Diluted magnetic semiconductor oxides (DMSOs) have received great attention recently due to their outstanding applications in optoelectronic and spintronic devices. Ever since the initial observation of ferromagnetism at room temperature in cobalt-doped titania, extensive effort is concentrated on preparation of transition metal doped wide band gap semiconductors, especially Mn- doped ZnO. Compared to Mn-doped ZnO, magnetic interactions in SnO! and In!O! semiconductors have been underexplored. SnO! and In!O! semiconductors have many applications, owing to their high charge carrier density and mobility as well as high optical transparency. Investigation on electronic structure changes induced by dopants during the synthesis procedure can effectively influence magnetic interactions between charge carriers. In this work, a combination of structural and spectroscopic methods was used to probe as-synthesized SnO! and In!O! nanocrystals doped with Mn!! and Mn!! as precursors. X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) spectroscopy are powerful techniques to explore formal oxidation state of manganese dopant, electronic environment, number of nearest neighbors around the absorbent, and bond lengths to the neighboring atoms. Analysis reveals the presence of multiple oxidation states in the doped nanocrystals, and establishes a relation between !"!! ratio and expansion or contraction of lattice parameters. !"!! Although doping semiconductors are crucial for manipulating the functional properties, the influence of dopants on nanocrystals structure is not well understood. Nanocrystalline films prepared from colloidal Mn-doped SnO! and In!O! nanocrystals through spin coating process exhibit ferromagnetic behavior in temperatures ranging from 5 K to 300 K. Magnetic transformation from paramagnetic in free-standing Mn-doped nanocrystals to strong ferromagnetic ordering in nanocrystalline films is attributed to the formation of extended structural defects, e.g., oxygen vacancies at the nanocrystals interface. Magnetic circular dichroism (MCD) studies clearly show that Mn!! occupies different symmetry sites in indium oxide, when bixbyite and rhombohedral In!O! nanocrystals (NCs) are compared.

Cavity enhanced absorption spectroscopies have earned themselves a place as one of the methods of choice for sensitive absorption measurements on gas-phase samples, but their application to liquid samples has so far been more limited. Sensitive short pathlength analysis of liquid samples is required for online analysis of microfluidic samples, which are processed in channels with dimensions of tens to hundreds of micrometres. Microfluidics is important for a range of applications including drug discovery and environmental sensing. This thesis explores the application of cavity enhanced absorption spectroscopies to short pathlength (0.010 mm to 2 mm) analysis of sub-microlitre volumes of liquids. Three experimental set-ups have been been examined. Firstly, a single-wavelength cavity ringdown (CRD) spectrometer operating at 532 nm was assembled using two 99.8% reflectivity mirrors. High optical quality flow cells with short pathlengths ranging from 0.1 mm to 2 mm were inserted into this cavity at Brewster’s angle. The detection limit of the set-up with each inserted flow cell was established using a concentration series of aqueous potassium permanganate (KMnO₄) solutions. For the 1 mm flow cell, a detection limit of 29 nM KMnO₄ or 1.4 x 10⁻⁴ cm⁻¹ was established. Several different types of microfluidic devices were also inserted into the cavity, and it was found that the losses arising from the inserted chip were highly dependent on the method of chip manufacture. The CRD set-up with inserted 1 mm flow cell was applied to the detection of two important species, nitrite and iron(II), via analyte-specific colourimetric reactions. Detection limits of 1.9 nM nitrite and 3.8 nM iron(II) were established. The second experimental set-up utilised broadband, supercontinuum light generated in a 20 m length of nonlinear photonic crystal fibre. Broadband mirrors with around 99% reflectivity over the wavelength range from 400 to 800 nm were used to form the cavity, and a miniature spectrometer was used to wavelength-resolve the time-integrated cavity output. Flow cells and microfluidic chips were inserted into the cavity either at normal incidence or at Brewster’s angle. This set-up was employed for reaction analysis of an iron complexation reaction with bathophenanthroline, and for a model organic reaction, the Diels-Alder reaction between anthracene and 4-phenyl-1,2,4-triazoline-3,5-dione. The same broadband set-up was also used for pH measurements using bromocresol green indicator solution. Using dual-wavelength CRD spectroscopy, the pH sensitivity was established to be around a few milli pH units. Finally, an alternative type of cavity, formed from a loop of optical fibre has been investigated. A novel light-coupler was designed and fabricated in 365 μm core diameter multimode optical fibre. Sample designs employing both direct and evanescent wave absorption were investigated in small-core and large-core optical fibres, and the lowest detection limit of 0.11 cm⁻¹ was determined in direct absorption measurements, with a pathlength of 180 μm, using our novel light coupler in 365 μm core diameter optical fibre.

