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Quantum dots are a part of very important our technological future because of their intriguing and useful properties. These properties are different in character from those of the corresponding bulk material. Quantum dots are inorganic artificial semiconductor nanocrystal whose electrons influence their physical and chemical properties. Zinc oxide quantum dots were synthesized through an ethanol based precipitation via colloidal synthesis method at various pH values. Various emission colors were obtained because the excited quantum dots of various sizes emitted specific wavelengths of light. The emission spectra indicated that the pH dependent quantum dots were successfully synthesized. Zinc oxide quantum dots were also encapsulated and the luminescence properties examined. The quantum dots that were immobilized in polyisoprene (PI) through chemiluminescence (CL) analyses were found to be stable and were capable of continuing their luminescence properties with extended uses and long- term storage. Linear calibration curves were acquired for concentration of 8.75 x 10-5 M H2O2 in TCPO-CL.

Microplastic (MP) pollution has recently been recognized as a threat to the biosphere including humans due to its widespread distribution, persistent nature and infinitesimal size. This study focused on the solid phase degradation of microplastic residues (particularly low density polyethylene, LDPE) in water through heterogeneous photocatalysis process by designed photocatalysts of zinc oxide nanorods (ZnO NRs) and platinum nanoparticles deposited on zincoxide nanorods (Pt NPs-ZnO NRs) under visible light irradiation. These photocatalysts were assessed following standard protocol (ISP 10678: 2010), and characterized using SEM, EDX andoptical spectroscopies (UV-VIS and PL). Deposition of Pt-NPs on ZnO NRs for certain minutes has been found optimum that enhanced the photodegradation process about 38% under UV irradiation and 16.5% under visible light irradiation by improving of both electrons-holes pair separation process and visible light absorption. Photocatalytic degradation of LDPE films was confirmed by FTIR spectroscopy, dynamic mechanical analyzer (DMA), optical and electron microscopes. When LDPE film irradiated in presence of Pt-ZnO, degradation was found quicker than ZnO alone of similar concentration which exhibited formation of a large number of wrinkles, cracks and cavities on the film surface. Dynamic mechanical analyzer (DMA) test indicated stiffness and embrittlement of exposed LDPE films in presence of photocatalysts. Thus, the present work provides a new insight about modified catalysts for the degradation of microplastics in water using visible light.

Growing demand for clean source of energy in the recent years has increased the manufacture of solar cells for converting sun energy directly into electricity. Research has been carried out around the world to make a cheaper and more efficient solar cell technology by employing new architectural designs and developing new materials to serve as light absorbers and charge carriers. Aluminum doped Zinc Oxide thin film, a Transparent conductive Oxides (TCO) is used as a window material in the solar cell these days. Its increased stability in the reduced ambient, less expensive and more abundance make it popular among the other TCO’s. It is the aim of this work to obtain a significantly low resistive ZnO:Al thin film with good transparency. Detailed electrical and materials studies is carried out on the film in order to expand knowledge and understanding. RF magnetron sputtering has been carried out at various substrate temperatures using argon, oxygen and hydrogen gases with various ratios to deposit this polycrystalline films on thermally grown SiO2 and glass wafer. The composition of the films has been determined by Xray Photoelectron Spectroscopy and the identification of phases present have been made using X-ray diffraction experiment. Surface imaging of the film and roughness calculations are carried out using Scanning Electron Microscopy and Atomic Force Microscopy respectively. Determination of resistivity using 4-Probe technique and transparency using UV spectrophotometer were carried out as a part of electrical and optical characterization on the obtained thin film.The deposited thin films were later annealed in vacuum at various high temperatures and the change in material and electrical properties were analyzed.

