In this dissertation, I have investigated applying the laser ablation of microparticle aerosol (LAMA) process to the production of nanocomposite polymer membranes for olefin/paraffin separation. Experimental results for three major thrusts are presented: 1) an investigation into the scalability of the LAMA process, 2) a new laser ablation technique for nanoparticle production from aqueous feedstocks, and 3) characterization of olefin-selective polymer nanocomposite membranes produced using LAMA. The propensity for Ag nanoparticles to form agglomerates in LAMA is investigated. Nanoparticle samples were collected on TEM grids at several feedstock aerosol densities. As the density increased, the particle morphology shifted from single nanoparticles 5 nm in diameter to chained agglomerates of 20 nm diameter primary particles. The results are in agreement with a numerical model of Brownian agglomeration and diffusion. Factors influencing nanoparticle morphology, such as temperature, initial nanoparticle charge, and feedstock aerosol density are discussed. It is shown that agglomeration occurs on a much longer timescale than the other processes, and can be treated independently. A new nanoparticle synthesis technique is presented: laser ablation of aqueous aerosols. A Collison nebulizer is used to generate a mist of ~10 [mu]m diameter water droplets containing dissolved transition metal salts. Water from the droplets quickly evaporates, leaving solid particles which are ablated by an excimer laser. Ablation results in plasma breakdown and photothermal decomposition of the feedstock material. For AgNO₃ ablated in He gas, metallic Ag nanoparticles were produced. For Cu(NO₃)₂ ablated in He gas, crystalline Cu₂O nanoparticles were produced. For Ni(NO₃)₂ ablated in He gas, crystalline NiO nanoparticles were produced. A combination of AgNO₃ and Cu(NO₃)₂ ablated in a reducing atmosphere of 10%H₂/He yielded nonequilibrium Ag-Cu alloy nanoparticles. Membranes composed of poly(ethylene glycol diacrylate) (PEGDA) and Ag nanoparticles were produced by the LAMA process. Permeation and sorption measurements for the light olefins and paraffins were conducted for these membranes. The membranes showed very little improvement in olefin/paraffin selectivity compared with neat PEGDA membranes. Using the LAMA implementation described here, it was impossible to produce membranes with high Ag loading. Whether membranes containing more Ag would exhibit improved selectivity remains an open question. / text

Nanotechnology has reached the status of the 21st century's leading science and technology based on fundamental and applied research during the last two decades. An important feature of nanotechnology is to bridge the crucial dimensional gap between the atomic and molecular fundamental sciences and microstructural scale of engineering. Accordingly, it is very important to have an in-depth understanding of the synthesis of nanomaterials for the use of state-of-the-art high technological devices with enhanced properties. Recently, the 'bottom-up' approach for the fabrication of nanomaterials has received a great deal of attention for its simplicity and cost effectiveness. Tailoring the various parameters during synthesis of selected nanoparticles can be used to fabricate technologically important components. During the last decade, carbon nanotubes (CNTs) have been envisioned for a host of different new applications. Although carbon nanotubes can be synthesized using a variety of techniques, large-scale synthesis is still a great challenge to the researchers. Three methods are commonly used for commercial and bulk productions of carbon nanotubes: arc-discharge, chemical vapor deposition and laser ablation. However, low-cost, large-scale production of high-quality carbon nanotubes is yet to be reported. One of the objectives of the present research is to develop a simplified synthesis method for the production of large-scale, low-cost carbon nanotubes with functionality. Herein, a unique, simple, inexpensive and one-step synthesis route of CNTs and CNTs decorated with nanoparticles is reported. The method is simple arc-discharge in solution (ADS). For this new method, a full-fledged optoelectronically controlled instrumen is reported here to achieve high efficiency and continuous bulk production of CNTs. In this system, a constant gap between the two electrodes is maintained using a photosensor which allows a continuous synthesis of the carbon nanostructures. The system operates in a feedback loop consisting of an electrode-gap detector and an analogue electronic unit, as controller. This computerized feed system was also used in single process step to produce in situ-decorated CNTs with a variety of industrially important nanoparticles. To name a few, we have successfully synthesized CNTs decorated with 3-4 nm ceria, silica and palladium nanoparticles for many industrially relevant applications. This process can be extended to synthesize decorated CNTs with other oxide