Les oscillateurs de référence de haute pureté sont actuellement utilisés dans un grand nombre d’applications allant du contrôle de fréquence aux horloges pour les radars, les GPS et l’espace... Les tendances actuelles dans ce domaine requièrent des architectures miniaturisées avec la génération de signaux directement dans la gamme de fréquences d’intérêt, autour de quelques GHz. Récemment, de nouvelles architectures basées sur les principes de l’optomécanique ont vu le jour dans ce but. De tels oscillateurs optomécanique génèrent non seulement des signaux hyperfréquences directement dans la gamme de fréquences GHz avec éventuellement un faible bruit de phase, mais permettent également un degré élevé d'intégration sur puce. Ce travail de thèse s'inscrit dans cette démarche. L’oscillateur optomécanique étudié se compose de cavités à cristaux photoniques suspendues couplées à des guides d’ondes silicium sur isolant intégrés dans une architecture tridimensionnelle. Ces cavités abritent des modes optiques fortement confinés autour de 1550nm et des modes mécaniques dans le GHz. De plus, ces structures présentent un recouvrement spatial entre phonon et photon élevé. Il en résulte un couplage optomécanique amélioré. Cette force de couplage optomécanique améliorée est ici sondée optiquement sur des structures à cristaux photoniques de conception optimisée. Ces cavités sont réalisées dans des matériaux semi-conducteurs III-V dont la piézoélectricité nous permet d'intégrer des outils supplémentaires pour sonder et contrôler les vibrations mécaniques via un pilotage capacitif, piézoélectrique ou acoustique. Ce contrôle total des modes mécaniques et de l’interaction optomécanique ouvre la voie à la mise en œuvre de circuits intégrés pour le verrouillage par injection et des boucles de rétroaction permettant de réduire le bruit de phase de l’oscillateur. / High purity reference oscillators are currently used in a wide variety of frequency control and timing applications including radar, GPS, space... Current trends in such fields call for miniaturized architectures with direct signal generation in the frequency range of interest, around few GHz. Recently, novel optomechanically-enhanced architectures have emerged with this purpose. Such optomechanically-driven oscillators not only generate microwave signals directly in the GHz frequency range with possibly low phase noise but also are amenable to a high degree of integration on single chip settings. This PhD work falls within this scope. The optomechanically-driven oscillator under study consists of suspended photonic crystal cavities coupled to integrated silicon-on-insulator waveguides in a three-dimensional architecture. These cavities harbor highly-confined optical modes around 1,55 µm and mechanical modes in the GHz and most importantly, feature a high phonon-photon spatial overlap, all resulting in an enhanced optomechanical coupling. This enhanced optomechanical coupling strength is here probed optically on photonic crystal structures with optimized design. These cavities are hosted in III-V semiconductor materials whose piezoelectricity enable us to integrate additional tools for probing and controlling mechanical vibrations via capacitive, piezoelectric or acoustic driving. This full control over the mechanical modes and optomechanical interaction, paves the way towards the implementation of integrated injection locking circuits of feedback loops for reducing the phase noise of the oscillator.

