1 |
Modeling Compact High Power Fiber Lasers and VECSELsLi, Hongbo January 2011 (has links)
Compact high power fiber lasers and the vertical-external-cavity surface-emitting lasers (VECSELs) are promising candidates for high power laser sources with diffraction-limited beam quality and are currently the subject of intensive research and development. Here three large mode area fiber lasers, namely, the photonic crystal fiber (PCF) laser, the multicore fiber (MCF) laser, and the multimode interference (MMI) fiber laser, as well as the VECSEL are modeled and designed.For the PCF laser, the effective refractive index and the effective core radius of the PCF are investigated using vectorial approaches and reformulated. Then, the classical step-index fiber theory is extended to PCFs, resulting in a highly efficient vectorial effective-index method for the design and analysis of PCFs. The new approach is employed to analyze the modal properties of the PCF lasers with depressed-index cores and to effectively estimate the number of guided modes for PCFs.The MCF laser, consisting of an active MCF and a passive coreless fiber, is modeled using the vectorial mode expansion method developed in this work. The results illustrate that the mode selection in the MCF laser by the coreless fiber section is determined by the MMI effect, not the Talbot effect. Based on the MMI and self-imaging in multimode fibers, the vectorial mode expansion approach is employed to design the first MMI fiber laser demonstrated experimentally.For the design and modeling of VECSELs, the optical, thermal, and structural properties of common material systems are investigated and the most reliable material models are summarized. The nanoscale heat transport theory is applied for the first time, to the best of my knowledge, to design and model VECSELs. In addition, the most accurate strain compensation approach is selected for VECSELs incorporating strained quantum wells to maintain structural stability. The design principles for the VECSEL subcavity are elaborated and applied to design a 1040nm VECSEL subcavity that has been demonstrated for high power operation of VECSELs where near diffraction-limited output over 20 W is obtained. Physical modeling of the VECSEL is also discussed and used to compare VECSEL subcavity designs on the laser level.
|
2 |
Thermal and thermoelectric properties of nanostructured materials and interfacesLiao, Hao-Hsiang 19 December 2012 (has links)
Many modern technologies are enabled by the use of thin films and/or nanostructured composite materials. For example, many thermoelectric devices, solar cells, power electronics, thermal barrier coatings, and hard disk drives contain nanostructured materials where the thermal conductivity of the material is a critical parameter for the device performance. At the nanoscale, the mean free path and wavelength of heat carriers may become comparable to or smaller than the size of a nanostructured material and/or device. For nanostructured materials made from semiconductors and insulators, the additional phonon scattering mechanisms associated with the high density of interfaces and boundaries introduces additional resistances that can significantly change the thermal conductivity of the material as compared to a macroscale counterpart. Thus, better understanding and control of nanoscale heat conduction in solids is important scientifically and for the engineering applications mentioned above.
In this dissertation, I discuss my work in two areas dealing with nanoscale thermal transport: (1) I describe my development and advancement of important thermal characterization tools for measurements of thermal and thermoelectric properties of a variety of materials from thin films to nanostructured bulk systems, and (2) I discuss my measurements on several materials systems done with these characterization tools.
First, I describe the development, assembly, and modification of a time-domain thermoreflectance (TDTR) system that we use to measure the thermal conductivity and the interface thermal conductance of a variety of samples including nanocrystalline alloys of Ni-Fe and Co-P, bulk metallic glasses, and other thin films. Next, a unique thermoelectric measurement system was designed and assembled for measurements of electrical resistivity and thermopower of thermoelectric materials in the temperature range of 20 to 350 °C. Finally, a commercial Anter Flashline 3000 thermal diffusivity measurement system is used to measure the thermal diffusivitiy and heat capacity of bulk materials at high temperatures. With regards to the specific experiments, I examine the thermal conductivity and interface thermal conductance of two different types of nanocrystalline metallic alloys of nickel-iron and cobalt-phosphorus. I find that the thermal conductivity of the nanocrystalline alloys is reduced by a factor of approximately two from the thermal conductivity measured on metallic alloys with larger grain sizes. With subsequent molecular dynamics simulations performed by a collaborator, and my own electrical conductivity measurements, we determine that this strong reduction in thermal conductivity is the result of increased electron scattering at the grain boundaries, and that the phonon component of the thermal conductivity is largely unchanged by the grain boundaries.
