Neste trabalho investigamos a dinâmica de formação de nanopartículas de Au por pulsos de femtossegundos formatados (800 nm, 30 fs, 1 kHz e 2 mJ), induzida pela ionização da molécula de quitosana. Inicialmente desenvolvemos um sistema de formatação de pulsos ultracurtos que faz uso de um modulador espacial de luz, constituído por um arranjo linear de cristais líquidos, com o qual somos capazes de impor distintas modulações de fase ao pulso laser. Para monitorar o processo de produção de nanopartículas, montamos um sistema de excitação (pulsos de femtossegundos) e prova (luz branca), o qual permite a observação em tempo real do aparecimento da banda de plásmon e, consequentemente, da dinâmica de formação das nanopartículas. Resultados obtidos para pulsos não formatados (limitados por Transformada de Fourier) demonstraram que a formação de nanopartículas deve-se à ionização não linear da quitosana, a qual está relacionada à oxidação do grupo hidroxila para o grupo carbonila. Medidas de microscopia eletrônica de transmissão forneceram os tamanhos (entre 20 e 100 nm) e formatos (esferas, pirâmides, hexágonos, bastões, etc) das nanopartículas geradas. Ainda, nossos resultados revelaram que esta ionização é iniciada por absorção multifotônica, mais especificamente por absorção de 4 fótons. Utilizando pulsos formatados com fase espectrais constante, degrau e cossenoidal com diferentes frequências, investigamos a influência destes na formação de nanopartículas. Concluímos que os pulsos mais longos são mais favoráveis ao processo de ionização, e consequente redução dos íons de Au para a formação de nanopartículas metálicas. Este comportamento se deve, provavelmente, à redistribuição da energia absorvida para os modos vibracionais, o que é mais provável para pulsos mais longos. Assim, o método apresentado pode abrir novas maneiras para a formação de nanopartículas de metálicas, as quais podem ser mais exploradas dos pontos de vista aplicado e fundamental. / In this work we have studied the synthesis of Au nanoparticles using shaped ultrashort pulses (800 nm, 30 fs, 1 kHz and 2 mJ), induced by the ionization of the chitosan. Initially we developed a pulse shaping setup that uses a spatial light modulator (liquid crystals array), with which we are able to impose distinct phase mask to the laser pulse. In order to monitor the nanoparticles production process, we used a pump-probe system, consisting of femtosecond pulses (pump) and white light (probe), which allows the observation of the plasmon band enhancement and hence the nanoparticles formation dynamics. The results obtained by Fourier Transform limited pulses have shown that the nanoparticles formation is due to the nonlinear ionization of chitosan, which is related to hydroxyl group oxidation to the carbonyl group. Transmission electron microscopy measurements provided the sizes (20-100 nm) and shapes (spheres, pyramids, hexagons, rods, etc.) of the produced nanoparticles. Moreover, our results revealed that ionization is initiated by multiphoton absorption, more specifically by four photons absorption. Using pulses shaped with constant, step and cossenoidal (with different frequencies) spectral phase masks, we investigated their influence in the nanoparticles formation. We conclude that longer pulses are more favorable to the ionization process and, consequently, to the gold ions reduction for the synthesis of the metallic nanoparticles. This behavior is probably due to the redistribution of the absorbed energy to the vibrational modes, which is more likely for longer pulses. Therefore, the approach presented here can open new ways to produce metallic nanoparticles, which can be further explored from applied and fundamental points of view.