Doping in bulk semiconductors (e.g., n- or p- type doping in silicon) allows for precise control of their properties and forms the basis for the development of electronic and photovoltaic devices. Recently, there have been reports on the successful synthesis of doped semiconductor nanocrystals (or quantum dots) for potential applications in solar cells and spintronics. For example, nanocrystals of ZnSe (with zinc-blende lattice structure) and CdSe and ZnO (with wurtzite lattice structure) have been doped successfully with transition-metal (TM) elements (Mn, Co, or Ni). Despite the recent progress, however, the underlying mechanisms of doping in colloidal nanocrystals are not well understood. This thesis reports a comprehensive theoretical analysis toward a fundamental kinetic and thermodynamic understanding of doping in ZnO, CdSe, and ZnSe quantum dots based on first-principles density-functional theory (DFT) calculations. The theoretical predictions of this thesis are consistent with experimental measurements and provide fundamental interpretations for the experimental observations. The mechanisms of doping of colloidal ZnO nanocrystals with the TM elements Mn, Co, and Ni is investigated. The dopant atoms are found to have high binding energies for adsorption onto the Zn-vacancy site of the (0001) basal surface and the O-vacancy site of the (0001) basal surface of ZnO nanocrystals; therefore, these surface vacancies provide viable sites for substitutional doping, which is consistent with experimental measurements. However, the doping efficiencies are affected by the strong tendencies of the TM dopants to segregate at the nanocrystal surface facets, as indicated by the corresponding computed dopant surface segregation energy profiles. Furthermore, using the Mn doping of CdSe as a case study, the effect of nanocrystal size on doping efficiency is explored. It is shown that Mn adsorption onto small clusters of CdSe is characterized by high binding energies, which, in conjunction with the Mn surface segregation characteristics on CdSe nanocrystals, explains experimental reports of high doping efficiency for small-size CdSe clusters. In addition, this thesis presents a systematic analysis of TM doping in ZnSe nanocrystals. The analysis focuses on the adsorption and surface segregation of Mn dopants on ZnSe nanocrystal surface facets, as well as dopant-induced nanocrystal morphological transitions, and leads to a fundamental understanding of the underlying mechanisms of dopant incorporation into growing nanocrystals. Both surface kinetics (dopant adsorption onto the nanocrystal surface facets) and thermodynamics (dopant surface segregation) are found to have a significant effect on the doping efficiencies in ZnSe nanocrystals. The analysis also elucidates the important role in determining the doping efficiency of ZnSe nanocrystals played by the chemical potentials of the growth precursor species, which determine the surface structure and morphology of the nanocrystals.

In recent years, interest in sustainability and being environmentally friendly has increased. Wood is a durable and renewable building material, which is becoming more common in the constructions industry. In 2002, the government in Sweden adopted a national strategy to promote an increased use of wood in buildings. However, the usage of wood in construction has a potential risk – wood is ignitable and has fire-spreading properties.  The aim of this project was to investigate whether a ZnO coating can reduce the risk of ignition on wooden surfaces exposed to a radiative heat source, focusing on the time to ignition of the wood. ZnO possess a wide combination of physical properties, such as ability to reflect infrared radiation and being thermally stable at extremely high temperatures. The study has been carried out through a literature review and laboratory experiments. In the laboratory experiments, a cone calorimeter was used and the tests were performed according to ISO 5660-1. In the cone calorimeter, two different amounts of ZnO applied to the wood surface were tested, 0.5 and 1 g ZnO per dm2 and an untreated piece of wood as a reference. The test was carried out in three different heat fluxes: 20, 35 and 50 kWm-2. After completed tests, the change in the wood’s morphology was examined in a scanning electron microscopy (SEM). The result shows that an application of ZnO on a wooden surface significantly increases the time to ignition for the wood. An application of 0.5 g ZnO per dm2increased the time to ignition by 26-33 % for the three different heat fluxes. On the other hand, 1 g of ZnO per dm2 created an increase of 37-40 %. The trend of the increase of time to ignition was similar for all heat fluxes. The result showed no clear tendency that the smoke production rate was reduced with the application of ZnO. The heat release rate was not affected by the addition of ZnO, which was expected because ZnO delays the time to ignition, but once it catches fire, the wood burns. The SEM images before and after combustion showed that there is no change in the morphology of ZnO, although some ZnO has agglomerated but remains intact after combustion. The conclusion of this study is that ZnO has the potential to protect wood from fireby increasing the time to ignition. But when the wood has ignited, there is no clear tendency for ZnO to affect the growth of the fire. The study has shown that in the future ZnO could be applied to a wooden surface to reduce the risk of fire ignition. Further studies are required to find effective methods to implement the usage of ZnO, as applying ZnO on vertical wooden surfaces.

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