Semiconductor photocatalysis has received extensive attention due to its wide applications in water and indoor air purification, solar fuel production, etc. Charge carrier separation is a crucial step in semiconductor photocatalysis and influences the overall efficiency. It has been demonstrated that internal depolarisiation field of ferroelectric materials can drive spatial separation of charge carriers, which results in spatial separation of reduction and oxidation reactions, and improved charge carrier separation. In this thesis, ferroelectric barium titanate was chosen and its photocatalytic performance in decolourisation of organic dye molecules was investigated. Photodeposition method was adopted to deposite silver nanoparticles on the surface of barium titanate. Silver modified barium titanate showed increased photodecolourisation rate compared with bare barium titanate due to its role of electron traps and hindered charge carrier recombination. A simple thermal treatment was used to alter the phase composition of the as-received barium titanate. Samples which contained more ferroelectric tetragonal phase were found to possess higher photocatalytic activity compared with non-ferroelectric samples. This was associated with stronger ferroelectricity after thermal treatment, which enhanced dye molecule adsorption and aid charge carrier separation. The mechanism and intermediates generated in photodegradation of Rhodamine B with silver modified ferroelectric barium titanate were studied. Cleavage of chromophore was demonstrated to dominate in the initial process. Benzoic acid was identified as the main intermediate and no siginificant discrepancy in intermediates distribution between ferroelectric photocatalytic system and non-ferroelectric system was observed. The influence of ferroelectric dipole of barium titanate on photocatalytic activity of heterostructured barium titanate/hematite was also studied. The synthesised heterostructured barium titanate/hematite showed higher photodcolourisation rate than both barium titanate and hematite. This phenomenon was attributed to the improved charge carrier separation and extended charge carrier lifetime arising from heterojunction and an interaction between the ferroelectric dipole and the carriers in the hematite.

Maintaining a constant supply of clean drinking water is among the most pressing global challenges in our time. About one-third of the population is affected by the water scarcity and it can only get worse with climate change, rapid industrialization, and the population growth. Even though nearly 70 percent of the planet is covered by water, the consumable freshwater content is only 2.5 percent of it. Unfortunately, the accessible portion of it is only 1 percent. Even so, most of the freshwater bodies are choked with pollution. Considering the vast availability of saline water on the planet and the increasing wastewater generation, seawater desalination, and wastewater treatment and recycling seem to have the potential to address current water-related issues. Therefore, it is necessary to find efficient techniques for seawater desalination and wastewater treatment. The use of nanostructured materials for these applications is becoming a popular approach due to the unique chemical and physical properties they possess compared to bulk materials Solar energy is the cleanest and most abundant renewable natural resource available. Materials for solar photothermal energy conversion are highly sought after for their cost savings, clean environment, and broad utility in providing water heating and/or steam for many applications including domestic water heating and solar-driven desalination. Extensive research efforts have been made to develop efficient solar absorbers with characteristics such as low weight, low thermal conductivity, broad solar absorption and porosity to be able to float on water to provide more efficient and cost-effective solar steam generation systems. Metal NPs have been proposed to take advantage of the high efficiency of the photothermal energy conversion associated with surface plasmon resonance absorption. Nanostructured carbon-based materials such as graphene oxide, carbon nanotubes, carbonized biomass are also in use due to their excellent photothermal energy conversion ability over the range of the visible and near infra-red region of the electromagnetic spectrum. In this dissertation, five projects based on the utility of nanostructured materials for desalination, photocatalysis and water treatment will be discussed. The first three projects involve the fabrication and design of plasmonic and carbon-based photothermal materials for applications in solar steam generation, water desalination, and wastewater treatment. In the fourth project, a unique shape of ZnO nanostructure was synthesized for photodegradation of organic dyes in industrial wastewater. The final project demonstrates the shape-controlled synthesis of iron carbide nanostructures and composite materials of aminated graphene oxide for the removal of Cr(VI) from wastewater.