Este trabalho teve como objetivo a montagem de um sistema de otimização de pulsos ultracurtos (oscilador laser modelocked de 15 fs), através de uma técnica de formatação de pulsos via absorção de dois fótons em compostos orgânicos. Está técnica utiliza uma estratégia evolucionária baseada em um algoritmo genético, onde se controla o formato do pulso pela deformação imposta a um espelho deformável, conjuntamente com o monitoramento de um sinal de realimentação. Desta forma, este sistema permite tanto a otimização do processo de absorção de dois fótons, quanto a otimização do próprio pulso do sistema laser. Após a montagem inicial do sistema de formatação de pulsos, foram implementados três métodos de otimização via monitoramento do processo de absorção de dois fótons, sendo que dois deles foram desenvolvidos nesta dissertação. Os métodos diferem entre si pelo emprego de distintos sinais de realimentação para o processo de otimização: (i) intensidade da fluorescência excitada por dois fótons; (ii) variação da transmitância não linear dos compostos orgânicos devido à absorção de dois fótons; e (iii) intensidade do efeito de lente térmica apresentada pelos compostos orgânicos após a absorção de dois fótons. Os três métodos de otimização apresentaram resultados similares e satisfatórios, aproximando a largura temporal do pulso ao final do processo de otimização da largura temporal dada pelo limite da transformada de Fourier, medidas através de técnicas de autocorrelação. Estes resultados apontam para a validade do uso dos métodos por nós desenvolvidos como alternativas para processos de otimização de pulsos ultracurtos. / In this work it is described the implementation of an ultrashort pulse optimization system (15 fs modelocked oscillator) that employs pulse shaping methods via two-photon absorption in organic materials. This technique uses an evolutionary strategy based on a Genetic Algorithm, where the pulse shape is controlled by a deformable mirror, while a feedback signal is monitored. In this way, this system allows both, the two-photon absorption process and pulse optimization. After the accomplishment of the pulse shaping system, we have implemented three distinct optimization methods via two-photon absorption monitoring, being two of them proposed in the present dissertation. These three methods differs from each other by the use of different feedback signals for the optimization process: (i) intensity of the two-photon excited fluorescence; (ii) nonlinear transmittance change in organic compounds due to the two-photon absorption; and (iii) intensity of the thermal lens effect. All optimization methods presented similar and satisfactory results, leading the ultrashort pulse, in the end of the optimization process, close to the Fourier transformed limit. In such cases, the pulse duration were determined through the autocorrelation technique. These results indicates that the new methods proposed here can be used as an alternative for both, pulse optimization and control of two-photon absorption process, specially for nonfluorescent samples.

Este trabalho teve como objetivo a montagem de um sistema de otimização de pulsos ultracurtos (oscilador laser modelocked de 15 fs), através de uma técnica de formatação de pulsos via absorção de dois fótons em compostos orgânicos. Está técnica utiliza uma estratégia evolucionária baseada em um algoritmo genético, onde se controla o formato do pulso pela deformação imposta a um espelho deformável, conjuntamente com o monitoramento de um sinal de realimentação. Desta forma, este sistema permite tanto a otimização do processo de absorção de dois fótons, quanto a otimização do próprio pulso do sistema laser. Após a montagem inicial do sistema de formatação de pulsos, foram implementados três métodos de otimização via monitoramento do processo de absorção de dois fótons, sendo que dois deles foram desenvolvidos nesta dissertação. Os métodos diferem entre si pelo emprego de distintos sinais de realimentação para o processo de otimização: (i) intensidade da fluorescência excitada por dois fótons; (ii) variação da transmitância não linear dos compostos orgânicos devido à absorção de dois fótons; e (iii) intensidade do efeito de lente térmica apresentada pelos compostos orgânicos após a absorção de dois fótons. Os três métodos de otimização apresentaram resultados similares e satisfatórios, aproximando a largura temporal do pulso ao final do processo de otimização da largura temporal dada pelo limite da transformada de Fourier, medidas através de técnicas de autocorrelação. Estes resultados apontam para a validade do uso dos métodos por nós desenvolvidos como alternativas para processos de otimização de pulsos ultracurtos. / In this work it is described the implementation of an ultrashort pulse optimization system (15 fs modelocked oscillator) that employs pulse shaping methods via two-photon absorption in organic materials. This technique uses an evolutionary strategy based on a Genetic Algorithm, where the pulse shape is controlled by a deformable mirror, while a feedback signal is monitored. In this way, this system allows both, the two-photon absorption process and pulse optimization. After the accomplishment of the pulse shaping system, we have implemented three distinct optimization methods via two-photon absorption monitoring, being two of them proposed in the present dissertation. These three methods differs from each other by the use of different feedback signals for the optimization process: (i) intensity of the two-photon excited fluorescence; (ii) nonlinear transmittance change in organic compounds due to the two-photon absorption; and (iii) intensity of the thermal lens effect. All optimization methods presented similar and satisfactory results, leading the ultrashort pulse, in the end of the optimization process, close to the Fourier transformed limit. In such cases, the pulse duration were determined through the autocorrelation technique. These results indicates that the new methods proposed here can be used as an alternative for both, pulse optimization and control of two-photon absorption process, specially for nonfluorescent samples.