We also examine four complex bulk metallic glass (BMG) materials with compositions of Zr₅₀Cu₄₀Al₁₀, Cu<sub>46.25</sub>Zr<sub>44.25</sub>Al<sub>7.5</sub>Er₂, Fe₄₈Cr₁₅Mo₁₄C₁₅B₆Er₂, and Ti<sub>41.5</sub>Zr<sub>2.5</sub>Hf₅Cu<sub>42.5</sub>Ni<sub>7.5</sub>Si₁. From these measurements, I find that the addition of even a small percentage of heavy atoms (i.e. Hf and Er) into complex disordered BMG structures can create a significant reduction in the phonon thermal conductivity of these materials. This work also indicates that the addition of these heavy atoms does not disrupt electron transport to the degree with which thermal transport is reduced. / Ph. D.
|
3 |
Heat Transport across Dissimilar MaterialsShukla, Nitin 08 June 2009 (has links)
All interfaces offer resistance to heat transport. As the size of a device or structure approaches nanometer lengthscales, the contribution of the interface thermal resistance often becomes comparable to the intrinsic thermal resistance offered by the device or structure itself. In many microelectronic devices, heat has to transfer across a metal-nonmetal interface, and a better understanding about the origins of this interface thermal conductance (inverse of the interface thermal resistance) is critical in improving the performance of these devices. In this dissertation, heat transport across different metal-nonmetal interfaces are investigated with the primary goal of gaining qualitative and quantitative insight into the heat transport mechanisms across such interfaces. A time-domain thermoreflectance (TDTR) system is used to measure the thermal properties at the nanoscale. TDTR is an optical pump-probe technique, and it is capable of measuring thermal conductivity, k, and interface thermal conductance, G, simultaneously.
The first study examines k and G for amorphous and crystalline Zr47Cu31Al13Ni9 metallic alloys that are in contact with poly-crystalline Y2O3. The motivation behind this study is to determine the relative importance of energy coupling mechanisms such as electron-phonon or phonon-phonon coupling across the interface by changing the material structure (from amorphous to crystalline), but not the composition. From the TDTR measurements k=4.5 W m-1 K-1 for the amorphous metallic glass of Zr47Cu31Al13Ni9, and k=5.0 W m-1 K-1 for the crystalline Zr47Cu31Al13Ni9. TDTR also gives G=23 MW m-2 K-1 for the metallic glass/Y2O3 interface and G=26 MW m-2 K-1 for the interface between the crystalline Zr47Cu31Al13Ni9 and Y2O3. The thermal conductivity of the poly-crystalline Y2O3 layer is found to be k=5.0 W m-1 K-1. Despite the small difference between k and G for the two alloys, the results are repeatable and they indicate that the structure of the alloy plays a role in the electron-phonon coupling and interface conductance.
The second experimental study examines the effect of nickel nanoparticle size on the thermal transport in multilayer nanocomposites. These nanocomposites consist of five alternating layers of nickel nanoparticles and yttria stabilized zirconia (YSZ) spacer layers that are grown with pulsed laser deposition. Using TDTR, thermal conductivities of k=1.8, 2.4, 2.3, and 3.0 W m-1 K-1 are found for nanocomposites with nickel nanoparticle diameters of 7, 21, 24, and 38 nm, respectively, and k=2.5 W m-1 K-1 for a single 80 nm thick layer of YSZ. The results indicate that the overall thermal conductivity of these nanocomposites is strongly influenced by the Ni nanoparticle size and the interface thermal conductance between the Ni particles and the YSZ matrix. An effective medium theory is used to estimate the lower limits for the interface thermal conductance between the nickel nanoparticles and the YSZ matrix (G>170 MW m-2 K-1), and the nickel nanoparticle thermal conductivity. / Ph. D.
|
4 |
Nanoscale thermal transport through solid-solid and solid-liquid interfacesHarikrishna, Hari 03 July 2013 (has links)
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.
|
Page generated in 0.0915 seconds