This research mainly includes two parts. First, monodispersed silica spheres with diameter about 58 and 73 nm were successfully synthesized. The tablet-like silica template could be made using a stainless steel mold by pressing the mold with a pressure ~ 10 MPa. The advantage of this molding process is it takes only a short time to accomplish the total fabrication. Second, infiltration of the carbon precursor was done using the monomers resorcinol (R) and furfural (F) in the interval of tablet-like silica template, and then polymerization and drying. It was subsequently carbonized in N2 atmosphere at 800 ¢J and then the silica template was removed by 20 wt % HF solution. The activated porous carbon material has larger specific surface area than the traditional powder carbon material. The chemical activation process by KOH plays a vital role in raising the specific surface area, since the KOH would etch the carbon pore surface to produce a large number of micropores (diameter < 2 nm), forming a macro-micro or meso-micro porous carbon materials. The F/R molar ratios for polymerization between 2.0 to 3.0 were applied and the carbon yields of these resins were higher than 51% in this range. An F/R ratio below 2.0 or 3.0 gave a lower carbon yield when carbonization at 800 ¢J. X-ray diffraction analyses on the macroporous carbon materials indicate a semi-crystalline structure which belong to the hexagonal crystal system with (002) d-spacing of = 0.373 nm, which is larger than the 0.339 nm of graphite. In Raman spectra analysis, the integral area of D-peak (ID) and G-peak (IG) is an index to define the degree of graphitization. The ratios ID/IG of lie between 1.7 - 1.8, which are larger than that of graphite (ID/IG = 0.1 - 0.3), so the FR series macroporous carbon is mostly amorphous and is far from highly crystallized structure. The un-activated macroporous carbon materials has open pore structure, the pore diameter is 56 nm which is classified to the macroporous scale. The nitrogen adsorption/desorption isotherm of the porous carbon materials belongs to the type IV, with H1 type hysteresis. The BET results show that the specific surface area increases with increasing KOH concentration; whereas the open pore structure remain the same. SEM observations reveal the pore structure doesn¡¦t collapse but the pore wall does become thinner. From this work, macroporous carbon materials with total pore volume as high as 2.23 cm3/g and the specific surface area as high as 658 m2/g have successfully been synthesized. Activation by KOH creates more micropores on its carbon walls, resulting in a macro-microporous carbon material having two scales of pores in the same time and with a high surface area of 1404 m2/g.

During the synthesis of well arrayed nano/micro structures through wet chemical methods, plenty of parameters are usually involved. Consequently, it is extremely time- and cost-consuming to find out the optimized synthesis conditions by using the conventional "changing one separate factor at a time" (COST) strategy. Instead, the "statistical experimental design" method has been proven in a few works to be an efficient method for experiments involving many parameters.  With this method, the responses could be optimized efficiently by using only a few experiments. Besides, several responses can be optimized simultaneously. Also, models could be built up and the changing tendency can be plotted to predict the required experimental settings for specific tasks. Two types of well arrayed structures including monolayer arrays of silica spheres and vertically aligned ZnO rod arrays were investigated in this work. Monolayer arrays of silica spheres were synthesized by using a dual-speed spin coating method. With assistance of statistical experimental design, the accelerating rate, the second rotation speed and time of the dual-speed spin coating system were found as non-significant parameters to the ordering degree of the obtained monolayer, and thus they can be fixed. This finding could remarkably increase the feasibility of optimizing the practical process. On the other hand, the relative humidity, the first rotation speed and the suspension concentration are identified as the significant parameters to the structures of the monolayer. Moreover, the optimal values for these three parameters were identified: 23% for the relative humidity, 1000 rpm for the first rotation speed and 30 wt.