41 |
CARACTERIZAÃÃO ÃTICA E ESTRUTURAL DE FILMES DE CdS DEPOSITADOS POR BANHO QUÃMICOWellington de Queiroz Neves 15 March 2013 (has links)
Neste trabalho estudamos as propriedades Ãticas de filmes de sulfeto de cÃdmio (CdS) crescidos sobre um substrato de vidro. Os filmes foram obtidos por meio da tÃcnica de deposiÃÃo por banho quÃmico (Chemical Bath Deposition, CBD). Os filmes de CdS sÃo preparados numa soluÃÃo aquosa, sob agitaÃÃo, a uma temperatura de 80 oC durante 60 minutos sobre substrato de vidro. Alguns dos filmes foram obtidos com duplo depÃsito em dois banhos sucessivos iguais. Como fonte de Ãons de cÃdmio à usado sulfato de cÃdmio (CdSO4,) como fonte de Ãons de enxofre à usado a tioureia, como tampÃo à usado cloreto de amÃnia, e como agente complexante o Ethylenediamine tetra acetic acid (Edta) em vÃrias concentraÃÃes. ApÃs o crescimento, os filmes foram submetidos a um tratamento tÃrmico no ar nas temperaturas de 300 ou 400 oC por uma hora. Foram realizadas medidas experimentais usando a tÃcnicas de difraÃÃo de raios-X, fototransmissÃo Ãtica UV-VIS e espectroscopia Raman. Os filmes de CdS obtidos possuem estrutura cÃbica e sÃo de coloraÃÃo amarelada, homogÃneos e muito aderentes ao substrato de vidro. SÃo analisados os efeitos da concentraÃÃo de Edta, tratamento tÃrmico no ar, tempo de deposiÃÃo e temperatura de crescimento dos filmes de CdS. Nossos resultados mostram que, sob as condiÃÃes estudadas, os filmes de CdS nÃo possuem fase hexagonal em sua estrutura. O gap dos filmes de CdS està em torno de 2,45 eV, com pequenas variaÃÃes (2,40 â 2,51 eV) devido Ãs condiÃÃes experimentais de crescimento ou tratamento tÃrmico apÃs o crescimento. Observamos o modo LO, de simetria A1, em torno de 300 cm-1 e atà trÃs sobremodos desse fÃnon. Em alguns casos, os espectros Raman aparecem sobre uma larga fotoemissÃo, dependendo das condiÃÃes experimentais.
|
42 |
Synthesis and characterisation of metal chalcogenide thin filmsPearce, Amber Marie January 2014 (has links)
There is much interest in the electronic potential of ‘nano’-semiconductors. The avenue of research pursued in this project was in inorganic analogues of graphene, namely metal chalcogenides MxEy (M = metal, E = S, Se, Te, x ≠ y = integer value). Thin films of these materials have been used in solar cells, ambient thermoelectric generators and IR detectors, due to their interesting properties, such as: optoelectronics, magnetooptic, piezoelectric, thermoelectric and photovoltaic, as well as electrical conductivity. The key issues with the use of these materials are the formation of controlled films, especially in terms of stoichiometry, crystallinity and uniformity, and also the precursor system used. The aim of this research was to synthesise and isolate novel precursor compounds for use in the deposition of metal sulfide thin films (for use with molybdenum and tungsten). The potential viability of the compounds as single source precursors (ssp) was judged following ThermoGravimetric Analysis (TGA). The compounds were also subjected to analysis using NMR (1H, 13C and 31P where applicable), infrared and UV-Vis spectroscopy, as well as elemental analysis. Cadmium sulfide (CdS) is one of the key direct band gap II-VI semiconductors, having vital optoelectronic applications for laser light-emitting diodes, and optical devices based on non-linear properties. The ratio of these films should ideally be 1:1, however, during the formation of cadmium sulfide films, particularly at elevated temperatures, a common problem encountered is the production of sulfur deficient films. These films have a formula consistent with 〖Cd〗_x S_y, where x is an integer value greater than y, but the sulfur deficiency is generally no greater than 10 %. In order to correct this sulfur deficiency, it was decided to investigate deposition making use of both a ssp and an additional sulfur source, with the aim of producing uniform films with 1:1 Cd:S.Molybdenum disulfide films have been deposited previously from multi source precursors and more recently using ssp. In this project MoS2 was deposited using novel ssps in both LP and AACVD on a variety of substrates with the aim of producing uniform thin films and assessing any differences in the morphology of the deposition. This work was continued with the deposition of WS2 and MoxW1-xS2 from ssps which had not been reported previously. The films deposited were analysed using XRD, SEM, EDX (when available) and Raman spectroscopy.
