The contactless electroreflectance¡]CER¡^ spectra of ZnO bulk has been measured at 300K. It was observed the difference between the CER spectra by using the polarization E of probe light perpendicular ( E¡æc) and parallel ( E¡üc) to the c-axis of the m-plane ZnO. In addition, a mercury lamp was focused on the sample to reduce its strength of electric field. It was observed that the CER spectrum was blue-shifted with Hg lamp being on. Hence, the observed features were attributed to excitonic transitions. The experimental spectra were fitted by Lorentzian lineshapes. The energies of the A ( B¡^, B¡]A¡^, and C excitonic transitions were determined as 3.329eV, 3.343eV and 3.387eV, respectively.

In this Ph.D. work, we investigate the optoelectronic properties of low-bandgap semiconducting polymers and project the potential for employing these materials in electronic and photonics devices, with a particular emphasis on use in organic solar cells. The field of organic solar cells is well developed and many of the fundamental aspects of device operation and material requirements have been established. However, there is still more work to be done in order for these devices to ultimately reach their full potential and achieve commercialization. Of immediate concern is the low power conversion efficiency demonstrated in these devices so far. In order to improve upon this efficiency, several routes are being explored. Because the optical bandgaps of semiconducting polymers are larger than in inorganic semiconductors, one of the most promising routes currently under exploration is the development of low-bandgap materials. Using polymers with lower band gaps will allow more of the solar irradiance spectrum to be absorbed and converted into electricity and thus possibly boost the overall efficiency. The bandgap of these semiconducting polymers is determined by the chemical structure, and therefore can be tailored through synthesis if the relevant structure-property relationships are well-understood. The materials studied in this work, a new series of Poly(thienylenevinylene) (PTV) derivatives, posses lower band gaps than conventional polymers through a design that incorporates aromatic-quinoid structural disturbances. This type of chemical structure delocalizes the electronic structure along the polymer backbone and reduces the energy of the lowest excited-state leading to a smaller band-gap. We investigate these materials through a variety of techniques including linear spectroscopy such as absorption and photoluminescence, pump-probe techniques like cw-photoinduced absorption and transient photo-induced absorption, and the non-linear electroasborption technique in order to interrogate the consequences of the delocalized electronic structure and its response to optical stimuli. We additionally consider the effects of environmental factors such as temperature, solvents and chemical doping agents. During the course of these investigations, we consider both of the two primary categorical descriptions of structure-property relationships for polymers within the molecular exciton model, namely the role of inter-molecular interactions on the electronic properties through the variation of supermolecular order and the fundamental determination of electronic structure due to specific intra-molecular interaction along the backbone of the polymer chain. We show that the dilution of aromaticity in semiconducting polymers, while being a viable means of reducing the optical band gap, results in a significant increase in the role of electron-electron interactions in determining the electronic properties. This is observed to be detrimental for device performance as the highly polarizable excited state common to polymers gives way to highly correlated state that extinguishes both the emissive properties and more importantly for solar cells, the charge-generating characteristics. This situation is shown to be predominant regardless of the nature of interchain interactions. We therefore show that the method of obtaining low-bandgap polymers here comes along with costly side-effects that inhibit their efficient application in solar cells. Further, we directly probe the efficacy of these materials in the common bulk-heterojunction architecture with both spectroscopy and device characterization in order to determine the limiting and beneficial factors. We show that, while from the point of view of absorption of solar radiation these low-bandgap polymers are more suited for solar cells, the ability to convert the absorbed photons into electron-hole pairs and generate electricity is lacking, due to the internal conversion into the highly correlated state and thus, the absorbed photon energy is lost. For completeness, we fabricate devices and verify that both the charge-transport properties and alignment of charge extraction levels with those of the contacts can not be responsible for the dramatic decrease in efficiency found from these devices as compared to other higher band gap polymers. We thus conclusively determine that the lack of power converison efficiency is governed by the inefficiency of charge-generation resulting from the intrinsic defective molecular structures rendering a low-lying optically forbidden state below the lowest optical allowed state that consumes the majority of the photogenerated excitons. It is emphasized that our means of investigation allow us to truly access the potential of these materials. In contrast, the direct application of these systems in devices and interpretation of the performance is exceedingly complex and may obscure their true potential. In other words, poor performance from a device may be extrinsic in nature and the optimization process may be very costly with respect to both time and materials. The methods used here however, allow us to determine the intrinsic potential. Not only is this beneficial in terms of preserving the resources that would be used on the trial-and-error method for devices, but it also allows us to learn more on a fundamental level about the structure-property relationships and their implications for device performance. The benefits of this increased understanding are two-fold. First, by learning about the fundamental response of a material, a new application may be realized. For example, the rapidly efficient internal conversion process that renders the materials in this study as poor candidates for solar cells may make them useful for photonics applications, as optical switches, for instance. Secondly, this type of investigation has implications for the whole organic electronics community instead of just being limited to the particular material system and the primary application attempted. In this case, we are essentially able to determine a threshold for aromaticty necessary in a structure that will preserve the stability of the ionic excited state that is useful for charge generation in solar cells.

