@phdthesis{Richter2021,
  author    = {Richter, Enrico Christian},
  title     = {Das letzte Kapitel des deutschen Zionismus},
  doi       = {10.25932/publishup-61575},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-615756},
  school      = {Universit{\"a}t Potsdam},
  pages     = {447},
  year      = {2021},
  abstract  = {Die Geschichtsschreibung terminiert das Ende des deutschen Zionismus bisher mit dem NS-Verbot der Zionistischen Vereinigung f{\"u}r Deutschland im Zuge des Novemberpogroms 1938. Zu diesem Zeitpunkt hatte er aber von seinem geographischen Kontext entgrenzt, in Erez Israel bereits neue Wurzeln geschlagen. Zionisten aus Deutschland schickten sich nun an, mit ihrem spezifischen Erfahrungshorizont und Wertemaßstab und mitgebrachtem ideologischen R{\"u}stzeug die Entwicklung des j{\"u}dischen Nationalheims mitzugestalten und einer umfassenden {\"o}konomischen, kulturellen und politischen Akkulturation der deutschen Alijah den Weg zu bahnen. Entgegen aller zionistischen Theorie gr{\"u}ndeten sie auf landsmannschaftlicher Basis im Jahr 1932 die Selbsthilfeorganisation Hitachduth Olej Germania und w{\"a}hrend des Weltkrieges die Partei Alija Chadascha. Die Dissertation beinhaltet die Gesamtschau des deutschen Zionismus in seiner letzten Phase in den Jahren 1932 bis 1948; zugleich beleuchtet sie die Geschichte der etwa 60.000 in Pal{\"a}stina eingewanderten Juden aus Deutschland in der f{\"u}r diese Abhandlung relevanten Zeitperiode. Im ersten Teil wird in chronologischer Folge die 1932 beginnende letztmalige Sammlung und Neuformierung des deutschen Zionismus in seiner neu-alten Heimat dargestellt. Wenn man so will, die formativen Jahre im personellen, organisatorischen und ideologisch-politischen Sinne, die schließlich nach dem fast g{\"a}nzlichen Scheitern der politischen Integration der deutschen Alijah mit der - in der R{\"u}ckschau - fast zwangsl{\"a}ufig erscheinenden Begr{\"u}ndung der Alija Chadascha ihren Abschluss fanden. Im zweiten Teil werden die Positionen der deutschen Zionisten zu den existenziellen Fragen der j{\"u}dischen Gemeinschaft in Pal{\"a}stina, hebr{\"a}isch Jischuw genannt, in der im Fokus stehenden Zeitperiode dargestellt. Im Einzelnen handelt es sich erstens um die Einwanderungsfrage, die untrennbar verbunden war mit der in der zionistischen Theorie unabdingbaren Forderung nach der Erlangung einer j{\"u}dischen Majorit{\"a}t in Pal{\"a}stina; zweitens um die der staatlichen Ausgestaltung des zuk{\"u}nftigen j{\"u}dischen Gemeinwesens und drittens um die Frage der ad{\"a}quaten Reaktion des Jischuw auf die Schoah. In diese jeweils in separaten Kapiteln behandelten Themenkomplexe wird die Frage nach dem anzustrebenden Verh{\"a}ltnis zur britischen Mandatsmacht mit einfließen. Hieran mussten die deutschen Zionisten ihr mitgebrachtes geistig-ideologisches R{\"u}stzeug einem Praxistest unterziehen und nach realpolitischen Antworten suchen. Dem kometenhaften Aufstieg der weiterhin landsmannschaftlich gepr{\"a}gten Alija Chadascha folgte dann in den ersten Nachkriegsjahren ein ebenso rapider Zerfall. Einige Monate nach der Staatsgr{\"u}ndung Israels l{\"o}ste sie sich dann sang- und klanglos auf und das Gros ihrer Aktivisten integrierte sich in das Parteiengef{\"u}ge des neuen Staates. Der deutsche Zionismus als politische Bewegung kam nun wirklich an sein Ende. Diese Abhandlung wird somit zum einen den Kampf der deutschen Alijah um gesellschaftliche Anerkennung und politische Partizipation im Jischuw nachzeichnen und zum anderen eine geistig-ideologische Verortung des deutschen Zionismus in seiner letzten Phase vollziehen und Tendenzen der ideologischen Neuausrichtung offenlegen. Dar{\"u}ber hinaus werden in der Historiographie vorhandene Allgemeinpl{\"a}tze wie die fast allseits anerkannte These vom Scheitern der deutschen Zionisten in der neuen Heimat einer {\"U}berpr{\"u}fung unterzogen. Die letzte vorhandene Leerstelle im wissenschaftlichen Kanon zur mehr als 50-j{\"a}hrigen Geschichte des deutschen Zionismus wird somit geschlossen.},
  language  = {de}
}
@phdthesis{Antonelli2021,
  author    = {Antonelli, Andrea},
  title     = {Accurate waveform models for gravitational-wave astrophysics: synergetic approaches from analytical relativity},
  doi       = {10.25932/publishup-57667},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-576671},
  school      = {Universit{\"a}t Potsdam},
  pages     = {XII, 259, LXXV},
  year      = {2021},
  abstract  = {Gravitational-wave (GW) astrophysics is a field in full blossom. Since the landmark detection of GWs from a binary black hole on September 14th 2015, fifty-two compact-object binaries have been reported by the LIGO-Virgo collaboration. Such events carry astrophysical and cosmological information ranging from an understanding of how black holes and neutron stars are formed, what neutron stars are composed of, how the Universe expands, and allow testing general relativity in the highly-dynamical strong-field regime. It is the goal of GW astrophysics to extract such information as accurately as possible. Yet, this is only possible if the tools and technology used to detect and analyze GWs are advanced enough. A key aspect of GW searches are waveform models, which encapsulate our best predictions for the gravitational radiation under a certain set of parameters, and that need to be cross-correlated with data to extract GW signals. Waveforms must be very accurate to avoid missing important physics in the data, which might be the key to answer the fundamental questions of GW astrophysics. The continuous improvements of the current LIGO-Virgo detectors, the development of next-generation ground-based detectors such as the Einstein Telescope or the Cosmic Explorer, as well as the development of the Laser Interferometer Space Antenna (LISA), demand accurate waveform models. While available models are enough to capture the low spins, comparable-mass binaries routinely detected in LIGO-Virgo searches, those for sources from both current and next-generation ground-based and spaceborne detectors must be accurate enough to detect binaries with large spins and asymmetry in the masses. Moreover, the thousands of sources that we expect to detect with future detectors demand accurate waveforms to mitigate biases in the estimation of signals' parameters due to the presence of a foreground of many sources that overlap in the frequency band. This is recognized as one of the biggest challenges for the analysis of future-detectors' data, since biases might hinder the extraction of important astrophysical and cosmological information from future detectors' data. In the first part of this thesis, we discuss how to improve waveform models for binaries with high spins and asymmetry in the masses. In the second, we present the first generic metrics that have been proposed to predict biases in the presence of a foreground of many overlapping signals in GW data. For the first task, we will focus on several classes of analytical techniques. Current models for LIGO and Virgo studies are based on the post-Newtonian (PN, weak-field, small velocities) approximation that is most natural for the bound orbits that are routinely detected in GW searches. However, two other approximations have risen in prominence, the post-Minkowskian (PM, weak- field only) approximation natural for unbound (scattering) orbits and the small-mass-ratio (SMR) approximation typical of binaries in which the mass of one body is much bigger than the other. These are most appropriate to binaries with high asymmetry in the masses that challenge current waveform models. Moreover, they allow one to "cover" regions of the parameter space of coalescing binaries, thereby improving the interpolation (and faithfulness) of waveform models. The analytical approximations to the relativistic two-body problem can synergically be included within the effective-one-body (EOB) formalism, in which the two-body information from each approximation can be recast into an effective problem of a mass orbiting a deformed Schwarzschild (or Kerr) black hole. The hope is that the resultant models can cover both the low-spin comparable-mass binaries that are routinely detected, and the ones that challenge current models. The first part of this thesis is dedicated to a study about how to best incorporate information from the PN, PM, SMR and EOB approaches in a synergistic way. We also discuss how accurate the resulting waveforms are, as compared against numerical-relativity (NR) simulations. We begin by comparing PM models, whether alone or recast in the EOB framework, against PN models and NR simulations. We will show that PM information has the potential to improve currently-employed models for LIGO and Virgo, especially if recast within the EOB formalism. This is very important, as the PM approximation comes with a host of new computational techniques from particle physics to exploit. Then, we show how a combination of PM and SMR approximations can be employed to access previously-unknown PN orders, deriving the third subleading PN dynamics for spin-orbit and (aligned) spin1-spin2 