and metallic nanoparticles. Sixty experimental runs were carried out for parametric analysis varying process parameters including voltage, current and precursors. The amount of yield with time, rate of erosion of the anode, and rate of deposition of carbonaceous materials on the cathode electrode were investigated. Normalized kinetic parameters were evaluated for different amperes from the sets of runs. The production rate of pristine CNT at 75 A is as high as 5.89 ± 0.28 g.min-1. In this study, major emphasis was given on the characterizations of CNTs with and without nanoparticles using various techniques for surface and bulk analysis of the nanostructures. The nanostructures were characterized using transmission electron microscopy, high resolution transmission electron microscopy, scanning transmission electron microscopy, energy dispersive spectroscopy and scanning electron microscopy, x-ray photo electron spectroscopy, x-ray diffraction studies, and surface area analysis. Electron microscopy investigations show that the CNTs, collected from the water and solutions, are highly pure except the presence of some amorphous carbon. Thermogravimetric analysis and chemical oxidation data of CNTs show the good agreement with electron microscopy analysis. The surface area analysis depicts very high surface area. For pristine multi-walled carbon nanotubes, the BET surface area is approximately 80 m2.g-1. X-ray diffraction studies on carbon nanotubes shows that the products are clean. Nano-sized palladium decorated carbon nanotubes are supposed to be very efficient for hydrogen storage. The synthesis for in-situ decoration of palladium nanoparticles on carbon nanotubes using the arc discharge in solution process has been extensively carried out for possible hydrogen storage applications and electronic device fabrication. Palladium nanoparticles were found to form during the reduction of palladium tetra-chloro-square planar complex. The formation of such a complex was investigated using ultraviolet-visible spectroscopic method. Pd-nanoparticles were simultaneously decorated on carbon nanotubes during the rolling of graphene sheets in the arc-discharge process. Zero-loss energy filtered transmission electron microscopy and scanning transmission electron microscopy confirm the presence of 3 nm palladium nanoparticles. The deconvoluted X-ray photoelectron spectroscopy envelope shows the presence of palladium. Surface area measurements using BET method show a surface area of 28 m2.g-1. The discrepancy with pristine CNTs can be explained considering the density of palladium (12023 kg.m-3). Energy dispersive spectroscopy suggests no functionalization of chlorine to the sidewall of carbon nanotubes. The presence of dislodged graphene sheets with wavy morphology as observed with high-resolution transmission electron microscopy supports the formation of CNTs through the 'scroll mechanism'.

No description available.

L’objectif de ce mémoire de maîtrise est de caractériser la distribution axiale des plasmas tubulaires à la pression atmosphérique créés et entretenus par une onde électromagnétique de surface ainsi que d’explorer le potentiel de ces sources pour la synthèse de matériaux et de nanomatériaux. Un précédent travail de thèse, qui avait pour objectif de déterminer les mécanismes à l’origine de la contraction radiale du plasma créé dans des gaz rares, a mis en lumière un phénomène jusque-là inconnu dans les plasmas d’onde de surface (POS). En effet, la distribution axiale varie différemment selon la puissance incidente ce qui constitue une différence majeure par rapport aux plasmas à pression réduite. Dans ce contexte, nous avons réalisé une étude paramétrique des POS à la pression atmosphérique dans l’Ar. À partir de nos mesures de densité électronique, de température d’excitation et de densité d’atomes d’Ar dans un niveau métastable (Ar 3P2), résolues axialement, nous avons conclu que le comportement axial de l’intensité lumineuse avec la puissance n’est pas lié à un changement de la cinétique de la décharge (qui est dépendante de la température des électrons et de la densité d’atomes d’Ar métastables), mais plutôt à une distribution anormale de dissipation de puissance dans le plasma (reliée à la densité d’électrons). Plus précisément, nos résultats suggèrent que ce dépôt anormal de puissance provient d’une réflexion de l’onde dans le fort gradient de densité de charges en fin de colonne, un effet plus marqué pour de faibles longueurs de colonnes à plasma. Ensuite, nous avons effectué une étude spectroscopique du plasma en présence de précurseurs organiques, en particulier le HMDSO pour la synthèse de matériaux organosiliciés et l’IPT pour la synthèse de matériaux organotitaniques. Les POS à la PA sont caractérisés par des densités de charges très élevées (>10^13 cm^-3), permettant ainsi d’atteindre des degrés de dissociation des précurseurs nettement plus élevés que ceux d'autres plasmas froids à la pression atmosphérique comme les décharges à barrière