% for the suspension concentration. With these optimized parameters, the area of the obtained silica sphere monolayers reached over 1 cm2 and the defect-free domain size reached over 4000 μm2. These values are considerably higher compared to the previously reported values. Vertically aligned ZnO rod arrays were fabricated by chemical bath deposition. Parameters including precursor concentration, pH value, reaction temperature, reaction time and addition of capping agent were optimized by using statistical experimental design to improve and optimize the growth quality of ZnO rod arrays. Through several stages of optimization, the growth quality of the obtained structures was remarkably enhanced from sparse or clustered ZnO rods to upright and dense ZnO rods. The boundary conditions to achieve vertically aligned ZnO rods, such as a neutral solution and a precursor concentration over 0.02M, were determined. The changing tendency of the texture coefficient and aspect ratio with the factors was also plotted to predict the required experimental settings for specific requests. The points or regions to achieve the optimal properties were identified as well. For instance, the concentration should be as close as to 0.1 M, while the reaction temperature should be limited to 80-90 ◦C, to achieve the ideal preferential growth. With the optimized parameters, the texture coefficient reached almost the perfect value 1, and the aspect ratio was elevated to 21. Moreover, to obtain a dense ZnO thin film, tri-sodium citrate was added to the reaction system. The diameter was systematically controlled through varying the parameters. When both the diameter and the texture coefficient reached the optimal values, the rods were merged together to form a dense ZnO thin film. Furthermore, comments on the statistical experimental method are proposed, and both the advantages and disadvantages are presented according to the present thesis work. This might help the researchers to avoid the disadvantages and thus to employ this method more efficiently in the future. / <p>QC 20150903</p>

Effective light energy conversion into other forms of energy in metal and metal compound nanoparticles has been of great interest in past decades. Being illuminated by incident light, electrons in the nanoparticles can be excited to higher energy states followed by deposition of energy into other molecules around their surface and the lattices in the following relaxation process. Ultrafine nanoparticles are thus preferred in these processes due to their high specific surface areas. Moreover, the portion of excited electrons with higher energies is higher in smaller nanoparticles than in larger ones. However, the overall light power absorbed by nanoparticles is proportional to the square of particle size, which causes the ultrafine nanoparticles not to efficiently absorb the incident light, or to drive further chemical or physical processes.Light antennae materials are usually employed to enhance the light absorption of these ultrafine nanoparticles. Plasmonic nanoparticles, e.g., Ag, Au, Cu, and Al nanoparticles, enhance the light absorption of loaded nanoparticles mainly through strong electromagnetic fields generated near their surfaces and have been proven to be effective light antennae to benefit the light energy conversion of ultrafine nanoparticles. On the other hand, spherical dielectric particles, e.g., silicon dioxide nanospheres, represent a different type of light antennae with the advantages of low cost, simple synthesis, and negligible Ohmic loss when being illuminated. When the sizes of high geometric symmetry dielectric nanospheres are comparable with the wavelength of the incident light, Mie scattering can happen based on the difference in refractive index between the sphere and the surrounding medium, generating size-dependent scattering resonances at various wavelengths. At these wavelengths, strong electric fields can be created on the surface of dielectric spheres to enhance the light absorption of the nanoparticles loaded on the surface. Previous works have shown that silica nanospheres with a diameter of several hundreds of nanometers can effectively enhance the light absorption of ultrafine Pt nanoparticles and benefit photocatalytic reactions, e.g., selective oxidation of benzyl alcohol. Over the past few years, this concept has been broadened to other ultrafine nanoparticles to study their novel photo-to-chemical/physical properties. However, the availability and comprehensive understanding of the optical properties of this class of composite particles still need to be improved. These challenges limit the further development of these composite materials in new light energy conversion processes. This dissertation aims at studying this class of novel ultrafine nanoparticles/dielectric sphere composite particles synthesis and optical properties. In Chapter 2, a synthesis protocol of ultrafine ruthenium oxyhydroxide nanoparticles on the surface of silica nanospheres’ surfaces is introduced. Unlike the traditional synthesis of nanoparticles in solution followed by a loading process, the method developed in this chapter only requires the injection of aqueous ruthenium salt solution into a silica nanosphere dispersion. The obtained ultrafine nanoparticles with sizes of 2-3 nm are characterized to be ruthenium oxyhydroxide (RuOOH) nanoparticles. The silica nanospheres are crucial in stabilizing these ultrafine RuOOH nanoparticles and enhancing their light absorption. Due to the presence of ruthenium-oxygen bonds in the nanoparticles, the absorbed photons are converted to heat and transferred to the