The main goal of the dissertation was to determine task-dependent modulation of corticospinal descending output. From this main goal, I conducted three different studies to determine how corticospinal output to muscles of the upper arm and hand changed as a function of the task demands. In study 1, I examined how a somatosensory-motor circuit changes when a muscle needs to be active in a task and found that this circuit may be dependent on the movement phase, type of afferent input, and the task demands. In study 2, I examined how this same somatosensory-motor circuit acts to both allow and prevent muscle activity before movement. I revealed that this somatosensory-motor circuit may function to prevent muscle activity when a muscle is not needed in a task and creates facilitation of corticospinal output when it needs to be active in a task. These effects, however, are dependent on the movement phase and the digit the muscle is controlling. Study 3 determined how corticospinal output is modulated to upper arm muscles when performing movements that required different combinations of segmental interactions to achieve the task successfully. Corticospinal output was increased when inertia and the BBC moment at a joint resisted the intended joint rotation and these effects were dependent on the muscle and movement phase. I propose a model of the connectivity between the primary motor and somatosensory cortices that would increase, modulate, or decrease corticospinal output to a muscle depending on its role in the task. The findings from this work provides information to guide future neural rehabilitative interventions for individuals who have movement disorders arising from altered somatosensory-motor processing such as Cerebellar Ataxia, Developmental Coordination Disorder, Focal Hand Dystonia, Parkinson’s disease, and stroke. / Dissertation / Doctor of Philosophy (PhD) / On a day to day basis, we perform a variety of movements without giving much thought to how complicated it is for our nervous system to perform said movements. There are many different areas of the brain that are responsible for controlling movement. This dissertation focuses on two key areas that are critical for movement performance, namely the primary motor and somatosensory cortices. The primary motor cortex is largely responsible for sending signals to the muscles to control movement, while the primary somatosensory cortex plays a crucial role in receiving and understanding sensory input from our body. The studies in this dissertation describe how these two areas of the brain communicate during finger and arm movements to produce or prevent muscle activity. This work has implications for individuals with disorders that impact their everyday movements.

A ballistic pendulum impulse generator was used to impact networks in primary culture growing on microelectrode arrays. This approach has the advantage of imparting pure tangential acceleration insults (50 to 300 g) with simultaneous morphological and electrophysiological multichannel monitoring for days before and after the impact. Action potential (AP) production, network activity patterns, and cell electrode coupling of individual units using AP waveshape templates were quantified. Network adhesion was maintained after tangential impacts up to 300g with minimal loss of pre-selected active units. Time lapse phase contrast microscopy revealed stable nuclei pre-impact, but post impact nuclear rotation in 95% of observations (n= 30). All recording experiments (n=31) showed a repeatable two-phase spike production response profile: recovery to near reference in 1-2 hrs, followed by a slow activity decay to a stable, level plateau approximately 30-40% below reference. Phase 1 consisted of a complex two-step recovery: rapid activity increase to an average 23.6% (range: 11-34%) below reference, forming a level plateau lasting from 5 to 20 min, followed by a climb to within 20% of reference where a second plateau was established for 1 to 2 hrs. Cross correlation profiles showed changes in firing hierarchy after impact, and in spontaneous network oscillatory activity. Native oscillations were found in the Delta band (2 to 3 Hz), and decreased by approximately 20% after impact. Under network disinhibition with bicuculline, oscillations were slower (0.8-1Hz) and decreased 40% after impact. These data link network performance deficits with microscopically observable subcellular changes.