diélectrique. Dans de tels cas, les matériaux synthétisés prennent la forme de nanopoudres organiques de taille inférieure à 100 nm. En présence de faibles quantités d’oxygène dans le plasma, nous obtenons plutôt des nanopoudres à base d’oxyde de silicium (HMDSO) ou à base de titanate de silicium (IPT), avec très peu de carbone. / The purpose of this master thesis is to characterize the axial distribution of tubular discharges at atmospheric pressure sustained by electromagnetic surface wave and to explore their potential for materials and nanomaterials synthesis. A previous doctoral thesis, aimed at determining the mechanisms driving radial plasma contraction in rare gas discharges shed light on a yet unknown phenomenon occurring in surface wave discharges (SWD). As a matter of fact, increasing the power injected into the system leads to a change of the axial distribution of the discharge, in sharp contrast with the behavior commonly observed in reduced-pressure plasmas. In this context, we have performed a parametric investigation of atmospheric pressure SWD sustained in Ar gas. Based on our axially-resolved measurements of the electron density, excitation temperature, and number density of Ar atoms in metastable state (Ar 3P2), we found that the peculiar change of the axial distribution of the light intensity with power is not linked to a modification in the discharge kinetics (linked to the electron temperature and metastable number density) but rather to an anomalous power deposition (linked to the electron density). More specifically, such anomalous power deposition can be attributed to a wave reflection in the high gradient of charged particle densities near the end of the plasma column; a behavior that is more apparent in short plasma columns. Then, we have realized a parametric investigation of the discharge with the addition of organic precursors. Particularly, we used HMDSO for organo-silicon material synthesis and TTIP for organo-titanium material synthesis. It is found that because SWD are characterized by high charged particle densities (>10^13 cm^-3), higher precursor dissociation rates can be achieved with respect to other cold, atmospheric-pressure plasmas such as low-density dielectric barrier discharges. In this case, powder-like nanomaterials with sizes below 100 nm are obtained. Moreover, the addition of small amounts of oxygen into the discharge leads to the formation of round-like silicon oxide or titanium oxide nanoparticles.

The thesis is divided into two parts. The first part deals with the research work carried out on the synthesis and chemical modification of nanomaterials whereas the second part describes the preparation and characterisation of polymer films and their use as separation membranes. Part I of the thesis describing the synthetic strategies and chemical manipulation schemes employed on various types of nanomaterials is divided into six chapters. Chapter 1 describes a chemist’s approach towards synthesizing and tuning the properties of different classes of nanomaterials along with a brief account of their potential applications. Chapter 2 of the thesis describes the synthesis and characterization of various metal nanostructures (viz. nanoparticles, nanorods, nanosheets etc.) of nickel, ruthenium, rhodium and iridium using a solvothermal procedure. Chapter 3 deals with the nanoparticles of the novel oxide metal ReO3. ReO3@Au, ReO3@Ag, ReO3@SiO2 and ReO3@TiO2 core-shell nanostructures with ReO3 as the core nanoparticle have been synthesized through a two-step process and characterized. Dependence of the plasmon band of the ReO3 nanoparticles on the interparticle separation has been examined by incorporating the nanoparticles in various polymer matrices and the results compared with those obtained with gold nanoparticles. Chapter 4 presents the dispersion of nanostructures of metal oxides such as TiO2, Fe3O4 and ZnO in solvents of differing polarity (water, DMF and toluene) in the presence of several surfactants. In Chapter 5 of the thesis, fluorous chemical method of separation of metallic and semiconducting single-walled carbon nanotubes is described. This method involves the selective reaction of the diazonium salt of a fluorous aniline with the metallic nanotubes in an aqueous medium and subsequent extraction of the same in a fluorous solvent leaving the semiconducting nanotubes in the aqueous layer. Chapter 6 presents the studies on the interaction of single walled nanotubes and graphene with various halogen molecules (I2, IBr, ICl and Br2) of varying electron affinity probed by employing Raman spectroscopy and electronic absorption spectroscopy. Part II of the thesis describes a general method of fabricating ultrathin free-standing cross-linked polymer films and their subsequent use as separation membranes. A particular class of 1-D nanomaterials namely cadmium hydroxide nanostrands were used in this method throughout, to generate a sacrificial layer upon which the polymer films were generated.

