Yes / Understanding the effect of physical parameters (e.g., temperature) on crystallisation dynamics is of paramount importance for the synthesis of nanocrystals of well‐defined sizes and geometries. However, imaging nucleation and growth is an experimental challenge owing to the resolution required and the kinetics involved. Here, by using an aberration‐corrected transmission electron microscope, we report the fabrication of precious metal nanocrystals from nuclei and the identification of the dynamics of their nucleation at three different temperatures (20, 50, and 100 °C). A fast, and apparently linear, acceleration of the growth rate is observed against increasing temperature (78.8, 117.7, and 176.5 pm min−1, respectively). This work appears to be the first direct observation of the effect of temperature on the nucleation and growth of metal nanocrystals. / The Royal Society. Grant Number: UF150295 Leverhulme Trust. Grant Number: ECF-2013-414 The Academy of Medical Sciences. Grant Number: SBF003\1170

Magic-sized nanocrystals (MSNs) are nanocrystals with a single size distribution. They have narrow spectral features that do not exhibit inhomogeneous line broadening. This enabled us to analyze homogeneous line broadening of CdSe and CdTe MSNs. In solution, we observed two aggregated configurations of CdSe and CdTe MSNs. Sub-peaks within MSN excitonic peaks were caused by these two aggregated configurations and surface states. A two-dimensional photoluminescence spectrum of a mixture of CdTe 427 nm and 500 nm MSNs gave direct evidence of Förster resonant energy transfer (RET) between the two sizes of MSNs. Normalized experimental overlap between donor emission and acceptor absorption spectra was on the order predicted by theory, confirming that there is sufficient overlap for RET to take place in this system. Additionally, within both aggregated configurations, the two sizes of MSNs were within sufficient distance from one another for RET to occur.

Magic-sized nanocrystals (MSNs) are nanocrystals with a single size distribution. They have narrow spectral features that do not exhibit inhomogeneous line broadening. This enabled us to analyze homogeneous line broadening of CdSe and CdTe MSNs. In solution, we observed two aggregated configurations of CdSe and CdTe MSNs. Sub-peaks within MSN excitonic peaks were caused by these two aggregated configurations and surface states. A two-dimensional photoluminescence spectrum of a mixture of CdTe 427 nm and 500 nm MSNs gave direct evidence of Förster resonant energy transfer (RET) between the two sizes of MSNs. Normalized experimental overlap between donor emission and acceptor absorption spectra was on the order predicted by theory, confirming that there is sufficient overlap for RET to take place in this system. Additionally, within both aggregated configurations, the two sizes of MSNs were within sufficient distance from one another for RET to occur.