A fundamental goal in neurobiology is to understand the development and organization of neural circuits that drive behavior. In the embryonic spinal cord, the first motor activity is a slow coiling of the trunk that is sensory-independent and therefore appears to be centrally driven. Embryos later become responsive to sensory stimuli and eventually locomote, behaviors that are shaped by the integration of central patterns and sensory feedback. In this thesis I used a simple vertebrate model, the zebrafish, to investigate in three manners how developing spinal networks control these earliest locomotor behaviors. For the first part of this thesis, I characterized the rapid transition of the spinal cord from a purely electrical circuit to a hybrid network that relies on both chemical and electrical synapses. Using genetics, lesions and pharmacology we identified a transient embryonic behavior preceding swimming, termed double coiling. I used electrophysiology to reveal that spinal motoneurons had glutamate-dependent activity patterns that correlated with double coiling as did a population of descending ipsilateral glutamatergic interneurons that also innervated motoneurons at this time. This work (Knogler et al., Journal of Neuroscience, 2014) suggests that double coiling is a discrete step in the transition of the motor network from an electrically coupled circuit that can only produce simple coils to a spinal network driven by descending chemical neurotransmission that can generate more complex behaviors. In the second part of my thesis, I studied how spinal networks filter sensory information during self-generated movement. In the zebrafish embryo, mechanosensitive sensory neurons fire in response to light touch and excite downstream commissural glutamatergic interneurons to produce a flexion response, but spontaneous coiling does not trigger this reflex. I performed electrophysiological recordings to show that these interneurons received glycinergic inputs during spontaneous fictive coiling that prevented them from firing action potentials. Glycinergic inhibition specifically of these interneurons and not other spinal neurons was due to the expression of a unique glycine receptor subtype that enhanced the inhibitory current. This work (Knogler & Drapeau, Frontiers in Neural Circuits, 2014) suggests that glycinergic signaling onto sensory interneurons acts as a corollary discharge signal for reflex inhibition during movement. v In the final part of my thesis I describe work begun during my masters and completed during my doctoral degree studying how homeostatic plasticity is expressed in vivo at central synapses following chronic changes in network activity. I performed whole-cell recordings from spinal motoneurons to show that excitatory synaptic strength scaled up in response to decreased network activity, in accordance with previous in vitro studies. At the network level, I showed that homeostatic plasticity mechanisms were not necessary to maintain the timing of spinal circuits driving behavior, which appeared to be hardwired in the developing zebrafish. This study (Knogler et al., Journal of Neuroscience, 2010) provided for the first time important in vivo results showing that synaptic patterning is less plastic than synaptic strength during development in the intact animal. In conclusion, the findings presented in this thesis contribute widely to our understanding of the neural circuits underlying simple motor behaviors in the vertebrate spinal cord. / Un objectif important en neurobiologie est de comprendre le développement et l'organisation des circuits neuronaux qui entrainent les comportements. Chez l'embryon, la première activité motrice est une lente contraction spontanée qui est entrainée par l'activité intrinsèque des circuits spinaux. Ensuite, les embryons deviennent sensibles aux stimulations sensorielles et ils peuvent éventuellement nager, comportements qui sont façonnées par l'intégration de l'activité intrinsèque et le rétrocontrôle sensoriel. Pour cette thèse, j'ai utilisé un modèle vertébré simple, le poisson zèbre, afin d'étudier en trois temps comment les réseaux spinaux se développent et contrôlent les comportements locomoteurs embryonnaires. Pour la première partie de cette thèse j'ai caractérisé la transition rapide de la moelle épinière d'un circuit entièrement électrique à un réseau hybride qui utilise à la fois des synapses chimiques et électriques. Nos expériences ont révélé un comportement embryonnaire transitoire qui précède la natation et qu'on appelle « double coiling ». J'ai démontré que les motoneurones spinaux présentaient une activité dépendante du glutamate corrélée avec le « double coiling » comme l'a fait une population d'interneurones glutamatergiques ipsilatéraux qui innervent les motoneurones à cet âge. Ce travail (Knogler et al., Journal of Neuroscience, 2014) suggère que le « double coiling » est une étape distincte dans la transition du réseau moteur à partir d'un circuit électrique très simple à un réseau