L’objectif de ce mémoire de maîtrise est de caractériser la distribution axiale des plasmas tubulaires à la pression atmosphérique créés et entretenus par une onde électromagnétique de surface ainsi que d’explorer le potentiel de ces sources pour la synthèse de matériaux et de nanomatériaux. Un précédent travail de thèse, qui avait pour objectif de déterminer les mécanismes à l’origine de la contraction radiale du plasma créé dans des gaz rares, a mis en lumière un phénomène jusque-là inconnu dans les plasmas d’onde de surface (POS). En effet, la distribution axiale varie différemment selon la puissance incidente ce qui constitue une différence majeure par rapport aux plasmas à pression réduite. Dans ce contexte, nous avons réalisé une étude paramétrique des POS à la pression atmosphérique dans l’Ar. À partir de nos mesures de densité électronique, de température d’excitation et de densité d’atomes d’Ar dans un niveau métastable (Ar 3P2), résolues axialement, nous avons conclu que le comportement axial de l’intensité lumineuse avec la puissance n’est pas lié à un changement de la cinétique de la décharge (qui est dépendante de la température des électrons et de la densité d’atomes d’Ar métastables), mais plutôt à une distribution anormale de dissipation de puissance dans le plasma (reliée à la densité d’électrons). Plus précisément, nos résultats suggèrent que ce dépôt anormal de puissance provient d’une réflexion de l’onde dans le fort gradient de densité de charges en fin de colonne, un effet plus marqué pour de faibles longueurs de colonnes à plasma. Ensuite, nous avons effectué une étude spectroscopique du plasma en présence de précurseurs organiques, en particulier le HMDSO pour la synthèse de matériaux organosiliciés et l’IPT pour la synthèse de matériaux organotitaniques. Les POS à la PA sont caractérisés par des densités de charges très élevées (>10^13 cm^-3), permettant ainsi d’atteindre des degrés de dissociation des précurseurs nettement plus élevés que ceux d'autres plasmas froids à la pression atmosphérique comme les décharges à barrière diélectrique. Dans de tels cas, les matériaux synthétisés prennent la forme de nanopoudres organiques de taille inférieure à 100 nm. En présence de faibles quantités d’oxygène dans le plasma, nous obtenons plutôt des nanopoudres à base d’oxyde de silicium (HMDSO) ou à base de titanate de silicium (IPT), avec très peu de carbone. / The purpose of this master thesis is to characterize the axial distribution of tubular discharges at atmospheric pressure sustained by electromagnetic surface wave and to explore their potential for materials and nanomaterials synthesis. A previous doctoral thesis, aimed at determining the mechanisms driving radial plasma contraction in rare gas discharges shed light on a yet unknown phenomenon occurring in surface wave discharges (SWD). As a matter of fact, increasing the power injected into the system leads to a change of the axial distribution of the discharge, in sharp contrast with the behavior commonly observed in reduced-pressure plasmas. In this context, we have performed a parametric investigation of atmospheric pressure SWD sustained in Ar gas. Based on our axially-resolved measurements of the electron density, excitation temperature, and number density of Ar atoms in metastable state (Ar 3P2), we found that the peculiar change of the axial distribution of the light intensity with power is not linked to a modification in the discharge kinetics (linked to the electron temperature and metastable number density) but rather to an anomalous power deposition (linked to the electron density). More specifically, such anomalous power deposition can be attributed to a wave reflection in the high gradient of charged particle densities near the end of the plasma column; a behavior that is more apparent in short plasma columns. Then, we have realized a parametric investigation of the discharge with the addition of organic precursors. Particularly, we used HMDSO for organo-silicon material synthesis and TTIP for organo-titanium material synthesis. It is found that because SWD are characterized by high charged particle densities (>10^13 cm^-3), higher precursor dissociation rates can be achieved with respect to other cold, atmospheric-pressure plasmas such as low-density dielectric barrier discharges. In this case, powder-like nanomaterials with sizes below 100 nm are obtained. Moreover, the addition of small amounts of oxygen into the discharge leads to the formation of round-like silicon oxide or titanium oxide nanoparticles.

