TY - THES A1 - Kappe, Philip T1 - Design and investigation of the emission dynamics of a mode-locked SBS-laser oscillator T1 - Steuerung und Untersuchung der Emissionsdynamik eines modengekoppelten SBS-Laser Oszillators N2 - The primary objective of this work was to develop a laser source for fundamental investigations in the field of laser – materials interactions. In particular it is supposed to facilitate the study of the influence of the temporal energy distribution such as the interaction between adjacent pulses on ablation processes. Therefore, the aim was to design a laser with a highly flexible and easily controllable temporal energy distribution. The laser to meet these demands is an SBS-laser with optional active mode-locking. The nonlinear reflectivity of the SBS-mirror leads to a passive Q-switching and issues ns-pulse bursts with µs spacing. The pulse train parameters such as pulse duration, pulse spacing, pulse energy and number of pulses within a burst can be individually adjusted by tuning the pump parameters and the starting conditions for the laser. Another feature of the SBS-reflection is phase conjugation, which leads to an excellent beam quality thanks to the compensation of phase distortions. Transverse fundamental mode operation and a beam quality better than 1.4 times diffraction limited can be maintained for average output powers of up to 10 W. In addition to the dynamics on a ns-timescale described above, a defined splitting up of each ns-pulse into a train of ps-pulses can be achieved by additional active mode-locking. This twofold temporal focussing of the intensity leads to single pulse energies of up to 2 mJ at pulse durations of approximately 400 ps which corresponds to a pulse peak power of 5 MW. While the pulse duration is of the same order of magnitude as those of other passively Q-switched lasers with simultaneous mode-locking, the pulse energy and pulse peak power exceeds the values of these systems found in the literature by an order of magnitude. To the best of my knowledge the laser presented here is the first implementation of a self-starting mode-locked SBS-laser oscillator. In order to gain a better understanding and control of the transient output of the laser two complementary numerical models were developed. The first is based on laser rate equations which are solved for each laser mode individually while the mode-locking dynamics are calculated from the resultant transient spectrum. The rate equations consider the mean photon densities in the resonator, therefore the propagation of the light inside the resonator is not properly displayed. The second model, in contrast, introduces a spatial resolution of the resonator and hence the propagation inside the resonator can more accurately be considered. Consequently, a mismatch between the loss modulation frequency and the resonator round trip time can be conceived. The model calculates all dynamics in the time domain and therefore the spectral influences such as the Stokes-shift have to be neglected. Both models achieve an excellent reproduction of the ns-dynamics that are generated by the SBS-Q-switch. Separately, each model fails to reproduce all aspects of the ps-dynamics of the SBS-laser in detail. This can be attributed to the complexity of the numerous physical processes involved in this system. But thanks to their complementary nature they provide a very useful tool for investigating the various influences on the dynamics of the mode-locked SBS-laser individually. These aspects can eventually be recomposed to give a complete picture of the mechanisms which govern the output dynamics. Among the aspects under scrutiny were in particular the start resonator quality which determines the starting condition for the SBS-Q-switch, the modulation depth of the AOM and the phonon lifetime as well as the Brillouin-frequency of the SBS-medium. The numerical simulations and the experiments have opened several doors inviting further investigations and promising a potential for further improvement of the experimental results: The results of the simulations in combination with the experimental results which determined the starting conditions for the simulations leave no doubt that the bandwidth generation can primarily be attributed to the SBS-Stokes-shift during the buildup of the Q-switch pulse. For each resonator round trip, bandwidth is generated by shifting a part of the revolving light in frequency. The magnitude of the frequency shift corresponds to the Brillouin-frequency which is a constant of the SBS material and amounts in the case of SF6 to 240 MHz. The modulation of the AOM merely provides an exchange of population between spectrally adjacent modes and therefore diminishes a modulation in the spectrum. By use of a material with a Brillouin-frequency in