Der erste Teil der Arbeit beschäftigt sich mit ultraschnellen Relaxationsprozessen in quasi-eindimensionalen organischen Molekülkristallen. Als Modellsystem wird das Perylenderivat MePTCDI untersucht. Mit verschiedenen Methoden der optischen Ultrakurzzeit-Spektroskopie werden Prozesse der Exzitonen- und Phononenrelaxation in der Zeit-Domäne untersucht. Die dafür aufgebauten Experimente erreichen eine Zeitauflösung von 20 Femtosekunden. Durch optische Anregung der niedrigsten elektronischen Übergänge werden in einem organischen Molekülkristall freie Exzitonen mit Wellenvektor k=0 gebildet. Dabei werden gleichzeitig zahlreiche intramolekulare und intermolekulare Schwingungsfreiheitsgrade angeregt. Die Anregung mit fs-Laserpulsen führt zum Aufbau kohärenter Schwingungswellenpakete. Es werden sowohl hochenergetische Oszillationen intramolekularer Vibrationen beobachtet, als auch erstmalig niedrigenergetische Oszillationen, die von Gittervibrationen (Phononen) stammen. Die kohärenten Vibrationen im elektronischen Grundzustand klingen bei Raumtemperatur im Bereich einiger Pikosekunden ab. Durch die optische Anregung mit fs-Laserpulsen wird nicht nur phononische Kohärenz, sondern auch elektronische Kohärenz der optischen Übergänge induziert. Die elektronische Kohärenz klingt mit der Dephasierungszeit T2 ab. Trotz der hohen Zeitauflösung war es letztendlich nicht möglich, die Dephasierung des niedrigsten exzitonischen Übergangs zeitlich aufzulösen - sie liegt jedoch im Bereich 17fs < T2 < 52fs. Die energetische Relaxation der freien Exzitonen zu den relaxierten, emittierenden Exzitonenzuständen erfolgt mit einer Zeitkonstante von ca. 50fs. Von diesen relaxierten Zuständen erfolgt die energetische Abregung in den elektronischen Grundzustand im ns-Bereich. Im zweiten Teil der Arbeit werden Untersuchungen an selbst-assemblierten Monoschichten (SAM) photochromer Moleküle vorgestellt. Als Modellsystem dienen Azobenzen-funktionalisierte Thiole auf Gold (111). Es konnten hochgeordnete Monoschichten dieser photochromen Moleküle erzielt werden, allerdings sind die bisherigen Schichten aufgrund der dichten Packung nicht photoaktivierbar. Mit Hilfe von Raster-Mikroskopie und Infrarot-Spektroskopie werden diese ultradünnen Schichten strukturell untersucht. Es wird ein kommensurates Wachstum mit zwei Molekülen in der nahezu rechteckigen Einheitszelle beobachtet, wobei die laubbaumförmigen Moleküle nahezu senkrecht auf der Oberfläche stehen. Als weitere Methode wurde die Generation der zweiten Harmonischen (Second Harmonic Generation, SHG) angewendet. Diese Technik eröffnet prinzipiell die Möglichkeit, photostimuliertes Schalten der Schicht zeitaufgelöst zu untersuchen. / The first part of this thesis is devoted to ultrafast relaxation processes in quasi-one-dimensional organic molecular crystals. Crystalline samples of the perylene derivative MePTCDI are employed as a model system. Processes concerning the excitonic and phononic relaxation are investigated in time domain using various experimental techniques of optical ultrafast spectroscopy. The experimental setups attain a time-resolution of 20 femtoseconds. Free excitons at wavevector k=0 are formed in a molecular crystal by optical excitation of the lowest electronic transitions. Thereby, various intramolecular and intermolecular vibrational degrees of freedom are excited simultaneously. The excitation by fs-laser pulses results in the composition of coherent vibrational wave packets. Both, higher-energetic oscillations caused by intramolecular vibrations (internal phonons) and, for the first time in a quasi-one-dimensional organic system, lower-energetic modulations which are related to coherent lattice phonons (external phonons) are observed. The coherence of both types of phonons in the electronic ground state is damped at room temperature within a few ps. Besides phononic coherence, optical excitation by fs-laser pulses additionally induces electronic coherence of the optical transitions. The electronic coherence decays with the dephasing time T2. In spite of the high time-resolution, finally it was not possible to time resolve the dephasing of the lowest excitonic transition - however, we can estimated it to be in the range of 17fs < T2 < 52fs. The energetic relaxation of free excitons to the relaxed, emitting exciton states takes place with a time constant of approx. 50fs. The subsequent energetic relaxation to the electronic ground state occurs on a ns-time scale. In the second part, investigations of self-assembled monolayers (SAM) of photochromic molecules are presented. Azobenzene-functionalized thiols on gold (111) are employed as a model system. Highly ordered monolayers of these photochromic molecules could be realized. However, these layers are not photoactive because of dense packing. By use of scanning tunneling microscopy and infra-red spectroscopy the structural properties of these ultrathin layers are investigated. A commensurate growth, yielding a lattice with two molecules within the nearly rectangular unit cell is observed. The molecules, shaped like a broad-leafed tree, are found to stand nearly upright on the surface. Second harmonic generation (SHG) is applied as another experimental method. This technique allows to time resolve photo-stimulated conformational changes of the layers in principle.