Neste trabalho investigamos a dinâmica de formação de nanopartículas de Au por pulsos de femtossegundos formatados (800 nm, 30 fs, 1 kHz e 2 mJ), induzida pela ionização da molécula de quitosana. Inicialmente desenvolvemos um sistema de formatação de pulsos ultracurtos que faz uso de um modulador espacial de luz, constituído por um arranjo linear de cristais líquidos, com o qual somos capazes de impor distintas modulações de fase ao pulso laser. Para monitorar o processo de produção de nanopartículas, montamos um sistema de excitação (pulsos de femtossegundos) e prova (luz branca), o qual permite a observação em tempo real do aparecimento da banda de plásmon e, consequentemente, da dinâmica de formação das nanopartículas. Resultados obtidos para pulsos não formatados (limitados por Transformada de Fourier) demonstraram que a formação de nanopartículas deve-se à ionização não linear da quitosana, a qual está relacionada à oxidação do grupo hidroxila para o grupo carbonila. Medidas de microscopia eletrônica de transmissão forneceram os tamanhos (entre 20 e 100 nm) e formatos (esferas, pirâmides, hexágonos, bastões, etc) das nanopartículas geradas. Ainda, nossos resultados revelaram que esta ionização é iniciada por absorção multifotônica, mais especificamente por absorção de 4 fótons. Utilizando pulsos formatados com fase espectrais constante, degrau e cossenoidal com diferentes frequências, investigamos a influência destes na formação de nanopartículas. Concluímos que os pulsos mais longos são mais favoráveis ao processo de ionização, e consequente redução dos íons de Au para a formação de nanopartículas metálicas. Este comportamento se deve, provavelmente, à redistribuição da energia absorvida para os modos vibracionais, o que é mais provável para pulsos mais longos. Assim, o método apresentado pode abrir novas maneiras para a formação de nanopartículas de metálicas, as quais podem ser mais exploradas dos pontos de vista aplicado e fundamental. / In this work we have studied the synthesis of Au nanoparticles using shaped ultrashort pulses (800 nm, 30 fs, 1 kHz and 2 mJ), induced by the ionization of the chitosan. Initially we developed a pulse shaping setup that uses a spatial light modulator (liquid crystals array), with which we are able to impose distinct phase mask to the laser pulse. In order to monitor the nanoparticles production process, we used a pump-probe system, consisting of femtosecond pulses (pump) and white light (probe), which allows the observation of the plasmon band enhancement and hence the nanoparticles formation dynamics. The results obtained by Fourier Transform limited pulses have shown that the nanoparticles formation is due to the nonlinear ionization of chitosan, which is related to hydroxyl group oxidation to the carbonyl group. Transmission electron microscopy measurements provided the sizes (20-100 nm) and shapes (spheres, pyramids, hexagons, rods, etc.) of the produced nanoparticles. Moreover, our results revealed that ionization is initiated by multiphoton absorption, more specifically by four photons absorption. Using pulses shaped with constant, step and cossenoidal (with different frequencies) spectral phase masks, we investigated their influence in the nanoparticles formation. We conclude that longer pulses are more favorable to the ionization process and, consequently, to the gold ions reduction for the synthesis of the metallic nanoparticles. This behavior is probably due to the redistribution of the absorbed energy to the vibrational modes, which is more likely for longer pulses. Therefore, the approach presented here can open new ways to produce metallic nanoparticles, which can be further explored from applied and fundamental points of view.