spinal entrainé par la neurotransmission chimique pour générer des comportements plus complexes. Pour la seconde partie de ma thèse, j'ai étudié comment les réseaux spinaux filtrent l'information sensorielle de mouvements auto-générés. Chez l'embryon, les neurones sensoriels mécanosensibles sont activés par un léger toucher et ils excitent en aval des interneurones sensoriels pour produire une réponse de flexion. Par contre, les contractions spontanées ne déclenchent pas ce réflexe même si les neurones sensoriels sont toujours activés. J'ai démontré que les interneurones sensoriels reçoivent des entrées glycinergiques pendant les contractions spontanées fictives qui les empêchaient de générer des potentiels d'action. L'inhibition glycinergique de ces interneurones, mais pas des autres neurones spinaux, est due à l'expression d'un sous-type de récepteur glycinergique unique qui augmente iii le courant inhibiteur. Ce travail (Knogler & Drapeau, Frontiers in Neural Circuits, 2014) suggère que la signalisation glycinergique chez les interneurones sensoriels agit comme un signal de décharge corolaire pour l'inhibition des réflexes pendant les mouvements auto- générés. Dans la dernière partie de ma thèse, je décris le travail commencé à la maîtrise et terminé au doctorat qui montre comment la plasticité homéostatique est exprimée in vivo aux synapses centrales à la suite des changements chroniques de l'activité du réseau. J'ai démontré que l'efficacité synaptique excitatrice de neurones moteurs spinaux est augmentée à la suite d’une diminution de l'activité du réseau, en accord avec des études in vitro précédentes. Par contre, au niveau du réseau j'ai démontré que la plasticité homéostatique n'était pas nécessaire pour maintenir la rythmicité des circuits spinaux qui entrainent les comportements embryonnaires. Cette étude (Knogler et al., Journal of Neuroscience, 2010) a révélé pour la première fois que l'organisation du circuit est moins plastique que l'efficacité synaptique au cours du développement chez l'embryon. En conclusion, les résultats présentés dans cette thèse contribuent à notre compréhension des circuits neuronaux de la moelle épinière qui sous-tendent les comportements moteurs simples de l'embryon.

Cette thèse a pour objectif l’investigation du circuit des récompenses, sur les plans comportementaux et neuronaux, chez des adolescents à risque parental élevé de dépression majeure et de trouble bipolaire, en comparaison à des jeunes à risque parental peu élevé. Plus précisément, le but est d’identifier des marqueurs comportementaux et neuronaux du risque de développer une dépression majeure ou un trouble bipolaire, afin d’être en mesure de détecter et de prévenir ces troubles le plus tôt possible pour éviter, ou du moins retarder, leur émergence. Pour ce faire, nous avons réalisé deux études, présentées ici dans deux articles empiriques. Dans le premier article, le fonctionnement comportemental et neuronal du circuit des récompenses a été investigué au moyen d’une tâche d’anticipation et d’obtention de gains et de pertes monétaires, chez des adolescents à risque parental de dépression majeure (i.e., jeunes asymptomatiques dont un des parents souffre de dépression majeure), des adolescents à risque parental de trouble bipolaire (i.e., jeunes asymptomatiques dont un des parents souffre de trouble bipolaire) et des adolescents contrôles (i.e., jeunes asymptomatiques dont les deux parents sont en bonne santé mentale). Au niveau comportemental, les résultats ont révélé une meilleure performance chez les jeunes à risque de dépression majeure lorsqu’ils devaient éviter d’obtenir des pertes monétaires de magnitude variée (0,20$, 1$ ou 5$), ainsi qu’une meilleure performance chez les jeunes à risque de trouble bipolaire sur les essais impliquant d’éviter des pertes monétaires de magnitude nulle (0$). Au niveau neuronal, les jeunes à risque de dépression majeure démontraient une diminution de l’activation du cortex préfrontal dorsolatéral lors de l’anticipation de potentielles pertes monétaires de magnitude variée, tandis que les jeunes à risque de trouble bipolaire démontraient une diminution de l’activation du cortex préfrontal dorsolatéral lors de l’anticipation de potentielles pertes monétaires de magnitude nulle. De plus, les jeunes à risque de dépression majeure tendaient à démontrer une augmentation de l’activité du cortex orbitofrontal durant l’évitement réussi de pertes monétaires, tandis que les jeunes à risque de trouble bipolaire tendaient à démontrer une augmentation de l’activité du cortex orbitofrontal lors de l’obtention de pertes monétaires. Dans le deuxième article, l’intégrité structurelle des régions fronto-limbiques a été investiguée, au moyen de mesures