couplings. Such new results can then be included in the EOB models currently used in GW searches and parameter estimation studies, thereby improving them when the binaries have high spins. Finally, we build an EOB model for quasi-circular nonspinning binaries based on the SMR approximation (rather than the PN one as usually done). We show how this is done in detail without incurring in the divergences that had affected previous attempts, and compare the resultant model against NR simulations. We find that the SMR approximation is an excellent approximation for all (quasi-circular nonspinning) binaries, including both the equal-mass binaries that are routinely detected in GW searches and the ones with highly asymmetric masses. In particular, the SMR-based models compare much better than the PN models, suggesting that SMR-informed EOB models might be the key to model binaries in the future. In the second task of this thesis, we work within the linear-signal ap- proximation and describe generic metrics to predict inference biases on the parameters of a GW source of interest in the presence of confusion noise from unfitted foregrounds and from residuals of other signals that have been incorrectly fitted out. We illustrate the formalism with simple (yet realistic) LISA sources, and demonstrate its validity against Monte-Carlo simulations. The metrics we describe pave the way for more realistic studies to quantify the biases with future ground-based and spaceborne detectors.},
  language  = {en}
}
@phdthesis{Forster2021,
  author    = {Forster, Florian},
  title     = {Continuous microgravity monitoring of the Þeistareykir geothermal field (North Iceland)},
  doi       = {10.25932/publishup-54851},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-548517},
  school      = {Universit{\"a}t Potsdam},
  pages     = {XVII, 164},
  year      = {2021},
  abstract  = {In my doctoral thesis, I examine continuous gravity measurements for monitoring of the geothermal site at Þeistareykir in North Iceland. With the help of high-precision superconducting gravity meters (iGravs), I investigate underground mass changes that are caused by operation of the geothermal power plant (i.e. by extraction of hot water and reinjection of cold water). The overall goal of this research project is to make a statement about the sustainable use of the geothermal reservoir, from which also the Icelandic energy supplier and power plant operator Landsvirkjun should benefit. As a first step, for investigating the performance and measurement stability of the gravity meters, in summer 2017, I performed comparative measurements at the gravimetric observatory J9 in Strasbourg. From the three-month gravity time series, I examined calibration, noise and drift behaviour of the iGravs in comparison to stable long-term time series of the observatory superconducting gravity meters. After preparatory work in Iceland (setup of gravity stations, additional measuring equipment and infrastructure, discussions with Landsvirkjun and meetings with the Icelandic partner institute ISOR), gravity monitoring at Þeistareykir was started in December 2017. With the help of the iGrav records of the initial 18 months after start of measurements, I carried out the same investigations (on calibration, noise and drift behaviour) as in J9 to understand how the transport of the superconducting gravity meters to Iceland may influence instrumental parameters. In the further course of this work, I focus on modelling and reduction of local gravity contributions at Þeistareykir. These comprise additional mass changes due to rain, snowfall and vertical surface displacements that superimpose onto the geothermal signal of the gravity measurements. For this purpose, I used data sets from additional monitoring sensors that are installed at each gravity station and adapted scripts for hydro-gravitational modelling. The third part of my thesis targets geothermal signals in the gravity measurements. Together with my PhD colleague Nolwenn Portier from France, I carried out additional gravity measurements with a Scintrex CG5 gravity meter at 26 measuring points within the geothermal field in the summers of 2017, 2018 and 2019. These annual time-lapse gravity measurements are intended to increase the spatial coverage of gravity data from the three continuous monitoring stations to the entire geothermal field. The combination of CG5 and iGrav observations, as well as annual reference measurements with an FG5 absolute gravity meter represent the hybrid gravimetric monitoring method for Þeistareykir. Comparison of the gravimetric data to local borehole measurements (of groundwater levels, geothermal extraction and injection rates) is used to relate the observed gravity changes to the actually extracted (and reinjected) geothermal fluids. An approach to explain the observed gravity signals by means of forward modelling of the geothermal production rate is presented at the end of the third (hybrid gravimetric) study. Further modelling with the help of the processed gravity data is planned by Landsvirkjun. In addition, the experience from time-lapse and continuous gravity monitoring will be used for future gravity measurements at the Krafla geothermal field 22 km south-east of Þeistareykir.},
  language  = {en}
}
@phdthesis{Canil2021,
  author    = {Canil, Laura},
  title     = {Tuning Interfacial Properties in Perovskite Solar Cells through Defined Molecular Assemblies},
  doi       = {10.25932/publishup-54633},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-546333},
  school      = {Universit{\"a}t Potsdam},
  pages     = {vii, 157},
  year      = {2021},
  abstract  = {In the frame of a world fighting a dramatic global warming caused by human-related activities, research towards the development of renewable energies plays a crucial role. Solar energy is one of the most important clean energy sources and its role in the satisfaction of the global energy demand is set to increase. In this context, a particular class of materials captured the attention of the scientific community for its attractive properties: halide perovskites. Devices with perovskite as light-absorber saw an impressive development within the last decade, reaching nowadays efficiencies comparable to mature photovoltaic technologies like silicon solar cells. Yet, there are still several roadblocks to overcome before a wide-spread commercialization of this kind of devices is enabled. One of the critical points lies at the interfaces: perovskite solar cells (PSCs) are made of several layers with different chemical and physical features. In order for the device to function properly, these properties have to be well-matched. This dissertation deals with some of the challenges related to interfaces in PSCs, with a focus on the interface between the perovskite material itself and the subsequent charge transport layer. In particular, molecular assemblies with specific properties are deposited on the perovskite surface to functionalize it. The functionalization results in energy level alignment adjustment, interfacial losses reduction, and stability improvement. First, a strategy to tune the perovskite's energy levels is introduced: self-assembled monolayers of dipolar molecules are used to functionalize the surface, obtaining simultaneously a shift in the vacuum level position and a saturation of the dangling bonds at the surface. A shift in the vacuum level corresponds to an equal change in work function, ionization energy, and electron affinity. The direction of the shift depends on the direction of the collective interfacial dipole. The magnitude of the shift can be tailored by controlling the deposition parameters, such as the concentration of the solution used for the deposition. The shift for different molecules is characterized by several non-invasive techniques, including in particular Kelvin probe. Overall, it is shown that it is possible to shift the perovskite energy levels in both directions by several hundreds of meV. Moreover, interesting insights on the molecules deposition dynamics are revealed. Secondly, the application of this strategy in perovskite solar cells is explored. Devices with different perovskite compositions ("triple cation perovskite" and MAPbBr3) are prepared. The two resulting model systems present different energetic offsets at the perovskite/hole-transport layer interface. Upon tailored perovskite surface functionalization, the devices show a stabilized open circuit voltage (Voc) enhancement of approximately 60 meV on average for devices with MAPbBr3, while the impact is limited on triple-cation solar cells. This suggests that the proposed energy level tuning method is valid, but its effectiveness depends on factors such as the significance of the energetic offset compared to the other losses in the devices. Finally, the above presented method is further developed by incorporating the ability to interact with the perovskite surface directly into a novel hole-transport material (HTM), named PFI. The HTM can anchor to the perovskite halide ions via halogen bonding (XB). Its behaviour is compared to that of another HTM (PF) with same chemical structure and properties, except for the ability of forming XB. The interaction of perovskite with PFI and PF is characterized through UV-Vis, atomic force microscopy and Kelvin probe measurements combined with simulations. Compared to PF, PFI exhibits enhanced resilience against solvent exposure and improved energy level alignment with the perovskite layer. As a consequence, devices comprising PFI show enhanced Voc and operational stability during maximum-power-point tracking, in addition to hysteresis reduction. XB promotes the formation of a high-quality interface by anchoring to the halide ions and forming a stable and ordered interfacial layer, showing to be a particularly interesting candidate for the development of tailored charge transport materials in PSCs. Overall, the results exposed in this dissertation introduce and discuss a versatile tool to functionalize the perovskite surface and tune its energy levels. The application of this method in devices is explored and insights on its challenges and advantages are given. Within this frame, the results shed light on XB as ideal interaction for enhancing stability and efficiency in perovskite-based devices.},