Complex optical pulse shapes are typically generated from ultrashort laser pulses by manipulating the optical spectrum of the input pulses. This generates complex but periodic time-domain waveforms. Optical Arbitrary Waveform Generation (OAWG) builds on the techniques of ultrashort pulse-shaping, with the goal of making non-periodic, truly arbitrary optical waveforms. Some applications of OAWG are coherently controlling chemical reactions on a femtosecond time scale, improving the performance of LADAR systems, high-capacity optical telecommunications and ultra wideband signals processing. In this work, an array of Vertical Cavity Surface Emitting Lasers (VCSELs) are used as modulators, by injection-locking each VCSEL to an individual combline from an optical frequency comb source. Injection-locking ensures that the VCSELs' emission is phase coherent with the input combline, and modulating its current modulates mainly the output optical phase. The multi-GHz modulation bandwidth of VCSELs updates the output optical pulse shape on a pulse-to-pulse time scale, which is an important step towards true OAWG. In comparison, it is about a million times faster than the liquid-crystal modulator arrays typically used for pulse shaping! Novel components and subsystems of Optical Arbitrary Waveform Generation (OAWG) are developed and demonstrated in this work. They include: 1. Modulators An array of VCSELs is packaged and characterized for use as a modulator for rapid?update pulse?shaping at GHz rates. The amplitude and phase modulation characteristics of an injection-locked VCSEL are simultaneously measured at GHz modulation rates. 2. Optical Frequency Comb Sources An actively mode-locked semiconductor laser was assembled, with a 12.5 GHz repetition rate, ~ 200 individually resolvable comblines directly out of the laser, and high frequency stability. In addition, optical frequency comb sources are generated by modulation of a single frequency laser. 3. High-resolution optical spectral demultiplexers The demultiplexers are implemented using bulk optics, and are used to spatially resolve individual optical comblines onto the modulator array. 4. Optical waveform measurement techniques Several techniques are used to measure generated waveforms, especially for spectral phase measurements, including multi-heterodyne phase retrieval. In addition, an architecture for discriminating between ultrashort encoded optical pulses with record high sensitivity is demonstrated.

Orthogonal Frequency Division Multiplexing (OFDM) is well known as an efficient technology for wireless communications and is widely used in many of the current and upcoming wireless and wireline communication standards. However, it has some intrinsic drawbacks, e.g., sensitivity to the inter-carrier interference (ICI) and high peak-to-average power ratio (PAPR). Additionally, the cyclic prefix (CP) is not spectrum efficient and fails when the channel delay spread exceeds the length of CP, which will result in inter-symbol interference (ISI). In order to combat or alleviate these drawbacks various techniques have been proposed, which can be categorised into two main classes: techniques that keep the structure of OFDM and meanwhile increase the system robustness or re-organise the symbol streams on each sub-carrier, and techniques that increase the ISI/ICI immunity by adopting well designed pulse shapes and/or resorting to general system lattices. The latter class are coined as Generalised FDM (GFDM) throughout this thesis to distinguish with the former class. To enable seamless handover and efficient usage of spectrum and energy, GFDM is expected to dynamically adopt pulse shapes that are optimal in doubly (time and frequency) dispersive fading channels. This is however not an easy task as the method of optimal pulse shape adaptation is still unclear, let alone efficient implementationmethods. Besides, performance of GFDM highly depends on the channel estimation quality, which is not straightforward in GFDM systems. This thesis addresses, among many other aspects of GFDM systems, measures of the time frequency localisation (TFL) property, pulse shape adaptation strategy, performance evaluation and channel estimation.  We first provide a comparative study of state-of-the-art GFDM technologies and a brief overview of the TFL functions and parameters which will be used frequently in later analysis and discussion. A framework for GFDM pulse shape optimisation is formulated targeting at minimising the combined ISI/ICI over doubly dispersive channels. We also propose a practical adaptation strategy utilising the extended Gaussian functions (EGF) and discuss the trade-off between performance and complexity.  One realisation under the umbrella of GFDM, namely OFDM/OQAM, is intensively studied and an efficient implementation method by direct discretisation of the continuous time model has been proposed.  Besides, a theoretical framework for a novel preamble-based channel estimation method has been presented and a new preamble sequence with higher gain is identified. Under the framework, an optimal pulse shape dependent preamble structure together with a suboptimal but pulse shape independent preamble structure have been proposed and evaluated in the context of OFDM/OQAM. / QC 20101108

