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A solid state laser system for Doppler-free spectroscopy of muoniumBakule, Pavel January 1998 (has links)
No description available.
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Study on molecular photoionization in femtosecond laser fieldLi, Hui January 1900 (has links)
Master of Science / Department of Physics / Matthias Kling / This thesis consists of two major parts. The first part concerns studies of the orientation dependence of the ionization of diatomic molecules in intense, femtosecond two-color laser fields. The second part is about studies on the ionization mechanisms of the C[subscript]6[subscript]0 molecule in femtosecond near-infrared and ultraviolet laser fields.
In the first part, experimental and theoretical results on the asymmetric ion emission of the heteronuclear molecules CO and NO in two-color laser fields are discussed. The two-color fields, which can be tailored by a relative phase, are used to ionize and dissociate CO and NO molecules, both of which are molecules with small polarizabilities. The resulting C[superscript]+, C[superscript]2[superscript]+, N[superscript]+ and O[superscript]+ ions are detected by a velocity map imaging (VMI) setup. The photoelectrons from above-threshold ionization (ATI) of Xe are studied under such a two-color field to assign the phase. For both CO and NO we find that enhanced ionization occurs when the molecule is oriented with the electric field pointing from the C or N atom toward the O atom. This is in agreement with the molecular orbital Ammosov-Delone-Krainov (MO-ADK) theory and the Stark-corrected strong-field-approximation (SFA) calculations.
The second part is devoted to the investigation of the ionization mechanism of neutral C[subscript]6[subscript]0 molecules with 30 fs laser pulses at about 800 nm and with 50 fs pulses at about 400 nm. The angular distributions of photoelectrons are measured utilizing VMI. Measurements under different intensities are carried out for the two wavelengths. In our work, thermal electron emission is highly suppressed by the use of short pulses. For near-infrared excitation, photoelectron angular distributions (PADs) that contain six lobes are observed for low energy electrons. This behavior is different from studies for longer pulses of about 120 fs [1]. Further analysis indicates that the PADs might originate from single photon ionization of a super atomic molecular orbital (SAMO), however, a detailed assignment requires further theoretical work. The PADs for the ultraviolet excitation show very similar structures to earlier results [1]. For the near-infrared excitation, we have carried out studies as a function of the chirp of the pulses and find effects on photoelectron spectra and on PADs, which are tentatively explained by sequential multiphoton ionization via “doorway” states.
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Photoionization and vibrational spectroscopy of sodium doped water clustersDierking, Christoph Wilhelm Hansjörn Ralf 07 February 2020 (has links)
No description available.
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Absorção cooperativa de dois fótons em átomos frios / Cooperative absorption of two-photon in cold atomsPeñafiel, Edwin Eduardo Pedrozo 27 July 2011 (has links)
Neste trabalho estudamos a absorção cooperativa de dois fótons em processos de colisão entre átomos frios de sódio aprisionados. Efeitos não-lineares exigem amostras de alta densidade para ser observados. Redesenhamos nosso sistema experimental para conseguir amostras de 1012 átomos/cm3. As principais alterações foram a construção de um desacelerador Zeeman em configuração spin-flip, a implementação de bombeamento diferencial entre o forno e a câmara principal, assim como redesenhar o forno. A fim de compreender e melhorar os processos de medição utilizamos a técnica de fotoionização nos estados 32P1/2 e 32P3/2. Com esses dados conseguimos calcular a seção transversal de ionização para cada um desses estados, que está de acordo com valores reportados na literatura. Estes resultados mostram que o novo desenho do sistema permite um grande ponto de partida para a medição da absorção de dois fótons. Uma tentativa de medir a absorção de dois fótons foi feita. Um pequeno aumento no número de íons produzidos por unidade de tempo foi observada em uma região deslocada para o vermelho de cerca de 4,5 GHz de onde inicialmente se esperava ocorrer a transição. Isto motiva a aprofundar o estudo da absorção de dois fótons, já que provavelmente essa medida seja um indício da ocorrência desse fenômeno. Assim, tanto a medição da seção de choque dos estados 32P1/2 e 32P3/2 e a tentativa de medir a absorção de dois fótons, fornecem uma base sólida para conhecer qual é a melhor maneira de obter resultados mais decisivos no que diz respeito à absorção cooperativa de dois fótons, e as vantagens do nosso sistema em futuros experimentos. / In this work we study the cooperative two-photon absorption in collisional processes between cold trapped sodium atoms. Nonlinear effects require high density samples to be observed. We redesign our experimental system to achieve samples up to 1012 atoms/ cm3 .The key changes were building a spin-flip Zeeman slower, implementing differential pumping between the oven and the chamber and changing the oven´s design. In order to understand and improve the measurement processes we did photoionization from the states 32P1/2 e 32P3/2. With this data we could calculate the ionization cross section for each of these states, which is in agreement with values reported in the literature. These results show that the new design of the system allows a great starting point for measuring of two-photon absorption. An attempt to measure the absorption of two-photon was made. A small increase in the number of ions produced per unit time was observed in a region shifted to the red of about 4.5 GHz from where we initially expected the transition to occur. This probably indicates two-photon absorption. Thus, both the measurement of cross section of states and the attempt to measure the absorption of two photons, provide a solid foundation for understanding what is the best way to obtain more decisive results with regard to cooperative absorption, and the advantages of performance of our system in future experiments.
