fluid occurs mutually via the coupling of the low frequency vibration modes.

Molecular Dynamics (MD) simulations of nano-scale flows typically utilize fixed lattice crystal interactions between the fluid and stationary wall molecules. This approach cannot properly model thermal interactions at the wall-fluid interface. In order to properly simulate the flow and heat transfer in nano-scale channels, an interactive thermal wall model is developed. Using this model, the Fourier’s law of heat conduction is verified in a 3.24 nm height channel, where linear temperature profiles with constant thermal conductivity is obtained. The thermal conductivity is verified using the predictions of Green-Kubo theory. MD simulations at different wall wettability ( εωf /ε ) and crystal bonding stiffness values (K) have shown temperature jumps at the liquid/solid interface, corresponding to the well known Kapitza resistance. Using systematic studies, the thermal resistance length at the interface is characterized as a function of the surface wettability, thermal oscillation frequency, wall temperature and thermal gradient. An empirical model for the thermal resistance length, which could be used as the jump-coefficient of a Navier boundary condition, is developed. Temperature distributions in the nano-channels are predicted using analytical solution of the continuum heat conduction equation subjected to the new temperature jump condition, and validated using the MD results. Momentum and heat transfer in shear driven nanochannel flows are also investigated. Work done by the viscous stresses heats the fluid, which is dissipated through the channel walls, maintained at isothermal conditions. Spatial variations in the fluid density, kinematic viscosity, shear- and energy dissipation rates are presented. The energy dissipation rate is almost a constant for εωf /ε < 0.6, which results in parabolic temperature profiles in the domain with temperature jumps due to the Kapitza resistance at the liquid/solid interfaces. Using the energy dissipation rates predicted by MD simulations and the continuum energy equation subjected to the temperature jump boundary conditions developed in this study, the analytical solutions are obtained for the temperature profiles, which agree well with the MD results.

Our study is focused on the behavior of grain boundaries in uranium dioxide system under irradiation conditions. The research can be seen as two parts: the study of interaction of the grain boundary and the damage cascade, and the calculation of Kapitza resistance of grain boundaries. The connection between these two parts lies in that damage cascades bring in changes in the structure and other properties of grain boundaries, and inevitably the Kapitza resistance of the grain boundary changes as well. For the first part, we studied interactions of grain boundaries and damage cascades in uranium dioxide system by simulating two types of bombardments: one direct bombardment into a grain boundary leading to ballistic-collision-mediated interface mixing; the other bombardment is in the close vicinity of a grain boundary causing interface biased defect migration. We found that more defects are trapped by the grain boundary followed by the first type of bombardment, resulting in enhanced grain boundary energy. By comparing with the second type of bombardment, we are able to reveal the mechanisms of the interaction between defects and grain boundaries. For the second part, we employed the non-equilibrium molecular dynamics method to calculate the Kapitza resistance of different coincident site lattice boundaries with or without defects loaded, and later we found that a universal positive correlation between the Kapitza resistance and the grain boundary energy can be well established, regardless of the cause of boundary energy changes. Our study provides a deeper understanding of the Kapitza resistance of the grain boundary and its evolutions under irradiation, which benefits multi-scale modeling of uranium dioxide thermal properties under extreme radiation conditions as well as experimental studies of fuel material thermal properties.

Many materials are made up of small crystals, or grains. Grain boundaries are the interfaces between two grains and affect the flow of heat through the material. These interfaces serve to interfere with the energy carriers by scattering or disrupting them. Because of the negative effect these interfaces have on these energy carriers, they inhibit heat flow and act as thermal resistors. The thermal boundary resistance between two grains of the same material is sometimes referred to as the Kapitza resistance, although this term is also used to describe the thermal resistance between solid/solid interfaces of different materials or solid/liquid interfaces. A better understanding of the heat transport process on a micro-scale is especially relevant to nuclear energy applications. Nuclear fuels are polycrystalline materials that experience large heat differences over small distances. An improved understanding of these grain boundaries and the role they play in transferring heat can help better predict nuclear fuel performance and improve nuclear reactor efficiency and safety. The study of the thermal resistance across crystal interfaces and their potential influence on nuclear fuels is a topic that has received relatively little attention. While the thermal resistance across a single grain boundary is rather small, the total resistance generated from many grain boundaries can have a big impact on the material. Smaller grains mean there are more interfaces, which will result in a lower overall thermal conductivity. For this study, Kapitza resistance across individual grain boundaries was measured using a laser-based measurement technique. The sample material was Cerium Oxide. It was used because of its similar properties to Uranium Oxide, which is a popular material used in nuclear fuel. The average interfacial thermal resistance measured at room temperature in this thesis study was 9.88∙10-9 �2�/�. The average measured value fit in an accepted range from other results found in similar studies.

