Synthesis and characterization of oxide materials

Nanostructured materials are central to the evolution of future electronics and biomedical applications amongst other applications. This thesis is focused on developing novel methods to prepare a number of nanostructured metal oxide particles and films by a number of different routes. Part of the aim was to see how techniques used in nanoparticle science could be applied to thin film methods to develop functional surfaces. Wet-chemical methods were employed to synthesize and modify the metal oxide nanostructures (CeO2 and SiO2) and their structural properties were characterized through advanced X-ray diffraction, electron microscopy, photoelectron spectroscopy and other techniques. Whilst particulates have uses in many applications, their attachment to surfaces is of importance and this is frequently challenging. We examined the use of block copolymer methods to form very well defined metal oxide particulate-like structures on the surface of a number of substrates. Chapter 2 describes a robust method to synthesize various sized silica nanoparticles. As-synthesized silica nanoparticles were further functionalized with IR-820 and FITC dyes. The ability to create size controlled nanoparticles with associated (optical) functionality may have significant importance in bio-medical imaging. Thesis further describes how non-organic modified fluorescent particles might be prepared using inorganic oxides. A study of the concentrations and distributions of europium dopants within the CeO2 nanoparticles was undertaken and investigated by different microscopic and spectroscopic techniques. The luminescent properties were enhanced by doping and detailed explanations are reported. Additionally, the morphological and structural evolution and optical properties were correlated as a function of concentrations of europium doping as well as with further annealing. Further work using positron annihilation spectroscopy allowed the study of vacancy type defects formed due to europium doping in CeO2 crystallites and this was supported by complimentary UV-Vis spectra and XRD work. During the last few years the interest in mesoporous silica materials has increased due to their typical characteristics such as potential ultra-low dielectric constant materials, large surface area and pore volume, well-ordered and uniform pores with adjustable pores between 2 and 50 nm. A simple, generic and cost-effective route was used to demonstrate the synthesis of 2D mesoporous silica thin films over wafer scale dimensions in chapter 5. Lithographic resist and in situ hard mask block copolymer followed by ICP dry etching were used to fabricate mesoporous silica nanostructures. The width of mesoporous silica channels can be varied by using a variety of commercially available lithographic resists whereas depth of the mesoporous silica channels can be varied by altering the etch time. The crystal structure, morphology, pore arrangement, pore diameters, thickness of films and channels were determined by XRD, SEM, ellipsometry and the results reported. This project also extended work towards the study of the antimicrobial study of nanopatterned silver nanodot arrays formed using the block copolymer approach defined above. Silver nanodot arrays were successfully tested for antimicrobial activity over S. aureus and P. aeruginosa biofilms and results shows silver nanodots has good antimicrobial activity for both S. aureus and P. aeruginosa biofilms. Thus, these silver nanodot arrays shows a potential to be used as a substitute for the resolution of infection complications in many areas

Defect chemistry and vacancy concentration of luminescent europium doped ceria nanoparticles by solvothermal method

Pure phase and europium-doped ceria nanocrystals have been synthesized by a single step simple solvothermal process. Different spectroscopic, diffractive, and microscopic techniques were used to determine the morphology, size, crystal structure, and phase of all the samples. Electron energy loss spectroscopy (EELS) for elemental mapping confirmed that good solid solutions were formed and that the particles had a homogeneous distribution of europium. The defect chemistry was more complex than might be expected with the incorporation of each Eu3+ ion resulting in the production of an anion vacancy since the doping results in charge compensating (i.e., for Eu3+) anion vacancies as well as vacancies due to oxygen removal from the crystallite surface. Variations in nanoparticles dimension and lattice parameters were measured as a function of dopant concentrations and their variations explained. The band gap of the samples could be tailored by the doping. The doped samples were found to be luminescent due to the substitution of Ce4+ ions in the cubic symmetric lattice by the dopant ions. The thermal stability of the fluorescence properties was also investigated

A positron annihilation spectroscopic investigation of europium-doped cerium oxide nanoparticles

Doping in ceria (CeO2) nanoparticles with europium (Eu) of varying concentrations (0, 0.1, 0.5, …, 50 atom%) is studied using complementary experimental techniques and novel observations were made during the investigation. The immediate observable effect was a distinct reduction in particle sizes with increasing Eu concentration attributed to the relaxation of strain introduced due to the replacement of Ce4+ ions by Eu3+ ions of larger radius. However, this general trend was reversed in the doping concentration range of 0.1–1 atom% due to the reduction of Ce4+ to Ce3+ and the formation of anion vacancies. Quantum confinement effects became evident with the increase of band gap energy when the particle sizes reduced below 7–8 nm. Positron annihilation studies indicated the presence of vacancy type defects in the form of vacancy clusters within the nanoparticles. Some positron annihilation was also seen on the surface of crystallites as a result of diffusion of thermalized positrons before annihilation. Coincidence Doppler broadening measurements indicated the annihilation of positrons with electrons of different species of atoms and the characteristic S–W plot showed a kink-like feature at the particle sizes where quantum confinement effects began