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Rôle des états de Rydberg dans la dynamique de photoionisation et de formation de paires d’ions (NO+,O-) de la molécule NO2 : photoémission induite par rayonnement synchrotron et impulsions lasers femtosecondes / The role of Rydberg states in photoionization of NO2 and (NO+,O-) ion pair formation : photoemission induced by synchotron radiation and femtosecond pulsesMarggi Poullain, Sonia 14 January 2014 (has links)
L’étude comparée des réactions de formation de paires d’ions et de simple photoionisation de la molécule NO2 induites par rayonnement synchrotron (RS) d’une part et par impulsions laser femtosecondes (fs) d’autre part, démontre le rôle remarquable de l’excitation résonante d’états de Rydberg dans la dynamique électronique et nucléaire induite. Trois réactions principales, la photoionisation non dissociative (NO2+ (X 1Σ+g) + e), la photoionisation dissociative (NO+ (X 1Σ+) + O(3P) + e) et la formation de paires d'ions, (NO+ (X 1Σ+) + O- (2P)), ont été caractérisées en utilisant la méthode des corrélations vectorielles ou spectroscopie en coïncidence des impulsions du photoélectron et des photoions, auprès des sources RS (SOLEIL, DESIRS) et lasers fs (CEA, Saclay), respectivement. Le diagramme de corrélation des énergies cinétiques électron-ion, première observable issue de ces mesures, met en évidence un partage de l’énergie en excès entre noyaux et électrons qui dépend fortement du mode d’excitation photonique. Les déviations significatives observées par rapport aux profils d’ionisation de type Franck Condon sont attribuées à des couplages vibroniques entre états excités NO2*, tels que ceux induits par une intersection conique. Les chemins réactionnels identifiés confirment le rôle de l’excitation des séries de Rydberg [R*(6a1)-1] et [R*(4b2)-1] intervenant comme états intermédiaires dans l’excitation multiphotonique ou dans le continuum d’ionisation exploré. Une étude complémentaire par spectroscopie à haute résolution des états [R*(6a1)-1] a été mise en œuvre (UBC, Vancouver).Pour une réaction de photoionisation dissociative (PID), l’observable la plus complète est la distribution angulaire des photoélectrons dans le référentiel lié à la vitesse de recul de l’ion fragment (RFPAD) déduite de la mesure de la corrélation vectorielle (Vi, Ve, P). Afin d’accéder aux éléments de matrice dipolaire décrivant la photoionisation de l’état électronique considéré, le formalisme développé en collaboration avec R. R. Lucchese (Texas A&M) décrivant la photoémission dans le référentiel moléculaire pour la simple PID d'une molécule linéaire par excitation à un photon, a été étendu à l'étude des réactions de PID par excitation multiphotonique d'une molécule polyatomique, telle que la molécule NO2 de symétrie C2v. L’analyse multivariée de la RFPAD multiphotonique proposée constitue une stratégie fructueuse en vue d’extraire l’information optimale sur la dynamique complexe de photoionisation et de réaliser une comparaison détaillée entre les résultats expérimentaux et les calculs de photoionisation des états excités de la molécule. / The comparative study of ion pair formation and simple photoionization of the NO2 molecule induced by synchrotron radiation (SR) on the one hand and by femtosecond (fs) pulses on the other hand reveals the remarkable role of Rydberg states in the induced electronic and nuclear dynamics. Three main reactions, namely (NO2+ (X 1Σ+g) + e) non dissociative photoionization, (NO+ (X 1Σ+) + O(3P) + e) dissociative photoionization and (NO+ (X 1Σ+) + O- (2P)) ion pair formation have been characterized using the vector correlation method, or photoion and photoelectron coincidence momentum spectroscopy, at SR sources (SOLEIL DESIRS) and at fs laser platforms (CEA, Saclay), respectively. The electron-ion kinetic energy correlation diagram, which is the first observable obtained from these measurements, highlights the excess energy sharing among nuclei and electrons, which strongly depends on the photon excitation mode. The observed remarkable deviations from Franck Condon ionization profiles are attributed to vibronic couplings such as those induced at a conical intersection. The identified reaction pathways confirm the role of the [R*(6a1)-1] and [R*(4b2)-1] Rydberg series excitation as stepping states in multiphoton excitation or in the explored ionization continua. A complementary study of high resolution spectroscopy of [R*(6a1)-1] Rydberg series has been performed (UBC, Vancouver). For a dissociative photoionization (DPI) process, the most complete observable is the photoelectron