Obtaining abundant, clean, sustainable energy has become an increasingly large need globally. To date, solar cells have had a limited impact in meeting energy demands. This is primarily due to their relatively high cost and low power conversion efficiencies. Sensitized solar cells, or Grätzel cells, have the potential for being made with low cost materials, and achieving power conversion efficiency high enough to economically compete with fossil fuels. Understanding the dynamics of charge carriers as they separate at the interface of the light absorbing donor and their semiconducting acceptor becomes an important first step in the realization of an inexpensive and efficient sensitized solar cell. Presented is the theory of treating electrons at donor-acceptor interfaces, and why time-resolved surface second harmonic generation (TR-SHG) is used to probe the dynamics of charge carriers at these interfaces. A series of experiments are described where various preparations of thin films of sensitizers on single crystal titanium dioxide, a common acceptor in Grätzel cells, are prepared and studied. TR-SHG studies of thin films of colloidal PbSe and CdSe QDs showed remarkably different electron cooling and transfer dynamics. The electron cooling in PbSe is thermally activated in PbSe QDs. By cooling samples, electron transfer from higher excited “hot” states was observed. Contrary, for CdSe QDs electron transfer rates were dependent on the energy of the excited state. When higher states were excited, charge transfer rates decreased, indicating that only low energy, electrically “cold”, states participate in charge transfer. When carbon based grapheme QDs are used, the electron dynamics mimic PbSe QDs. In this system, increasing the pump energy leads to slower recombination rates, indicating that electrons have to drift further back to the interface. / text