Orientador: Maria do Carmo Gonçalves / Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Química / Made available in DSpace on 2018-08-20T11:02:43Z (GMT). No. of bitstreams: 1 Taipina_MarciadeOliveira_M.pdf: 4509830 bytes, checksum: a4492786879a5c950122cf7b0b637caa (MD5) Previous issue date: 2012 / Resumo: Neste trabalho, a evolução da degradação da fibra de curuá submetida à hidrólise ácida foi acompanhada em diferentes tempos. Foi possível observar que a hidrólise se inicia por um processo de fibrilação, permitindo um maior acesso do ácido ao longo da estrutura da fibra. As micrografias obtidas das fibras embutidas sugeriram que o ataque ácido na célula vegetal se dá no sentido da lamela média a regiões mais internas da parede celular. Após apenas 10 minutos de hidrólise foi possível observar a exposição de nanocristais presos à parede celular, bem como aglomerados de nanocristais já isolados. Esses resultados também revelaram que há formação de nanocristais após um terço do tempo de hidrólise estabelecido pela literatura. Após 30 minutos de hidrólise os nanocristais de celulose se apresentavam isolados em sua maioria. Nanocristais de celulose foram obtidos a partir da hidrólise ácida da celulose proveniente de diferentes fontes, sendo elas algodão, curauá e celulose microcristalina. Os nanocristais apresentaram formato de agulha, com dimensões dependentes da fonte de celulose utilizada. A modificação da superfície dos nanocristais foi realizada com 3- isocianatopropiltrietoxissilano (IPTS). Resultados de análises de espectroscopia no infravermelho sugeriram a modificação de superfície dos nanocristais. O mapeamento de silício feito por ESI-TEM mostrou a presença do silício na superfície dos nanocristais. Como propósito secundário, foi feito o processamento de nanocompósitos com os nanocristais em matriz de PLA. Os nanocompósitos preparados com nanocristais obtidos por hidrólise ácida com HCl apresentaram um ganho mais significativo em propriedades mecânicas e os resultados evidenciaram a necessidade de modificação de superfície, bem como a escolha do ácido mais adequado para a hidrólise do material celulósico / Abstract: In this work, degradation evolution of curauá fiber, subjected to acid hydrolysis, was monitored at different times. It was observed that the hydrolysis is initiated by a fibrilation process, allowing the access of acid throughout the fiber structure. The cross-section micrographs of the embedded fibers suggested that the acid attack in plant cells takes place towards the middle lamella to the inner regions of the cell wall. Exposure of nanocrystals that attached to the cell wall, as well as, clusters of isolated nanocrystals were observed after only 10 minutes of hydrolysis. These results also showed the formation of nanocrystals after one third of the time established in literature for hydrolysis. The cellulose nanocrystals were completly isolated after 30 minutes of hydrolysis. Cellulose nanocrystals were obtained by acid hydrolysis of cellulose from different sources, such as cotton, curauá and cellulose microcrystalline. The nanocrystals showed a needle-like shape, with dimensions dependent on the cellulose source. The surface modification of nanocrystals was performed with 3-isocyanatepropyltriethoxysilane (IPTS). Results from infrared spectroscopy analysis suggested the surface modification of the nanocrystals. The silicon mapping made by ESI-TEM showed the presence of silicon on the surface of the nanocrystals. As a secondary purpose, the processing of nanocomposites with nanocrystals in a PLA matrix was carried out. The nanocomposites with nanocrystals obtained by acid hydrolysis with HCl showed a more significant improvement in mechanical properties and the results showed the need for surface modification as well as the most suitable choice of acid for the hydrolysis of cellulosic material / Mestrado / Físico-Química / Mestre em Química

Metal and semiconducting nanocrystals have received a great deal of attention from fundamental scientists and application-oriented researchers due to their physical and chemical properties, which differ from those of bulk materials. Nanocrystals are essential building blocks in the development of nanostructured devices for energy conversion. Colloidal metals and metal chalcogenides have been developed for use as nanocrystal inks to produce efficient solar cells with lower costs. All high-performing photovoltaic nanocrystals contain toxic elements, such as Pb, or scarce elements, such as In; thus, the production of solution-processable nanocrystals from earth-abundant materials using environmentally benign synthesis and processing methods has become a major challenge for the inorganic semiconductor-based solar field. This dissertation, divided into two parts, addresses several aspects of these emerging challenges. The first portion of the thesis describes the synthesis and characterization of nanocrystals of antimony sulfide, which is composed of non-scarce and non-toxic elements, and examines their performance in photovoltaic devices. The effect of various synthetic parameters on the final morphology is explored. The structural, optical and morphological properties of the nanocrystals were investigated, and Sb2S3 nanocrystal-based solid-state semiconductor-sensitized solar cells were fabricated using different deposition processes. We achieved promising power conversion efficiencies of 1.48%. The second part of the thesis demonstrates a novel method for the in situ synthesis and patterning of nanocrystals via reactive inkjet printing. The use of low-cost manufacturing approaches for the synthesis of nanocrystals is critical for many applications, including photonics and electronics. In this work, a simple, low-cost method for the synthesis of nanocrystals with minimum size variation and waste using reactive inkjet printing is introduced. As a proof of concept, the method was used for the in situ synthesis of gold nanoparticles as a model system. Relatively monodisperse gold nanoparticles were produced. The size and shape of gold nanoparticles can be controlled by the gold precursor and surfactant concentration in the ‘ink.’ This approach can be extended to the synthesis of other nanocrystals and is thus a truly impactful process for the low-cost synthesis of materials and devices incorporating nanocrystals.

No description available.

