<p>Optical parametric oscillators (OPOs) and optical parametricamplifiers (OPAs) constitute a class of optical frequencyconverting devices that have many possible applications, e.g.in range finding, molecular spectroscopy and medicine. They canconvert the frequency of the incident pump field with highefficiency, and generate two waves at new frequencies that willbe continuously tuneable over a wide spectral range. Virtuallyany wavelengths within the transparency region of the nonlinearmaterial can be generated if the material can bequasi-phasematched (QPM). In addition, QPM gives thepossibility to utilise the largest nonlinear tensor element ofthe material and allows walk-off free interaction between thewaves.</p><p>The aims of this thesis have been to investigate thepossibility to use QPM KTiOPO₄crystals as nonlinear material in nanosecond OPOsand OPAs operating at room-temperature, and to explore theadvantages and shortcomings of these devices. The technique ofelectric field poling has been employed to implement the QPMstructure in flux grown KTiOPO₄(KTP).</p><p>The main conclusion is that periodically poled KTP (PPKTP)is a suitable material to use in nanosecond OPOs and OPAs. Thematerial properties that foremost make KTP into an attractivenonlinear material are: The large value of the nonlinearcoefficient d₃₃, the high resistance to optically inducedbreakdown, the low susceptibility to grey-track formation, theinsensitivity to the photorefractive effect, the widetransparency and the low coercive field.</p><p>The thesis shows that it is possible to pole large volumesof KTP with a high quality of the QPM structure. Highlyefficient nanosecond OPOs have been constructed during thisproject. Maximum conversion efficiencies have reached 45 % inthe case of a singly resonant OPO (SRO) built around a 3 mmthick PPKTP crystal. Total pulse energies for both the signal(1.72 µm) and the idler (2.8 µm) of up to 18 mJ wasreached and an average output power of 2 W was obtained forthis sample. However, up to 24 W was produced in a doublyresonant OPO operating close to degeneracy. The efficiencyreached 48 % for that case. Truly continuous and very widespectral tuning has also been demonstrated, as well as a narrowbandwidth OPO operating on one single longitudinal mode.</p><p><b>Keywords:</b>optical parametric oscillators, opticalparametric amplifiers, quasi-phasematching, KTiOPO₄, nonlinear optics, frequency conversion, periodicelectric field poling, ferroelectrics, high-order secondharmonic generation, electro-optic effect.</p>

<p>This thesis deals with the fabrication and the characterization of periodically-poled crystals for use in lasers to generate visible and UV radiation by second-harmonic generation (SHG) through quasi-phasematching (QPM). Such lasers are of practical importance in many applications like high-density optical storage, biomedical instrumentation, colour printing, and for laser displays.</p><p>The main goals of this work were: (1) to develop effective monitoring methods for poling of crystals from the KTiOPO₄ (KTP) family, (2) to develop useful non-destructive domain characterization techniques, (3) to try to find alternative crystals to KTP for easier, periodic poling, (4) to investigate the physical mechanisms responsible for optical damage in KTP. The work shows that the in-situ SHG technique used together with electro-optic monitoring, makes it possible to obtain reliable, real-time information regarding the poling quality over the whole crystal aperture during the electric-field poling process. Using this combined monitoring method, both KTP and Rb-doped KTP (RKTP) crystals were successfully poled. By comparing these two crystals, we found that a low-doped KTP has a substantially reduced ionic conductivity and, thus, a high-quality periodic poling can be obtained