Consideramos os efeitos de desordem ou aperiodicidade sobre três sistemas magnéticos distintos. Inicialmente, apresentamos um modelo fenomenológico para descrever a dependência térmica da magnetização remanente induzida por diluição numa classe de antiferromagnetos quase-unidimensionais. O modelo trata exatamente as correlações ao longo da direção dominante, levando em conta as demais interações por meio de um campo efetivo. Em seguida, utilizamos uma aproximação autoconsistente de Bethe-Peierls para avaliar os efeitos de um campo cristalino aleatório sobre os diagramas de fases de um modelo de Ising de spins mistos. Mostramos que a desordem é capaz de modificar a natureza dos pontos multicríticos existentes no limite uniforme do modelo. Finalmente, estudamos os efeitos de interações aleatórias ou aperiódicas sobre o comportamento da cadeia XX quântica em baixas temperaturas, através de câlculos numéricos baseados no mapeamento do sistema em um modelo de férmions livres. Apontamos evidências de que, em temperatura zero, existe um único ponto fixo universal, característico de uma fase de singleto aleatório, que governa o comportamento do modelo na presença de interações desordenadas. No caso de interações aperiódicas,obtemos resultados consistentes com previsões de grupo de renormalização, indicando, para uma certa classe de seqüências de substituição, um comportamento semelhante àquele associado à desordem. / We consider effects of disorder or aperiodicity on three different magnetic systems. First, we present a phenomenological model to describe the thermal dependence of the dilution-induced remanent magnetization in a class of quasi-one-dimensional antiferromagnets. The model treats correlations along the dominant direction in an exact way, while including the remaining inte-. i ractions via an effective field. Then, we use a self-consistent Bethe-Peierls ~ j .. approximation to gauge the effects of a random crystal field on the phase diagram of a mixed-spin Ising mode!. We show that disorder may have profound effects on the multicritical behavior associated with the uniform limit of the mo de!. Finally, we study effects of random or aperiodic interactions on the behavior of the quantum XX chain at low temperatures, by performing numerical calculations based on a mapping of the system onto a free-fermion mo de!. . We present evidence that, at zero temperature, there exists a single, universal fixed-point, associated with a random-singlet phase, which governs the behavior of the model in the presence of disordered interactions. In the case of aperiodic interactions, our results are consistent with renormalizationgroup predictions, indicating, for a certain class of substitution sequences, a behavior similar to the one induced by disorder.

Consideramos os efeitos de desordem ou aperiodicidade sobre três sistemas magnéticos distintos. Inicialmente, apresentamos um modelo fenomenológico para descrever a dependência térmica da magnetização remanente induzida por diluição numa classe de antiferromagnetos quase-unidimensionais. O modelo trata exatamente as correlações ao longo da direção dominante, levando em conta as demais interações por meio de um campo efetivo. Em seguida, utilizamos uma aproximação autoconsistente de Bethe-Peierls para avaliar os efeitos de um campo cristalino aleatório sobre os diagramas de fases de um modelo de Ising de spins mistos. Mostramos que a desordem é capaz de modificar a natureza dos pontos multicríticos existentes no limite uniforme do modelo. Finalmente, estudamos os efeitos de interações aleatórias ou aperiódicas sobre o comportamento da cadeia XX quântica em baixas temperaturas, através de câlculos numéricos baseados no mapeamento do sistema em um modelo de férmions livres. Apontamos evidências de que, em temperatura zero, existe um único ponto fixo universal, característico de uma fase de singleto aleatório, que governa o comportamento do modelo na presença de interações desordenadas. No caso de interações aperiódicas,obtemos resultados consistentes com previsões de grupo de renormalização, indicando, para uma certa classe de seqüências de substituição, um comportamento semelhante àquele associado à desordem. / We consider effects of disorder or aperiodicity on three different magnetic systems. First, we present a phenomenological model to describe the thermal dependence of the dilution-induced remanent magnetization in a class of quasi-one-dimensional antiferromagnets. The model treats correlations along the dominant direction in an exact way, while including the remaining inte-. i ractions via an effective field. Then, we use a self-consistent Bethe-Peierls ~ j .. approximation to gauge the effects of a random crystal field on the phase diagram of a mixed-spin Ising mode!. We show that disorder may have profound effects on the multicritical behavior associated with the uniform limit of the mo de!. Finally, we study effects of random or aperiodic interactions on the behavior of the quantum XX chain at low temperatures, by performing numerical calculations based on a mapping of the system onto a free-fermion mo de!. . We present evidence that, at zero temperature, there exists a single, universal fixed-point, associated with a random-singlet phase, which governs the behavior of the model in the presence of disordered interactions. In the case of aperiodic interactions, our results are consistent with renormalizationgroup predictions, indicating, for a certain class of substitution sequences, a behavior similar to the one induced by disorder.