|
43 |
Photoluminescent properties of novel colloidal quantum dotsEspinobarro Velazquez, Daniel January 2015 (has links)
In this thesis type II colloidal quantum dots (CQDs) with zinc blende crystal structure were investigated. The optical properties were characterized by steady state absorption and photoluminescence (PL) spectroscopy for all the samples, and the PL quantum yield was measured for selected samples by using both absolute and relative methods. Exciton dynamics and interactions were investigated by time-resolved PL (TRPL).The exciton-exciton interaction energy for CdSe, CdSe/CdTe and CdSe/CdTe/CdS CQDs was investigated using TRPL spectroscopy, an established method. The TRPL results were compared with previous results from ultrafast transient absorption (TA) measurements and theoretical predictions. The discrepancies between the TRPL and TA results and the theoretical calculations suggest that TRPL data has been misinterpreted in the literature. The single exciton recombination dynamics for CdSe, CdSe/CdTe and CdSe/CdTe/CdS CQDs were investigated. The effects of non-radiative recombination were identified from the PL transients by using a theoretically-calculated radiative lifetime as a fitting parameter. The combined rate of the non-radiative processes thus found was consistent with the localisation of holes into shallow traps by an Auger-mediated process. A rate equation analysis also showed how shallow trapping can give rise to the tri-exponential PL dynamics observed experimentally. Chloride passivation of CdTe CQDs resulted in a near-complete suppression of surface traps, producing a significant enhancement of the optical properties. PL quantum yield (PLQY) and PL lifetime in particular benefit from the chloride treatment. The radiative recombination rate that now could be extracted from PL transients for chloride treated samples was used to calculate the non-radiative recombination rate for the untreated samples. In addition, a study of the effects of air exposure on the PL, observed for both treated and untreated samples was undertaken and revealed the importance of the influence of the dielectric environment surrounding the traps states on recombination dynamics.
|
44 |
Designing Selectivity in Metal-Semiconductor Nanocrystals: Synthesis, Characterization, and Self-AssemblyPavlopoulos, Nicholas George, Pavlopoulos, Nicholas George January 2017 (has links)
This dissertation contains six chapters detailing recent advances that have been made in the synthesis and characterization of metal-semiconductor hybrid nanocrystals (HNCs), and the applications of these materials. Primarily focused on the synthesis of well-defined II-VI semiconductor nanorod (NR) and tetrapod (TP) based constructs of interest for photocatalytic and solar energy applications, the research described herein discusses progress towards the realization of key design rules for the synthesis of functional semiconductor nanocrystals (NCs). As such, a blend of novel synthesis, advanced characterization, and direct application of heterostructured nanoparticles are presented. Additionally, for chapters two through six, a corresponding appendix is included containing supporting data pertinent to the experiments described in the chapter.