without otherwise affecting the properties of the crystal. RKTP is a good alternative candidate to KTP for poling purpose. We have also shown that Atomic Force Microscopy (AFM) is an informative tool for investigating domain nucleation, growth, and merging. Furthermore, we have demonstrated a simple technique for 3D characterization of QPM samples. It utilizes a group-velocity mismatched, type-II SHG of femtosecond pulses for layer-by-layer monitoring of the effective nonlinearity along the propagation direction of the beam. The quality of these crystals was finally reflected in a number of SHG experiments with a variety of laser sources. High energies and high efficiencies were thus demonstrated using CW, mode-locked and Q-switched lasers. Gratings with pitches smaller than 3 µm, were demonstrated for first-order UV generation. Type-II QPM SHG was demonstrated as a technique for reducing the fabrication constraints.</p><p>High intensity light in the visible and the UV leads to modification of the material properties and, eventually, to optical damage. In KTP and its isomorphs, the first sign of material change is an optically-induced absorption. We have used thermal-lens spectroscopy with a common-path interferometer for high-sensitivity measurements of green light-induced infrared absorption dynamics in single-domain and periodically-poled KTP (PPKTP). The saturated, green light-induced absorption has been shown to be consistently higher in periodically-poled crystals, and is attributed to the creation of stoichiometric and interstitial defects in the crystals during the poling process. Finally, irreversible bulk damage thresholds in PPKTP have been determined for pulsed frequency converters. As the characteristics of optical damage are closely related to the material quality, this investigation can provide useful information for crystal manufactures and will help to optimise the crystal growth conditions.</p>

In der vorliegenden Arbeit wird dargestellt, wie sich mit Methoden der nuklearen Festkörperphysik Defekte und Deformationen selbst in kristallographisch komplexen Materialien wie den MAX-Phasen, einer Klasse von Komplexcarbiden bzw. -nitriden, in-situ nachweisen lassen. Die sensitive Messgröße bildet dabei der elektrische Feldgradient (EFG), der ein Maß für die Asymmetrie der den jeweiligen Sondenkern umgebenden Ladungsverteilung darstellt. Es werden zwei Wechselwirkungsmechanismen zwischen Defekt und EFG diskutiert: Einerseits die langreichweitigen Auswirkungen elastischer Verzerrungen, andererseits der direkte Einfluss eines Defektes auf seine lokale elektronische Umgebung. Die Bestimmung der elastischen Antwort des Feldgradienten erfolgt mittels Ab-initio-Methoden im Rahmen der Dichtefunktionaltheorie. Der dabei vorgestellte Ansatz erlaubt es, die Ursachen der Dehnungsabhängigkeit zu klären und andere, speziellere Dehnungsabhängigkeiten wie die Volumenabhängigkeit oder die Strukturabhängigkeit des Feldgradienten zu bestimmen. Die in der Umgebung bestimmter Defekte oder Deformationen auftretenden EFG-Verteilungen werden anhand der allgemeinen Dehnungsabhängigkeit mittels Monte-Carlo-Simulationen bestimmt. Die so vorhergesagten Verteilungen werden durch ein Experiment im Rahmen der gestörten $\gamma$-$\gamma$-Winkelkorrelation (PAC) sichtbar gemacht, indem polykristalline MAX-Phasen unter uniaxialer Last verformt werden. Eine quantitative Auswertung erlaubt es schließlich, Defektdichten in-situ abzuschätzen. Die lokalen Auswirkungen auf den EFG werden anhand verschiedener MAX-Phasen-Mischkristalle systematisch untersucht. Im Zuge dessen wird die Synthese eines bisher unbekannten MAX-Phasen-Mischkristalls, Ti$_2$(Al$_{0,5}$,In$_{0,5}$)C, beschrieben. Die Zugehörigen Gitterkonstanten werden mittels Röntgendiffraktometrie im Rahmen der Rietveld-Methode bestimmt.

