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Yes / Coprecipitation method was used to prepare non-stoichiometric pristine copper and iron layered double hydroxide (LDH) doped with zirconium and embedded with reduced graphene oxide. The composite materials (ZrRGOCuFe LDHs) were studied for the photodegradation of methylene blue (MB) dye as a model contaminant from an aqueous solution. These composites were fully characterized by X-rays diffraction (XRD), Scanning electron microscopy (SEM), Energy Dispersive X-ray Spectroscopy (EDX), Fourier transform infrared spectroscopy (FTIR), Photoluminescence (PL), Raman spectroscopy and Electrochemical Impedance Spectroscopy (EIS). The results of Raman, Photoluminescence and Electrochemical Impedance Spectroscopy revealed the presence of oxygen defects level in the composites. Such defects are believed to be essential for boosting the catalytic potential of the composites. The secondary pollution manifested by transition metal ions is usually tackled by inducing heterogeneous catalysis. Herein, pristine CuFe LDH has been doped with Zr and RGO moieties to realize heterogeneous catalysis within ZrRGOCuFe LDH dopants. An admirable band ranging between 1.74 and 2.0 eV was obtained for the doped materials. The remarkable photodegradation efficiency of 95.2% was achieved by using heterogeneous photocatlyst Zr0.6RGOCuFe LDH within 75 min at a pH of 7, photocatalyst dosage of 1.0 g/L and methylene blue dye solution of 10 ppm under visible light irradiation. The total organic content (TOC) analysis has revealed removal of 92% organic content. Moreover, the catalyst has the potentia to maitain sufficient stability and reusability capacity even after three successive cycles. The reaction kinetics and proposed photocatalytic mechanism were also explained in detail.

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Les processus photocatalytiques à la surface d’oxydes métalliques semi-conducteurs font l’objet d’intensesrecherches au niveau mondial car ils constituent des alternatives efficaces, respectueuses de l’environnement etpeu coûteuses aux méthodes conventionnelles dans les domaines de la purification de l’eau et de l’air, et de laproduction « verte » d’hydrogène. Cependant, certaines limitations pour atteindre des efficacitésphotocatalytiques élevées ont été mises en évidence avec les matériaux semiconducteurs classiques du fait de larecombinaison rapide des porteurs de charge générés par illumination. Le développement de photocatalyseurs àbase d’héterostuctures obtenues par dépôt de métaux à la surface de matériaux semiconducteurs ou parassociation de deux semiconducteurs possédant des bandes d’énergie bien positionnées devrait permettre delimiter ces phénomènes de recombinaison via un transfert de charge vectoriel. Dans ce contexte, trois typesd’hétérostructures telles que des nanomatériaux à base d’hétérojonction semiconducteur n/semiconducteur n(SnO2/ZnO), metal/semiconducteur n (RuO2/TiO2 and RuO2/ZnO) et semiconducteur p/semiconducteur n(NiO/TiO2) ont été synthétisées avec succès par différentes voies liquides. Leur composition, leur texture, leurstructure et leur morphologie ont été caractérisées par spectroscopies FTIR et Raman, par diffraction des rayonsX, microscopie électronique en transmission (MET) et porosimétrie de sorption d’azote. Par ailleurs, unecombinaison judicieuse des données issues de mesures effectuées par spectroscopie UV-visible en réflexiondiffuse (DRS) et par spectroscopies de photoélectrons X (XPS) et UV (UPS) a permis de déterminer lediagramme d’énergie des bandes pour chaque système étudié. Les catalyseurs ainsi obtenus ont conduit à desefficacités photocatalytiques plus élevées qu’avec le dioxyde de titane P25 pour la dégradation de colorantsorganiques (bleu de méthylène, l’orangé de méthyle) et la production d’hydrogène. En particulier, lesnanocomposites RuO2/TiO2 et NiO/TiO2 contenant une quantité optimale de RuO2 (5 % en masse) et de NiO(1% en masse), respectivement, ont conduit aux efficacités photocatalytiques les plus importantes pour laproduction d’hydrogène. Ces excellentes performances photocatalytiques ont été interprétées en termesd’alignement adéquat des bandes d’énergies des matériaux associé à des propriétés texturales et structuralesfavorables. Ce concept de photocatalyseurs à base d’hétérojonctions semiconductrices d’activité élevée devrait àl’avenir trouver des débouchés industriels dans les domaines de l’élimination de l’environnement de composésorganiques indésirables et de la production « verte » d’hydrogène. / Photocatalytic processes over semiconducting oxide surfaces have attracted worldwide attention aspotentially efficient, environmentally friendly and low cost methods for water/air purification as well as forrenewable hydrogen production. However, some limitations to achieve high photocatalytic efficiencies havebeen found due to the fast recombination of the charge carriers. Development of heterostucture photocatalystsby depositing metals on the surface of semiconductors or by coupling two semiconductors with