  language  = {en}
}
@phdthesis{Andjelkovic2021,
  author    = {Andjelkovic, Marko},
  title     = {A methodology for characterization, modeling and mitigation of single event transient effects in CMOS standard combinational cells},
  doi       = {10.25932/publishup-53484},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-534843},
  school      = {Universit{\"a}t Potsdam},
  pages     = {xxiv, 216},
  year      = {2021},
  abstract  = {With the downscaling of CMOS technologies, the radiation-induced Single Event Transient (SET) effects in combinational logic have become a critical reliability issue for modern integrated circuits (ICs) intended for operation under harsh radiation conditions. The SET pulses generated in combinational logic may propagate through the circuit and eventually result in soft errors. It has thus become an imperative to address the SET effects in the early phases of the radiation-hard IC design. In general, the soft error mitigation solutions should accommodate both static and dynamic measures to ensure the optimal utilization of available resources. An efficient soft-error-aware design should address synergistically three main aspects: (i) characterization and modeling of soft errors, (ii) multi-level soft error mitigation, and (iii) online soft error monitoring. Although significant results have been achieved, the effectiveness of SET characterization methods, accuracy of predictive SET models, and efficiency of SET mitigation measures are still critical issues. Therefore, this work addresses the following topics: (i) Characterization and modeling of SET effects in standard combinational cells, (ii) Static mitigation of SET effects in standard combinational cells, and (iii) Online particle detection, as a support for dynamic soft error mitigation. Since the standard digital libraries are widely used in the design of radiation-hard ICs, the characterization of SET effects in standard cells and the availability of accurate SET models for the Soft Error Rate (SER) evaluation are the main prerequisites for efficient radiation-hard design. This work introduces an approach for the SPICE-based standard cell characterization with the reduced number of simulations, improved SET models and optimized SET sensitivity database. It has been shown that the inherent similarities in the SET response of logic cells for different input levels can be utilized to reduce the number of required simulations. Based on characterization results, the fitting models for the SET sensitivity metrics (critical charge, generated SET pulse width and propagated SET pulse width) have been developed. The proposed models are based on the principle of superposition, and they express explicitly the dependence of the SET sensitivity of individual combinational cells on design, operating and irradiation parameters. In contrast to the state-of-the-art characterization methodologies which employ extensive look-up tables (LUTs) for storing the simulation results, this work proposes the use of LUTs for storing the fitting coefficients of the SET sensitivity models derived from the characterization results. In that way the amount of characterization data in the SET sensitivity database is reduced significantly. The initial step in enhancing the robustness of combinational logic is the application of gate-level mitigation techniques. As a result, significant improvement of the overall SER can be achieved with minimum area, delay and power overheads. For the SET mitigation in standard cells, it is essential to employ the techniques that do not require modifying the cell structure. This work introduces the use of decoupling cells for improving the robustness of standard combinational cells. By insertion of two decoupling cells at the output of a target cell, the critical charge of the cell's output node is increased and the attenuation of short SETs is enhanced. In comparison to the most common gate-level techniques (gate upsizing and gate duplication), the proposed approach provides better SET filtering. However, as there is no single gate-level mitigation technique with optimal performance, a combination of multiple techniques is required. This work introduces a comprehensive characterization of gate-level mitigation techniques aimed to quantify their impact on the SET robustness improvement, as well as introduced area, delay and power overhead per gate. By characterizing the gate-level mitigation techniques together with the standard cells, the required effort in subsequent SER analysis of a target design can be reduced. The characterization database of the hardened standard cells can be utilized as a guideline for selection of the most appropriate mitigation solution for a given design. As a support for dynamic soft error mitigation techniques, it is important to enable the online detection of energetic particles causing the soft errors. This allows activating the power-greedy fault-tolerant configurations based on N-modular redundancy only at the high radiation levels. To enable such a functionality, it is necessary to monitor both the particle flux and the variation of particle LET, as these two parameters contribute significantly to the system SER. In this work, a particle detection approach based on custom-sized pulse stretching inverters is proposed. Employing the pulse stretching inverters connected in parallel enables to measure the particle flux in terms of the number of detected SETs, while the particle LET variations can be estimated from the distribution of SET pulse widths. This approach requires a purely digital processing logic, in contrast to the standard detectors which require complex mixed-signal processing. Besides the possibility of LET monitoring, additional advantages of the proposed particle detector are low detection latency and power consumption, and immunity to error accumulation. The results achieved in this thesis can serve as a basis for establishment of an overall soft-error-aware database for a given digital library, and a comprehensive multi-level radiation-hard design flow that can be implemented with the standard IC design tools. The following step will be to evaluate the achieved results with the irradiation experiments.},
  language  = {en}
}
@phdthesis{MathieuGaedke2021,
  author    = {Mathieu-Gaedke, Maria},
  title     = {Grafting-to and grafting-from proteins - synthesis and characterization of protein-polymer conjugates on the way to biohybrid membrane materials},
  doi       = {10.25932/publishup-54292},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-542921},
  school      = {Universit{\"a}t Potsdam},
  pages     = {XVIII, 149},
  year      = {2021},