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Nonlinear optics is well known to be a highly powerful tool to investigate the properties of the materials. In this thesis we used two important nonlinear optical techniques known as Electric Field Induced Second Harmonic Generation (EFISH) and Harmonic Light Scattering (HLS) to study the first hyperpolarizability of various molecular objects. Firstly, we evidenced the pi donor conjugation in cyclometallated Ir complexes. We have also explored the series of trinuclear organometallic triaryl-1, 3, 5-triazinane-2, 4, 6-triones functionalized by d6-transition metal acetylides complexes at their periphery- large hyperpolarizabilities, far higher than those of related purely organic derivatives are reported. Secondly, a series of dipolar and octupolar dithienylethene (DTE)-containing 2, 2-bipyridine ligands with different metal ions featuring two, four and six photochromic dithienylethene units have been synthesized and fully characterized. The study reveals a large increase in the hyperpolarizability after UV irradiation and subsequent formation of ring-closed isomers. This efficient enhancement clearly reflects the delocalization of the pi-electron system and the formation of strong push&pull chromophores in the closed forms. Thirdly, we have investigated NLO properties of bis (phthalocyaninato) lanthanide-(III) double-decker complexes with crosswise ABAB (phthalocyanine bearing alternating electron-donor and electron-acceptor groups), AB3 (3 donor groups), A4 (4 donor groups) and B4 (no donor groups) ligands. First-order hyperpolarizability is measured and displays the highest quadratic hyperpolarizability ever reported for an octupolar molecule. The direct contribution of f-electrons in coordinated lanthanides ions is also observed on second order nonlinear activity. Finally, gold nanospheres (AuNSs) and gold nanorods (AuNRs) with different aspect ratios (AR) ranging from 1.7 to 3.2 nm have been synthesized by Radiolysis method. Second harmonic intensity collected from AuNRs is clearly higher than that of the nanospheres and reveals their dependence on the AR. We have also mixed the chromophore 4-dimethylamino-N-methyl-4-stilbazolium tosylate (DAST) derivative with AuNRs and observed the enhancement of DAST NLO properties in the presence of AuNRs. A clear increase in the hyperpolarizability (by a factor of 8) of DAST derivatives has been evidence.

The aim of the study presented in this thesis is to explore the electrical and physical properties of films of tin and lead clusters. Understanding the novel conductance properties of cluster films and related phenomenon such as coalescence is important to fabricate any cluster based devices. Coalescence is an important phenomenon in metallic cluster films. Due to coalescence the morphology of the films changes with time which changes their properties and could lead to failure in cluster devices. Coalescence is studied in Sn and Pb cluster films deposited on Si$_3$N$_4$ surfaces using Ultra High Vacuum (UHV) cluster deposition system. The conductance of the overall film is linked to the conductance of the individual necks between clusters by simulations. It is observed that the coalescence process in Sn and Pb films follows a power law in time with an exponent smaller than reported in literature. These results are substantiated by the results from previous experimental and Kinetic Monte Carlo (KMC) simulation studies at UC. Percolating films of Sn show unique conductance properties. These films are characterized using various electrode configurations, applied voltages and temperatures. The conductance measurements are performed by depositing clusters on prefabricated gold electrodes on top of Si$_3$N$_4$ substrates. Sn cluster films exhibit a variety of conductance behaviours during and after the end of deposition. It is observed that the evolution of conductance during the onsets at percolation threshold is dependent on the film morphology. Samples showing difference responses in onset also behave differently after the end of deposition. Therefore all samples were categorized according to their onset behaviour. After the end of deposition, when a bias voltage is applied, the conductance of Sn films steps up and down between various well-defined conductance levels. It is also observed that in many cases the conductance levels between which these devices jump are close to integral multiples of the conductance quantum. There are many possible explanations for the steps in conductance. One of the explanations is formation and breaking of conducting paths in the cluster films by electric field induced evaporation and electromigration respectively. The stepping behaviour is similar to that in non-volatile memory devices and hence very interesting to explore due to potential applications.