suitable bandedge position can reduce recombination phenomena by vectorial transfer of charge carriers. To draw newprospects in this domain, three different kinds of heterostructures such as n-type/n-type semiconductor(SnO2/ZnO), metal/n-type semiconductor (RuO2/TiO2 and RuO2/ZnO) and p-type/n-type semiconductor(NiO/TiO2) heterojunction nanomaterials were successfully prepared by solution process. Their composition,texture, structure and morphology were thoroughly characterized by FTIR, X-ray diffraction (XRD), Ramanspectroscopy, transmission electron microscopy (TEM) and N2 sorption measurements. On the other hand, asuitable combination of UV–visible diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy(XPS) and ultraviolet photoemission spectroscopy (UPS) data provided the energy band diagram for eachsystem. The as-prepared heterojunction photocatalysts showed higher photocatalytic efficiency than P25 TiO2for the degradation of organic dyes (i.e. methylene blue and methyl orange) and the production of hydrogen.Particularly, heterostructure RuO2/TiO2 and NiO/TiO2 nanocomposites with optimum loading of RuO2 (5 wt %)and NiO (1 wt %), respectively, yielded the highest photocatalytic activities for the production of hydrogen.These enhanced performances were rationalized in terms of suitable band alignment as evidenced by XPS/UPSmeasurements along with their good textural and structural properties. This concept of semiconductingheterojunction nanocatalysts with high photocatlytic activity should find industrial application in the future toremove undesirable organics from the environment and to produce renewable hydrogen.

M. Tech. (Department of Chemical Engineering, Faculty of Engineering and Technology), Vaal University of Technology / Water pollution caused by organic and inorganic contaminants represents an important ecological and health hazard. Simultaneous treatment of organic and inorganic contaminants had gradually gained great scientific interest. Advanced oxidation processes such as photocatalysis, using TiO2 as a photocatalyst, have been shown to be very robust in the removal of biorecalcitrant pollutants. These methods offer the advantage of removing the pollutants, in contrast to conventional techniques. At present, the main technical challenge that hinder its commercialization remained on the post-recovery of the photocatalyst particles after water treatment. Supporting of the photocatalyst on the adsorbent surface is important as it assists during the filtration step, reducing losses of the materials and yielding better results in degrading pollutants. To overcome this challenge, in this study composite photocatalysts of TiO2/zeolite and TiO2/silica were prepared and investigated to explore the possible application in the simultaneous removal of organic and inorganic compounds from contaminated water. The main objective of this study was to investigate the heterogeneous photocatalytic degradation of organic compounds in the presence of metal ions using composite photocatalysts. The Brunauer–Emmett–Teller (BET), Scanning Electron Microscopy and Energy Dispersive X-ray (SEM-EDX), Raman spectroscopy (RS) and zeta potential (ZP) analyses were used to characterize the prepared composite photocatalysts. The successive composite photocatalysts were used in a semi-batch reactor under an irradiation intensity of 5.5 mW/m2 (protected by a quartz sleeve) at 25 ± 3°C for the photocatalytic degradation of synthetic textile (methyl orange) and agricultural (atrazine) wastewater in the presence of ions. The effect of operating parameters such as TiO2 composition on supporting material, particle size, composite photocatalyst loading, initial pollutant concentration and pH were optimized. The effects of inorganic salts and humic acid on dye and pesticides degradation were also studied, respectively. The performance of the photocatalyst reactor was evaluated on the basis of color removal, metal ion reduction, total organic carbon (TOC) reduction, intermediates product analysis and modeling of kinetics and isotherms. Different kinetic and isotherm models were introduced and applied in this work. Important aspects such as error functions with the optimal magnitude were used for the selection of the best suitable model. / European Union. City of Mikkeli, Finland. Water Research Commission (RSA)