This dissertation presents an experimental investigation of heat transport through solid- solid and solid-liquid interfaces. Heat transport is a process initiated by the presence of a thermal gradient. All interfaces offer resistance to heat flow in the form of temperature drop at the interface. In micro and nano scale devices, the contribution of this resistance often becomes comparable to, or greater than, the intrinsic thermal resistance offered by the device or structure itself. In this dissertation, I report the resistance offered by the interfaces in terms of interface thermal conductance, G, which is the inverse of Kapitza resistance and is quantified by the ratio of heat flux to the temperature drop. For studying thermal transport across interfaces, I adapted a non-contact optical measurement technique called Time-Domain Thermoreflectance (TDTR) that relies on the fact that the reflectivity of a metal has a small, but measurable, dependence on temperature. The first half of this dissertation is focused on investigating heat transport through thin films and solid-solid interfaces. The samples in this study are thin lead zirconate- titanate (PZT) piezoelectric films used in sensing applications and dielectric films such as SiOC:H used in semiconductor industry. My results on the PZT films indicate that the thermal conductivity of these films was proportional to the packing density of the elements within the films. I have also measured thermal conductivity of dielectric films in different elemental compositions. I also examined thermal conductivity of dielectric films for a variety of different elemental compositions of Si, O, C, and H, and varying degrees of porosity. My measurements showed that the composition and porosity of the films played an important role in determining the thermal conductivity. The second half of this dissertation is focused on investigating heat transport through solid-liquid interfaces. In this regard, I functionalize uniformly coated gold surfaces with a variety of self-assembled monolayers (SAMs). Heat flows from the gold surface to the sulfur molecule, then through the hydrocarbon chain in the SAM, into the terminal group of the SAM and finally into the liquid. My results showed that by changing the terminal group in a SAM from hydrophobic to hydrophilic, G increased by a factor of three in water. By changing the number of carbon atoms in the SAM, I also report that the chain length does not present a significant thermal resistance. My results also revealed evidence of linear relationship between work of adhesion and interface thermal conductance from experiments with several SAMs on water. By examining a variety of SAM-liquid combination, I find that this linear dependency does not hold as a unified hypothesis. From these experiments, I speculate that heat transport in solid-liquid systems is controlled by a combination of work of adhesion and vibrational coupling between the omega-group in the SAM and the liquid. / Ph. D.

This thesis documents research done in the development and the exploration of feasibility for a high-throughput method to measure local thermal properties. The present capabilities in the measurement of local thermophysical properties such as thermal conductivity, thermal diffusivity, and Kapitza resistance are very inefficient and impractical to fully understand and characterize heat transport through certain materials and features. This work follows up on past work in local thermal property measurement via the spatial domain thermoreflectance (SDTR) method, and explores the possibility of parallelizing the process. The parallelized SDTR (P-SDTR) method involves using laser projector sources to periodically heat and measure the changes of reflectivity of a sample surface at multiple locations simultaneously. These measurements are made possible by the development of a lock-in camera that can measure the characteristics of modulated light using lock-in amplification at several spots across an area with an advanced camera sensor. This method allows for the measurement of local thermal properties across features such as grain boundaries, or directional properties in anisotropic materials. An experimental setup is developed to determine at which heating and probing parameters a thermoreflectance signal can be measured. A finite element model is also made to simulate the P-SDTR process, and validate that the assumptions made in SDTR can be made in P-SDTR measurements. It is shown that at an appropriate separation of heating/measurement locations, the solutions from the simulation approach that of a single measurement spot. An initial device design is proposed and tested. Future work in the development of the P-SDTR device is also laid out.