L'oxyde de zinc (ZnO) est un matériau connu et intensivement étudié pour des applications optoélectroniques dans le domaine de l’ultraviolet en raison de son large gap énergétique (3,34 eV). Cependant, les applications UV basées sur des matériaux nanostructurés représentent un véritable défi : la diminution en taille des particules obtenues généralement par des voie de chimie en solution permet d’accroître la surface spécifique mais en stabilisant des défauts à l’origine d’émissions visibles. Au cours des dernières décennies, des progrès concernant la qualité des particules ont été enregistrés au moyen des techniques physiques basées sur les dépôts en phase gazeuse à haute température. Cependant, la taille et le contrôle de la morphologie des particules restent difficiles. En prenant en compte l'état de l'art portant sur les propriétés optiques des particules de ZnO, c’est la voie supercritique qui a été mise en œuvre dans cette étude. Tout d'abord des réacteurs micro/millifluidiques ont été développés de façon à accroître la quantité de matériaux produits (gramme/jour) tout en conservant des propriétés d’émission dans l’ultraviolet. Puis les caractéristiques physico-chimiques des particules ont été étudiées au regard de l'influence de la dimension des réacteurs et de l'hydrodynamique des systèmes. Les propriétés de luminescence sont reportées à température ambiante et basses températures et comparées expérimentalement à la réponse d’un monocristal et des données de la littérature. Les mécanismes de formation (nucléation et croissance) des nanoparticules ont été élucidés et ont permis de comprendre les réponses optiques uniques de ces particules. / Zinc oxide (ZnO) is a well-known and intensively studied material for optoelectronic applications in the ultraviolet (UV) spectrum region due to its wide band gap energy - 3.34 eV. However, the UV applications based on nanostructured ZnO present a big challenge due to the small size of the nanostructures i.e. a large surface-to-volume ratio resulting the appearance of the visible emission originated from the surface defects. In the last decades, the progress concerning the fabrication of UV-emitting ZnO nanostructures was carried out through the high temperature gas phase based approach. However, the size and shape control of ZnO nanostructures obtained with this approach is still difficult. Taking into account the state of the art in the optics based on ZnO nanomaterials, this Ph.D. thesis demonstrates the development of new supercritical fluids based approach for the synthesis of ZnO nanostructures with UV-emitting only PL properties. First of all in this thesis, we have developed continuous supercritical set up from micro- up to millifluidic reactor dimension for the synthesis of a larger quantity of UV-emitting ZnO nanocrystals (a gram scale per day). The influence of reactor dimension associated with hydrodynamics on physico-chemical characteristics was investigated. ZnO nanocrystals formation mechanism was studied as a function of the residence time in our continuous supercritical fluids process for the understanding of the nucleation and growth of the nanocrystals. Moreover, ZnO nanocrystals formation mechanism determines UV-emitting properties of this material. The optical properties at room and low temperature were deeply investigated with comparing to the PL emission of several types of ZnO particles and single crystal for the understanding of the nature of UV emission.

This thesis is concerned with quantum properties of excitonic energy transport in nanostructures that are embedded in a noisy environment. Of principal interests are ways to exploit this environment to facilitate the transport of energetic excitations. The first research chapter deals with an extension to the 'standard' open quantum system picture, where the Hilbert space is split into three: system, environment, and a wider universe. This division is natural for many biological and artificial nanostructures. A new analytical method, based on a phase space representation of the density matrix, is developed for studying such division. The effects of the wider universe are shown to be captured by a simple correction of the environmental response function. The second research chapter addresses the question: when do second-order perturbative approaches to open quantum systems, which are intuitive and simple to compute, provide adequate accuracy? A simple analytical criterion is developed, and its validity is verified for the case of the much-studied FMO dynamics as well as the canonical spin-boson model. In the third research chapter, an intuitive model of a photocell is studied. The model comprises two light-absorbing molecules coupled to an idealised reaction centre, showing asymmetric dimers are capable of providing a significant enhancement of light-to-current conversion under ambient conditions. This is done by 'parking' the energy of an absorbed photon in a dark state which neither absorbs nor emits light. In the final research chapter, a basic model for what can be thought as a "quantum brachistochrone" problem is investigated. Exotic energy configurations are found to yield considerable enhancement to the exciton's transfer probability, due to similar mechanisms studied in the previous chapter.