The first chapter is a review summarizing the design, synthesis, properties, and applications of multicomponent nanomaterials composed of disparate semiconductor and metal domains. By coupling two compositionally distinct materials onto a single nanocrystal, synergistic properties can arise that are not present in the isolated components, ranging from self-assembly to photocatalysis. While much progress was made in the late 1990s and early 2000s on the preparation of a variety of semiconductor/metal hybrids towards goals of photocatalysis, comprehensive understanding of nanoscale reactivity and energetics required the development of synthetic methods to prepare well-defined multidimensional constructs. For semiconductor nanomaterials, this was first realized in the ability to tune nanomaterial dimensions from 0-D quantum dot (QD) structures to cylindrical (NR) and branched (TP) structures by exploitation of advanced colloidal synthesis techniques and understandings of NC facet reactivities. Another key advance in this field was the preparation of "seeded" NR and TP constructs, for which an initial semiconductor QD (often CdSe) is used to "seed" the growth of a second semiconductor material (for example, CdS). These advances led to exquisite levels of control of semiconductor nanomaterial composition, shape, and size. Concurrently, many developments were made in the functionalization of these NCs with metallic nanoparticles, allowing for precise tuning of metal nanoparticle deposition position on the surface of preformed semiconductor NCs. To date, photoinduced and thermally induced methods are most widely used for this, providing access to metal-semiconductor hybrid structures functionalized with Au, Pt, Ag2S, Pd, Au/Pt, Ni, and Co nanoparticles (to name a few). With colloidal nanomaterial preparation becoming analogous to traditional molecular systems in terms of selectivity, property modulation, and compositional control, the field of nanomaterial total synthesis has thus emerged in the past decade. With a large toolbox of reactions which afford selectivity at the nanoscale developed, to date it is possible to design a wider array of materials than ever before. Only recently (the past ~ 5 years), however, has the transition from design of model systems for fundamental characterization to realization of functional materials with optimized properties begun to be demonstrated. The emphasis of chapter 1 is thus on the key advances in the preparation of metal-semiconductor hybrid nanoparticles made to date, with seminal synthetic, characterization, and application milestones being highlighted.
The second chapter is focused on the synthesis and characterization of well-defined CdSe-seeded-CdS (CdSe@CdS) NR systems synthesized by overcoating of wurtzite (W) CdSe quantum dots with W-CdS shells. 1-dimensional NRs have been interesting constructs for applications such as solar concentrators, optical gains, and photocatalysis. In each of these cases, a critical step is the localization of photoexcited excitons from the light-harvesting CdS NR "antenna" into the CdSe QD seed, from which emission is primarily observed. However, effects of seed size and NR length on this process remained unexplored prior to this work. Previous work had demonstrated that, for core@shell CdSe@CdS systems, small CdSe seed sizes (< 2.8 nm in diameter) resulted in quasi-type II alignment between semiconductor components (with photoexcited electrons delocalized across the structure and holes localized in the CdSe seed), and large seed sizes (> 2.8 nm) resulted in type I alignment (with photoexcited electrons and holes localized in the CdSe seed). Through synthetic control over CdSe@CdS NR systems, materials with small and large CdSe seeds were prepared, and for each seed size, multiple NR lengths were prepared. Through transient absorption studies, it was found that band alignment did not affect the efficiency of charge localization in the CdSe core, whereas NR length had a profound effect. This work indicated that longer NRs resulted in poor exciton localization efficiencies owing to ultrafast trapping of photoexcited excitons generated in the CdS NR. Thus, with increasing rod length, poorer efficiencies were observed. This work served to highlight the ideal size range for CdSe@CdS NR constructs targeted towards photocatalysis, with ~ 40 nm NRs exhibiting the best rod-to-seed localization efficiencies. Additionally, it served to expand the understanding of exciton trapping in colloidal NC systems, allowing development of a predictive model to help guide the preparation of other nanorod based photocatalytic systems.