Lithium niobate (LiNbO3) and KTiOPO4 (KTP) are ferroelectric crystals of considerable interest in different fields of optics and optoelectronics. Due to its large values of the nonlinear optical, electro-optic (EO), piezoelectric and acousto-optical coefficients, LiNbO3 is widely used for laser frequency conversion using the quasiphase matching (QPM) approach where the sign of nonlinearity has been periodically modulated by electric field poling (EFP). In the microwave and telecommunication field LiNbO3 is used for surface acoustic devices and integrated optical modulators. KTP and its isomorphs, on the other hand, exhibit slightly lower nonlinear coefficients but have much higher photorefractive damage thresholds, so that it is mainly used in the fabrication of QPM devices for both UV, IR and visible light generation and in high power applications. This thesis focus on different key issues: (1) accurate characterization of specific optical properties of LiNbO3, which are of interest in nonlinear and EO applications; (2) in-situ visualization and characterization of domain reversal by EFP in LiNbO3 and KTP crystals for a through understanding of the ferroelectric domain switching; (3) fabrication of periodic surface structures at sub-micron scale in LiNbO for photonic applications. An interferometric method is used for accurate measurement of ordinary and extraordinary refractive indices in uniaxial crystals, which is of great interest in the proper design of QPM crystals. A digital holography (DH) based method is presented here for 2D characterization of the EO properties of LiNbO , which is considerably interesting in the applications where the proper design of the EO device requires a spatially resolved information about the EO behaviour and the existing pointwise techniques are not sufficient. A DH method for novel in-situ monitoring of domain reversal by EFP in both LiNbO3 and KTP, is also presented here. The technqiue could be used as a tool for high fidelity periodic domain engineering but also provides information about domain kinetics, internal field and crystals defects. 3 3 3 Finally this thesis presents novel results concerning nanoscale periodic surface structuring of congruent LiNbO3. Holographic lithography (HL) is used for sub-micron period resist patterning and electric overpoling for surface domain reversal. Surface structures are obtained by selective etching. Moiré effect is also used in the HL to fabricate complicated structures with multiple periods. The depth compatibility with waveguide implementation allows foreseeing possible applications of these structures for Bragg gratings or innovative photonic crystal devices, exploiting the additional nonlinear and EO properties typical of LiNbO3. / QC 20100824

Nonlinear optical frequency conversion is one of the most important key techniques in order to obtain lasers with wavelengths targeted for specific applications. In order to realize efficient and tailored lasers, the quasi-phase-matching (QPM) approach using periodically-poled ferroelectric crystals is getting increasingly important. Also understanding of damage mechanisms in nonlinear materials is necessary to be able to design reliable and well working lasers. This is especially true for high power application lasers, which is a rapidly growing field, where the damage problem normally is the ultimate limiting factor. In this thesis work, several promising novel ferroelectric materials have been investigated for nonlinear optical applications and the emphasis has been put on QPM devices consisting of periodically-poled structures. The materials were selected from three different types of ferroelectric materials: 1) MgO-doped stoichiometric LiNbO3 (MgO:SLN) and LiTaO3 (MgO:SLT), and non-doped stoichiometric LiTaO3 (SLT), 2) KTiOPO4 (KTP) and its isomorphs RbTiOPO4 (RTP), and 3) KNbO3 (KN). The focus in our investigations have been put on the spontaneous polarization switching phenomena, optimization of the periodic poling conditions, and the photochromic optical damage properties which were characterized by the help of blue light-induced infrared absorption (BLIIRA) measurements. With electrical studies of the spontaneous polarization switching, we were able to determine quantitatively, and compare, the coercive field values of different materials by applying triangularly shaped electric fields. We found that the values of the coercive fields depended on the increase rate of the applied electric field. The coercive field of KN was the lowest (less than 0.5 kV/mm) followed by the ones of KTP, SLT, and MgO:SLT (1.5 to 2.5 kV/mm). MgO:SLN, and RTP had relatively high coercive fields, approximately 5.0 to 6.0 kV/mm, respectively. Based on the domain switching characteristics we found, we successfully fabricated periodically-poled devices in all of the investigated materials with 30 μm periodicities and sample thickness of 1 mm. Blue light-induced infrared absorption (BLIIRA) has been characterized for unpoled bulk and