III-nitride semiconductors have garnered significant attention due to their diverse applications in the fields of optics and electronics. As GaN-based visible light-emitting diodes (LEDs) and laser technologies continue to advance, there has been a surge of interest in the development of ultraviolet (UV) devices. In order to explore the UV range, extensive research has been conducted on BN-based materials and their alloys with conventional III-nitrides, driven by the quest for materials exhibiting larger bandgaps and enhanced refractive index contrast. Additionally, the incorporation of boron into III-nitrides through alloying provides a promising avenue for effectively modulating lattice parameters and manipulating the crystalline structure. This offers a novel approach for strain engineering, lattice matching, and structural manipulation, facilitating the optimization of device performance and expanding the capabilities of III-nitride semiconductors in the realm of UV device development. In this work, we optimize and investigate the epitaxial growth of BGaN using metalorganic chemical vapor deposition, and characterize the physical and electronic properties of the grown films using several techniques such as X-ray diffraction, atomic force microscopy, UV-Visible spectroscopy, X-ray Photoelectron Spectroscopy (XPS), electron energy loss spectroscopy (EELS) and more. We have explored different metalorganic chemical vapor deposition techniques —such as continuous growth and pulsed-flow modulation, high temperature and low temperature growths, hydrogen-containing and hydrogen-free growths, trimethylgallium (TMG) and triethylgallium (TEG) sourced growths, Triethylborane (TEB) and borazine (BRZN) sourced growths— to grow BGaN alloys. Samples grown using continuous-flow method, low temperatures, TEG source and hydrogen-free carrier gas show higher boron content and better crystalline quality when having TEB as a boron source. BRZN is used to reduce carbon impurities for the purpose of film doping. With BRZN, TMG was found as a preferred gallium source. Additionally, we have characterized the electronic properties of the grown films in details using XPS, EELS and other related techniques. We have studied the band offset of BGaN with AlN using traditional methods. Furthermore, we have developed a statistical technique to find small offsets at interfaces at the precision of the measuring instrument.

abstract: In this dissertation, the interface chemistry and electronic structure of plasma-enhanced atomic layer deposited (PEALD) dielectrics on GaN are investigated with x-ray and ultraviolet photoemission spectroscopy (XPS and UPS). Three interrelated issues are discussed in this study: (1) PEALD dielectric growth process optimization, (2) interface electronic structure of comparative PEALD dielectrics on GaN, and (3) interface electronic structure of PEALD dielectrics on Ga- and N-face GaN. The first study involved an in-depth case study of PEALD Al2O3 growth using dimethylaluminum isopropoxide, with a special focus on oxygen plasma effects. Saturated and self-limiting growth of Al2O3 films were obtained with an enhanced growth rate within the PEALD temperature window (25-220 ºC). The properties of Al2O3 deposited at various temperatures were characterized to better understand the relation between the growth parameters and film properties. In the second study, the interface electronic structures of PEALD dielectrics on Ga-face GaN films were measured. Five promising dielectrics (Al2O3, HfO2, SiO2, La2O3, and ZnO) with a range of band gap energies were chosen. Prior to dielectric growth, a combined wet chemical and in-situ H2/N2 plasma clean process was employed to remove the carbon contamination and prepare the surface for dielectric deposition. The surface band bending and band offsets were measured by XPS and UPS for dielectrics on GaN. The trends of the experimental band offsets on GaN were related to the dielectric band gap energies. In addition, the experimental band offsets were near the calculated values based on the charge neutrality level model. The third study focused on the effect of the polarization bound charge of the Ga- and N-face GaN on interface electronic structures. A surface pretreatment process consisting of a NH4OH wet chemical and an in-situ NH3 plasma treatment was applied to remove carbon contamination, retain monolayer oxygen coverage, and potentially passivate N-vacancy related defects. The surface band bending and polarization charge compensation of Ga- and N-face GaN were investigated. The surface band bending and band offsets were determined for Al2O3, HfO2, and SiO2 on Ga- and N-face GaN. Different dielectric thicknesses and post deposition processing were investigated to understand process related defect formation and/or reduction. / Dissertation/Thesis / Ph.D. Physics 2014