The third chapter describes the synthesis of Au-tipped CdSe NRs and studies of the effects of selective metal nanoparticle deposition on the band edge energetics of these model photocatalytic systems. Previous studies had demonstrated ultrafast localization of photoexcited electrons in Au nanoparticles (AuNP) (and PtNP) deposited at the termini of CdSe and CdSe@CdS NR constructs. Also, for similar systems, the hydrogen evolution reaction (HER) had been studied, for which it was found that noble metal nanoparticle tips were necessary to extract photoexcited electrons from the NR constructs and drive catalytic reactions. However, in these studies, energetic trap states, generally ascribed to surface defects on the NC surface, are often cited as contributing to loss of catalytic efficiency. In this study, we found that the literature trend of assuming the band-edge energetics of the parent semiconductor NC applies to the final metal-functionalized catalyst did not present a complete picture of these systems. Through a combination of ultraviolet photoelectron spectroscopy and waveguide based spectroelectrochemistry on films of 40 nm long CdSe NRs before and after AuNP functionalization, we found that metal deposition resulted in the formation of mid-gap energy states, which were assigned as metal-semiconductor interface states. Previously these states had only been seen in single particle STS studies, and their identification in this study from complementary characterization techniques highlighted a need to further understand the nature of the interface between metal/semiconductor components for the design of photoelectrochemical systems with appropriate band alignments for efficient photocatalysis.
The fourth chapter transitions from NR constructs to highly absorbing CdSe@CdS TP materials, for which a single zincblende (ZB) CdSe NC is used to seed the growth of four identical CdS arms. These arms act as highly efficient light absorbers, resulting in absorption cross sections an order of magnitude greater than for comparable NR systems. In the past, many studies have been published on the striking properties of TP nanocrystals, such as dual wavelength fluorescence, multiple exciton generation, and inherent self-assembly owing to their unique geometry. Nonetheless, these materials have not been exploited for photocatalysis, primarily owing to challenges in preparing TP from ultrasmall ZB-CdSe seed size (owing to phase instability of the zincblende crystal structure), thus preventing access to quasi-type II structures necessary for efficient photocatalysis. In this study, we successfully break through the type I/quasi-type II barrier for TP NCs, reclaiming lost ground in this field and demonstrating for the first time quasi-type II behavior in CdSe@CdS TPs through transient absorption measurements. This was enabled by new synthetic protocols for the synthesis and stabilization of ultrasmall (1.8 – 2.8 nm) ZB-CdSe seeds, as well as for the synthesis of CdSe@CdS TPs with arm lengths of 40 nm. Easily scalable, TPs were prepared on gram scales, and the quasi-type II systems showed dramatically enhanced rates of selective photodeposition of AuNP tips under ultraviolet and solar irradiation. These are promising materials for photocatalytic and solar energy applications.
The fifth chapter continues with the study of CdSe@CdS TPs, and elaborates on a new method for the selective functionalization of the highly symmetrical TP construct. Previous studies had demonstrated that access to single noble metal NP tips was vital for efficient photocatalytic HER from NR constructs. However, TP materials have been notoriously difficult to selectively functionalize, owing to their symmetric nature. Using a novel photoinduced electrochemical Ostwald ripening process, we found that initially randomly deposited AuNPs could be ripened to a single, large (~ 7 nm) AuNP tip at the end of one arm of a type I CdSe@CdS TP with 40 nm arms. To demonstrate the selectivity of this tipping process, dipolar cobalt was selectively overcoated onto the AuNP tips of these TPs, resulting in dipolar Au@Co-CdSe@CdS TP nanocrystals. These particles were observed to spontaneous self-assemble into 1-D mesoscopic chains, owing to pairing of N-S dipoles of the ferromagnetic CoNPs, resulting in the first example of “colloidal polymers” (CPs) bearing bulky, tetrapod ("giant t-butyl") pendant groups.