du volume, de l’épaisseur corticale et de la superficie corticale. Les résultats ont mis en évidence, chez les jeunes à risque de trouble bipolaire, un volume plus élevé du cortex préfrontal dorsolatéral, par rapport aux jeunes à risque de dépression majeure et contrôles. De plus, les jeunes à risque de trouble bipolaire présentaient un volume plus élevé du cortex cingulaire postérieur, en comparaison aux jeunes à risque de dépression majeure. Enfin, une diminution de l’épaisseur corticale du cortex orbitofrontal et du gyrus frontal moyen a été observée chez les adolescents à risque de trouble bipolaire, en comparaison au groupe contrôle. L’ensemble de ces résultats démontre ainsi l’existence de particularités comportementales et d’altérations neuronales sur les plans fonctionnel et structurel, chez des jeunes à risque élevé de troubles de l’humeur, et ce, avant même l’émergence des premiers symptômes thymiques. Plus particulièrement, ces caractéristiques pourraient constituer des marqueurs du risque de développer un trouble de l’humeur. Par conséquent, ces marqueurs pourraient aider à mieux identifier les jeunes qui sont le plus à risque de développer un trouble de l’humeur, et ainsi permettre la mise en place précoce de stratégies préventives adaptées, afin d’éviter des trajectoires développementales psychopathologiques. / This thesis aims to investigate the behavioral and neural reward circuitry, in youths at high parental risk for major depressive and bipolar disorder, in comparison to youths at low parental risk for mood disorders. More specifically, the goal is to identify behavioral and neural markers of the risk to develop a major depressive or a bipolar disorder in order to early detect and prevent these disorders, and ultimately to avoid, or at least delay, their emergence. To do so, we conducted two experiments, presented herein in two empirical articles. In the first article, behavioral and neuronal reward circuitry were investigated in youths at high parental risk for major depressive disorder (i.e, asymptomatic youths which one of the parents is suffering from major depression), youths at high parental risk for bipolar disorder (i.e, asymptomatic youths which one of the parents is suffering from bipolar disorder) and control youths (i.e, asymptomatic youths from mentally healthy parents). Therefore, we used a monetary incentive delay task allowing the assessment of monetary gain and loss anticipation and outcome. Behaviorally, results revealed a better performance in youths at risk for major depressive disorder on trials involving potential losses of various magnitude (0,20$, 1$ or 5$), as well as a better performance in youths at risk for bipolar disorder on trials involving potential null losses (0$). Regarding imaging data, youths at risk for major depressive disorder demonstrated a reduced activity in the dorsolateral prefrontal cortex during the anticipation of potential monetary losses of various magnitude, while youths at risk for bipolar disorder showed a reduced activity in the dorsolateral prefrontal cortex during the anticipation of potential null losses. Moreover, youths at risk for major depressive disorder tended to have an increased activity in the orbitofrontal cortex during successful avoidance of monetary losses, while youths at risk for bipolar disorder tended to demonstrate an increased activity in the orbitofrontal cortex during feedback of monetary losses. In the second article, structural integrity of fronto-limbic regions was investigated, through volumetric, cortical thickness and surface area measures. Results have highlighted, in youths at risk for bipolar disorder, an increased volume in the dorsolateral prefrontal cortex, compared to both youths at risk for major depressive disorder and controls. Moreover, youths at risk for bipolar disorder showed an increased volume in the posterior cingulate cortex, in comparison to youths at risk for major depressive disorder. Finally, a reduced thickness in the orbitofrontal cortex and middle frontal gyrus were observed in youths at risk for bipolar disorder, in comparison to control youths. Taken together, these results demonstrate the existence of behavioral particularities, and neuronal alterations regarding functional and structural data, in youths at high risk for mood disorders, and this, even before the emergence of the first mood symptoms. More specifically, these characteristics might constitute markers of the risk to develop a mood disorder. Consequently, these markers could help to better identify youths who are most at risk to develop a mood disorder, and thus allow the early implementation of adapted preventive strategies to avoid psychopathological developmental trajectories.