the GHz range the bandwidth generation can be considerably accelerated thereby shortening the pulse duration. Also, it was demonstrated that yet another nonlinear effect of the SBS can be exploited: If the phonon lifetime is short compared to the resonator round trip time we obtain a modulation in the SBS-reflectivity that supports the modulation of the AOM. The application of an external optical feedback by a conventional mirror turns out to be an alternative to the AOM in synchronizing the longitudinal resonator modes. The interesting feature about this system is that it is ― although highly complex in the physical processes and the temporal output dynamics ― very simple and inexpensive from a technical point of view. No expensive modulators and no control electronics are necessary. Finally, the numerical models constitute a powerful tool for the investigation of emission dynamics of complex laser systems on arbitrary timescales and can also display the spectral evolution of the laser output. In particular it could be demonstrated that differences in the results of the complementary models vanish for systems of lesser complexity. N2 - Ziel der Arbeit ist die Entwicklung einer Laserstrahlquelle, die zur Untersuchung von Laser-Material-Wechselwirkungen eingesetzt werden soll. Im Mittelpunkt des Interesses steht hierbei der Einfluss der zeitlichen Pulsstruktur des Lasers auf Materialabtragsprozesse. Daraus ergibt sich die Anforderung einer möglichst hohen Flexibilität in der Pulsstruktur des Lasers sowie einer möglichst guten Strahlqualität. Eine gute Strahlqualität zeichnet sich durch eine homogene räumliche Intensitätsverteilung aus und ist Voraussetzung für eine gezielte Energiedeponierung auf dem Material. Diese Anforderungen wurden mit einem SBS-Laser erfüllt. Dabei handelt es sich um einen Laser, der einen SBS-Spiegel verwendet, dessen Reflektivität auf der Streuung des Lichts an Schallwellen beruht, die von dem einfallenden Licht selbst erzeugt werden. Als Resultat hat dieser Spiegel eine Reflektivität, die abhängig von der Energie des eingestrahlten Lichts ist. In einem Laser verwendet führt diese energieabhängige Reflektivität zu einer sogenannten Güteschaltung, die sich in der Ausbildung von kurzen Lichtpulsen mit Dauern von etwa 100 Nanosekunden äußert. Die Abstände zwischen den Pulsen, die Pulsdauern und die Pulsenergien können sehr leicht durch die Randbedingungen, wie etwa die Reflektivität der konventionellen Spiegel des Lasers, gesteuert werden. Durch eine zusätzliche, aktiv herbeigeführte Verlustmodulation im Laserresonator wird eine Aufspaltung der Nanosekundenpulse in eine Reihe von Pulsen mit Dauern von nur noch einigen 100 Pikosekunden erreicht. Diese Technik ist unter dem Begriff Modenkopplung bekannt. Es liegt jetzt also eine doppelte Pulsstruktur vor: Nanosekundenpulse, die sich jeweils aus vielen Pikosekundenpulsen zusammensetzen. Durch diese doppelte zeitliche Bündelung der Ausgangsleistung werden während der Pulse Spitzenleistungen von bis zu 5 MW erreicht. Die Pulsenergien der ps-Pulse erreichen bis zu 2 mJ. Diese Werte liegen um den Faktor 10 über denen vergleichbarer Systeme. Meines Wissens ist dies die erste Umsetzung eines selbsttätigen SBS-Lasers mit zusätzlicher Modenkopplung. Um die verschiedenen Einflüsse auf diese Emissionsdynamik besser verstehen und kontrollieren zu können, wurden zwei Modelle mit komplementären Ansätzen entwickelt, auf deren Basis diese Dynamik durch numerische Simulationen wiedergegeben werden kann. Insbesondere können auf diese Weise auch die Einflüsse von einzelnen Materialparametern isoliert betrachtet werden, was im Experiment im allgemeinen nicht möglich ist. Der SBS-Laser wurde bereits erfolgreich in Laser-Materialbearbeitungsexperimenten eingesetzt. So konnte beispielsweise gezeigt werden, dass sich die Bearbeitungsdauer beim Wendelbohren durch die Verwendung von Pulszügen, also einer Reihe kurz aufeinander folgender Pulse, gegenüber dem Einsatz von Pulsen mit gleichmäßigen Abständen erheblich verbessern lässt. KW - Laser KW - Pulszugformung KW - Stimulierte Brillouin Streuung KW - Modenkopplung KW - Laser KW - tailored pulse trains KW - stimulated Brillouin scattering KW - mode-locking Y1 - 2006 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-11514 ER - TY - GEN A1 - Löhmannsröben, Hans-Gerd A1 - Beitz, Toralf A1 - Luadien, Robert A1 - Schultze, Rainer T1 - Laser-based ion mobility spectrometry for sensing of aromatic compounds N2 - The drift time spectra of polycyclic aromatic hydrocarbons (PAH), alkylbenzenes and alkylphenylethers were recorded with a laser-based ion mobility (IM) spectrometer. The ion mobilities of all compounds were determined in helium as drift gas. This allows the calculation of the diffusion cross sections (Omegacalc) on the basis of the exact hard