For more than seventy years, semiconductor devices have functioned as the cornerstone for technological advancement, and as the defining transition into the information age. The III-Nitride family of semiconductors, in particular, underwent an impressive maturation over the past thirty years, which allowed for efficient light- emitting devices, photo-detectors, and power electronic devices. As researchers try to push the limits of semiconductor devices, and in particular, as they aim to design ultraviolet light emitters and high threshold power devices, the search for new materials with high band gaps, high breakdown voltages, unique optical properties, and variable lattice parameters is becoming a priority. Two interesting candidates that can help in achieving the aforementioned goals are the wurtzite BAlN and BGaN alloy systems, which are currently understudied due to difficulties associated with their growth in epitaxial settings. In our research, we will investigate the band alignment between BAlN and BGaN alloys, and other wurtzite III-Nitride semiconductors from first principle simulations. Through an understanding of band alignment types and a quantification of the band offset values, researchers will be able to foresee the applicability of a particular interface. As an example, a type-I band alignment with a high conduction band offset and a low valence band offset is a potential electron blocking layer to be implemented in standard LED designs. This first principle investigation will be aided by simulations using Density Functional Theory (DFT) as implemented in the Vienna Ab Initio Simulation Package (VASP) environment. In addition, we will detail an experiment from the literature that uses X- ray Photoelectron Spectroscopy on multiple samples to infer and quantify the band alignment between different materials of interest to us. We aim in this study to anticipate the band alignment in interfaces involving materials at the cutting edge of research. Our hope is to set a theoretical ground for future experimental studies on this same matter in parallel to the current efforts to improve the quality and stability of wurtzite BAlN and BGaN alloy crystals.

Two-dimensional (2D) layered materials such as MoS2 have been recognized as high on-off ratio semiconductors which are promising candidates for electronic and optoelectronic devices. In addition to the use of individual 2D materials, the accelerated field of 2D heterostructures enables even greater functionalities. Device designs differ, and they are strongly controlled by the electronic band alignment. For example, photovoltaic cells require type II heterostructures for light harvesting, and light-emitting diodes benefit from multiple quantum wells with the type I band alignment for high emission efficiency. The vertical tunneling field-effect transistor for next-generation electronics depends on nearly broken-gap band alignment for boosting its performance. To tailor these 2D layered materials toward possible future applications, the understanding of 2D heterostructure band alignment becomes critically important. In the first part of this thesis, we discuss the band alignment of 2D heterostructures. To do so, we firstly study the interlayer coupling between two dissimilar 2D materials. We conclude that a post-anneal process could enhance the interlayer coupling of as-transferred 2D heterostructures, and heterostructural stacking imposes similar symmetry changes as homostructural stacking. Later, we precisely determine the quasi particle bandgap and band alignment of the MoS2/WSe2 heterostructure by using scan tunneling microscopy/spectroscopy (STM/S) and micron-beam X-ray photoelectron spectroscopy (μ-XPS) techniques. Lastly, we prove that the band alignment of 2D heterojunctions can be accurately predicted by Anderson’s model, which has previously failed to predict conventional bulk heterostructures. In the second part of this thesis, we develop a new Chemical Vapor Deposition (CVD) method capable of precisely controlling the growth area of p- and n-type transition metal dichalcogenides (TMDCs) and further form lateral or vertical 2D heterostructures. This method also allows p- and n-type TMDCs to separately grow in a selective area in one step. In addition, we demonstrate a first bottom-up 2D complementary inverter based on hetero-TMDCs.