Yes / Metal nanocrystals offer new concepts for the design of nanodevices with a range of potential applications. Currently the formation of metal nanocrystals cannot be controlled at the level of individual atoms. Here we describe a new general method for the fabrication of multi-heteroatom-doped graphitic matrices decorated with very small, ångström-sized, three-dimensional (3D)-metal crystals of defined size. We irradiate boron-rich precious-metal-encapsulated self-spreading polymer micelles with electrons and produce, in real time, a doped graphitic support on which individual osmium atoms hop and migrate to form 3D-nanocrystals, as small as 15 Å in diameter, within 1 h. Crystal growth can be observed, quantified and controlled in real time. We also synthesize the first examples of mixed ruthenium–osmium 3D-nanocrystals. This technology not only allows the production of ångström-sized homo- and hetero-crystals, but also provides new experimental insight into the dynamics of nanocrystals and pathways for their assembly from single atoms. / We thank the Leverhulme Trust (Early Career Fellowship No. ECF-2013-414 to NPEB), the University of Warwick (Grant No. RDF 2013-14 to NPEB), the Swiss National Science Foundation (Grant No. PA00P2_145308 to NPEB and PBNEP2_142949 to APB), the ERC (Grant No. 247450 to PJS), EPSRC (EP/G004897/1 to RKOR, and EP/F034210/1 to PJS) and Science City (AWM/ERDF) for support. We thank the Wellcome Trust (Grant No. 055663/Z/98/Z) for funding the Electron Microscopy Facility, School of Life Sciences, University of Warwick. We also thank COST Action CM1105 for stimulating discussions, Thomas Wilks for supplying the micelle image for Figure 1, and the Australian Synchrotron and the University of Monash for allocation of time on the SAXS/ WAXS beamline and funding. The 2000FX Gatan Orius digital TEM camera used in this research was funded by Science City: Creating and Characterizing Next Generation Advanced Materials, with support from Advantage West Midlands and part funded by the European Regional Development Fund.