sphere scattering model (EHSSM) and their comparison with the experimentally determined diffusion cross sections (Omegaexp). These Omegaexp/Omegacalc-correlations are presented for molecules with a rigid structure like PAH and prove the reliability of the theoretical model and experimental method. The increase of the selectivity of IM spectrometry is demonstrated using resonance enhanced multiphoton ionisation (REMPI) at atmospheric pressure, realized by tuneable lasers. The REMPI spectra of nine alkylbenzenes and alkylphenylethers are investigated. On the basis of these spectra, the complete qualitative distinction of eight compounds in a mixture is shown. These experiments are extended to alkylbenzene isomer mixtures. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - paper 003 KW - Laser KW - REMPI KW - Ion mobility spectrometry KW - PAH Y1 - 2004 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-11892 ER - TY - JOUR A1 - Villatoro, José Andrés A1 - Zühlke, Martin A1 - Riebe, Daniel A1 - Beitz, Toralf A1 - Weber, Marcus A1 - Riedel, Jens A1 - Löhmannsröben, Hans-Gerd T1 - IR-MALDI ion mobility spectrometry: physical source characterization and application as HPLC detector JF - International journal for ion mobility spectrometry : official publication of the International Society for Ion Mobility Spectrometry N2 - Infrared matrix-assisted laser dispersion and ionization (IR-MALDI) in combination with ion mobility (IM) spectrometry enables the direct analysis of biomolecules in aqueous solution. The release of ions directly from an aqueous solution is based on a phase explosion, induced by the absorption of an IR laser pulse, which disperses the liquid as vapor, nano-and micro-droplets. The ionization process is characterized initially by a broad spatial distribution of the ions, which is a result of complex fluid dynamics and desolvation kinetics. These processes have a profound effect on the shape and width of the peaks in the IM spectra. In this work, the transport of ions by the phase explosion-induced shockwave could be studied independently from the transport by the electric field. The shockwave-induced mean velocities of the ions at different time scales were determined through IM spectrometry and shadowgraphy. The results show a deceleration of the ions from 118 m.s(-1) at a distance of 400 mu m from the liquid surface to 7.1 m.s(-1) at a distance of 10 mm, which is caused by a pile-up effect. Furthermore, the desolvation kinetics were investigated and a first-order desolvation constant of 325 +/- 50 s(-1) was obtained. In the second part, the IR-MALDI-IM spectrometer is used as an HPLC detector for the two-dimensional separation of a pesticide mixture. KW - Ion mobility spectrometry KW - IR-MALDI KW - Shadowgraphy KW - Laser KW - Imaging KW - HPLC Y1 - 2016 U6 - https://doi.org/10.1007/s12127-016-0208-1 SN - 1435-6163 SN - 1865-4584 VL - 19 SP - 197 EP - 207 PB - Springer CY - Heidelberg ER - TY - JOUR A1 - Villatoro, José Andrés A1 - Zühlke, Martin A1 - Riebe, Daniel A1 - Riedel, Jens A1 - Beitz, Toralf A1 - Löhmannsröben, Hans-Gerd T1 - IR-MALDI ion mobility spectrometry JF - Analytical and bioanalytical chemistry : a merger of Fresenius' journal of analytical chemistry and Analusis N2 - The novel combination of infrared matrix-assisted laser dispersion and ionization (IR-MALDI) with ion mobility (IM) spectrometry makes it possible to investigate biomolecules in their natural environment, liquid water. As an alternative to an ESI source, the IR-MALDI source was implemented in an in-house-developed ion mobility (IM) spectrometer. The release of ions directly from an aqueous solution is based on a phase explosion, induced by the absorption of an IR laser pulse (lambda = 2.94 mu m, 6 ns pulse width), which disperses the liquid as nano- and micro-droplets. The prerequisites for the application of IR-MALDI-IM spectrometry as an analytical method are narrow analyte ion signal peaks for a high spectrometer resolution. This can only be achieved by improving the desolvation of ions. One way to full desolvation is to give the cluster ions sufficient time to desolvate. Two methods for achieving this are studied: the implementation of an additional drift tube, as in ESI-IM-spectrometry, and the delayed extraction of the ions. As a result of this optimization procedure, limits of detection between 5 nM and 2.5 mu M as well as linear dynamic ranges of 2-3 orders of magnitude were obtained for a number of substances. The ability of this method to analyze simple mixtures is illustrated by the separation of two different surfactant mixtures. KW - Ion mobility spectrometry KW - IR-MALDI KW - Laser Y1 - 2016 U6 - https://doi.org/10.1007/s00216-016-9739-x SN - 1618-2642 SN - 1618-2650 VL - 408 SP - 6259 EP - 6268 PB - Springer CY - Heidelberg ER -