The present work provides a micromechanics approach based on the generalized self-consistent composite cylinders method as a non-Eshelby approach towards for assessing the impact of carbon nanotubes on the multi-functional nature of nanocom-posites in which they are a constituent. Emphasis is placed on the effective elastic properties as well as electrical and thermal conductivities of nanocomposites con-sisting of randomly oriented single walled carbon nanotubes in epoxy. The effective elastic properties of aligned, as well as clustered and well-dispersed nanotubes in epoxy are discussed in the context of nanotube bundles using both the generalized self-consistent composite cylinders method as well as using computational microme-chanics techniques. In addition, interphase regions are introduced into the composite cylinders assemblages to account for the varying degrees of load transfer between nanotubes and the epoxy as a result of functionalization or lack thereof. Model pre-dictions for randomly oriented nanotubes both with and without interphase regions are compared to measured data from the literature with emphasis placed on assessing the bounds of the effective nanocomposite properties based on the uncertainty in the model input parameters. The generalized self-consistent composite cylinders model is also applied to model the electrical and thermal conductivity of carbon nanotube-epoxy nanocomposites. Recent experimental observations of the electrical conductivity of carbon nanotube polymer composites have identified extremely low percolation limits as well as a per-ceived double percolation behavior. Explanations for the extremely low percolation limit for the electrical conductivity of these nanocomposites have included both the creation of conductive networks of nanotubes within the matrix and quantum effects such as electron hopping or tunneling. Measurements of the thermal conductivity have also shown a strong dependence on nanoscale effects. However, in contrast, these nanoscale effects strongly limit the ability of the nanotubes to increase the thermal conductivity of the nanocomposite due to the formation of an interfacial thermal resistance layer between the nanotubes and the surrounding polymer. As such, emphasis is placed here on the incorporation of nanoscale effects, such as elec-tron hopping and interfacial thermal resistance, into the generalized self-consistent composite cylinder micromechanics model.

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Les problèmes liés au réchauffement climatique, conséquences de la production d'énergie et de la pollution, rendent ce thème de recherche un des plus importants du moment. La course pour trouver de nouveaux matériaux pour mettre au point des applications innovantes est à son apogée, et de grands progrès voient le jour dans chaque domaine de recherche. Par exemple, les chercheurs en physique se concentrent sur la fabrication de matériaux ou de couples de matériaux avec des propriétés électriques/thermiques supérieures pour améliorer les systèmes électroniques aux échelles nano- et micro- métriques. Certains de ces éléments sont formés de couches simples, de multicouches ou de membranes. Ainsi, des techniques expérimentales appropriées sont essentielles pour mesurer les propriétés thermophysiques de ces nouveaux composants. Dans cette thèse, la caractérisation thermique de diverses sortes de matériaux est réalisée en utilisant une technique de radiométrie photothermique (PTR). PTR est une méthode sans contact dans laquelle la réponse thermique de matériaux induite par rayonnement est mesurée. Deux types de configurations ont été utilisées, la première avec une modulation dans le domaine fréquentiel jusqu'à 10 MHz et l’autre avec une modulation hybride fréquence/spatial jusqu'à 2 MHz avec ~ 30 µm de résolution. Avec ces méthodes, il est possible d'extraire indépendamment des paramètres thermophysiques comme la diffusivité thermique, l’effusivité thermique ou la résistance de Kapitza. Ces deux configurations sont utilisées pour caractériser thermiquement des combinaisons particulières de matériaux comme des nanocomposites, des couches minces organiques, des matériaux irradiés, des matériaux à changement de phase ou les résistances thermiques à l’interfaces métal/semiconducteur. Les résultats obtenus donnent de nouvelles pistes de recherche sur le transport thermique et la gestion de la chaleur à l’échelle nanométrique. / The recognition of problems connected to the global warming linked to energy production and pollution, makes it the most important research topic of the moment. The race of finding new materials for improved applications is at its peak, while big advancements in technologies within each field of research have seen the light. For example, researchers in physics are focusing on making superior materials or couple of materials with enhanced thermo-/electric- physical properties for nano- and micro- electronic devices. The constituents in question, embody simple or complicated multiscale layers or membranes. Thus, proper experimental techniques are essential to measure the thermophysical properties of these new components. In this thesis, thermal characterization of diverse kinds of materials is made using a photothermal radiometry (PTR) technique. PTR is a contactless method which measures the thermal response of materials induced by optical heating. Two types of PTR setups were utilized, one using frequency domain modulation up to 10 MHz and one based upon hybrid frequency/spatial domain modulation up to 2 MHz with ~30 µm resolution. With these methods, it is possible to extract independent thermophysical parameters like the thermal diffusivity, thermal effusivity or Kapitza resistance. These two setups are used jointly to thermally characterize peculiar combinations of materials like: nanocomposite, organic, irradiated, phase changing and silicide materials. The results grasp new insights on the thermal transport and heat management across these set of materials and encourages novel ways to apply them in diverse applications throughout many research fields.

No description available.