  abstract  = {The incorporation of proteins in artificial materials such as membranes offers great opportunities to avail oneself the miscellaneous qualities of proteins and enzymes perfected by nature over millions of years. One possibility to leverage proteins is the modification with artificial polymers. To obtain such protein-polymer conjugates, either a polymer can be grown from the protein surface (grafting-from) or a pre-synthesized polymer attached to the protein (grafting-to). Both techniques were used to synthesize conjugates of different proteins with thermo-responsive polymers in this thesis. First, conjugates were analyzed by protein NMR spectroscopy. Typical characterization techniques for conjugates can verify the successful conjugation and give hints on the secondary structure of the protein. However, the 3-dimensional structure, being highly important for the protein function, cannot be probed by standard techniques. NMR spectroscopy is a unique method allowing to follow even small alterations in the protein structure. A mutant of the carbohydrate binding module 3b (CBM3bN126W) was used as model protein and functionalized with poly(N-isopropylacrylamide). Analysis of conjugates prepared by grafting-to or grafting-from revealed a strong impact of conjugation type on protein folding. Whereas conjugates prepared by grafting a pre-formed polymer to the protein resulted in complete preservation of protein folding, grafting the polymer from the protein surface led to (partial) disruption of the protein structure. Next, conjugates of bovine serum albumin (BSA) as cheap and easily accessible protein were synthesized with PNIPAm and different oligoethylene glycol (meth)acrylates. The obtained protein-polymer conjugates were analyzed by an in-line combination of size exclusion chromatography and multi-angle laser light scattering (SEC-MALS). This technique is particular advantageous to determine molar masses, as no external calibration of the system is needed. Different SEC column materials and operation conditions were tested to evaluate the applicability of this system to determine absolute molar masses and hydrodynamic properties of heterogeneous conjugates prepared by grafting-from and grafting-to. Hydrophobic and non-covalent interactions of conjugates lead to error-prone values not in accordance to expected molar masses based on conversions and extents of modifications. As alternative to this method, conjugates were analyzed by sedimentation velocity analytical ultracentrifugation (SV-AUC) to gain insights in the hydrodynamic properties and how they change after conjugation. Within a centrifugal field, a sample moves and fractionates according to the mass, density, and shape of its individual components. Conjugates of BSA with PNIPAm were analyzed below and above the cloud point temperature of the thermo-responsive polymer component. It was identified that the polymer characteristics were transferred to the conjugate molecule which than showed a decreased ideality - defined as increased deviation from a perfect sphere model - below and increased ideality above the cloud point temperature. This effect can be attributed to an arrangement of the polymer chain pointing towards the solvent (expanded state) or snuggling around the protein surface depending on the applied temperature. The last project dealt with the synthesis of ferric hydroxamate uptake protein component A (FhuA)-polymer conjugates as building blocks for novel membrane materials. The shape of FhuA can be described as barrel and removal of a cork domain inside the protein results in a passive channel aimed to be utilized as pores in the membrane system. The polymer matrix surrounding the membrane protein is composed of a thermo-responsive and a UV-crosslinkable part. Therefore, an external trigger for covalent immobilization of these building blocks in the membrane and switchability of the membrane between different states was incorporated. The overall performance of membranes prepared by a drying-mediated self-assembly approach was evaluated by permeability and size exclusion experiments. The obtained membranes displayed an insufficiency in interchain crosslinking and therefore a lack in performance. Furthermore, the aimed switch between a hydrophilic and hydrophobic state of the polymer matrix did not occur. Correspondingly, size exclusion experiments did not result in a retention of analytes larger than the pores defined by the dimension of the used FhuA variant. Overall, different paths to generate protein-polymer conjugates by either grafting-from or grafting-to the protein surface were presented paving the way to the generation of new hybrid materials. Different analytical methods were utilized to describe the folding and hydrodynamic properties of conjugates providing a deeper insight in the overall characteristics of these seminal building blocks.},
  language  = {en}
}
@phdthesis{Dahmani2021,
  author    = {Dahmani, Ismail},
  title     = {Influenza A virus matrix protein M1},
  doi       = {10.25932/publishup-52740},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-527409},
  school      = {Universit{\"a}t Potsdam},
  pages     = {XI, 147},
  year      = {2021},
  abstract  = {Influenza A virus (IAV) is a pathogen responsible for severe seasonal epidemics threatening human and animal populations every year. During the viral assembly process in the infected cells, the plasma membrane (PM) has to bend in localized regions into a vesicle towards the extracellular side. Studies in cellular models have proposed that different viral proteins might be responsible for inducing membrane curvature in this context (including M1), but a clear consensus has not been reached. M1 is the most abundant protein in IAV particles. It plays an important role in virus assembly and budding at the PM. M1 is recruited to the host cell membrane where it associates with lipids and other viral proteins. However, the details of M1 interactions with the cellular PM, as well as M1-mediated membrane bending at the budozone, have not been clarified. In this work, we used several experimental approaches to analyze M1-lipids and M1-M1 interactions. By performing SPR analysis, we quantified membrane association for full-length M1 and different genetically engineered M1 constructs (i.e., N- and C-terminally truncated constructs and a mutant of the polybasic region). This allowed us to obtain novel information on the protein regions mediating M1 binding to membranes. By using fluorescence microscopy, cryogenic transmission electron microscopy (cryo-TEM), and three-dimensional (3D) tomography (cryo-ET), we showed that M1 is indeed able to cause membrane deformation on vesicles containing negatively-charged lipids, in the absence of other viral components. Further, sFCS analysis proved that simple protein binding is not sufficient to induce membrane restructuring. Rather, it appears that stable M1-M1 interactions and multimer formation are required to alter the bilayer three-dimensional structure through the formation of a protein scaffold. Finally, to mimic the budding mechanism in cells that arise by the lateral organization of the virus membrane components on lipid raft domains, we created vesicles with lipid domains. Our results showed that local binding of M1 to spatial confined acidic lipids within membrane domains of vesicles led to local M1 inward curvature.},
  language  = {en}
}
@phdthesis{Saretia2021,
  author    = {Saretia, Shivam},
  title     = {Modulating ultrathin films of semi-crystalline oligomers by Langmuir technique},
  doi       = {10.25932/publishup-54210},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-542108},
  school      = {Universit{\"a}t Potsdam},
  pages     = {XIII, 109},
  year      = {2021},
  abstract  = {Polymeric films and coatings derived from semi-crystalline oligomers are of relevance for medical and pharmaceutical applications. In this context, the material surface is of particular importance, as it mediates the interaction with the biological system. Two dimensional (2D) systems and ultrathin films are used to model this interface. However, conventional techniques for their preparation, such as spin coating or dip coating, have disadvantages, since the morphology and chain packing of the generated films can only be controlled to a limited extent and adsorption on the substrate used affects the behavior of the films. Detaching and transferring the films prepared by such techniques requires additional sacrificial or supporting layers, and free-standing or self supporting domains are usually of very limited lateral extension. The aim of this thesis is to study and modulate crystallization, melting, degradation and chemical reactions in ultrathin films of oligo(ε-caprolactone)s (OCL)s with different end-groups under ambient conditions. Here, oligomeric ultrathin films are assembled at the air-water interface using the Langmuir technique. The water surface allows lateral movement and aggregation of the oligomers, which, unlike solid substrates, enables dynamic physical and chemical interaction of the molecules. Parameters like surface pressure (π), temperature and mean molecular area (MMA) allow controlled assembly and manipulation of oligomer molecules when using the Langmuir technique. The π-MMA isotherms, Brewster angle microscopy (BAM), and interfacial infrared spectroscopy assist in detecting morphological and physicochemical changes in the film. Ultrathin films can be easily transferred to the solid silicon surface via Langmuir Schaefer (LS) method (horizontal substrate dipping). Here, the films transferred on silicon are investigated using atomic force microscopy (AFM) and optical microscopy and are compared to the films on the water surface. The semi-crystalline morphology (lamellar thicknesses, crystal number densities, and lateral crystal dimensions) is tuned by the chemical structure of the OCL end-groups (hydroxy or methacrylate) and by the crystallization temperature (Tc; 12 or 21 °C) or MMAs. Compression to lower MMA of ~2 {\AA}2, results in the formation of a highly crystalline film, which consists of tightly packed single crystals. Preparation of tightly packed single crystals on a cm2 scale is not possible by conventional