In this thesis the morphology and the atomic structure of quasi-one-dimensional structures grown on Si were determined by means of diffraction experiments in combination with kinematic diffraction theory calculations. In the first and the second study a formerly unknown superstructure of Dy/Tb on Si(111) was characterized by means of STM, DFT, SPA-LEED experiments and kinematic diffraction calculations. Here, a structure model could be proposed which contains half as many subsurface Si vacancies as compared to the well-known superstructure of Dy/Tb on Si(111) it was derived from. Due to the decreased number of subsurface Si vacancies the reconstruction is subject to an uni-axial strain which is mitigated by the formation of domains separated by anti-phase domain boundaries. It could be shown that two different types of domains alternate across the surface forming quasi-one-dimensional domains. Additionally, the distribution of the domains could be derived by comparison with kinematic diffraction calculations. In the third study a deeper insight into the complex system of bundled rare-earth silicide nanowires on Si(001) was given. Here, the distributions of the NW width, the bundle width and the bundle distance were deduced from the diffraction patterns collected by SPA-LEED and the subsequent comparison to kinematic diffraction theory calculations. Additionally, it was shown that the (2 x 1) reconstruction sometimes observed on top of the NWs by STM cannot exist over larger parts of the sample and instead a (1 x 1) reconstruction needs to be assumed to explain the experimentally observed diffraction data. In the fourth study the atomic structure of the gold induced atomic wires of the Si(111)-(5 x 2)-Au system was analyzed. The Patterson function of the in-plane SXRD data was compared to the Patterson functions derived from the atomic structure models proposed in literature (AN, EBH, KK) ruling out the AN-model. By comparison of the experimental out-of-plane SXRD data to the corresponding (calculated) SXRD data for the EBH- and the KK-model the KK-model could be identified as the most probable model. Additionally, a refined atomic structure model was derived for the KK-model. In conclusion, the results presented in this thesis clearly display the power of diffraction experiments especially in conjunction with the comparison to kinematic diffraction theory calculations and prove that they are applicable even to low dimensional (e.g., quasi-one-dimensional) structures. Furthermore, it was shown that diffraction experiments can deliver complementary information (e.g., information on deeper atomic layers) as compared to local probing methods (e.g. STM or Atomic Force Microscopy) and especially the combination of local probing methods, DFT calculations and diffraction experiments allows for the explanation of even very complicated material systems.