Electronic band structure in the solid and its relation to the energy gap of the monomer is all about studying how intermolecular interactions change electronic structure. In experimental studies this results in broader absorption bands and by extension a lowering of the LUMO and raising of HOMO energy to the conduction and valence band edges respectively. This electronic change involves splitting of the molecular energy levels into bands of non-degenerate energies and can be calculated either quantum mechanically (QM) or by classical force field models through the change in ionization potential (IP) and electron affinity (EA), called the apparent polarization energy, and its relation to HOMO and LUMO through Koopman’s and Janak’s theorem. The study of the formation of a ‘band’ like structure is important in regimes and systems where conventional quantum mechanical (QM) methods become infeasible. Specifically, when systems are non-periodic and plane wave approximations fail, such as in amorphous structures, or in regimes between where the plane wave bulk approximation and the gas phase single molecule QM methods where the scaling of conventional gas phase atomic orbital methods becomes exorbitantly costly and the plane wave approximation fails for open systems. Therefore, the objective of this work is to highlight the changing optoelectronic properties of molecular solids within this regime using both density functional theory and molecular mechanics. The scalability of DFT limits it to multimer systems, leaving the larger nanoscale materials to be studied using molecular mechanics. Here we have utilized a variety of dispersion sensitive functionals in order to characterize the intermolecular interactions and splitting energies in small multimers of some of the smallest oligoacene species, benzene and anthracene. Benzene and anthracene nanoclusters from 0.8 to 5.0 nm in radius have had their changes in electronic band energy calculated due to polarization using the AMOEBA force field and bulk values have also been extrapolated. AMOEBA’s explicit polarization terms allow for direct handling of the polarization energy, control of nanocluster size and shape in a regime that QM methods cannot probe efficiently, and the ability to specify the position of charge carriers in order to examine specific electronic surface behavior. Using differing DFT methods the change in the HOMO and LUMO energy from the single molecule state to multimers of the size of 10 and 12 units for anthracene and benzene respectively. The HOMO band of benzene was raised by ~0.3 eV and LUMO lowered by 0.35 eV. In anthracene the HOMO was lowered by ~0.1 eV and the LUMO by ~0.15 eV. These values remain within 0.1 eV across all dispersion functionals. Using Ren’s parameterization procedure and MP2 for the AMOEBA force field he apparent polarization was calculated. The extrapolated values for the change in the HOMO and LUMO of benzene from single molecule to bulk were 1.42 eV and 0.49 eV respectively. For anthracene the crystalline bulk changes the HOMO and LUMO by 1.34 eV and 1.16 eV respectively. The regression for bulk extrapolation also predicts that benzene clusters of 12 units will be 0.77 eV for HOMO and -0.41 eV for LUMO. Similarly for an anthracene cluster made up of 10 molecular units the apparent polarization is predicted through linear regression to be 0.58 eV for HOMO and 0.53 eV for LUMO.

No description available.

Condensed matter systems exhibit a variety of dynamical phenomena at low energy scales, from gigahertz (GHz) to terahertz (THz) frequencies in particular, arising from complex interplay between charge, spin, and lattice. A large number of collective and elementary excitations in solids occur in this frequency range, which are further modified and enriched by scattering, interactions, and disorder. Recent advancements in spectroscopic methods for probing low-energy dynamics allow us to investigate novel aspects of charge and spin dynamics in solids. In this dissertation work, we used direct current (DC) conductivity, GHz, THz, and mid-infrared (MIR) techniques to provide significant new insights into interaction and disorder effects in low-dimensional systems. Specifically, we have studied temperature-dependent magnetoresistance (MR) and electron spin resonance (ESR) in single-wall carbon nanotubes (SWCNTs), intra-exciton scattering in InGaAs quantum wells, and high-field MIR-induced band gaps in graphene. Temperature-dependent resistance and MR were measured in an ensemble of SWCNTs from 0.3 to 350 K. The resistance temperature behavior followed a 3D variable range hopping (VRH) behavior from 0.3 to ~100 K. A positive MR was observed at temperatures above 25 K and could be fit with a spin-dependent VRH model; negative MR was seen at low temperatures. In the GHz regime, the ESR linewidth for SWCNTs was observed to narrow by as much as ~50% as the temperature was increased from 3 to 300 K, a phenomenon known as motional narrowing, suggesting that we are detecting the ESR of hopping spins. From the linewidth change versus temperature, we find the hopping frequency to be 285 GHz. For excitons in InGaAs quantum wells, we demonstrate the manipulation of intra-excitonic populations using intense, narrow-band THz pulses. The THz radiation temporarily quenches the 1s emission, which is then followed by an enhancement and subsequent decay of 2s emission. After the quenching, the 1s emission recovers and then eventually becomes enhanced, a demonstration of energy storage in intra-exciton states known as excitonic shelving. We show that the diffusive Coulomb scattering between the 2p and 2s states produces a symmetry breaking, leading to a THz-field-induced 1s-to-2s exciton population transfer.