The rotational spectrum of ScO (X-2 Sigma(+)) has been measured in the gas phase in the frequency range 30-493 GHz using a combination of Fourier transform microwave/millimeter-wave (FTM/mmW) and submillimeter direct absorption methods. This work is the first pure rotational study of this radical. Both the ground vibrational and v=1 states were observed. ScO was created from the reaction of metal vapor, produced either by a laser ablation source or a Broida-type oven, and N2O, in the former case heavily diluted in argon. Extensive hyperfine structure was observed in the FTM/mmW data, although the spin-rotation splitting was found to be small (similar to 3 MHz). In the mm-wave spectra, however, the fine and hyperfine structure was blended together, resulting in broad, single lines for a given transition N + 1 <- N. The data were analyzed in a combined fit using the very accurate hyperfine measurements of Childs and Steimle (1988), employing a Hund's case b Hamiltonian, and an improved set of rotational and centrifugal distortion constants were determined. These measurements improve the accuracy of predicted frequencies for astronomical searches by 14-18 MHz, or 16-20 km/s, in the 1 mm region - a difference of half to a full linewidth for certain interstellar sources. This work also demonstrates the capabilities of the FTM/mmW spectrometer at 61 GHz.

A source-modulation microwave spectrograph was utilized to measure line width parameters for several spectral lines in the pure rotational spectrum of formaldehyde (H₂CO). The spectrograph featured high-gain ac amplification and phase-sensitive detection, and was capable of measuring microwave lines having absorption coefficients as small as 10⁻⁷ cm⁻¹ with a frequency resolution on the order of 30 kHz. Center frequencies of the measured lines varied from 4,830 MHz to 72,838 MHz; hence, most of the observations were made on transitions between K-doublets in the rotational spectrum. Corrections were applied to the measured line width parameters to account for Doppler broadening and, where possible, for deviations due to magnetic hyperfine structure in some of the K-doubled lines. Low modulation voltages and low microwave power levels were used to minimize modulation and saturation broadenings; other extraneous broadenings were found to be insignificant. The primary broadening mechanism at low gas pressure is pressure broadening, and a review of this topic is included. Line width parameters for the several observed transitions were determined by graphing half-widths versus pressure for each spectral line, and performing a linear least-squares fit to the data points. Repeatability measurements indicated the accuracy of the line width parameters to be better than ±10 percent. The reasons for this repeatability spread are discussed, Broadening of each line was measured for self- and foreign-gas broadening by atomic helium and diatomic hydrogen. Effective collision diameters were calculated for each broadening interaction, based on the observed rates of broadening.