Oxide dielectric breakdown is an old problem that has been studied over decades. It causes power dissipations and irreversible damage to the electronic devices. The aggressive downscaling of the device size exponentially increases the leakage current density, which also raises the risk of dielectric breakdown. It has been proposed that point defects, current leakages, impurity diffusions, etc. all contribute to the change of oxide chemical composition and ultimately lead to the dielectric breakdown. However, the conclusive cause and a clear understanding of the entire process of dielectric breakdown are still under debate. In this research, the electronic structure at metal/oxide interfaces is studied using first-principle calculations within the framework of Density Functional Theory (DFT) to investigate any possible key signature that would trigger the dielectric breakdown. A classical band alignment method, the Van de Walle method, is applied to the case study of the Al/crystal-SiO2 (Al/c-SiO2) interface. Point defects, such as oxygen vacancy (VO) and hydrogen impurity (IH), are introduced into the Al/c-SiO2 interface to study the effects on band offset and electronic structure caused by point defects at metal/oxide interfaces. It is shown that the bonding chemistry at metal/oxide interfaces, which is mainly ionic bond, polarizes the interface. It results in many interface effects such as the interface dipole, built-in voltage, band bending, etc. Charge density analysis also indicates that the interface can localize charge due to such ionic bonding. It is also found that VO at the interface traps metal electrons which closes the open -sp3 orbital. The analysis on local potential shows that the metal potential penetrates through a few layers of oxide starting from the interface, which metalizes the interfacial region and induces unoccupied states in the oxide band gap. In addition, it is shown that higher oxygen content at metal/oxide interfaces minimizes such metal potential invasion. In addition, an oxygen vacancy is created at multiple sites through the Al/c-SiO2 and Al/a-SiO2 interface systems, separately. The oxygen local pressure is also calculated before its removal using Quantum Stress Density theory. Correlations among electronic structure, stress density, and vacancy formation energy are found, which provide informative insights into the defect generation controlling and dielectric breakdown analysis. A new band alignment approach based on the projection of plane-waves (PWs) into the space-dependent atomic orbital (LCAO) basis is presented and tested against classical band offset methods -- the Van de Walle method. It is found that the new band alignment approach can provide a quantitative and reliable band alignment and can be applied to the heterojunctions consisting of amorphous materials. The new band alignment approach reveals the real-space dependency of the electronic structure at interfaces. In addition, it includes all interface effects, such as the interface dipole, built-in voltage, virtual oxide thinning, and band deformation, which cannot be derived using classical band offset methods. This new band alignment approach is applied to the case study of both the Al/amorphous-SiO2 (Al/a-SiO2) interface and the Al/c-SiO2. We have found that at extremely low dimensions, the reduction of the insulator character due to the virtual oxide thinning is a pure quantum effect. I highlight that the quantum tunneling current leakage is more critical than the decrease of the potential barrier height on the failure of the devices. / PHD

abstract: In this dissertation, in-situ X-ray and ultraviolet photoemission spectroscopy have been employed to study the interface chemistry and electronic structure of potential high-k gate stack materials. In these gate stack materials, HfO2 and La2O3 are selected as high-k dielectrics, VO2 and ZnO serve as potential channel layer materials. The gate stack structures have been prepared using a reactive electron beam system and a plasma enhanced atomic layer deposition system. Three interrelated issues represent the central themes of the research: 1) the interface band alignment, 2) candidate high-k materials, and 3) band bending, internal electric fields, and charge transfer. 1) The most highlighted issue is the band alignment of specific high-k structures. Band alignment relationships were deduced by analysis of XPS and UPS spectra for three different structures: a) HfO2/VO2/SiO2/Si, b) HfO2-La2O3/ZnO/SiO2/Si, and c) HfO2/VO2/ HfO2/SiO2/Si. The valence band offset of HfO2/VO2, ZnO/SiO2 and HfO2/SiO2 are determined to be 3.4 ± 0.1, 1.5 ± 0.1, and 0.7 ± 0.1 eV. The valence band offset between HfO2-La2O3 and ZnO was almost negligible. Two band alignment models, the electron affinity model and the charge neutrality level model, are discussed. The results show the charge neutrality model is preferred to describe these structures. 2) High-k candidate materials were studied through comparison of pure Hf oxide, pure La oxide, and alloyed Hf-La oxide films. An issue with the application of pure HfO2 is crystallization which may increase the leakage current in gate stack structures. An issue with the application of pure La2O3 is the presence of carbon contamination in the film. Our study shows that the alloyed Hf-La oxide films exhibit an amorphous structure along with reduced carbon contamination. 3) Band bending and internal electric fields in the gate stack structure were observed by XPS and UPS and indicate the charge transfer during the growth and process. The oxygen plasma may induce excess oxygen species with negative charges, which could be removed by He plasma treatment. The final HfO2 capping layer deposition may reduce the internal potential inside the structures. The band structure was approaching to a flat band condition. / Dissertation/Thesis / Ph.D. Physics 2012

The band alignment of Atomic Layer Deposited SiO 2 on (In x Ga1−x) 2 O 3 at varying indium concentrations is reported before and after annealing at 450 °C and 600 °C to simulate potential processing steps during device fabrication and to determine the thermal stability of MOS structures in high-temperature applications. At all indium concentrations studied, the valence band offsets (VBO) showed a nearly constant decrease as a result of 450 °C annealing. The decrease in VBO was −0.35 eV for (In0.25Ga 0.75) 2 O 3 , −0.45 eV for (In0.42Ga 0.58) 2 O 3 , −0.40 eV for (In0.60Ga 0.40) 2 O 3 , and −0.35 eV (In0.74 Ga0.26) 2 O 3 for 450 °C annealing. After annealing at 600 °C, the band alignment remained stable, with <0.1 eV changes for all structures examined, compared to the offsets after the 450 °C anneal. The band offset shifts after annealing are likely due to changes in bonding at the heterointerface. Even after annealing up to 600 °C, the band alignment remains type I (nested gap) for all indium compositions of (In x Ga1−x ) 2 O 3 studied.