Les propriétés spécifiques des milieux fluides supercritiques sont exploitées depuis denombreuses années dans les domaines de la séparation, de la chimie et des matériaux.Aujourd’hui, les activités de recherche se focalisent vers une meilleure compréhension et unmeilleur contrôle des processus thermodynamiques, physiques et chimiques mis en jeu, ce quinous a naturellement amené à développer la microfluidique supercritique. C’est dans cecontexte que s’inscrivent ces travaux de thèse ayant pour objet le développement et l’utilisationde l’outil microfluidique pour l’étude de la réactivité chimique et de la germination-croissance enmilieux fluides supercritiques.Notre premier objectif a concerné le développement de l’outil microfluidique supercritique etde microsystèmes résistants aux conditions de température et de pression. Quelquescaractéristiques physiques associées à ces dispositifs sont proposées de manière à observerclairement les avantages attendus du couplage de la microfluidique et des fluides supercritiques.Nous avons ensuite validé l’apport de la microfluidique supercritique sur la réactivité chimiqueet la chimie des matériaux via, d’une part, l’étude de l’oxydation hydrothermale du méthanol et,d’autre part, l’élaboration de nanocristaux de ZnO. Les propriétés de photoluminescence de cesnanocristaux de ZnO ont été caractérisées; nous avons montré que l’outil microfluidiquesupercritique permet de synthétiser des nanocristaux de ZnO avec une luminescenceexcitonique. / The unique properties of supercritical fluids (SCFs) have been widely used since the 1980’sin a wide range of applications including separation, chemistry and materials synthesis.Currently, the research activities are focused toward a better understanding and tailoring ofthermodynamical, physical and chemical phenomena involved in SCFs processes. In thiscontext, this is why we have chosen to develop supercritical microfluidics in the frame of thisPhD work, which aims at developing and using microfluidic tools in order to study the chemicalreactivity and the nucleation-growth in supercritical fluids.First of all, our strategy aimed at fabricating microsystems which could handle to the SCFsoperating conditions (high pressure and high temperature). Then, we have studied somephysical characteristics of these devices and in particular we determined the expectedadvantages associated with the combination of microfluidic tools and supercritical fluids.Afterwards, we have demonstrated the benefits of the supercritical microfluidics to materialssynthesis and chemical reactivity through the hydrothermal oxidation of methanol and thesynthesis of ZnO nanocrystals. This last point was also the subject of a photoluminescencestudy, demonstrating that supercritical microfluidics tools can be used as “precision synthesis”reactors.

This dissertation has two intersecting foci; firstly, the discovery of a new methodology for the growth of high surface area cuprous oxide (Cu2O) substrates. Secondly, the synthesis and characterization of electron-accepting molecules, and their incorporation into excitonic solar cells (XSCs) using the Cu2O substrates as electrodes. Increasing the surface area of the semiconductor creates more locations for charge transfer to occur thus increasing the overall efficiency of the device. Zinc oxide (ZnO) has been widely studied, and can be easily grown into many different films with high surface area morphologies. The ZnO films serve as sacrificial templates that allow us to electrochemically grow new semiconductors with the same high surface area morphologies but composed of a material having more desirable electronic properties. A polymer can be applied over the surface of the ZnO nanorod films before etching the ZnO with a weak acid, thereby leaving a polymer nanopore membrane. Cathodic electrodeposition of Cu2O into the membrane nanopores gives Cu2O nanorods. Electron-accepting dyes are designed with tethers that allow for direct attachment to metal oxide semiconductors. After soaking, the semiconductor is coated with a monolayer of a dye and then the coated semiconductor films were made into various dye-sensitized solar cells (DSCs). These cells were studied to determine the electron transport properties at the semiconductor/sensitizer/electrolyte interface.