periodically-poled samples using a high-sensitivity, thermal-lens spectroscopy technique. SLT showed a large photorefraction effect and the BLIIRA signal could not be properly measured because of the large distortion of the probe beam. The rise and relaxation time of BLIIRA, after switching the blue light on and off was in a time span of 10 to 30 sec except for KTP and its isomorphs, which needed minutes to hours in order to saturate at a fixed value. KN and MgO:SLN showed the lowest susceptibility to the induced absorption. Periodic poling slightly increased the susceptibility of KTP, MgO:SLT, and KN. Relatively high thresholds were observed in MgO:SLT and KN. By increasing the peak-power intensity of the blue light, the induced absorption for MgO:SLN, KTP and KN saturated at a constant value while that of MgO:SLT increase in a constant fashion. This trend is critical issue for the device reliability at high-power applications. / QC 20100830

Cette thèse se concentre sur l'étude de composés magnétiques géométriquement frustrés où les ions magnétiques se situent aux sommets d'un réseau de tétraèdres partageant leurs sommets: les composés pyrochlores. Deux familles de formule chimique R2M2O7, où R est un lanthanide et M= Ti, Sn, sont particulièrement intéressantes puisqu'elles présentent une grande variété d'états magnétiques exotiques. Premièrement, nous avons étudié le champ cristallin agissant au site de la terre rare dans l'approximation de Stevens où uniquement le terme fondamental est considéré. Un jeu unique de paramètres a été déterminé pour chaque famille considérée grâce à une analyse globale incluant des spectres de neutrons inélastiques de plusieurs composés. Ensuite, nous avons caractérisé avec un large éventail de techniques les propriétés physiques à basse température de Nd2Sn2O7. En dessous de la température de transition Tc=0.91 K, ce composé possède un ordre magnétique à longue portée dans la configuration de spins dite "all-in-all-out". Une persistance de la dynamique de spins a été révélée dans la phase ordonnée, attribuée à des excitations unidimensionnelles de spins. Une dynamique de spins anormalement lente est également reportée dans la phase paramagnétique. Enfin, nous avons apporté quelques informations sur les deux états fondamentaux proposés pour le composé très étudié Tb2Ti2O7: premièrement, l'apparition d'une transition Jahn-Teller à basse température est suggérée mais l'absence d'élargissement des pics de Bragg réfute la présence d'une transition structurale. Enfin ce composé pourrait être un exemple d'une glace de spin quantique mais l'existence d'un plateau d'aimantation n'est pas évident jusqu'à T=20 mK. / This Phd thesis focuses on the study of magnetically frustrated compounds where magnetic ions lie at the vertices of a corner-sharing tetrahedra network: the pyrochlore compounds. The two series of chemical formula R2M2O7, where R is a lanthanide and M=Ti, Sn, are of peculiar interest since they display a large variety of exotic magnetic ground states. First, we have studied the crystal-electric-field acting at the rare earth within the Stevens approximation where only the ground state multiplet is considered. A single set of parameters for each families of interest has been determined through a global analysis including several inelastic neutron scattering spectra of various compounds. Then, we have characterised with a large panel of techniques the low temperature physical properties of Nd2Sn2O7. This compound enters a long-range magnetic order at transition temperature Tc=0.91 K with an ``all-in-all-out'' spin configuration. A persistence of spin dynamics has been found in the ordered phase, ascribed to one-dimensional spin loops excitations. Anomalously slow paramagnetic spin fluctuations are also reported. Finally, we have brought information on the two proposed ground states of the widely studied compound Tb2Ti2O7: first, a Jahn-Teller transition is claimed to occur at low temperatures but no broadening of the Bragg peaks is seen down to T=4 K precluding premises of a structural transition. Secondly, this compound could be a realisation of a quantum spin-ice but no definitive evidence of a magnetisation plateau is found down to T=20 mK.

Bismuth ferrite (BFO) is a multiferroic material with cross-correlation between magnetic and electric orders. With no applied external fields the spin structure of BFO is anitferromagnetic and cycloidal. This ordering prevents the detection of the weak ferromagnetism known to exist in the material. The application of magnetic and electric fields of suitable strength and direction is capable of compelling the Fe3+ spins to align in a homogeneous, antiferromagnetic fashion. This report details how numerical methods were used to simulate the spin alignment of a BFO system under different fields. The results were compiled into electric field-magnetic field phase diagrams of BFO to show the divide between cycloidal and homogeneous systems. / Graduate / 0607 / 0611 / marca@uvic.ca