Functional nanomaterials are gaining attention due to their excellent shape and size dependent optical, electrical and catalytic properties. Synthesizing nanoparticles is no longer novel with the availability of a host of synthesis protocols for a variety of shapes and sizes of particles. What is currently needed is an understanding the fundamentals of shape and size controlled synthesis to produce functional nanomaterials that is simple and general. In addition to simple metallic nanostructures, synthesizing bimetallic and hybrid nanostructures are important for applications. Instead of trying to add functionality to the preformed nanomaterials, it is advantageous to look for cost effective and general synthetic protocols that can yield bimetallic, hybrid nanostructures along with the shape and size control. In this dissertation, a novel synthetic protocol for the synthesis of ultrfine single crystalline nanowires, metallic and bimetallic nanostructures and hybrid nanostructures has been investigated. The key point of the synthesis is that all different functional nanostructures are achieved by the use of noble metal intermediates in organic medium without phase transfer reagents. The roles of capping agents, oriented attachment and aggregation phenomenon have been studied in order to understand the formation mechanisms. Along with the synthesis, formation mechanisms, the optical and catalytic properties of the functional, noble metal, bimetallic and hybrid nanostructures have been studied. The entire thesis based on the results and findings obtained from the present investigation is organized as follows: Chapter I provides a general introduction to functional nanomaterials, their properties and some general applications, along with a brief description of conventional methods for size and shape-controlled synthesis. Chapter II deals with the materials and methods which essentially gives the information about the materials used for the synthesis and the techniques utilized to characterize the materials chosen for the investigation. Chapter III presents a novel method of for synthesizing noble metals nanostructures starting from an intermediate solid phase. The method involves the direct synthesis of noble metal intermediates in organic medium without the use of any phase transfer reagent. Controlled reduction of these intermediates leads to the formation of ultrafine nanocrystallite building blocks. Controlled aggregation of the nanocrystallites under different conditions leads to the formation of different nanostructures ranging from single crystalline nanowires to porous metallic clusters. In this chapter, the details of synthesis of the intermediate phase of gold are presented. This intermediate phase is the rocksalt phase of AuCl that has been experimentally realized for the first time. Manipulation of the AuCl nanocubes leads to the formation of a variety of nanostructures of Au starting from hollow cubes to extended porous structures. Mechanistic details of the formation of the intermediate and the nanostructures are presented in this chapter. Chapter IV deals with the symmetry breaking of an FCC metal (gold) by oriented attachment of metal nanoparticles by the preferential removal of capping agent from certain facets and followed by the attachment of gold nanoparticles along those bare facets. This kind of oriented attachment leads to the formation of 1D nanostructures with high aspect ratios. In this chapter, the synthesis, characterisation, formation mechanism and optical properties of high aspect ratio, molecular scale single crystalline gold nanowires has been described. This represent the first ever successful method to produce ultrafine 1D metallic nanostructures