angular distribution in the reference frame attached to the recoil ion fragment velocity (RFPAD) deduced from the measured (Vi, Ve, P) vector correlation. In order to get access to the dipole matrix elements describing photoionization of the considered excited electronic state, the formalism developed in collaboration with R. R. Lucchese (Texas A&M) describing molecular frame photoemission for a DPI of a linear molecule by one-photon excitation has been extended to the study of DPI processes induced by multiphoton excitation for a polyatomic molecule, such as the NO2 molecule of C2v symmetry. The proposed multivariate analysis of the multiphoton RFPAD constitutes a successful strategy to extract the optimal information on the complex photoionization dynamics and to perform a detailed comparison between experimental results and calculations of photoionization of the molecular excited states.
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Laser Cooling and Trapping of Metastable Neon and Applications to PhotoionizationAshmore, Jonathan P, n/a January 2005 (has links)
This thesis presents an in-depth study into the characterization and enhancement of a metastable neon laser cooled and trapped atomic beam. The apparatus consists of a standard Zeeman slowed atomic beam loaded into a magneto-optical trap and was designed for applications to electron scattering experiments and photoionization. The efficiency of the metastable neon atomic source was investigated to determine the ideal cathode type for maximum metastable production and optimal atomic beam velocity haracteristics. A series of characterization measurements were performed on the MOT, and the trap volume and population were investigated for a range of trapping and slowing laser intensities and detunings, together with the MOT and Zeeman slower magnetic fields. The volume measurements were compared to standard Doppler theory and it was found that the Doppler model inadequately explained the trap behaviour. It was found that the MOT population characteristics were governed by two processes: two-body losses that limit the trap population at high densities, and the efficiency of the atom capture process which limits the operational range of the MOT over the various parameters. The trap temperature was determined to be 1.3mK via a time-of-flight technique. This was nearly twice that predicted by Doppler theory and the lack of agreement once again suggests the inadequacies in the Doppler theory to correctly model the experiment. The application of the MOT to the photoionization cross-section measurement of the (2p53p)3D3 state of neon was investigated. The MOT decay technique was utilized to measure cross-section values of o351 = 2.9+0.2 -0.3 x 10 -18cm2 and o363 = 3.1 +0.3 -0.4 x 10-18cm2 at the wavelengths of 351nm and 363nm respectively. This is an increase in accuracy of around a factor of five from previous measurements and it was found that the results agreed well with the values predicted by current theories.
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Simulations of laser-induced correlated many-electron dynamics in molecular systemsKlinkusch, Stefan January 2011 (has links)
In this thesis, simulations of laser-driven many-electron dynamics in molecules are presented, i.e., the interaction between molecules and an electromagnetic field is demonstrated. When a laser field is applied to a molecular system, a population of higher electronic states takes place as well as other processes, e.g. photoionization, which is described by an appropriate model. Also, a finite lifetime of an excited state can be described by such a model.
In the second part, a method is postulated that is capable of describing electron correlation in a time-dependent scheme. This is done by introducing a single-electron entropy that is at least temporarily minimized in a further step. / Im Rahmen dieser Doktorarbeit werden Simulationen lasergetriebener Vielelektronendynamik in Molekülen präsentiert, d.h., die Wechselwirkung zwischen Molekülen und einem elektromagnetischen Feld wird demonstriert. Bei Laseranregungen finden nicht nur elektronische Übergänge statt, sondern auch weitere Prozesse wie die Photoionisation, die mit einem geeigneten Modell beschrieben wird. Auch die endliche Lebensdauer angeregter Zustände kann mit einem solchen Modell beschrieben werden.
Im zweiten Teil wird eine Methode postuliert, die fähig ist, die Elektronenkorrelation zeitabhängig zu beschreiben. Dies wird durch die Einführung einer Einelektronenentropie erreicht, die in einem weiteren Schritt zumindest kurzzeitig minimiert wird.