The mammalian spinal cord contains the neuronal circuitry necessary to generate rhythmic locomotor activity in the absence of inputs from the higher brain centre or sensory system. This circuitry is regulated by local neuromodulatory inputs, which can adjust the strength and timing of locomotor output. The free radical gas nitric oxide has been shown to act as an important neuromodulator of spinal circuits, which control locomotion in other vertebrate models such as the tadpole and lamprey. Despite this, the involvement of the NO-mediated soluble guanylate cyclase/cyclic guanosine monophosphate secondary messenger-signalling pathway (NO/sGC/cGMP) in mammalian locomotion has largely been under-investigated. The NADPH diaphorase histochemical reaction was used to identify sources of NO in the lumbar spinal cord. The largest population NADPH diaphorase reactive neurons were located in the dorsal horn, followed by the laminae of the ventral horn, particularly around the central canal (lamina X) and lamina VII. NADPH diaphorase reactive neurons were found along a rostrocaudal gradient between lumbar segments L1 to L5. These results show that that discrete neuronal sources of NO are present in the developing mouse spinal cord, and that these cells increase in number during the developmental period postnatal day P1 – P12. NADPH diaphorase was subsequently used to identify NADPH diaphorase reactive neurons at P12 in the mouse model of ALS using the SODG93A transgenic mouse. Physiological recordings of ventral root output were made to assess the contribution of NO to the regulation induced rhythmic fictive locomotion in the in vitro isolated spinal cord preparation. Exogenous NO inhibits central pattern generator (CPG) output while facilitating and inhibiting motor neuron output at low and high concentrations respectively. Removal of endogenous NO increases CPG output while decreasing motor neuron output and these effects are mediated by cGMP. These data suggest that an endogenous tone of NO is involved in the regulation of fictive locomotion and that this involves the NO/sGC/cGMP pathway. Intracellular recordings from presumed motor neurons and a heterogeneous, unidentified sample of interneurons shows that NO modulates the intrinsic properties of spinal neurons. These data suggest that the net effect of NO appears to be a reduction in motor neuron excitability.

La récupération d'énergie thermique basée sur les générateurs thermoélectriques (TEG) est utilisée dans de nombreuses applications telles que les dispositifs médicaux auto-alimentés. La sûreté de fonctionnement et la continuité de service de ces systèmes sont aujourd'hui des préoccupations majeures. Ainsi, toute défaillance au niveau d'un des interrupteurs commandables de la circuiterie électronique d'interface peut provoquer de graves dysfonctionnements du système. Tout défaut non détecté et non compensé peut mettre en danger l'ensemble du système et interrompt l'alimentation en énergie de la charge. Par conséquent, la mise en œuvre d'une compensation de défaut efficace et rapide est impérative afin d'assurer la continuité de service. Dans ces travaux de recherche, nous étudions la continuité de service d'une interface électronique pour TEG basée sur une conversion à deux étages Buck/Buck-Boost cascadés. Une modélisation électrique générique (modèle de Thévenin) du TEG sous différentes conditions de fonctionnement et prenant en compte l'ensemble des résistances thermiques de contact est tout d'abord présentée. Ensuite, une méthode de compensation de défaut de type circuit-ouvert au niveau de l'interrupteur commandable de l'un des deux convertisseurs DC-DC est également proposée. Nous présentons une topologie originale de convertisseur DC-DC à tolérance de pannes, sans redondance matérielle classique. Cette topologie permet d'assurer la continuité de service du système de récupération d'énergie en mode nominal. Les études théoriques ont été validées par simulation et par des tests expérimentaux / Thermal energy harevsting based on thermoelectric generators is used in many applications such as self-powered medical devices. The reliability and continuity of service of these systems are now major concerns. Furthermore, any failure in the controllable switch of the electronic interface circuitry can cause serious system malfunctions. Any undetected and uncompensated fault can endanger the entire system and interrupt the power supply to the load. Therefore, the implementation of an efficient and rapid fault compensation is imperative in order to ensure the continuity of service. In this research, we study the continuity of service of an electronic interface for TEG, based on a two-stage conversion cascaded Buck/Buck-Boost. A generic electrical modeling of the TEG model under different operating conditions and with taking into account all the thermal contact resistances is first presented. Next, an open-circuit fault compensation method of the controllable switch of one of the two DC-DC converters is also proposed. We present an original fault-tolerant DC-DC converter topology with no conventional hardware redundancy. This topology ensures the continuity of service of the energy recovery system in nominal mode. Theoretical studies were validated by simulation and experimental tests