Der erste Teil der Arbeit beschäftigt sich mit ultraschnellen Relaxationsprozessen in quasi-eindimensionalen organischen Molekülkristallen. Als Modellsystem wird das Perylenderivat MePTCDI untersucht. Mit verschiedenen Methoden der optischen Ultrakurzzeit-Spektroskopie werden Prozesse der Exzitonen- und Phononenrelaxation in der Zeit-Domäne untersucht. Die dafür aufgebauten Experimente erreichen eine Zeitauflösung von 20 Femtosekunden. Durch optische Anregung der niedrigsten elektronischen Übergänge werden in einem organischen Molekülkristall freie Exzitonen mit Wellenvektor k=0 gebildet. Dabei werden gleichzeitig zahlreiche intramolekulare und intermolekulare Schwingungsfreiheitsgrade angeregt. Die Anregung mit fs-Laserpulsen führt zum Aufbau kohärenter Schwingungswellenpakete. Es werden sowohl hochenergetische Oszillationen intramolekularer Vibrationen beobachtet, als auch erstmalig niedrigenergetische Oszillationen, die von Gittervibrationen (Phononen) stammen. Die kohärenten Vibrationen im elektronischen Grundzustand klingen bei Raumtemperatur im Bereich einiger Pikosekunden ab. Durch die optische Anregung mit fs-Laserpulsen wird nicht nur phononische Kohärenz, sondern auch elektronische Kohärenz der optischen Übergänge induziert. Die elektronische Kohärenz klingt mit der Dephasierungszeit T2 ab. Trotz der hohen Zeitauflösung war es letztendlich nicht möglich, die Dephasierung des niedrigsten exzitonischen Übergangs zeitlich aufzulösen - sie liegt jedoch im Bereich 17fs < T2 < 52fs. Die energetische Relaxation der freien Exzitonen zu den relaxierten, emittierenden Exzitonenzuständen erfolgt mit einer Zeitkonstante von ca. 50fs. Von diesen relaxierten Zuständen erfolgt die energetische Abregung in den elektronischen Grundzustand im ns-Bereich. Im zweiten Teil der Arbeit werden Untersuchungen an selbst-assemblierten Monoschichten (SAM) photochromer Moleküle vorgestellt. Als Modellsystem dienen Azobenzen-funktionalisierte Thiole auf Gold (111). Es konnten hochgeordnete Monoschichten dieser photochromen Moleküle erzielt werden, allerdings sind die bisherigen Schichten aufgrund der dichten Packung nicht photoaktivierbar. Mit Hilfe von Raster-Mikroskopie und Infrarot-Spektroskopie werden diese ultradünnen Schichten strukturell untersucht. Es wird ein kommensurates Wachstum mit zwei Molekülen in der nahezu rechteckigen Einheitszelle beobachtet, wobei die laubbaumförmigen Moleküle nahezu senkrecht auf der Oberfläche stehen. Als weitere Methode wurde die Generation der zweiten Harmonischen (Second Harmonic Generation, SHG) angewendet. Diese Technik eröffnet prinzipiell die Möglichkeit, photostimuliertes Schalten der Schicht zeitaufgelöst zu untersuchen. / The first part of this thesis is devoted to ultrafast relaxation processes in quasi-one-dimensional organic molecular crystals. Crystalline samples of the perylene derivative MePTCDI are employed as a model system. Processes concerning the excitonic and phononic relaxation are investigated in time domain using various experimental techniques of optical ultrafast spectroscopy. The experimental setups attain a time-resolution of 20 femtoseconds. Free excitons at wavevector k=0 are formed in a molecular crystal by optical excitation of the lowest electronic transitions. Thereby, various intramolecular and intermolecular vibrational degrees of freedom are excited simultaneously. The excitation by fs-laser pulses results in the composition of coherent vibrational wave packets. Both, higher-energetic oscillations caused by intramolecular vibrations (internal phonons) and, for the first time in a quasi-one-dimensional organic system, lower-energetic modulations which are related to coherent lattice phonons (external phonons) are observed. The coherence of both types of phonons in the electronic ground state is damped at room temperature within a few ps. Besides phononic coherence, optical excitation by fs-laser pulses additionally induces electronic coherence of the optical transitions. The electronic coherence decays with the dephasing time T2. In spite of the high time-resolution, finally it was not possible to time resolve the dephasing of the lowest excitonic transition - however, we can estimated it to be in the range of 17fs < T2 < 52fs. The energetic relaxation of free excitons to the relaxed, emitting exciton states takes place with a time constant of approx. 50fs. The subsequent energetic relaxation to the electronic ground state occurs on a ns-time scale. In the second part, investigations of self-assembled monolayers (SAM) of photochromic molecules are presented. Azobenzene-functionalized thiols on gold (111) are employed as a model system. Highly ordered monolayers of these photochromic molecules could be realized. However, these layers are not photoactive because of dense packing. By use of scanning tunneling microscopy and infra-red spectroscopy the structural properties of these ultrathin layers are investigated. A commensurate growth, yielding a lattice with two molecules within the nearly rectangular unit cell is observed. The molecules, shaped like a broad-leafed tree, are found to stand nearly upright on the surface. Second harmonic generation (SHG) is applied as another experimental method. This technique allows to time resolve photo-stimulated conformational changes of the layers in principle.