techniques. Upon transfer to a solid surface, these films retain their crystalline morphology whereas amorphous films undergo dewetting. The melting temperature (Tm) of OCL single crystals at the water and the solid surface is found proportional to the inverse crystal thickness and is generally lower than the Tm of bulk PCL. The impact of OCL end-groups on melting behavior is most noticeable at the air-solid interface, where the methacrylate end-capped OCL (OCDME) melted at lower temperatures than the hydroxy end-capped OCL (OCDOL). When comparing the underlying substrate, melting/recrystallization of OCL ultrathin films is possible at lower temperatures at the air water interface than at the air-solid interface, where recrystallization is not visible. Recrystallization at the air-water interface usually occurs at a higher temperature than the initial Tc. Controlled degradation is crucial for the predictable performance of degradable polymeric biomaterials. Degradation of ultrathin films is carried out under acidic (pH ~ 1) or enzymatic catalysis (lipase from Pseudomonas cepcia) on the water surface or on a silicon surface as transferred films. A high crystallinity strongly reduces the hydrolytic but not the enzymatic degradation rate. As an influence of end-groups, the methacrylate end-capped linear oligomer, OCDME (~85 ± 2 \% end-group functionalization) hydrolytically degrades faster than the hydroxy end capped linear oligomer, OCDOL (~95 ± 3 \% end-group functionalization) at different temperatures. Differences in the acceleration of hydrolytic degradation of semi-crystalline films were observed upon complete melting, partial melting of the crystals, or by heating to temperatures close to Tm. Therefore, films of densely packed single crystals are suitable as barrier layers with thermally switchable degradation rates. Chemical modification in ultrathin films is an intricate process applicable to connect functionalized molecules, impart stability or create stimuli-sensitive cross-links. The reaction of end-groups is explored for transferred single crystals on a solid surface or amorphous monolayer at the air-water interface. Bulky methacrylate end-groups are expelled to the crystal surface during chain-folded crystallization. The density of end-groups is inversely proportional to molecular weight and hence very pronounced for oligomers. The methacrylate end-groups at the crystal surface, which are present at high concentration, can be used for further chemical functionalization. This is demonstrated by fluorescence microscopy after reaction with fluorescein dimethacrylate. The thermoswitching behavior (melting and recrystallization) of fluorescein functionalized single crystals shows the temperature-dependent distribution of the chemically linked fluorescein moieties, which are accumulated on the surfaces of crystals, and homogeneously dispersed when the crystals are molten. In amorphous monolayers at the air-water interface, reversible cross-linking of hydroxy-terminated oligo(ε-caprolactone) monolayers using dialdehyde (glyoxal) lead to the formation of 2D networks. Pronounced contraction in the area occurred for 2D OCL films in dependence of surface pressure and time indicating the reaction progress. Cross linking inhibited crystallization and retarded enzymatic degradation of the OCL film. Altering the subphase pH to ~2 led to cleavage of the covalent acetal cross-links. Besides as model systems, these reversibly cross-linked films are applicable for drug delivery systems or cell substrates modulating adhesion at biointerfaces.},
  language  = {en}
}
@phdthesis{Jentsch2021,
  author    = {Jentsch, Anna},
  title     = {Soil gas analytics in geothermal exploration and monitoring},
  doi       = {10.25932/publishup-54403},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-544039},
  school      = {Universit{\"a}t Potsdam},
  pages     = {xxxi, 162},
  year      = {2021},
  abstract  = {Major challenges during geothermal exploration and exploitation include the structural-geological characterization of the geothermal system and the application of sustainable monitoring concepts to explain changes in a geothermal reservoir during production and/or reinjection of fluids. In the absence of sufficiently permeable reservoir rocks, faults and fracture networks are preferred drilling targets because they can facilitate the migration of hot and/or cold fluids. In volcanic-geothermal systems considerable amounts of gas emissions can be released at the earth surface, often related to these fluid-releasing structures. In this thesis, I developed and evaluated different methodological approaches and measurement concepts to determine the spatial and temporal variation of several soil gas parameters to understand the structural control on fluid flow. In order to validate their potential as innovative geothermal exploration and monitoring tools, these methodological approaches were applied to three different volcanic-geothermal systems. At each site an individual survey design was developed regarding the site-specific questions. The first study presents results of the combined measurement of CO2 flux, ground temperatures, and the analysis of isotope ratios (δ13CCO2, 3He/4He) across the main production area of the Los Humeros geothermal field, to identify locations with a connection to its supercritical (T > 374◦C and P > 221 bar) geothermal reservoir. The results of the systematic and large-scale (25 x 200 m) CO2 flux scouting survey proved to be a fast and flexible way to identify areas of anomalous degassing. Subsequent sampling with high resolution surveys revealed the actual extent and heterogenous pattern of anomalous degassing areas. They have been related to the internal fault hydraulic architecture and allowed to assess favourable structural settings for fluid flow such as fault intersections. Finally, areas of unknown structurally controlled permeability with a connection to the superhot geothermal reservoir have been determined, which represent promising targets for future geothermal exploration and development. In the second study, I introduce a novel monitoring approach by examining the variation of CO2 flux to monitor changes in the reservoir induced by fluid reinjection. For that reason, an automated, multi-chamber CO2 flux system was deployed across the damage zone of a major normal fault crossing the Los Humeros geothermal field. Based on the results of the CO2 flux scouting survey, a suitable site was selected that had a connection to the geothermal reservoir, as identified by hydrothermal CO2 degassing and hot ground temperatures (> 50 °C). The results revealed a response of gas emissions to changes in reinjection rates within 24 h, proving an active hydraulic communication between the geothermal reservoir and the earth surface. This is a promising monitoring strategy that provides nearly real-time and in-situ data about changes in the reservoir and allows to timely react to unwanted changes (e.g., pressure decline, seismicity). The third study presents results from the Aluto geothermal field in Ethiopia where an area-wide and multi-parameter analysis, consisting of measurements of CO2 flux, 222Rn, and 220Rn activity concentrations and ground temperatures was conducted to detect hidden permeable structures. 222Rn and 220Rn activity concentrations are evaluated as a complementary soil gas parameter to CO2 flux, to investigate their potential to understand tectono-volcanic degassing. The combined measurement of all parameters enabled to develop soil gas fingerprints, a novel visualization approach. Depending on the magnitude of gas emissions and their migration velocities the study area was divided in volcanic (heat), tectonic (structures), and volcano-tectonic dominated areas. Based on these concepts, volcano-tectonic dominated areas, where hot hydrothermal fluids migrate along permeable faults, present the most promising targets for future geothermal exploration and development in this geothermal field. Two of these areas have been identified in the south and south-east which have not yet been targeted for geothermal exploitation. Furthermore, two unknown areas of structural related permeability could be identified by 222Rn and 220Rn activity concentrations. Eventually, the fourth study presents a novel measurement approach to detect structural controlled CO2 degassing, in Ngapouri geothermal area, New Zealand. For the first time, the tunable diode laser (TDL) method was applied in a low-degassing geothermal area, to evaluate its potential as a geothermal exploration method. Although the sampling approach is based on profile measurements, which leads to low spatial resolution, the results showed a link between known/inferred faults and increased CO2 concentrations. Thus, the TDL method proved to be a successful in the determination of structural related permeability, also in areas where no obvious geothermal activity is present. Once an area of anomalous CO2 concentrations has been identified, it can be easily complemented by CO2 flux grid measurements to determine the extent and orientation of the degassing segment. With the results of this work, I was able to demonstrate the applicability of systematic and area-wide soil gas measurements for geothermal exploration and monitoring purposes. In particular, the combination of different soil gases using different measurement networks enables the identification and characterization of fluid-bearing structures and has not yet been used and/or tested as standard practice. The different studies present efficient and cost-effective workflows and demonstrate a hands-on approach to a successful and sustainable exploration and monitoring of geothermal resources. This minimizes the resource risk during geothermal project development. Finally, to advance the understanding of the complex structure and dynamics of geothermal systems, a combination of comprehensive and cutting-edge geological, geochemical, and geophysical exploration methods is essential.},