This study seeks to evaluate the temperature effects on the electronic properties of thermoelectric materials, using first principles Density Functional Theory (DFT) calculations by incorporating the temperature effects on structural properties of the material. Using the electronic properties attained, the charge carrier scattering relaxation times were determined. The effect of interface between PbTe and SrTe on the charge carrier mobility was studied by finding out the relative alignment of energy bands at the semiconductor heterojunction. The crystal shape of the SrTe precipitates in the PbTe host matrix was evaluated from the interface energies using the Wulffman construction. We also attempted to develop a relation between the interface energies and electronic band alignment for different interface orientations. In this research, we incorporated the temperature effects on the structural properties of PbTe to get the temperature dependence of electronic properties like energy bandgap and effective masses of charge carriers. We used the values of bandgap and effective masses to determine the charge carrier scattering relaxation time at different temperatures which is used in evaluating the transport properties of thermoelectric materials like the Seebeck coefficient and electrical conductivity. / Master of Science

<p>In this dissertation core level electron spectroscopy has been employed to study various aspects of metal oxide films grown under ultra-high vacuum conditions. </p><p>Studies on <i>in situ</i> ion insertion of lithium into thin TiO₂ systems were performed. The electronic and geometric properties are investigated in detail, along with an estimation of charge transfer from Li to Ti. </p><p>A detailed study of chemical vapour deposition of ZrO₂ on Si(100)-(2x1) was performed. ZrO₂ is found to be an insulator, i.e. its electronic levels are decoupled from the substrate and the Zr levels are best referenced to the local vacuum level. The alignment of the valence and conduction band has been determined. </p><p>Combinatorial chemical vapour deposition of TiO₂ and ZrO₂ on Si(100)-(2x1) was realized. A film with graded stoichiometry consisting of pure TiO₂ and ZrO₂ on the opposing ends and mixed composition of both oxides in the middle was obtained. A detailed study of the electronic levels revealed that ZrO₂ remains an insulator in the monolayer regime and that modification of ZrO₂ with a small amount of TiO₂ leads to a more symmetric alignment of the bands relative to Si. </p><p>The influence of a core hole on the O 1s x-ray absorption spectrum in TiO₂ and ZrO₂ is elucidated. Supported by O 1s photoemission measurements and <i>ab initio</i> calculations it is concluded that the static final state picture as well as dynamical threshold effects must be considered in order to determine the location of the conduction band minimum within the XAS framework. </p><p>Finally a Co modified Co:ZnO film was shown to display ferromagnetic properties. It could be evidenced that Co with oxygen as nearest neighbours was responsible for the magnetism and not metallic Co.</p>

In this dissertation core level electron spectroscopy has been employed to study various aspects of metal oxide films grown under ultra-high vacuum conditions. Studies on in situ ion insertion of lithium into thin TiO2 systems were performed. The electronic and geometric properties are investigated in detail, along with an estimation of charge transfer from Li to Ti. A detailed study of chemical vapour deposition of ZrO2 on Si(100)-(2x1) was performed. ZrO2 is found to be an insulator, i.e. its electronic levels are decoupled from the substrate and the Zr levels are best referenced to the local vacuum level. The alignment of the valence and conduction band has been determined. Combinatorial chemical vapour deposition of TiO2 and ZrO2 on Si(100)-(2x1) was realized. A film with graded stoichiometry consisting of pure TiO2 and ZrO2 on the opposing ends and mixed composition of both oxides in the middle was obtained. A detailed study of the electronic levels revealed that ZrO2 remains an insulator in the monolayer regime and that modification of ZrO2 with a small amount of TiO2 leads to a more symmetric alignment of the bands relative to Si. The influence of a core hole on the O 1s x-ray absorption spectrum in TiO2 and ZrO2 is elucidated. Supported by O 1s photoemission measurements and ab initio calculations it is concluded that the static final state picture as well as dynamical threshold effects must be considered in order to determine the location of the conduction band minimum within the XAS framework. Finally a Co modified Co:ZnO film was shown to display ferromagnetic properties. It could be evidenced that Co with oxygen as nearest neighbours was responsible for the magnetism and not metallic Co.