Le rôle du désordre sur les phases onde de densité de spin induites par le champ magnétique (ODSIC) a été étudié sur un monocristal de (TMTSF)2ClO4. Les propriétés à basse température de ce conducteur organique quasi-unidimensionnel dépendent de la vitesse de refroidissement au passage de la transition de mise en ordre des anions qu'il subit à 24 kelvins. Nous avons utilisé cet effet de cinétique pour contrôler le taux de désordre dans l'échantillon. Nos investigations ont été effectuées à l'aide de mesures calorimétriques: d'une part, des mesures simultanées de la chaleur spécifique et de l'effet magnétocalorique en champ variable, et d'autre part, des mesures de la chaleur spécifique en champ fixe. Nous avons mis en évidence un nouveau comportement multicritique en un point de la ligne de transition du second ordre, qui sépare la phase métallique et les sous-phases ODSIC. La criticité de ce point passe de "tétracritique" à bicritique lorsque le désordre augmente. Le point "tétracritique" peut être interprété comme le résultat de la superposition de deux sous phases-ODSIC adjacentes. Nous rapportons aussi un effet de dépairage de paires électron-trou induit par le désordre non magnétique Ce dépairage diffère du comportement universel. De plus l'écart par rapport à ce dernier dépend du champ magnétique. Enfin il n'est pas monotone en fonction du champ. Par ailleurs, les mesures que nous avons effectuées montrent que la mise en ordre des anions n'influence pas directement les réentrances partielles de l'état métallique dans les sous-phases ODSIC entre 3 et 7 teslas. Ceci permet de penser que, dans ce domaine de champs magnétiques, la bande interdite ouverte dans le spectre d'énergie du fait de la mise en ordre des anions ne serait pas directement responsable des réentrances.

Le transport des ondes joue un rôle majeur dans les systèmes de communication comme le Wifi ou les fibres optiques. Les principaux problèmes rencontrés dans ces systèmes concernent la protection contre les intrusions, la consommation d’énergie et le filtrage modal. Nous proposons différentes expériences micro-ondes mettant toutes en œuvre une mise en forme des ondes, pour traiter ces problèmes. Dans une cavité micro-ondes, des états de diffusion particuliers sont générés en s’appuyant uniquement sur des mesures de transmission et sur le formalisme du temps de retard de Wigner-Smith. Ces états sont capables d’éviter une région déterminée de la cavité, de se concentrer sur un point particulier, ou de suivre une trajectoire d’une particule classique. Le filtrage de mode est mis en œuvre dans un guide d’ondes aux frontières ondulées et en présence de pertes dépendant de la position. Le profil du guide est choisi de façon à ce que les deux modes de Bloch qui se propagent encerclent un point exceptionnel. Cette trajectoire s’accompagne d’une transition non-adiabatique entre les deux modes et d'un filtrage asymétrique de ces modes. La thèse présente également des travaux liés à la problématique des algorithmes de « recherche quantique », notamment l’algorithme de Grover. Cette recherche est mise en œuvre dans un réseau en nid d’abeilles de résonateurs micro-ondes couplés, bien décrits par un modèle de liaisons fortes (le système constitue un analogue micro-ondes du graphène). Une expérience de preuve de principe propose la recherche de deux résonateurs distincts reliés au réseau. La loi d’échelle attendue pour cet algorithme est expérimentalement obtenue dans une chaîne linéaire / Transport of waves plays an important role in modern communication systems like Wi-Fi or optical fibres. Typical problems in such systems concern security against possible intruders, energy consumption, time efficiency and the possibility of mode filtering. Microwave experiments are suited to study this kind of problems, because they offer a good control of the experimental parameters. Thus we can implement the method of wave shaping to investigate atypical transport phenomena, which address the mentioned problems. Wave front shaping solely based on the transmission together with the Wigner-Smith time delay formalism allows me to establish special scattering states in situ. These scattering states avoid a pre-selected region, focus on a specific spot or follow trajectories of classical particles, so called particle-like scattering states. Mode filtering is induced inside a waveguide with wavy boundaries and position dependent loss. The boundary profiles are chosen in such a way that the two propagating modes describe an encircling of an exceptional point in the Bloch picture. The asymmetric mode filtering is found due to the appearing non-adiabatic transitions. Another part of my work deals with Grover’s quantum search. I put such a search into practice in a two-dimensional graphene-lattice using coupled resonators, which form a tight-binding analogue. In this proof of principle experiment we search for different resonators attached to the graphene-lattice. Furthermore, the scaling behaviour of the quantum search is quantified for a linear chain of resonators