Thesis (MSc)--University of Stellenbosch, 2011. / ENGLISH ABSTRACT: The selective excitation of an arbitrary vibrational level of a polyatomic molecule, without passage through an intermediary electronic excited state is demonstrated. This was achieved by simulating the interaction of a shaped, femtosecond pulse with one vibrational mode of the molecule. The carrier frequency of the pulse is chosen near resonant to the ground-to- rst-excited vibrational transition of the mode, and the pulse shape is optimized via closed-loop feedback. The simulation concentrates on the rst few vibrationally excited states since the density of states is still low, thus ensuring that the inter-vibrational decoherence time is relatively long compared to the pulse length. While various molecules were investigated this study focuses onUF6 for which detailed spectroscopic data for the v3 vibrational mode is available in literature. A multilevel model was developed and can be adapted for any number of levels. The model reported here was limited to a vibrational quantum number of four. The spectroscopic data included anharmonic splitting as well as forbidden transitions. The effect of rotational levels was not included. A density matrix approach was followed because this will allow for the introduction of dephasing of the coherent excitation via thermalizing collisions with the reservoir, as well as inter-vibrational relaxation. The time evolution of the density matrix is given by the Von Neumann equations. / AFRIKAANSE OPSOMMING: Die selektiewe opwekking van 'n arbitrêre vibrasionele vlak van 'n poliatomies molekule sonder oorgang na 'n intermediëre elektroniese opgewekte toetstand word gedemonstreer. Dit was bereik deur die interaksie te simuleer van 'n gevormde, femtosekonde pulse met een vibrasionele mode van 'n molekule. Die draer frekwensie van die pulse is so gekies dat dit naby resonansie van die grond-tot-eerste-opgewekte vibrasionele oorgang van die mode is, die puls vorm word geoptimeer deur 'n geslote-lus terugvoer. Die simulasie konsentreer op die eerste paar vibrasionele opgewekte toestande, omdat die digtheid van toestande nog steeds laag is, dus verseker dit dat inter-vibrasionele de-koherensie tyd relatief lank is in vergelyking met die puls se lengte. Verskillende molekules was ondersoek vir die studie. Die fokus is op UF6 waarvoor gedetaileerde spektroskopiese data vir die v3 vibrasionele beskikbaar is in die literatuur. 'n Multivlak model was ontwikkel en kan aangepas word vir enige aantal van vlakke. Die model wat hier aangemeld is, is beperk tot die vibrasionele kwantum getal van vier. Die spektroskopiese data het anharmonies splitting so wel as nie toegelaatbare oorgange bevat. Die effek van rotasionele vlakke was nie in berekening geneem nie. 'n Digtheids matriks benadering was gevolg, omdat dit toelaat vir die dekoherensie. Die tyd evolusie van die digtheids matriks word gegee deur die Von Neumann vergelykings.

In this thesis the control of ultrafast (10⁻¹³ s) optical pulses used for metrological applications has been investigated. Two different measurement set-ups have been considered, both based around the `pump-probe' technique, where an optical pulse is divided into two parts, one to `pump' or excite a physical system of interest, the other to `probe' or measure the outcome. In both cases the measurement uses electro-optic sampling (EOS), where an electric field is measured by detecting changes in the optical probe pulse polarisation after interaction with the field. In the first study, a method for wavelength metrology in the terahertz (THz) region has been demonstrated by producing an optical pulse shaper and genetic algorithm to control pump pulses and so indirectly influence the THz spectra they generate. In the second study an OPO (optical parametric oscillator) has been developed to provide ultrafast optical pulses for the generation of < 100 fs electrical pulses for metrology using quantum interference control (QUIC). QUIC electrical signals have been demonstrated successfully by charge accumulation measurements and the QUIC electrical pulse temporally measured using EOS, though the low signal levels due to power restrictions mean the QUIC electrical pulse is unsuitable for metrology at this time. Finally, a portable optical pulse measurement device based around frequency-resolved optical gating (FROG) has been designed, built and tested. This has been shown to be capable of retrieving amplitude and phase information in both the temporal and spectral domains for optical pulses as short as 20 fs duration. The ability to characterise shaped pulses also has been demonstrated successfully, with the requirements for full automation identified.