approaching molecular dimensions. Chapter V deals with the formation of hybrid nanostructures by attaching the cubic intermediate phase to a substrate like carbon nanotubes followed by the reduction of the attached intermediates on the tubes. The Pt intermediates have been synthesized and attached on the wall of functionalized CNTs and reduced. The PtCNT nanocomposites been characterized by several spectroscopic and microscopic techniques. The electrocatalytic activity of these nanocomposites towards the methanol oxidation has also been investigated. The composites exhibit high catalytic activity and good long term performance. The presence of functional groups on the CNT surface overcomes some of the limitations of current single metal catalysts that suffer from CO poisoning. Chapter VI deals with the formation of palladium nanostructures ranging from nanoparticles to hierarchical aggregates by controlled aggregation of nanoparticles in an organic medium that is tuned by the dielectric constant of the system. A crystalline intermediate of palladium salt has been synthesized and this intermediate of palladium has been used as the precursor solution for the synthesis of palladium nanostructures. The formation mechanism of the nanoporous Pd cluster is investigated using the modified DLVO approach. The catalytic efficiency of the Pd nanostructures has been investigated using the reduction of pnitrophenol and electrocatalytic hydrogen storage as model reactions. Chapter VII discusses the possibility of achieving functional bimetallic alloys by simultaneous reduction of the cubic intermediate of two different metals with experimental evidences. The synergistic effect of the two different metals gives rise to better catalytic activity. This chapter mainly deals with the synthesis of bimetallic porous nanoclusters of goldpalladium and goldplatinum in an organic medium. Detailed microstructural and spectroscopic characterisation of the bimetallic nanoclusters has been carried out and their electrocatalytic performance, morphological stability also investigated.

The thesis consists of eight chapters of which the first chapter presents a brief overview of inorganic nanostructures. Synthesis and magnetic properties of MnO and NiO nanocrystals are described in Chapter 2, with emphasis on the low-temperature ferromagnetic interactions in these antiferromagnetic oxides. Chapter 3 deals with the synthesis and characterizations of nanocrystals of ReO3, RuO2 and IrO2 which are oxides with metallic properties. Pressure-induced phase transitions of ReO3 nanocrystals and the use of the nanocrystals for carrying out surface-enhanced Raman spectroscopy of the molecules form Chapter 4. Use of ionic liquids to synthesize different nanostructures of semiconducting metal sulfides and selenides is described in Chapter 5. Synthesis of Mn-doped GaN nanocrystals and their magnetic properties are described in Chapter 6. A detailed investigation has been carried out on the growth kinetics of nanostructures of a few inorganic materials by using small-angle X-ray scattering and other techniques (Chapter 7). The study includes the growth kinetics of nanocrystals of Au, CdS and CdSe as well as of nanorods of ZnO. Results of a synchrotron X-ray study of the formation of nanocrystalline gold films at the organic-aqueous interface are also included in this chapter. Chapter 8 discuses the use of the organic-aqueous interface to generate Janus nanocrystalline films of inorganic materials where one side of the film is hydrophobic and other side is hydrophilic. This chapter also includes the formation of nanostructured peptide fibrils at the organic-aqueous interface and their use as templates to prepare inorganic nanotubes.