  language  = {en}
}
@phdthesis{Schutjajew2021,
  author    = {Schutjajew, Konstantin},
  title     = {Electrochemical sodium storage in non-graphitizing carbons - insights into mechanisms and synthetic approaches towards high-energy density materials},
  doi       = {10.25932/publishup-54189},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-541894},
  school      = {Universit{\"a}t Potsdam},
  pages     = {v, 148},
  year      = {2021},
  abstract  = {To achieve a sustainable energy economy, it is necessary to turn back on the combustion of fossil fuels as a means of energy production and switch to renewable sources. However, their temporal availability does not match societal consumption needs, meaning that renewably generated energy must be stored in its main generation times and allocated during peak consumption periods. Electrochemical energy storage (EES) in general is well suited due to its infrastructural independence and scalability. The lithium ion battery (LIB) takes a special place, among EES systems due to its energy density and efficiency, but the scarcity and uneven geological occurrence of minerals and ores vital for many cell components, and hence the high and fluctuating costs will decelerate its further distribution. The sodium ion battery (SIB) is a promising successor to LIB technology, as the fundamental setup and cell chemistry is similar in the two systems. Yet, the most widespread negative electrode material in LIBs, graphite, cannot be used in SIBs, as it cannot store sufficient amounts of sodium at reasonable potentials. Hence, another carbon allotrope, non-graphitizing or hard carbon (HC) is used in SIBs. This material consists of turbostratically disordered, curved graphene layers, forming regions of graphitic stacking and zones of deviating layers, so-called internal or closed pores. The structural features of HC have a substantial impact of the charge-potential curve exhibited by the carbon when it is used as the negative electrode in an SIB. At defects and edges an adsorption-like mechanism of sodium storage is prevalent, causing a sloping voltage curve, ill-suited for the practical application in SIBs, whereas a constant voltage plateau of relatively high capacities is found immediately after the sloping region, which recent research attributed to the deposition of quasimetallic sodium into the closed pores of HC. Literature on the general mechanism of sodium storage in HCs and especially the role of the closed pore is abundant, but the influence of the pore geometry and chemical nature of the HC on the low-potential sodium deposition is yet in an early stage. Therefore, the scope of this thesis is to investigate these relationships using suitable synthetic and characterization methods. Materials of precisely known morphology, porosity, and chemical structure are prepared in clear distinction to commonly obtained ones and their impact on the sodium storage characteristics is observed. Electrochemical impedance spectroscopy in combination with distribution of relaxation times analysis is further established as a technique to study the sodium storage process, in addition to classical direct current techniques, and an equivalent circuit model is proposed to qualitatively describe the HC sodiation mechanism, based on the recorded data. The obtained knowledge is used to develop a method for the preparation of closed porous and non-porous materials from open porous ones, proving not only the necessity of closed pores for efficient sodium storage, but also providing a method for effective pore closure and hence the increase of the sodium storage capacity and efficiency of carbon materials. The insights obtained and methods developed within this work hence not only contribute to the better understanding of the sodium storage mechanism in carbon materials of SIBs, but can also serve as guidance for the design of efficient electrode materials.},
  language  = {en}
}
@phdthesis{Hechenbichler2021,
  author    = {Hechenbichler, Michelle},
  title     = {New thermoresponsive amphiphilic block copolymers with unconventional chemical structure and architecture},
  doi       = {10.25932/publishup-54182},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-541822},
  school      = {Universit{\"a}t Potsdam},
  pages     = {XIX, 186},
  year      = {2021},
  abstract  = {Das Aggregationsverhalten von amphiphilen Blockcpoolymeren ist wichtig f{\"u}r zahlreiche Anwendungen, beispielsweise in der Waschmittelindustrie als Verdicker oder in der Pharmazie zur kontrollierten Freisetzung von Wirkstoffen. Wenn einer der Bl{\"o}cke thermoresponsiv ist, kann das Aggregationsverhalten zus{\"a}tzlich {\"u}ber die Temperatur gesteuert werden. W{\"a}hrend sich die bisherigen Untersuchungen solcher „intelligenten" Systeme zumeist auf einfache Diblockcopolymere beschr{\"a}nkt haben, wurde in der vorliegenden Arbeit die Komplexit{\"a}t der Polymere und damit die Vielseitigkeit dieser Systeme erh{\"o}ht. Dazu wurden spezifische Monomere, verschiedene Blockl{\"a}ngen, unterschiedliche Architekturen und zus{\"a}tzliche funktionelle Gruppen eingef{\"u}hrt. Durch systematische {\"A}nderungen wurde das Struktur-Wirkungsverhalten solcher thermoresponsiver amphiphiler Blockcopolymere untersucht. Dabei sind die Blockcopolymere typischerweise aus einem permanent hydrophoben „Sticker", einem permanent hydrophilen Block sowie einem thermoresponsiven Block, der ein Lower Critical Solution Temperature (LCST) Verhalten zeigt, aufgebaut. W{\"a}hrend der permanent hydrophile Block aus N,N Dimethylacrylamid (DMAm) bestand, wurden f{\"u}r den thermoresponsiven Block unterschiedliche Monomere, n{\"a}mlich N n Propylacrylamid (NPAm), N iso Propylacrylamid (NiPAm), N,N Diethylacrylamid (DEAm), N,N Bis(2 methoxyethyl)acrylamid (bMOEAm), oder N Acryloylpyrrolidin (NAP) mit entsprechend unterschiedlichen LCSTs von 25, 32, 33, 42 und 56 °C verwendet. Die Blockcopolymere wurden mittels aufeinanderfolgender reversibler Additions-Fragmentierungs-Ketten{\"u}bertragungspolymerisation (RAFT Polymerisation) hergestellt, um Polymere mit linearer, doppelt hydrophober sowie symmetrischer Quasi Miktoarm Architektur zu erhalten. Dabei wurden wohldefinierte Blockgr{\"o}ßen, Endgruppen und enge Molmassenverteilungen (Ɖ ≤ 1.3) erzielt. F{\"u}r komplexere Architekturen, wie die doppelt thermoresponsive und die nicht symmetrische Quasi Miktoarm Architekturen, wurde RAFT mit Atomtransfer-Radikalpolymerisation (ATRP) oder Single Unit Monomer Insertion (SUMI), kombiniert. Die dabei erhaltenen Blockcopolymere hatten ebenfalls wohldefinierte Blockl{\"a}ngen, allerdings war die Molmassenverteilung generell breiter (Ɖ ≤ 1.8) und Endgruppen gingen zum Teil verloren, da komplexere Syntheseschritte n{\"o}tig waren. Das thermoresponsive Verhalten in w{\"a}ssriger L{\"o}sung wurde mittels Tr{\"u}bungspunktmessung und Dynamischer Lichtstreuung (DLS) untersucht. Unterhalb der Phasen{\"u}berganstemperatur waren die Polymere l{\"o}slich in Wasser und mizellare Strukturen waren in der DLS sichtbar. Oberhalb der Phasen{\"u}bergangstemperatur war das Aggregationsverhalten dann stark abh{\"a}ngig von der Architektur und der chemischen Struktur des thermoresponsiven Blocks. Thermoresponsive Bl{\"o}cke aus PNAP und PbMOEAm mit einer Blockl{\"a}nge von DPn = 40 zeigten keinen Tr{\"u}bungspunkt (CP) bis hin zu 80 °C, da durch den angebrachten hydrophilen PDMAm Block die bereits hohe LCST der entsprechenden Homopolymere bei den Blockcopolymeren weiter erh{\"o}ht wurde. Blockcopolymere mit PNiPAm, PDEAm und PNPAm hinggeen zeigten abh{\"a}ngig von der Architektur und Blockgr{\"o}ße unterschiedliche CP's. Oberhalb der CP's waren gr{\"o}ßere Aggregate vor allem f{\"u}r die Blockcopolymere mit PNiPAm und PDEAm sichtbar, wohingegen der Phasen{\"u}bergang f{\"u}r Blockcopolymere mit PNPAm stark abh{\"a}ngig von der jeweiligen Architektur war und entsprechend kleinere oder gr{\"o}ßere Aggregate zeigte. Um das Aggregationsverhalten besser zu verstehen, wurden Fluoreszenzstudien an PDMAm und PNiPAm Homo und Blockcopolymeren mit linearer Architektur durchgef{\"u}hrt, welche mit komplement{\"a}ren Fluoreszenzfarbstoffen an den entgegengesetzten Kettenenden funktionalisiert wurden. Das thermoresponsive Verhalten wurde dabei sowohl in Wasser als auch in {\"O}l-in-Wasser Mikroemulsion untersucht. Die Ergebnisse zeigten, dass das Blockcopolymer sich, {\"a}hnlich wie die anderen hergestellten Architekturen, bei niedrigen Temperaturen wie ein Polymertensid verh{\"a}lt. Dabei bilden die hydrophoben Stickergruppen den Kern und die hydrophilen Arme die Corona der Mizelle. Oberhalb des Phasen{\"u}bergangs des PNiPAm Blocks verhielten sich die Blockcopolymere allerdings wie assoziative Telechele mit zwei nicht symmetrischen hydrophoben Endgruppen, die sich untereinander nicht mischten. Daher bildeten die Blockcopolymere anstatt aggregierter „Blumen"-Mizellen gr{\"o}ßere, dynamische Aggregate. Diese sind einerseits {\"u}ber die urspr{\"u}nglichen Mizellkerne bestehend aus den hydrophoben Sticker als auch {\"u}ber Cluster der kollabierten thermoresponsiven Bl{\"o}cke miteinander verkn{\"u}pft. In Mikroemulsion ist diese Art der Netzwerkbildung noch st{\"a}rker ausgepr{\"a}gt.},