Plasmonic circuitry is considered as a promising solution-effectivetechnology for miniaturizing and integrating the next generation ofoptical nano-devices. The realization of a practical plasmonic circuitry strongly depends on the complete understanding of the propagation properties of two key elements: surface plasmons and electrons. The critical part constituting the plasmonic circuitry is a waveguide which can sustain the two information-carriers simultaneously. Therefore, we present in this thesis the investigations on the propagation of surface plasmons and the co-propagation of surface plasmons and electrons in single crystalline metal nanowires. This thesis is therefore divided into two parts. In the first part, we investigate surface plasmons propagating in individual thick penta-twinned crystalline silver nanowires using dual-plane leakage radiation microscopy. The effective index and the losses of the mode are determined by measuring the wave vector content of the light emitted in the substrate. Surface plasmon mode is determined by numerical simulations and an analogy is drawn with molecular orbitals compound with similar symmetry. Leaky and bound modes selected by polarization inhomogeneity are demonstrated. We further investigate the effect of wire geometry (length, diameter) on the effective index and propagation losses. On the basis of the results obtained during the first part, we further investigate the effect of an electron flow on surface plasmon properties. We investigate to what extend surface plasmons and current-carrying electrons interfere in such a shared circuitry. By synchronously recording surface plasmons and electrical output characteristics of single crystalline silver and gold nanowires, we determine the limiting factors hindering the co-propagation of electrical current and surface plasmons in these nanoscale circuits. Analysis of wave vector distributions in Fourier images indicates that the effect of current flow on surface plasmons propagation is reflected by the morphological change during the electromigration process. We further investigate the possible crosstalk between co-propagating electrons and surface plasmons by applying alternating current bias

Pas de résumé en français / Plasmonic circuitry is considered as a promising solution-effectivetechnology for miniaturizing and integrating the next generation ofoptical nano-devices. The realization of a practical plasmonic circuitry strongly depends on the complete understanding of the propagation properties of two key elements: surface plasmons and electrons. The critical part constituting the plasmonic circuitry is a waveguide which can sustain the two information-carriers simultaneously. Therefore, we present in this thesis the investigations on the propagation of surface plasmons and the co-propagation of surface plasmons and electrons in single crystalline metal nanowires. This thesis is therefore divided into two parts. In the first part, we investigate surface plasmons propagating in individual thick penta-twinned crystalline silver nanowires using dual-plane leakage radiation microscopy. The effective index and the losses of the mode are determined by measuring the wave vector content of the light emitted in the substrate. Surface plasmon mode is determined by numerical simulations and an analogy is drawn with molecular orbitals compound with similar symmetry. Leaky and bound modes selected by polarization inhomogeneity are demonstrated. We further investigate the effect of wire geometry (length, diameter) on the effective index and propagation losses. On the basis of the results obtained during the first part, we further investigate the effect of an electron flow on surface plasmon properties. We investigate to what extend surface plasmons and current-carrying electrons interfere in such a shared circuitry. By synchronously recording surface plasmons and electrical output characteristics of single crystalline silver and gold nanowires, we determine the limiting factors hindering the co-propagation of electrical current and surface plasmons in these nanoscale circuits. Analysis of wave vector distributions in Fourier images indicates that the effect of current flow on surface plasmons propagation is reflected by the morphological change during the electromigration process. We further investigate the possible crosstalk between co-propagating electrons and surface plasmons by applying alternating current bias

No description available.