Due to the aggressive downscaling of the CMOS technology, power and current densities are increasing inside the chip. The limiting current conduction capacity(106 Acm−2)and thermal conductivity(201Wm−1K−1 for Al and 400 Wm−1K−1 for Cu) of the existing interconnects materials has given rise to different electro-thermal issues such a shot-spot formation, electromigration, etc. Exploration of new materials with high thermal conductivity and current conduction has thus attracted much attention for future integrated circuit technology. Among all the elemental materials, carbon nanomaterials (graphene and carbon nanotube) possess exceptionally high thermal (600-7000 Wm−1K−1) and current( ~108 -109 Acm−2)conduction properties at room temperature, which makes them potential candidate for interconnect materials. At the same time development of efficient energy harvesting techniques are also becoming important for future wireless autonomous devices. The excess heat generated at the hot-spot location could be used to drive an electronic circuit through a suitable thermoelectric generator. As the See beck coefficient of graphene is reported to be the highest among all elementary semiconductors, exploration of thermoelectric properties of graphene is very important. This thesis investigates the electrothermal and thermoelectric properties of metallic single walled carbon nanotube (SWCNT) and single layer graphene (SLG) for their possible applications in thermal management in next generation integrated circuits. A closed form analytical solution of Joule-heating equation in metallic SWCNTs is thus proposed by considering a temperature dependent lattice thermal conductivity (κ) on the basis of three-phonon Umklapp, mass-difference and boundary scattering phenomena. The solution of which gives the temperature profile over the SWCNT length and hence the location of hot-spot(created due to the self-heating inside the chip) can be predicted. This self-heating phenomenon is further extended to estimate the electromigration performance and mean-time-to-failure of metallic SWCNTs. It is shown that metallic SWCNTs are less prone to electromigration. To analyze the electro-thermal effects in a suspended SLG, a physics-based flexural phonon dominated thermal conductivity model is developed, which shows that κ follows a T1.5 and T−2 law at lower(<300 K) and higher temperature respectively in the absence of isotopes(C13 atoms). However in the presence of isotopic impurity, the behavior of κ sharply deviates from T−2 at higher temperatures. The proposed model of κ is found to be in excellent match with the available experimental data over a wide range of temperatures and can be utilized for an efficient electro-thermal analysis of encased/supported graphene. By considering the interaction of electron with in-plane and flexural phonons in a doped SLG sheet, a physics-based electrical conductance(σ) model of SLG under self-heating effect is also discussed that particularly exhibits the variation of electrical resistance with temperature at different current levels and matches well with the available experimental data. To investigate the thermoelectric performance of a SLG sheet, analytical models for See beck effect coefficient (SB) and specific heat (Cph) are developed, which are found to be in good agreement with the experimental data. Using those analytical models, it is predicted that one can achieve a thermoelectric figure of merit(ZT) of ~ 0.62 at room temperature by adding isotopic impurities(C13 atoms) in a degenerate SLG. Such prediction shows the immense potential of graphene in waste-heat recovery applications. Those models for σ, κ, SB and Cph are further used to determine the time evolution of temperature distribution along suspended SLG sheet through a transient analysis of Joule-heating equation under the Thomson effect. The proposed methodology can be extended to analyze the graphene heat-spreader theory and interconnects and graphene based thermoelectrics.

The present thesis entitled “Design, Synthesis and Characterization of Novel Nanomaterials” is divided into five chapters, staring with a general introduction. The remaining chapters focus on four different areas/projects that I have worked on. Chapter 1: Introduction to nanomaterials This chapter reviews the basic concepts of nanomaterials and their fabrication methods. Nanomaterials are defined as materials whose dimensions (at least one) are below 100 nm. One of the most exciting aspects of nanomaterials is that their properties may differ significantly from those of the corresponding bulk materials. Nanomaterials fabrication methods can be broadly classified according to whether the assembly follows either i) the bottom-up approach or ii) the top-down approach. These methods have been discussed with various examples including the self-assembly of proteins, peptides and small molecules. In the top-down approach synthetic procedures for Graphene Oxide and its application are discussed. All characterization techniques that are used for characterizing the nanomaterials are also described briefly. Chapter 2 Section A: Self-assembly of 1-Hydroxy benzotriazole (HOBT) in water The studies presented in Chapter 2 identifies HOBT as the smallest non-peptide building block that spontaneously self-assembles into hollow micro tubular structures upon evaporation of water. The tubes form under ambient conditions by rolling over of crystalline sheets of HOBT. The packing of