  language  = {en}
}
@phdthesis{Lood2021,
  author    = {Lood, Kajsa},
  title     = {Stereoselective Construction of C-C Double Bonds via Olefin Metathesis: From Tethered Reactions to Water-Soluble Catalysts for Stereoretentive Metathesis},
  doi       = {10.25932/publishup-53914},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-539142},
  school      = {Universit{\"a}t Potsdam},
  pages     = {95},
  year      = {2021},
  abstract  = {Natural products have proved to be a major resource in the discovery and development of many pharmaceuticals that are in use today. There is a wide variety of biologically active natural products that contain conjugated polyenes or benzofuran structures. Therefore, new synthetic methods for the construction of such building blocks are of great interest to synthetic chemists. The recently developed one-pot tethered ring-closing metathesis approach allows for the formation of Z,E-dienoates in high stereoselectivity. The extension of this method with a Julia-Kocienski olefination protocol would allow for the formation of conjugated trienes in a stereoselective manner. This strategy was applied in the total synthesis of conjugated triene containing (+)-bretonin B. Additionally, investigations of cross metathesis using methyl substituted olefins were pursued. This methodology was applied, as a one-pot cross metathesis/ring-closing metathesis sequence, in the total synthesis of benzofuran containing 7-methoxywutaifuranal. Finally, the design and synthesis of a catalyst for stereoretentive metathesis in aqueous media was investigated.},
  language  = {en}
}
@phdthesis{Diab2021,
  author    = {Diab, Momen},
  title     = {Enabling astrophotonics: adaptive optics and photonic lanterns for coupling starlight into the single-mode regime},
  doi       = {10.25932/publishup-53901},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-539012},
  school      = {Universit{\"a}t Potsdam},
  pages     = {xvii, 177},
  year      = {2021},
  abstract  = {Ground-based astronomy is set to employ next-generation telescopes with apertures larger than 25 m in diameter before this decade is out. Such giant telescopes observe their targets through a larger patch of turbulent atmosphere, demanding that most of the instruments behind them must also grow larger to make full use of the collected stellar flux. This linear scaling in size greatly complicates the design of astronomical instrumentation, inflating their cost quadratically. Adaptive optics (AO) is one approach to circumvent this scaling law, but it can only be done to an extent before the cost of the corrective system itself overwhelms that of the instrument or even that of the telescope. One promising technique for miniaturizing the instruments and thus driving down their cost is to replace some, or all, of the free space bulk optics in the optical train with integrated photonic components. Photonic devices, however, do their work primarily in single-mode waveguides, and the atmospherically-distorted starlight must first be efficiently coupled into them if they are to outperform their bulk optic counterparts. This is doable by two means: AO systems can again help control the angular size and motion of seeing disks to the point where they will couple efficiently into astrophotonic components, but this is only feasible for the brightest of objects and over limited fields of view. Alternatively, tapered fiber devices known as photonic lanterns — with their ability to convert multimode into single-mode optical fields — can be used to feed speckle patterns into single-mode integrated optics. They, nonetheless, must conserve the degrees of freedom, and the number of output waveguides will quickly grow out of control for uncorrected large telescopes. An AO-assisted photonic lantern fed by a partially corrected wavefront presents a compromise that can have a manageable size if the trade-off between the two methods is chosen carefully. This requires end-to-end simulations that take into account all the subsystems upstream of the astrophotonic instrument, i.e., the atmospheric layers, the telescope, the AO system, and the photonic lantern, before a decision can be made on sizing the multiplexed integrated instrument. The numerical models that simulate atmospheric turbulence and AO correction are presented in this work. The physics and models for optical fibers, arrays of waveguides, and photonic lanterns are also provided. The models are on their own useful in understanding the behavior of the individual subsystems involved and are also used together to compute the optimum sizing of photonic lanterns for feeding astrophotonic instruments. Additionally, since photonic lanterns are a relatively new concept, two novel applications are discussed for them later in this thesis: the use of mode-selective photonic lanterns (MSPLs) to reduce the multiplicity of multiplexed integrated instruments and the combination of photonic lanterns with discrete beam combiners (DBCs) to retrieve the modal content in an optical waveguide.},
  language  = {en}
}
@phdthesis{Krumbholz2021,
  author    = {Krumbholz, Julia},
  title     = {Identification of chemical mediators that regulate the specialized metabolism in Nostoc punctiforme},
  doi       = {10.25932/publishup-54024},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-540240},
  school      = {Universit{\"a}t Potsdam},
  pages     = {xxiii, 187},
  year      = {2021},
  abstract  = {Specialized metabolites, so-called natural products, are produced by a variety of different organisms, including bacteria and fungi. Due to their wide range of different biological activities, including pharmaceutical relevant properties, microbial natural products are an important source for drug development. They are encoded by biosynthetic gene clusters (BGCs), which are a group of locally clustered genes. By screening genomic data for genes encoding typical core biosynthetic enzymes, modern bioinformatical approaches are able to predict a wide range of BGCs. To date, only a small fraction of the predicted BGCs have their associated products identified. The phylum of the cyanobacteria has been shown to be a prolific, but largely untapped source for natural products. Especially multicellular cyanobacterial genera, like Nostoc, harbor a high amount of BGCs in their genomes. A main goal of this study was to develop new concepts for the discovery of natural products in cyanobacteria. Due to its diverse setup of orphan BGCs and its amenability to genetic manipulation, Nostoc punctiforme PCC 73102 (N. punctiforme) appeared to be a promising candidate to be established as a model organism for natural product discovery in cyanobacteria. By utilizing a combination of genome-mining, bioactivity-screening, variations of culture conditions, as well as metabolic engineering, not only two new polyketides were discovered, but also first-time insights into the regulation of the specialized metabolism in N. punctiforme were gained during this study. The cultivation of N. punctiforme to very high densities by utilizing increasing light intensities and CO2 levels, led to an enhanced metabolite production, causing rather complex metabolite extracts. By utilizing a library of CFP reporter mutant strains, each strain reporting for one of the predicted BGCs, it was shown that eight out of 15 BGCs were upregulated under high density (HD) cultivation conditions. Furthermore, it could be demonstrated that the supernatant of an HD culture can increase the expression of four of the influenced BGCs, even under conventional cultivation conditions. This led to the hypothesis that a chemical mediator encoded by one of the affected BGCs is accumulating in the HD supernatant and is able to increase the expression of other BGCs as part of a cell-density dependent regulatory circuit. To identify which of the BGCs could be a main trigger of the presumed regulatory circuit, it was tried to activate four BGCs (pks1, pks2, ripp3, ripp4) selectively by overexpression of putative pathway-specific regulatory genes that