Photocatalytic processes over semiconducting oxide surfaces have attracted worldwide attention aspotentially efficient, environmentally friendly and low cost methods for water/air purification as well as forrenewable hydrogen production. However, some limitations to achieve high photocatalytic efficiencies havebeen found due to the fast recombination of the charge carriers. Development of heterostucture photocatalystsby depositing metals on the surface of semiconductors or by coupling two semiconductors with suitable bandedge position can reduce recombination phenomena by vectorial transfer of charge carriers. To draw newprospects in this domain, three different kinds of heterostructures such as n-type/n-type semiconductor(SnO2/ZnO), metal/n-type semiconductor (RuO2/TiO2 and RuO2/ZnO) and p-type/n-type semiconductor(NiO/TiO2) heterojunction nanomaterials were successfully prepared by solution process. Their composition,texture, structure and morphology were thoroughly characterized by FTIR, X-ray diffraction (XRD), Ramanspectroscopy, transmission electron microscopy (TEM) and N2 sorption measurements. On the other hand, asuitable combination of UV-visible diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy(XPS) and ultraviolet photoemission spectroscopy (UPS) data provided the energy band diagram for eachsystem. The as-prepared heterojunction photocatalysts showed higher photocatalytic efficiency than P25 TiO2for the degradation of organic dyes (i.e. methylene blue and methyl orange) and the production of hydrogen.Particularly, heterostructure RuO2/TiO2 and NiO/TiO2 nanocomposites with optimum loading of RuO2 (5 wt %)and NiO (1 wt %), respectively, yielded the highest photocatalytic activities for the production of hydrogen.These enhanced performances were rationalized in terms of suitable band alignment as evidenced by XPS/UPSmeasurements along with their good textural and structural properties. This concept of semiconductingheterojunction nanocatalysts with high photocatlytic activity should find industrial application in the future toremove undesirable organics from the environment and to produce renewable hydrogen.

Water pollution has become an environmental catastrophe due to the rapid urbanization. The treatment of dumping of waste chemicals in water bodies has contributed to the increase in pollution. In addition to the pollution caused by waste chemicals, faecal bacteria such as Escherichia, Staphylococcus, Pseudomonas etc., can cause serious health issues. Techniques such as filtration and chlorination provide clean water but are associated with disadvantages such as toxic by-products. Although clean water can be still obtained by these techniques, the development of resistance by microorganisms with such conventional treatments of antibiotics is inevitable and poses a new threat. Various researches have taken place in the past few decades to provide clean drinking water. Photocatalysis is considered to be a promising viable alternative for the existing methods to solve the menace of water pollution. It is an advanced oxidation process where the reactive oxygen species are generated by using nanomaterials that can cause degradation of chemicals and pathogens. Particularly, photocatalysis using semiconductors and their composites have been tested for their use in the destruction of contaminants. Several methods have been used in the synthesis of nanomaterials and the variations in their morphologies have resulted in different applications such as photocatalysis and electrocatalysis. Among all semiconductors, TiO2 has been widely used in this application owing to their non-toxicity and abundance in availability. However, TiO2 can be activated only in the presence of UV light. Therefore, the formation of heterojunctions, doping of metals/no- metals in TiO2 has enabled the activation of TiO2 in the visible region. The former approach has also been studied with ceria and silver salts combination. Besides conventional metal oxides, other transitional metal oxides such as copper oxide and bismuth oxide have also been studied owing to its conducting property and facile growth on substrates respectively for enhanced photocatalysis. All the above tweaking has enabled efficient charge separation, band gap reduction, and prevention of recombination. In this thesis, all the nanomaterials and their composites have been synthesized using simple methods such as solution combustion, hydrothermal, solution co-precipitation, and chemical deposition. The primary aim of this thesis is to synthesize various effective nanomaterials with different morphologies, bandgap engineered nanocomposites, metal or non-metal doped metal oxides for efficient waste water treatment of dyes, antibiotics, phenols, and bacteria. Besides, relying on photocatalytic ability, the photoconductivity and intrinsic conducting properties of nanomaterials were exploited to perform photoelectrocatalysis that enhances the rate of decontamination to several orders than photocatalysis. In addition to focusing on increasing the rate of degradation, the main drawback of photocatalysis which is catalyst retrieval has been overcome using conducting substrates and nanomaterial coated substrates for efficient photocatalytic and photoelectrocatalytic decontamination of waste water. All the structural, morphological, chemical and optical properties were thoroughly studied using various characterization techniques such as XRD, SEM, TEM, XPS, UV-DRS, PL respectively. The rate kinetics of dye, antibiotic and phenol degradation was examined. Experimental data was tested with the proposed model in the case of photoelectrocatalytic degradation. The photocatalysts were also studied for its reusability for many cycles. All the proposed works have analyzed the reason for the enhanced activity