This thesis consists of two parts. The first part deals with the magnetic properties of Fe3O4 nanocrystals and their possible application in water remediation. The second part is on the delamination of layered materials and the preparation of new layered hybrids from the delaminated sheets. In recent years, nanoscale magnetic particles have attracted considerable attention because of their potential applications in industry, medicine and environmental remediation. The most commonly studied magnetic nanoparticles are metals, bimetals and metal oxides. Of these, magnetite, Fe3O4, nanoparticles have been the most intensively investigated as they are, non-toxic, stable and easy to synthesize. Magnetic properties of nanoparticles such as the saturation magnetization, coercivity and blocking temperature are influenced both by size and shape. Below a critical size magnetic particles can become single domain and above a critical temperature (T B , the blocking temperature) thermal fluctuations can induce random flipping of magnetic moments resulting in loss of magnetic order. At temperatures above the blocking temperature the particles are superparamagnetic. Magnetic nanocrystals of similar dimensions but with different shapes show variation in magnetic properties especially in the value of the blocking temperature, because of differences in the surface anisotropy contribution. The properties of magnetic nanoparticles are briefly reviewed in Chapter 1. The objective of the present study was to synthesize Fe3O4 nanocrystals of different morphologies, to understand the difference in magnetic properties associated with shape and to explore the possibility of using Fe3O4 nanocrystals in water remediation. In the present study, oleate capped magnetite (Fe3O4) nanocrystals of spherical and cubic morphologies of comparable dimensions (∼10nm) have been synthesized by thermal decomposition of FeOOH in high-boiling octadecene solvent (Chapter 2). The nanocrystals were characterized by XRD, TEM and XPS spectroscopy. The nanoparticles of different morphologies exhibit very different blocking temperatures. Cubic nanocrystals have a higher blocking temperature (T B = 190 K) as compared to spheres (T B = 142 K). From the shift in the hysteresis loop it is demonstrated that the higher blocking temperature is a consequence of exchange bias or exchange anisotropy that manifests when a ferromagnetic material is in physical contact with an antiferromagnetic material. In nanoparticles, the presence of an exchange bias field leads to higher blocking temperatures T B because of the magnetic exchange coupling induced at the interface between the ferromagnet and antiferromagnet. It is shown that in these iron oxide nanocrystals the exchange bias field originates from trace amounts of the antiferromagnet wustite, FeO, present along with the ferrimagnetic Fe3O4 phase. It is also shown that the higher FeO content in nanocrystals of cubic morphology is responsible for the larger exchange bias fields that in turn lead to a higher blocking temperature. Magnetic nanoparticles with moderate magnetization can be easily separated from dispersions by applying low intensity magnetic fields. Oleate capped spherical and cubic iron oxide nanocrystals have considerable magnetic moment and hence have the potential as host-carriers for magnetic separation in environmental remediation. These nanocrystals are, however, dispersible only in non-polar solvents like chloroform, toluene, etc. Environmental remediation requires that the nanocrystals be water dispersible. This was achieved by functionalizing the surface of the iron oxide nanocrystals by coordinating carboxymethyl-β-cyclodextrin (CMCD) cavities (Chapter 3). The hydroxyl groups located at the rim of the anchored cyclodextrin cavity renders the surface of the functionalized nanocrystal hydrophilic. The integrity of the anchored CMCD molecules are preserved on capping and their hydrophobic cavities available for host-guest chemistry. The CMCD capped iron oxide particles are water dispersible and separable in modest magnetic fields (<0.5 T). Small molecules like naphthalene and naphthol can be removed from aqueous media by forming inclusion complexes with the anchored cavities of the CMCD-Fe3O4 nanocrystals followed by separation of the nanocrystals by application of a magnetic field. The adsorption properties of the iron oxide surface towards arsenic ions are unaffected by the CMCD capping so it too can be simultaneously removed in the separation process. To extend the application of the iron oxide nanocrystals so that they can both capture and destroy organic contaminants present in water, cyclodextrin functionalized water dispersible core-shell Fe3O4@TiO2 (CMCD-Fe3O4@TiO2) nanocrystals have been synthesized (Chapter 4). The application of these particles for the photocatalytic degradation of endocrine disrupting chemicals (EDC), bisphenol A and dibutyl phthalate, in water is demonstrated. EDC molecules that may be present in water are captured by the CMCD-Fe3O4@TiO2 nanoparticles by inclusion within the anchored cavities. Once included they are photocatalytically destroyed by the TiO2 shell on UV light illumination. The magnetism associated with the crystalline Fe3O4 core allows for the magnetic separation of the particles from the aqueous dispersion once photocatalytic degradation is complete. An attractive feature of these ‘capture and destroy’ nanomaterials is that they may be completely removed from the dispersion and reused with little or no loss of catalytic activity. The second part of the thesis deals with the intercalation of surfactants in inorganic layered solids and their subsequent delamination of the functionalized solid in non-polar solvents. The solids investigated were - the anionic layered double hydroxides (LDH), the 2:1 smectite clay, montmorillonite (MMT), layered metal thiophosphates (CdPS3) and graphite oxide (GO). Layered Double Hydroxides (LDH) are lamellar solids of the general chemical formula [M0(1−x)Mx(OH)2], where M0 is a divalent metal ion and M a trivalent ion. The structure of the Mg-Al layered double hydroxide (Mg-Al LDH) may be derived from that of brucite, Mg(OH)2, by isomorphous substitution of a part of the Mg2+ by trivalent Al3+ ions with electrical neutrality maintained by interlamellar exchangeable ions like nitrate or carbonate. The ion exchange intercalation of the anionic surfactant dodecyl sulfate (DDS) in an Mg-Al LDH and the subsequent delamination of the surfactant intercalated LDH in non-polar solvent is reviewed in Chapter 5. Delamination results in a clear dispersion of neutral nanosheets. The delaminated sheets are neutral as the surfactant chains remain anchored to the inorganic sheet. On solvent evaporation, the sheets re-stack to give back the original surfactant intercalated solid. This strategy for delamination of layered solids by intercalation of an appropriate surfactant followed by dispersing in a non-polar solvent has been extended to montmorillonite (MMT) and cadmium thiophosphates (CdPS3) by ion-exchange intercalation of the cationic surfactant dioctadecyldimethylammonium bromide (DODMA) followed by sonication in non-polar solvents e.g. toluene or chloroform as in the case of the LDH (Chapter 6). The nanosheets of the MMT and CdPS3 are electrically neutral as the surfactant chains remain anchored to the inorganic sheet even after exfoliation. Graphite oxide (GO) too can be delaminated by functionalizing the sheets by covalently linking oleylamine chains to the GO sheets via an amide bond. The oleylamine functionalized GO is easily delaminated in non-polar solvents to give electrically neutral GO nanosheets. It is shown in Chapter 7 that the 1:1 mixtures of dispersions of montmorillonite-DODMA with Mg-Al LDH-DDS nanosheets can self assemble, on solvent evaporation, to give a new layered solid with periodically alternating montmorillonite and LDH layers. In this method attractive forces between the neutral exfoliated nanosheets of cationic and anionic ensures self-assembly of a perfectly periodic alternating layered structure. The method has been extended to synthesize new layered solids in which surfactant tethered cationic and anionic inorganic sheets alternate. The hybrid solids synthesized are CdPS3—MgAl-LDH, CdPS3—CoAl-LDH, GO—MgAl-LDH, GO—CoAl-LDH. The procedure outlined in Chapter 7 allows for a simple, but versatile, method for generating new periodically ordered layered hybrid solids by self-assembly.