surrounding media with a photo-to-thermal conversion efficiency close to the unity. Experimental results have shown that heat can be effectively used in accelerating the reaction rate of selective oxidation of benzyl alcohol by molecular oxygen. Kinetics data also have shown that these ultrafine RuOOH nanoparticles are able to activate molecular oxygen adsorbed on their surfaces, which represents a novel property of these ultrafine RuOOH nanoparticles that is not observed in other traditional ruthenium catalysts. In Chapter 3, a more general synthesis method of ultrafine metal and metal oxyhydroxide nanoparticles on silica nanospheres is developed, inspired by the synthetic route in Chapter 2. Instead of functionalizing silica surfaces with silane agents with amino groups, the silica surfaces are selectively etched by an aqueous base to create a high density of surface hydroxyl groups. These hydroxyl groups can provide basic sites to stabilize metal ions in aqueous dispersion, which are nuclei for the further growth of larger metal oxyhydroxide nanoparticles. In this chapter, more than ten kinds of metal ions are loaded onto silica spheres, forming oxyhydroxide nanoparticles with average sizes below 5 nm. Some oxyhydroxide nanoparticles can be reduced by 5% H2/N2 to form metal nanoparticles with their ultrafine sizes maintained. The synthesis protocol is promising in preparation of bimetallic samples. The composition and optical absorption of all obtained composite particles are analyzed, demonstrating the practicability of utilizing the reported method to prepare high-quality light-absorbing composite particles. In Chapter 4, the optical absorption property of the composite particle is systematically studied. Using ultrafine Pt nanoparticles as the light absorbing material, the light absorptions of composite particles consisting of silica spheres with diameters from 100 to 1100 nm loaded with these Pt nanoparticles are studied. Through the combination of theoretical calculation based on Mie theory and the measured optical absorption spectra, the scattering resonance peaks are successfully located in each sample. It is also found that the photonic crystal effect and the general absorption of Pt nanoparticles can contribute to the light absorption spectra, especially at higher wavelengths. The relationship between the general absorption of Pt nanoparticles and the packing density of the powder is further studied. The successful deconvolution of several components in the absorption spectra can guide the further rational design of composite particles in optical-related applications. In Chapter 5, the composite particle system is further broadened to using high refractive index zinc sulfide nanospheres as a light antenna. The use of a higher refractive index light antenna is promising for obtaining higher light absorption enhancement in loaded ultrafine nanoparticles, even though the sample is dispersed in organic media with a high refractive index as well. After the successful loading of Pt nanoparticles to the surface of silica-coated zinc sulfide nanospheres, a protocol for analyzing their light absorption spectra in organic media is proposed. Size-dependent scattering resonance peaks are observed in bare zinc sulfide nanospheres and can be utilized to enhance the light absorption of Pt nanoparticles, even when the sample is sealed in high refractive index polymeric matrices. The composite particles are further employed in photothermal tests, the results prove that the better light absorption enhancement using zinc sulfide than silica nanospheres. The results introduced in this dissertation represent the first systematic and comprehensive study of ultrafine metal and metal oxyhydroxide nanoparticles loaded on the surface of dielectric light antenna particles. The conclusions open an avenue to further rational design of high-performance light-absorbing composite particles to be used in photo-to-thermal/chemical processes. / Chemistry

No / Cd3P2 quantum dots (QDs) have been synthesized in both aqueous and high boiling point surfactant solutions via a gas-bubbling method. The synthesized QDs exhibit photoluminescent wavelengths spanning across the visible red to the near-infrared (NIR) spectral region. Two types of shell materials, SiO2 nanobeads and PS micro-spheres, have been employed to encapsulate the Cd3P2 QDs which provide protecting layers against physiological solutions. The coating layers are proven to enhance the optical and chemical stability of Cd3P2 QDs, and make the fluorescent particles capable of sustaining long-term photo-oxidation. To demonstrate the applicability of the bio-labelling, the fluorescent composite particles (PS@QDs, SiO2@QDs) were injected into a culture medium of colorectal carcinoma (LoVo) cells. The results demonstrated that the PS@QDs exhibited a brighter fluorescence, but the SiO2@QDs provided a better photostability which consequently led to long-term cancer cell detection as well as a much lower release of toxic Cd2+ into the PBS solutions.