Synthesis and stability of IR-820 and FITC doped silica nanoparticles

Fluorescent silica nanoparticles (NPs) have potential in biomedical applications as diagnostics and traceable drug delivery agents. In this study, we have synthesized fluorescent dye grafted silica NPs in two step process. First, a stable method to synthesize various sizes of silica NPs ranging from 20 to 52, 95, 210 and 410 nm have been successfully demonstrated. Secondly, as-synthesized silica NPs are readily grafted with some fluorescent dyes like IR-820 and fluorescein isothiocyanate (FITC) dyes by simple impregnation method. IR-820 and FITC dyes are ‘activated’ by (3-mercaptopropyl)trimethoxysilane (MPTMS) and (3-aminopropyl)triethoxysilane (APTS) respectively prior to the grafting on silica NPs. UV–vis spectroscopy is used to test the stability of dye grafted silica NPs. The fluorescent dye grafted silica NPs are quite stable in aqueous solution. Also, a new type of dual dye-doped hybrid silica nanoparticles has been developed. The combination of microscopic and spectroscopic techniques shows that the synthesis parameters have significant effects on the particle shape and size and is tuneable from a few nanometers to a few hundred nanometers. The ability to create size controlled nanoparticles with associated (optical) functionality may have significant importance in bio-medical imaging

Defect chemistry and vacancy concentration of luminescent europium doped ceria nanoparticles by solvothermal method

Pure phase and europium-doped ceria nanocrystals have been synthesized by a single step simple solvothermal process. Different spectroscopic, diffractive, and microscopic techniques were used to determine the morphology, size, crystal structure, and phase of all the samples. Electron energy loss spectroscopy (EELS) for elemental mapping confirmed that good solid solutions were formed and that the particles had a homogeneous distribution of europium. The defect chemistry was more complex than might be expected with the incorporation of each Eu3+ ion resulting in the production of an anion vacancy since the doping results in charge compensating (i.e., for Eu3+) anion vacancies as well as vacancies due to oxygen removal from the crystallite surface. Variations in nanoparticles dimension and lattice parameters were measured as a function of dopant concentrations and their variations explained. The band gap of the samples could be tailored by the doping. The doped samples were found to be luminescent due to the substitution of Ce4+ ions in the cubic symmetric lattice by the dopant ions. The thermal stability of the fluorescence properties was also investigated

A positron annihilation spectroscopic investigation of europium-doped cerium oxide nanoparticles

Doping in ceria (CeO2) nanoparticles with europium (Eu) of varying concentrations (0, 0.1, 0.5, …, 50 atom%) is studied using complementary experimental techniques and novel observations were made during the investigation. The immediate observable effect was a distinct reduction in particle sizes with increasing Eu concentration attributed to the relaxation of strain introduced due to the replacement of Ce4+ ions by Eu3+ ions of larger radius. However, this general trend was reversed in the doping concentration range of 0.1–1 atom% due to the reduction of Ce4+ to Ce3+ and the formation of anion vacancies. Quantum confinement effects became evident with the increase of band gap energy when the particle sizes reduced below 7–8 nm. Positron annihilation studies indicated the presence of vacancy type defects in the form of vacancy clusters within the nanoparticles. Some positron annihilation was also seen on the surface of crystallites as a result of diffusion of thermalized positrons before annihilation. Coincidence Doppler broadening measurements indicated the annihilation of positrons with electrons of different species of atoms and the characteristic S–W plot showed a kink-like feature at the particle sizes where quantum confinement effects began

Defect Chemistry and Vacancy Concentration of Luminescent Europium Doped Ceria Nanoparticles by the Solvothermal Method

Pure phase and europium-doped ceria nanocrystals have been synthesized by a single step simple solvothermal process. Different spectroscopic, diffractive, and microscopic techniques were used to determine the morphology, size, crystal structure, and phase of all the samples. Electron energy loss spectroscopy (EELS) for elemental mapping confirmed that good solid solutions were formed and that the particles had a homogeneous distribution of europium. The defect chemistry was more complex than might be expected with the incorporation of each Eu³⁺ ion resulting in the production of an anion vacancy since the doping results in charge compensating (i.e., for Eu³⁺) anion vacancies as well as vacancies due to oxygen removal from the crystallite surface. Variations in nanoparticles dimension and lattice parameters were measured as a function of dopant concentrations and their variations explained. The band gap of the samples could be tailored by the doping. The doped samples were found to be luminescent due to the substitution of Ce⁴⁺ ions in the cubic symmetric lattice by the dopant ions. The thermal stability of the fluorescence properties was also investigated