Inserido no contexto de fontes de energia renováveis, este trabalho consiste na síntese e caracterização de filmes de bastões de ZnO modificados com quantum dots de CdTe a fim de serem aplicados em células fotoeletroquímicas. Bastões de ZnO são materiais interessantes, porque este tipo de estrutura facilita o transporte de portadores de carga, minimizando a perda destes nos contornos de grão, sua recombinação e aniquilação. A modificação do filme de ZnO com nanocristais de CdTe deve aumentar a eficiência da fotoconversão, facilitando a separação de carga e transferência de elétrons, e isso aumenta a estabilidade dos nanocristais, impedindo a corrosão anódica e a decomposição destes. O filme de ZnO foi eletrodepositado potenciostaticamente sobre a superfície de ITO. As análises de MEV e EDX indicaram que filme de ZnO obtido é homogêneo e consiste de bastões com razão atômica de Zn e O de acordo com a estequiometria 1:1. O resultado de DRX apresentou três planos característicos do ZnO na forma cristalina wurtzita. O plano (002) foi o predominante, indicando a orientação dos bastões no eixo c vertical ao substrato. O filme de ZnO tem espessura de 550 nm, bandgap 3,27 eV, potencial de banda plana de 0,4 V e densidade de portadores de carga de 8,9 x 1019 cm-3. O procedimento sintético dos pontos quânticos de CdTe ocorreu a partir da dissolução de óxido de cádmio em ácido tetradecilfosfônico e octadeceno (ODE) a 300 &deg;C. Subsequentemente, a solução precursora de cádmio foi resfriada a 260 &deg;C e então a solução precursora de telúrio, preparada pela dissolução de telúrio e tributilfosfina em ODE, foi injetada. Os nanocristais obtidos foram dispersos em hexano, precitados com etanol e finalmente os quantum dots foram armazenados em tolueno. A partir das análises de UV-Vis e TEM foi possível estimar o tamanho dos pontos quânticos de CdTe com aproximadamente 4 nm. O DRX dos nanocristais de CdTe apresentou os planos característicos principais da estrutura da blenda de zinco. O eletrodo de ZnO modificado com os quantum dots de CdTe (ZnO/CdTe) foi obtido após 24 h de imersão em uma solução de acetonitrila contendo ácido mercaptopropiônico e ácido propiônico. Subsequentemente, o filme de ZnO modificado com o ligante foi imerso por 48 h na dispersão de pontos quânticos de CdTe. O espectro de FTIR revelou a ausência do estiramento simétrico de C=O em 1700 cm-1. Por outro lado o espectro revelou a presença dos modos assimétrico e simétrico vas(CO2-) e vs(CO2-) que foram observados em 1631 e 1417 cm-1, respectivamente. A transformação de Kulbeka-Munk do espectro de reflectância do eletrodo ZnO/CdTe apresentou a banda relativa ao CdTe no mesmo comprimento de onda observado quando este encontrava-se na dispersão. O eletrodo ZnO/CdTe mostrou um valor de fotocorrente de 138 &micro;A, um valor 10 vezes maior que o obtido para o ZnO. Nos experimentos de IPCE (eficiência de conversão do fóton incidente à corrente) um aumento de aproximadamente cinco vezes também foi observado para o eletrodo de ZnO/CdTe. A dinâmica dos portadores de carga foi investigada por TAS (Espectroscopia de Absorção Transiente) nas escalas de tempo fs e &micro;s para os eletrodos de ZnO e de ZnO/CdTe. A análise TAS indicou um tempo de vida menor para o filme ZnO/CdTe em comparação com filme ZnO. A medidas com o eletrodo de Clark demonstraram uma produção de oxigênio pelo eletrodo de ZnO/CdTe. Assim, o filme de ZnO/CdTe proposto apresenta-se como um material promissor para aplicações fotoeletroquímicas. / Placed in the context of renewable energy sources, this work consists of the synthesis and characterization of ZnO films modified CdTe quantum dots to be applied in photoelectrochemical cells. ZnO rods are interesting materials because this kind of structure facilitates the charge carriers transport, minimizing the loss of these at grain boundaries and their recombination and annihilation. The ZnO film modification with CdTe nanocrystals should increase the photoconversion efficiency by facilitating charge separation and electron transfer, and it increases the nanocrystals stability, preventing it from anodic corrosion and decomposition. The ZnO film was electrodeposited potenciostatically on ITO surface. SEM and EDX analysis indicated that the ZnO film obtained is homogeneous and it consists of rods with atomic ratio of Zn and O according to 1:1 stoichiometry. XRD result showed three characteristic planes of ZnO in wurtzite crystalline form. The (002) plane is the predominant, indicating the rods orientation in the c-axis vertical to the substrate. The ZnO film also has a thickness of 550 nm, bandgap of 3.27 eV, flat band potential of 0.4 V and density of charge carriers 8,9 x 1019 cm-3. The synthetic procedure of CdTe quantum dots occurred from the dissolution cadmium oxide in tetradecylphosphonic acid and octadecene (ODE) to 300 &deg;C. Subsequently, cadmium precursor solution of was cooled to 260 &deg;C and then the tellurium precursor solution, prepared by dissolving tellurium in tributylphosphine and in ODE was injected. The obtained nanocrystals were dispersed in hexane, precipitated with ethanol and finally the quantum dots were stored in toluene. From UV-Vis and TEM analysis was possible to estimate the quantum dots size of CdTe as 4 nm. The XRD of CdTe nanocrystals presented the main characteristic planes of zinc blend structure. ZnO electrode modified with CdTe quantum dots (ZnO/CdTe) was obtained by 24 h immersion in a solution of acetonitrile containing mecaptopropionic acid and propionic acid. Subsequently, the ZnO film modified with the linker was immersed for 48 h in CdTe quantum dots dispersion. FTIR spectrum reveals the absence of a symmetrical C=O stretching mode at approximately 1700 cm-1. Instead, the spectrum shows the presence of the asymmetric and symmetric vas(CO2-) and vs(CO2-) modes were observed at 1631 and 1417 cm-1, respectively. Kulbeka-Munk transformation of the reflectance spectrum of the ZnO/CdTe electrode presented the band related to CdTe in the same wavelength observed when this was in the dispersion. The ZnO/CdTe electrode showed a photocurrent value of 138 &micro;A, a value 10 times greater than that obtained for ZnO. At IPCE experiments (incident photon-to-current efficiency) an increase of approximately five times was also noticed to the electrode of ZnO/CdTe. Dynamics of charge carriers was investigated by fs and &micro;s TAS (Transient Absorption Spectroscopy) for ZnO and ZnO/CdTe electrodes. TAS analyses indicate a short life time to ZnO/CdTe electrode compared to ZnO film. Clark electrode measurements showed oxygen production by ZnO/CdTe electrode. Thus, ZnO/CdTe proposed electrode is presented as promising material for photoelectrochemical applications.