Water pollution is a major concern in vast countries such as India and other developing nations. Several methods of water purification have been practiced since many decades, Semiconductor photocatalysis is a promising technique, for photodegradation of various hazardous chemicals that are encountered in waste waters. The great significance of this technique is that, it can degrade (detoxify) various complex organic chemicals, which has not been addressed by several other methods of purification. This unique advantage made this field of research to attract many investigators particularly in latter eighties and after. This thesis incorporates the studies on the various semiconductor photocatalysts that have been employed for the detoxification purposes. The fundamental principles involved in the photoelectrochemistry, reactions at the interface (solid - liquid or solid - gas) and photocatalytic reactions on fine particles are briefed. General nature and size quantization in semiconductor particles, photocatalytically active semiconductors, TiCh and ABO3 systems, chemical systems and modifications for solar energy conversions are brought out in the introduction chapter besides giving brief description about photocatalytic mineralization of water pollutants with mechanism involved, formation of reactive species and the factors influencing photomineralization reactions. Scope of the present work is given at the end of the first chapter. Second chapter deals with the materials used for the preparation of photocatalyst, preparative techniques, methods of analysis, instruments employed for the photodegradation experiments and a brief description of material characterization methods such as X-ray diffraction, transmission electron microscopy, thermogravimetric analysis, differential thermal analysis, optical absorption spectro photometry, Electron paramagnetic resonance (EPR), and gas chromatograph - mass spectroscopy (GC - MS). Various preparative routes such as wet chemical and hydrothermal methods for obtaining TiO2 (both rutile and anatase forms), BaTiOs and SrTiO3 fine particles and the chemical analysis of their constituents have been described in brief. Third chapter presents the results of materials characterization. T1O2 (rutile and anatase), BaTiO3 and SrTiO3 have been characterized separately using various techniques. Different routes of obtaining the photocatalyst fine particles, heat treatment at various temperature ranges, experimental procedures and the results of characterization are brought out in this chapter. Fourth and fifth chapters present the details of degradation studies carried out on the photomineralization of chlorophenol, trichloroethylene and formaldehyde. Studies include photodegradation of the pollutants with different catalysts varying experimental conditions to check the effects of change in concentration of pollutants, oxidizer, pH, surface hydroxylation, etc. The most favorable conditions for the complete mineralization of the pollutants have been studied. In case of TiO2, anatase form has shown greater photoactivity when compared to rutile and complete mineralization of chlorophenols has been achieved at low pollutant concentrations, neutral pH, with H2O2 and UV illumination. Retarding effects of surface hydroxylation and the formation of peroxotitanium species during photodegradation have been presented. TCE and HCHO degradation with BaTiO3/SrTiO3 has been studied. Photocatalyst heat-treated at 1100°G-1300°C is found to be highly active in combination with H2O2 as electron scavenger. HCHO is not getting degraded to its completeness in aqueous conditions owing to the strong competition in surface adsorption posed by H2O molecules. Vapour-solid phase reaction however gave good results in the detoxification of HCHO via disproportionation. Summary and conclusions are given at the end of the thesis.

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This thesis reports the successful rational design of three highly active photocatalytic semiconductor nanocrystal (SNC) systems by exploiting morphology effects and the electronic properties of type II semiconductor heterojunctions. Novel architectures of colloidal SNCs are produced with the aim of suppressing exciton recombination and improving charge extraction for the successful initiation of desirable redox chemistry. Rod-shaped niobium pentoxide Nb₂O₅ nanocrystals (NCs) are shown to exhibit significantly enhanced activity (10-fold increase in rate constant) relative to spherical-shaped NCs of the same material. The increase is attributed to Nb5⁺ Lewis acid site rich (001) surfaces, present in higher proportions in the rod morphology, which bind organic substrates from solution resulting in direct interaction with photogenerated charges on the surface of the NC. Building on the insights into morphology-activity dependence, type II semiconductor heterojunctions are exploited for their ability to increase exciton lifetimes and spatially separate charges. Two novel II-VI heterostructured semiconductor nanocrystals (HSNCs) systems are investigated: a series of CdX/ZnO (X = S, Se, Te) HSNCs and ZnS/ZnO HSNCs capped with two different surface ligands. In the first case, substantial photocatalytic activity improvement is observed for HSNCs (relative to pure ZnO analogues) according to the following trend: CdTe/ZnO > CdS/ZnO > CdSe/ZnO. The observed trend is explained in terms of heterojunction structure and fundamental chalcogenide chemistry. In the second case, both ZnS/ZnO HSNCs exhibit activity enhancement over analogous pure ZnO, but the degree of enhancement is found to be a function of surface ligand chemistry. Photocatalytic activity testing of all the materials investigated in this work is performed via the photodecomposition of methylene blue dye in aerated aqueous conditions under UVA (350 nm) irradiation. The synthetic techniques employed for the synthesis of colloidal SNCs investigated in this thesis range from chemical precipitation and solvothermal techniques to several different organometallic approaches. A wide variety of analytical techniques are employed for the chemical, structural and optical characterisation of SNC photocatalysts including: XRD, XPS, TEM, UV-vis absorption, PL spectroscopy and FTIR. Atom Probe Tomography (APT) is employed for the first time in the structural characterisation of II-VI heterojunctions in colloidal HSNCs. Overall, this thesis provides a useful contribution to the growing body of knowledge pertaining to the enhancement of photocatalytic SNCs for useful applications including: solar energy conversion to chemical fuels, the photodecomposition of pollutants and light-driven synthetic chemistry.