The sixth chapter elaborates further on the preparation of colloidal polymers, further extending the analogy between molecular and colloidal levels of synthetic control. One challenge in the field of colloidal science is the realization of new modes of self-assemble for compositionally distinct nanoparticles. In this work, it was found that Au@Co nanoparticle dipole strength could be systematically varied by tuning of AuNP size on CdSe@CdS nanorods/tetrapods. In the first example of a colloidal analogue to reactivity ratios observed for traditional chain growth polymerization systems, highly disparate AuNP tip sizes (and thus final Au@Co NP dipole strength) were found to result in segmented colloidal copolymers upon dipolar self-assembly, whereas similar AuNP tip sizes ultimately led to random dipolar assemblies. Clearly visualized through incorporation of NR and TP sidechains into these colloidal polymers, this study presented a compelling case for continued exploration of colloidal analogues to traditional molecular levels of synthetic control.
|
45 |
Kreditní swapy a CDO a jejich využití ve finančním prostředí 21. století / Credit swaps and CDOs and their use in the financial environment of the 21st centuryVágó, Ádám January 2015 (has links)
The topic of this thesis is Credit swaps and CDOs and their use in the financial environment of the 21st century. The aim of this thesis is to examine how the market of these instruments works, show how they are traded and how diversely they can be used but also warns about the potential negative consequences in case these instruments are not handled with the required caution. The practical part of this thesis concentrates on the current situation on the credit derivatives market focusing on the above mentioned instruments. The role of CDSs and CDOs in the 2008 global financial crisis is examined with emphasis on the AIG case.
|
46 |
Finanční krize a morální hazard / Financial crisis and moral hazardValtr, Jiří January 2015 (has links)
This diploma thesis focuses on moral hazard in the recent financial crisis which was caused by the burst of the housing bubble in the United States of America almost nine years ago. The main contribution of this thesis is providing evidence of possibility to measure moral hazard. This measuring possibility is achieved by establishing key indicators which are linked to various types of moral hazard according to its origin or closest relation. The thesis also in part drafts a solution to moral hazard in the form of an effective regulation. This thesis is written comprehensibly and does not provide information about every detail of the financial crisis. Regardless of that it still provides most readers interesting and useful piece of information, which they probably have not encountered elsewhere.
|
47 |
Credit valuation adjustments with application to credit default swapsMilwidsky, Cara 03 July 2012 (has links)
The credit valuation adjustment (CVA) on an over-the-counter derivative transaction is the price of the risk associated with the potential default of the counterparties to the trade. This dissertation provides an introduction to the concept of CVA, beginning with the required backdrop of counterparty risk and the basics of default risk modelling. Right and wrong way risks are central themes of the dissertation. A model for the pricing of both the unilateral and the bilateral CVA on a credit default swap (CDS) is implemented. Each step of this process is explained thoroughly. Results are reported and discussed for a range of parameters. The trends observed in the CDS CVA numbers produced by the model are all justified and the right and wrong way nature of the exposures captured. In addition, the convergence and stability of the numerical schemes utilised are shown to be appropriate. A case study, in which the model is applied to a set of market scenarios, concludes the dissertation. Since the field is far from established, a number of areas are suggested for further research. Copyright / Dissertation (MSc)--University of Pretoria, 2012. / Mathematics and Applied Mathematics / unrestricted
|
48 |
Modeling and monitoring of the price process of Credit Default SwapsLoshkina, Anna, Malysheva, Elena January 2008 (has links)
Credit derivatives are very popular on financial markets in recent days. The most liquid credit derivative is a credit default swap (CDS). In this research we investigate methods for modeling and monitoring of the price process of CDS. We study Hull and White model to calculate CDS spread and have data for our analysis. We consider different methods for monitoring of the price process of CDS. In particular we study CUSUM method. And we calculate more commonly used perfomance measures for this method.
|
49 |
Investigation of Optoelectronic Properties in Thin-Film and Crystalline Cadmium SulfideBhowmick, Mithun 26 June 2007 (has links)
No description available.
|
50 |
CdS Reflection Coefficient Determination via Photocurrent SpectroscopyWang, Yang 19 September 2008 (has links)
No description available.
|
Page generated in 1.2828 seconds