by performing scavenger reactions to determine the responsible reactive oxygen species. Thus, this thesis exhibits a thorough understanding of how to design and engineer nanomaterials for photocatalytic and photoelectrocatalytic water remediation. The following are the chapters discussed in this thesis. Chapter 1 discusses the drawbacks associated with the current waste water treatment methods and the possibilities of photocatalysis to replace the existing treatments. The advantages of certain transition metals, conventional methods of synthesis and various other properties of the nanomaterials have been discussed. Chapter 2 explains the synthesis of TiO2 nanobelts using combustion synthesized TiO2 under UV and solar irradiation. The catalyst has been characterized for its structural, morphological, chemical and optical properties. The degradation of anionic and cationic dyes and their activity against E.coli bacteria have been evaluated. The efficiency of this catalyst has been compared with commercial Degussa P25. This study shows the morphological influence of nanomaterials on photocatalytic activity. Chapter 3 describes the synthesis of Ag3PO4 impregnated combustion synthesized TiO2 nanobelts using co-precipitation technique. The activity of this material has been studied under solar light. The catalyst has been characterized for its structural, morphological, chemical and optical properties. Similar to the previous chapter, the degradation of dyes and the antibacterial activity of this catalyst has been compared with commercial Degussa P25. This study explains the importance of morphology and charge carrier facilitation in the case of heterojunction formation. Chapter 4 explains the synthesis of ceria nanoflakes by solution combustion method using ascorbic acid as fuel and PEG assisted sonochemical method. The catalyst has been characterized for its structural, morphological, chemical and optical properties. The effect of silver salts such as AgBr on ceria/Ag3PO4 under visible region for degradation of dyes and antibacterial activity has been evaluated. This work elucidates the effect of band engineering in the charge carrier dynamics between interfaces of components within the catalysts. Chapter 5 elucidates the synthesis of vanadium, nitrogen co doped TiO2 catalysts for the simultaneous degradation of microbes and antibiotics. The primary aim of this work is to understand whether interstitial or substituted doped nitrogen will be effective in the presence of vanadium. The photoactivity of this novel catalyst was studied for its synergistic degradation of antibiotics and bacteria simultaneously towards the prevention of microbial resistance towards antibiotics. Chloramphenicol and E.coli were subjected to photodegradation under visible light. Chapter 6 explains the synthesis of copper oxide based nanomaterial for antibiotic and bacterial degradation by photoelectrocatalysis. In order to enhance the rate of photodegradation, photocatalysis has been upgraded with the application of a potential to photocatalytic systems that possess better charge conducting capability. Highly network like copper oxide has been synthesized using conventional combustion synthesis method and compared with copper oxide nanorods synthesized by hydrothermal method. The rate kinetics of photocatalytic and photoelectrocatalytic degradation of antibiotics has been examined thoroughly and validated based on a cyclic network model. This work demonstrates the synergistic rate enhancing capacity upon combining photocatalysis and electrocatalysis. Chapter 7 discusses the fabrication of Cu/CuO/FTO (fluorine doped tin oxide) based substrates for bacterial degradation. Considering the difficulties in photocatalyst retrieval processes and realizing the importance of electrocatalysis, conducting substrates such as Cu strip, FTO were subjected to antibacterial treatment. Formation of copper oxide onto copper strip during the course of reaction forced us to develop CuO/Cu and CuO/FTO interfaces to examine the photocatalytic and photoelectrocatalytic killing of E.coli. Chapter 8 investigates the fabrication of Bi2O3/Ag based material for photocatalytic and photoelectrocatalytic degradation for phenols and substituted phenols. This work starts with fabrication of Bi2O3 working electrodes by chemical deposition. Photodegradation experiments were conducted under UV irradiation and enhancement of the rate of degradation was observed when the working electrode was deposited with silver nanoparticles via chemical reduction method. Formation of the intermediate Bi(OH)x on Bi2O3 or Bi2O3/Ag has resulted in better hydroxyl radical generation upon excitation. Similarly, surface plasmon resonance due to silver nanoparticles was found to be responsible for augmentation in degradation efficiency of phenol. Chapter 9 briefly summarizes the work and provides future directions. The research work thus attempts to design and engineer photocatalytic nanomaterials that are better than the existing materials and emphasizes the importance towards water remediation.