Metal oxides and (oxy)hydroxides, particularly those containing two or more metals have many uses as electronic materials and catalyst, especially in energy applications. In this dissertation, the structure-property relationships of these mixed-metal materials are explored in order to understand how these materials work and to guide design of materials with even higher efficiency for a given application. Chapter I introduces the materials and studies undertaken. Chapter II presents a fundamental analysis of the electronic and local atomic properties of mixed-transition-metal aluminum oxide thin films. The final three chapters focus on water electrolysis for hydrogen production, which is limited in part by the slow kinetics of the oxygen evolution reaction (OER). Nickel-iron and cobalt-iron (oxy)hydroxides have been shown to be the most active in alkaline conditions. Although it is evident that Fe is essential for high activity, its role is still unclear. Chapter III investigates the role of Fe in NiOOH by comparing the effects of Ti, Mn, La, and Ce incorporation on the OER activity of NiOOH in base. Chapter IV evaluates the OER activity and Tafel behavior of Fe3+ impurities on different noble metal substrates. Chapter V describes the results of in situ and in operando X-ray spectroscopy experiments, which shows that the local structure around Fe atoms in Co(Fe)OOH changes during OER while that of Co stays the same. This work adds to the growing body of literature that suggests Fe is essential to the catalytic active site for the OER on transition-metal (oxy)hydroxides. This dissertation contains previously published and un-published coauthored material. / 2020-01-11