Cellulose nanocrystals (CNCs) are crystalline nanoparticles that are extracted from renewable sources such as trees or bacteria through mechanical or chemical treatments of their source. CNCs are of interest to several research communities concerned with sustainable technologies. Specifically, CNCs have attracted great interest in the polymer composite community given their high theoretical specific strength and modulus. Two key obstacles surround the use of CNCs in polymer composites, namely their comparatively lower thermal stability and hydrophilicity render their dispersion, and therefore mechanical reinforcement, in polymer matrices challenging. This research considered a waterborne epoxy and a polyurethane elastomer for CNC/polymer composites since these composites are seldom reported in literature or often suffer from degraded mechanical properties. In the epoxy/CNC composites, samples were prepared by two methods, first an epoxy emulsion was mixed with an amine crosslinker and an aqueous based CNC suspension (1-step mixing), and second, the epoxy emulsion was premixed with the aqueous based CNCs and the amine crosslinker was added some time later (2-step mixing). Both composites were mixed by magnetic stirring, however the samples prepared by the 2-step mixing method exhibited enhanced dispersion and mechanical properties, specifically the storage modulus (E’), tensile strength, and work of fracture. Zeta potential measurements and chemical analysis by FTIR indicated that the dispersion mechanism was physical in nature, rather than chemical. In the second composite system, CNCs were chemically modified with an isophorone diisocyanate (IPDI) monomer having unequally reactive isocyanate groups. The goal of the modification step was to react only one isocyanate group with the CNC surface and have a free isocyanate group available for further modification. The chemical structure of one linked isocyanate (urethane bond) and one free isocyanate was confirmed by FTIR and 13C NMR. The particles modified by IPDI (m-CNC) and the neat particles (um-CNC) were incorporated into a polyurethane matrix based on IPDI and a triol crosslinker. Upon visual inspection of the cured composites, it was clear that the modification step produced homogeneously dispersed nanoparticles in the polyurethane while the um-CNCs were aggregated. When the mechanical properties were tested by uniaxial tensile testing, it was determined that the m-CNC composites resulted in improvements in the tensile strength and work of fracture without degradation of the elongation of break property when compared to the neat matrix. Overall the findings in this research highlight important considerations for designing CNC/thermoset composites with enhanced dispersion and mechanical performance.

The focus of this study was to explore process-structure-property relationships in biodegradable polymer nanocomposite films in order to eliminate the commonly used trial and error approach to materials design and to enable manufacturing of composites with tailored properties for targeted applications. The nanofiller type and concentration, manufacturing method and compounding technique, as well as processing conditions were systematically altered in order to study the process-structure-property relationships. Polylactic acid (PLA) was used as the polymer and exfoliated graphite nanoplatelets (GNP), carbon nanotubes (CNT), and cellulose nanocrystals (CNC) were used as reinforcement. The nanocomposite films were fabricated using three different methods: 1) melt compounding and melt fiber spinning followed by compression molding, 2) solution mixing and solvent casting, and 3) solution mixing and electrospinning followed by compression molding. Furthermore, the physical properties of the polymer, namely the crystallization characteristics were altered by using two different cooling rates during compression molding. The electrical response of the composite films was examined using impedance spectroscopy and it was shown that by altering the physical properties of the insulating polymer matrix, increasing degree of crystallinity, the percolation threshold of the GNP/PLA films is significantly reduced. Additionally, design of experiments was used to examine the influence of nanofiller type (CNT versus GNP), nanofiller content, and processing conditions (cooling rate during compression molding) on the elastic modulus of the composite films and it was concluded that the cooling rate is the primary factor influencing the elastic modulus of both melt compounded CNT/PLA and GNP/PLA films. Furthermore, the effect of nanofiller geometry and compounding method was examined and it was shown that the high nanofiller aspect ratio in the CNT/PLA films led to decreased percolation threshold compared to the GNP/PLA films. The melt compounded GNP/PLA films displayed a lower percolation threshold than the solution cast GNP/PLA films most likely due to the more homogeneous distribution and dispersion of GNP in the solution cast films. Fully biodegradable and biorenewable nanocomposite films were fabricated and examined through the incorporation of CNC in PLA. Through the addition of CNC, the degree of crystallinity of the matrix was significantly increased. Focusing the design space through investigation of process-structure-property relationships in PLA nanocomposites, can help facilitate nanocomposites with tailored properties for targeted applications.