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Photoionization of the Be Isoelectronic Sequence: Relativistic and Nonrelativistic R-Matrix CalculationsChu, Wei-Chun 25 August 2009 (has links)
The photoionization of the beryllium-like isoelectronic series has been studied. The bound state wave functions of the target ions were built with CIV3 program. The relativistic Breit-Pauli R-matrix method was used to calculate the cross sections in the photon energy range between the ionization threshold and 1s24f7/2 threshold for each ion. For the total cross sections of Be, B+, C+2, N+3, and O+4, our results match experiment well. The comparison between the present work and other theoretical works are also discussed. We show the comparison with our LS results as it indicates the importance of relativistic effects on different ions. In the analysis, the resonances converging to 1s22lj and 1s23lj were identified and characterized with quantum defects, energies and widths using the eigenphase sum methodology. We summarize the general appearance of resonances along the resonance series and along the isoelectronic sequence. Partial cross sections are also reported systematically along the sequence. All calculations were performed on the NERSC system.
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Photoionization of the Potassium Isoelectronic Sequence: Ca+ and Transition Metal Ionssossah, ayao m 15 December 2010 (has links)
Photoionization cross section calculations are performed for the ground ([Ne]3s23p63d 2D ) and the first two excited ([Ne]3s23p63d 2D and [Ne]3s23p64s 2S ) states of potassium-like transition metal ions (Sc+2, Ti+3, V+4, Cr+5, Mn+6, Fe+7), along with photoionization calculations for K-like Ca+ ions in the ground ([Ne]3s23p64s 2S ) state and the first two excited ([Ne]3s23p63d 2D and [Ne]3s23p63d 2D ) states. The discrete N-electron final state ion system orbitals are generated using the computer program AUTOSTRUCTURE; 24 configurations are included in the configuration-interaction (CI) calculation for transition metal ions, and 30 configurations for the case of Ca+ ions. The initial and final (N+1)-electron wavefunctions are generated using R-matrix along with photoionization cross sections. In addition to the non-relativistic (LS-coupling) R-matrix, we have used the relativistic (Breit-Pauli) R -matrix method to carry out these calculations to focus on relativistic effects. Relativistic and non-relativistic results are compared to demonstrate the influence of relativistic effects. The prominent 3p → 3d giant resonances are analyzed and identified, and our calculated positions and widths are compared with experimental results for K-like ions such as Ca+, Sc+2 and Ti+3. In the case of lower Z (22 Z 20) ions (Ca+, Sc+2 and Ti+3), the photoionization cross section spectra are dominated by the giant (3p 3d excitation) resonances, while in cases of higher Z (26 Z 23) ions (V+4, Cr+5, Mn+6 and Fe+7), the 3p 3d resonances lie below the ionization threshold, and the cross sections are dominated by 3p53d nd and 3p53d n’s Rydberg series of resonances. Comparison of the Ca+, Sc+2 and Ti3+ results with available theoretical and experimental data shows good agreement.
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Größenselektive Untersuchungen zur Kristallisation und Struktur von Wasserclustern / A size resolved investigation on crystallization and structures of water clustersPradzynski, Christoph Czeslaw 06 February 2015 (has links)
IR-Spektren von neutralen Na(H2O)n-Clustern wurden im OH-Streckschwingungsbereich (2800 – 3800 cm-1) größenselektiv bis n=575±25 gemessen. Die Infrarot-anregungsmodulierte, durch chemische Vorionisation verstärkte Photoionisation beruht auf dem Effekt einer Signalverstärkung durch IR-Absorption bei schwellennaher Photoionisation. Die Strukturinformation kann anhand eines Vergleichs mit quantenchemischen Rechnungen gewonnen werden.
Die mit dieser Methode erhaltenen IR-Spektren können für verschiedene Größenbereiche mit durch andere Verfahren generierten Spektren verglichen werden. Für mittlere Clustergrößen (~n=20-50) sind die erhaltenen IR-Signaturen sehr ähnlich zu RIDIR-Spektren von phenoldotierten Clustern. Die Spektren großer amorpher Cluster (n=250) sind vergleichbar mit denen ionischer Cluster.
Die Variation der Expansionsbedingungen (z. B. die Änderung des Trägergases) beeinflusst nicht nur das Einsetzten der Kristallisation (beginnend zwischen n=200 und n=400), sondern auch die Isomerenzusammensetzung für kleinere Clustergrößen. Auf dieser Grundlage wurden Strukturen für die Größen (H2O)20, (H2O)25 und (H2O)32 untersucht.
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