by Lai Yuen Kwan. / Thesis (M.Phil.)--Chinese University of Hong Kong, 1997. / Includes bibliographical references (leaves 41-45). / Abstract --- p.i / Acknowledgement --- p.ii / Contents --- p.iii / List of Figures --- p.vi / List of Tables --- p.vii / Chapter 1. --- INTRODUCTION / Chapter 1.1 --- Air Pollution in Hong Kong --- p.1 / Chapter 1.2 --- Lead in Air and its Harmful Effects on Human --- p.3 / Chapter 1.3 --- Sampling of Air Particulates --- p.6 / Chapter 1.3.1 --- Principles of filter sampling --- p.6 / Chapter 1.3.2 --- Filter media for air sampling --- p.7 / Chapter 1.4 --- Sample Treatment --- p.9 / Chapter 1.4.1 --- Acid digestion - standard method for analysis of metals --- p.9 / Chapter 1.4.2 --- Slurry sampling - direct method for analysis of metals --- p.9 / Chapter 1.4.3 --- Literature survey on slurry sampling --- p.10 / Chapter 1.4.4 --- Comparison between acid digestion and slurry sampling methods --- p.10 / Chapter 1.5 --- Instrumental Analysis --- p.11 / Chapter 1.5.1 --- Graphite furnace atomic absorption spectrometry --- p.11 / Chapter 1.5.2 --- Background correction by the Zeeman effect --- p.12 / Chapter 2. --- EXPERIMENTAL / Chapter 2.1 --- Apparatus --- p.14 / Chapter 2.2 --- Reagents --- p.14 / Chapter 2.3 --- Procedure --- p.15 / Chapter 2.3.1 --- Selection of sample introduction technique --- p.15 / Chapter 2.3.2 --- Recovery study of lead in standard reference material (SRM) in 1-decanol --- p.16 / Chapter 2.3.3 --- Study of suspension behavior of solvents with SRM --- p.16 / Chapter 2.3.4 --- Recovery study of lead in SRM in ethylene glycol --- p.17 / Chapter 2.3.5 --- Determination of lead in SRM by the developed method --- p.17 / Chapter 2.3.6 --- Determination of lead in SRM by the acid digestion method --- p.18 / Chapter 2.3.7 --- Application of the developed method on the analysis of real sample --- p.18 / Chapter 3. --- RESULTS AND DISCUSSION / Chapter 3.1 --- Choice of Solvents for Suspension of Air Particulates --- p.20 / Chapter 3.2 --- Sample Introduction Technique --- p.20 / Chapter 3.3 --- Recovery Study of lead in SRM in 1-Decanol --- p.22 / Chapter 3.3.1 --- Drying stage of the temperature program for analysis --- p.23 / Chapter 3.3.2 --- Effect of 1-decanol on the absorbance signal of the analyte --- p.24 / Chapter 3.3.3 --- Sample injection volume --- p.25 / Chapter 3.3.4 --- Design of temperature program for analysis --- p.25 / Chapter 3.4 --- Study of Suspension Behavior of Solvents --- p.27 / Chapter 3.5 --- Recovery Study of lead in SRM in Ethylene Glycol --- p.32 / Chapter 3.6 --- Evaluation of the Developed Method --- p.33 / Chapter 3.6.1 --- Determination of lead in SRM --- p.33 / Chapter 3.6.2 --- Application of non-linear standard addition method --- p.35 / Chapter 3.6.3 --- precision and accuracy of the developed method --- p.36 / Chapter 3.7 --- Recovery Study with the Acid Digestion Method --- p.36 / Chapter 3.8 --- Analysis of Real Sample by the Developed Method --- p.37 / Chapter 3.8.1 --- Principles of TEOM® on mass measurement --- p.37 / Chapter 3.8.2 --- Selection of filter media for air sampling --- p.37 / Chapter 3.8.3 --- Study of dislodging efficiency of air particulates from Teflon filter --- p.38 / Chapter 3.8.4 --- Comparison with the acid digestion method --- p.39 / Chapter 4. --- CONCLUSION --- p.40 / Chapter 5. --- REFERENCES --- p.41 / Chapter 6. --- APPENDIX --- p.46

No description available.

京都大学 / 新制・課程博士 / 博士(人間・環境学) / 甲第23996号 / 人博第1048号 / 新制||人||246(附属図書館) / 2022||人博||1048(吉田南総合図書館) / 京都大学大学院人間・環境学研究科相関環境学専攻 / (主査)教授 内本 喜晴, 教授 高木 紀明, 教授 白井 理, 教授 光島 重徳 / 学位規則第4条第1項該当 / Doctor of Human and Environmental Studies / Kyoto University / DFAM

High-energy ion beam based proton induced x-ray (PIXE) is an ideal analytical tool suitable for simultaneous quantification of trace elements with high accuracy. The quantification of trace elements in solids using PIXE has been well established for over two decades. The main objective of this study is to extend this capability to solids with an inhomogeneous internal structure. In this study, pure GAC and PAC samples were soaked in known concentration of arsenic (As) solution and the trace amount of As uptake was determined during these exposures using PIXE, neutron activation analysis (NAA) and atomic absorption spectroscopy (AAS). There is a good agreement between the values and adsorption mechanisms derived from the NAA and pelletised PIXE measurements and some AAS measurements. Micro-PIXE was used to understand the discrepancies in the As adsorption on the pore and flat surfaces of GAC samples. / Master of Science (Hons) (Physics)