HOBT in the tubes seem to be predominantly driven by intermolecular π-stacking interactions between the aromatic rings of HOBT. These structural and packing patterns are similar to those found in nanotubes formed by the self-assembly of peptides and other larger molecules. The cavities of these thermolabile microtubes act as molds for casting gold nanoparticles for the synthesis of gold microrods with monodisperse dimensions. The non-reacting inner surfaces of the cavities have been used to uniquely synthesize R6G-functionalized gold microrods. With these features, HOBT is an important novel non-peptide building block for accessing micro and nanometric materials for their applications in medicine, biology and molecular biotechnology. Section B: Controlling the orientation of self-assembly of HOBT microtubes The studies presented in this chapter address the self-assembly of HOBT into microtubular structures in different solvents of varying polarities (H2O and DCM:MeOH) to understand the role of solvent volatility and its direction on the orientation of the HOBT microtubes. HOBT self-assembles from DCM:MeOH mixtures in its bipolar canonical form and is coordinated with its water of hydration, similar to its crystals obtained from water. FTIR and TGA data shows that MeOH is also integrated with the microtubes. We observe for the first time that the orientation of microtubular self-assembly is controlled in the direction of evaporation of the solvent. We demonstrate further this feature by controlling the orientation of HOBT self-assembly in exclusively vertical direction through controlled vertical evaporation of the solvent mixture DCM:MeOH (9:1). Additionally, the unique transition between vertical and horizontal orientations for self-assembled HOBT microtubes is achieved by simple change of solvation between aqueous and organic solvents. These results reveal a dynamic relationship between the rate of evaporation of solvent and the rates of formation of different self-assembled morphologies. The rate of evaporation of the solvent primarily governs the rate of formation of the tubes, rather than their orientations in three dimensions. Chapter 3: Chemical origins of debris in Graphene Oxide (GO) This chapter is focused on the investigation of the carbonyl rich fragments arising from GO and provides an understanding of its formation. The fragments are expelled from GO due to an uncontrolled nucleophile driven reaction in aqueous medium leaving the holes on the sheet. These fragments are carbonyl rich small (5 ± 2 nm) nonaromatic molecules that form as by-products of oxidative chemical reactions that occur at the sp3 clusters on the basal surface of GO sheets when they are treated with nucleophilic bases under aqueous conditions. The structure and size of the debris, and hence that of the hole, depend on the size of the sp3 cluster on the sheet. These debris fall out of the GO sheet surface, leading to formation of nanometer sized holes. Formation of debris and hence the holes can be avoided by using anhydrous polar solvents. This work sheds new light on the fundamental structure of GO and the prevention of debris from it during redox reactions enabling better control over functionalization of the GO surface. Chapter 4: Measurement of mechanical properties of polypeptide fragment from Insulin like growth factor binding protein nanotubes by the Peak Force QNM method This chapter describes the discovery of Polypeptide fragment from an IGFBP-2. This fragment self-assembles spontaneously and reversibly into nanotubular structures under oxidizing conditions. These nanotubes were characterized by using Transmission electron microscopy. Notably as compared to the monomer, an increase in intrinsic fluorescence upon self-assembly. The thermal stability of these nanotubes is realized form the fluorescence studies. Peak Force Quantitative Nanomechanical Mapping method of AFM was used to measure the Young’s modulus of the nanotubes. These nanotubes were found to have Young’s modulus value of ~10 Gpa, which is comparable to those of bones presumably due to intermolecular disulphide bonds. These nanotubes will have potential applications in tissue engineering. Chapter 5: Probing the pathways of n→π* interaction in peptides This chapter deals with the theoretical study of n→π* interaction in designed peptidomimetics. The n→π* interaction involves the delocalization of the lone pair of the donor group into the antibonding orbital (π*) of a carbonyl group. However despite beeing extensively studied there exists a debate over the validation of these n→π* interaction which is reminiscent to Bürgi and Dunitz trajectory. This chapter present our findings that peptidomimetics containing the 5,6-dihydro-4H-1,3-oxazine (Oxa) and 5,6-dihydro-4H-1,3-thiazine (Thi) functional groups at the C-terminus of Pro selectively stabilizes the cis conformer by reverse n→πi-1* interaction. These systems have been used to study the n→πi1* interaction using Natural Bond Orbital (NBO) method. Our study reveals that the energetically most favorable trajectory of a nucleophile for a favorable n→π* interaction presumably to facilitate the overlap between the lonepair of the nucleophile and the antibonding orbital of the carbonyl group. The geometrical requirements for the optimum n→π* interaction depends on the relative orientations of the orbitals that are involved. This study has implications for more accurately identifying long distant n→π* interaction.