This thesis describes the use of counterpropagating pulse trains to quasi-phase-match high-harmonic generation (HHG). Two novel techniques for generating trains of ultrafast pulses are described and demonstrated. The first method makes use of a birefringent crystal array to split a single pulse into a sequence of pulses. The second method makes use of the time-varying polarisation of a chirped pulse passed through a multiple-order wave plate to generate a train of pulses by the addition of a polariser. It is demonstrated that this second technique can be used to make pulse trains with non-uniform pulse separation by using an acousto-optic programmable dispersive filter to manipulate the higher-order dispersion encountered by the chirped pulse. The crystal array method is used to demonstrate quasi-phase-matching of HHG in a gas-filled capillary, using one and two counterpropagating pulses. Enhancements of up to 60% of the intensity of the 27th harmonic of the 800,nm driving laser light are observed. Information on the spatial and dynamic properties of the HHG process is obtained from measurements of the coherence length in the capillary. Simulations of HHG in a capillary waveguide have been performed. These agree well with the results of the quasi-phase-matching experiments. The effect of mode-beating on the generation process in a capillary and its use as a quasi-phase-matching mechanism are investigated.

Técnicas de formatação de pulsos permitem o controle das propriedades espectrais e temporais de um feixe laser criando novas possibilidades de estudo da interação luz-matéria. Neste trabalho estudamos as propriedades ópticas não-lineares via formatação de pulsos ultracurtos de três semicondutores: Óxido de Zinco, Silício e Nitreto de Gálio; em três abordagens diferentes. Discutimos também as consequências da distorção de fase em processos não lineares devido à natureza discreta do dispositivo modulador. Primeiramente, investigamos a otimização da emissão excitônica em um cristal de Óxido de Zinco através de uma técnica de otimização que utiliza algoritmo genético, observamos que a fase espectral que otimiza o processo cria um perfil temporal do pulso que indica um acoplamento do tipo éxciton-fônon no cristal. Estudamos ainda o efeito da aplicação de uma máscara de fase senoidal, criando um trem de pulsos, no processo de formação de estruturações superficiais periódicas induzidas a laser no Silício - o fator de eficácia das estruturações foi controlado através dos tempos de separação entre os sub-pulsos, resultado que pôde ser interpretado usando a teoria de Sipe-Drude. Por fim, estudamos a influência da formatação de pulsos em processos de absorção multi-fotônicos em um filme fino de GaN onde verificamos, inicialmente, que o material apresenta um coeficiente de absorção não-linear atípico. Modelamos este comportamento usando equações de taxa e investigamos sua modificação aplicando uma fase quadrática. / Pulse shaping techniques allows the control of spectral and temporal properties of a laser beam, creating new possibilities for the study of the light-matter interaction. In this work we study the nonlinear optical properties, via ultrashort pulses, of three semiconductors; Zinc Oxide, Silicon and Gallium Nitride in three different approaches. We also discuss the consequences of phase distortion in nonlinear processes due to the discrete nature of the light modulator device. Initially, we investigated the optimization of exciton emission in a zinc oxide crystal through using a genetic algorithm; we observed that the spectral phase that optimizes the process creates a temporal pulse profile that indicates an exciton-phonon coupling in the crystal. We also studied the effect of the application of a sinusoidal phase mask, creating a pulse train, in the process of laser induced periodic surface structures in Silicon; the efficacy factor of the produced structures was controlled through the separation time between the sub-pulses and interpreted using the Sipe-Drude theory. Finally, we study the influence of pulse shaping on multi-photon absorption processes in a thin film of GaN; we found, initially, that the material exhibits an atypical nonlinear absorption coefficient. We model this behavior using rate equations and investigate its modification by applying a quadratic phase.