were found inside the gene clusters. Transcriptional analysis of the mutants revealed that only the mutant strain targeting the pks1 BGC, called AraC_PKS1, was able to upregulate the expression of its associated BGC. From an RNA sequencing study of the AraC_PKS1 mutant strain, it was discovered that beside pks1, the orphan BGCs ripp3 and ripp4 were also upregulated in the mutant strain. Furthermore, it was observed that secondary metabolite production in the AraC_PKS1 mutant strain is further enhanced under high-light and high-CO2 cultivation conditions. The increased production of the pks1 regulator NvlA also had an impact on other regulatory factors, including sigma factors and the RNA chaperone Hfq. Analysis of the AraC_PKS1 cell and supernatant extracts led to the discovery of two novel polyketides, nostoclide and nostovalerolactone, both encoded by the pks1 BGC. Addition of the polyketides to N. punctiforme WT demonstrated that the pks1-derived compounds are able to partly reproduce the effects on secondary metabolite production found in the AraC_PKS1 mutant strain. This indicates that both compounds are acting as extracellular signaling factors as part of a regulatory network. Since not all transcriptional effects that were found in the AraC_PKS1 mutant strain could be reproduced by the pks1 products, it can be assumed that the regulator NvlA has a global effect and is not exclusively specific to the pks1 pathway. This study was the first to use a putative pathway specific regulator for the specific activation of BGC expression in cyanobacteria. This strategy did not only lead to the detection of two novel polyketides, it also gave first-time insights into the regulatory mechanism of the specialized metabolism in N. punctiforme. This study illustrates that understanding regulatory pathways can aid in the discovery of novel natural products. The findings of this study can guide the design of new screening strategies for bioactive compounds in cyanobacteria and help to develop high-titer production platforms for cyanobacterial natural products.},
  language  = {en}
}
@phdthesis{Muench2021,
  author    = {M{\"u}nch, Steffen},
  title     = {The relevance of the aeolian transport path for the spread of antibiotic-resistant bacteria on arable fields},
  doi       = {10.25932/publishup-53608},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-536089},
  school      = {Universit{\"a}t Potsdam},
  pages     = {XVI, 140},
  year      = {2021},
  abstract  = {The spread of antibiotic-resistant bacteria poses a globally increasing threat to public health care. The excessive use of antibiotics in animal husbandry can develop resistances in the stables. Transmission through direct contact with animals and contamination of food has already been proven. The excrements of the animals combined with a binding material enable a further potential path of spread into the environment, if they are used as organic manure in agricultural landscapes. As most of the airborne bacteria are attached to particulate matter, the focus of the work will be the atmospheric dispersal via the dust fraction. Field measurements on arable lands in Brandenburg, Germany and wind erosion studies in a wind tunnel were conducted to investigate the risk of a potential atmospheric dust-associated spread of antibiotic-resistant bacteria from poultry manure fertilized agricultural soils. The focus was to (i) characterize the conditions for aerosolization and (ii) qualify and quantify dust emissions during agricultural operations and wind erosion. PM10 (PM, particulate matter with an aerodynamic diameter smaller than 10 µm) emission factors and bacterial fluxes for poultry manure application and incorporation have not been previously reported before. The contribution to dust emissions depends on the water content of the manure, which is affected by the manure pretreatment (fresh, composted, stored, dried), as well as by the intensity of manure spreading from the manure spreader. During poultry manure application, PM10 emission ranged between 0.05 kg ha-1 and 8.37 kg ha-1. For comparison, the subsequent land preparation contributes to 0.35 - 1.15 kg ha-1 of PM10 emissions. Manure particles were still part of dust emissions but they were accounted to be less than 1\% of total PM10 emissions due to the dilution of poultry manure in the soil after manure incorporation. Bacterial emissions of fecal origin were more relevant during manure application than during the subsequent manure incorporation, although PM10 emissions of manure incorporation were larger than PM10 emissions of manure application for the non-dried manure variants. Wind erosion leads to preferred detachment of manure particles from sandy soils, when poultry manure has been recently incorporated. Sorting effects were determined between the low-density organic particles of manure origin and the soil particles of mineral origin close above the threshold of 7 m s-1. In dependence to the wind speed, potential erosion rates between 101 and 854 kg ha-1 were identified, if 6 t ha-1 of poultry manure were applied. Microbial investigation showed that manure bacteria got detached more easily from the soil surface during wind erosion, due to their attachment on manure particles. Although antibiotic-resistant bacteria (ESBL-producing E. coli) were still found in the poultry barns, no further contamination could be detected with them in the manure, fertilized soils or in the dust generated by manure application, land preparation or wind erosion. Parallel studies of this project showed that storage of poultry manure for a few days (36 - 72 h) is sufficient to inactivate ESBL-producing E. coli. Further antibiotic-resistant bacteria, i.e. MRSA and VRE, were only found sporadically in the stables and not at all in the dust. Therefore, based on the results of this work, the risk of a potential infection by dust-associated antibiotic-resistant bacteria can be considered as low.},
  language  = {en}
}
@phdthesis{Kraemer2021,
  author    = {Kr{\"a}mer, Kai Hauke},
  title     = {Towards a robust framework for recurrence analysis},
  doi       = {10.25932/publishup-53874},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-538743},
  school      = {Universit{\"a}t Potsdam},
  pages     = {xlii, 217},
  year      = {2021},
  abstract  = {In our daily life, recurrence plays an important role on many spatial and temporal scales and in different contexts. It is the foundation of learning, be it in an evolutionary or in a neural context. It therefore seems natural that recurrence is also a fundamental concept in theoretical dynamical systems science. The way in which states of a system recur or develop in a similar way from similar initial states makes it possible to infer information about the underlying dynamics of the system. The mathematical space in which we define the state of a system (state space) is often high dimensional, especially in complex systems that can also exhibit chaotic dynamics. The recurrence plot (RP) enables us to visualize the recurrences of any high-dimensional systems in a two-dimensional, binary representation. Certain patterns in RPs can be related to physical properties of the underlying system, making the qualitative and quantitative analysis of RPs an integral part of nonlinear systems science. The presented work has a methodological focus and further develops recurrence analysis (RA) by addressing current research questions related to an increasing amount of available data and advances in machine learning techniques. By automatizing a central step in RA, namely the reconstruction of the state space from measured experimental time series, and by investigating the impact of important free parameters this thesis aims to make RA more accessible to researchers outside of physics. The first part of this dissertation is concerned with the reconstruction of the state space from time series. To this end, a novel idea is proposed which automates the reconstruction problem in the sense that there is no need to preprocesse the data or estimate parameters a priori. The key idea is that the goodness of a reconstruction can be evaluated by a suitable objective function and that this function is minimized in the embedding process. In addition, the new method can process multivariate time series input data. This is particularly important because multi-channel sensor-based observations are ubiquitous in many research areas and continue to increase. Building on this, the described minimization problem of the objective function is then processed using a machine learning approach. In the second part technical and methodological aspects of RA are discussed. First, we mathematically justify the idea of setting the most influential free parameter in RA, the recurrence threshold ε, in relation to the distribution of all pairwise distances in the data. This is especially important when comparing different RPs and their quantification statistics and is fundamental to any comparative study. Second, some aspects of recurrence quantification analysis (RQA) are examined. As correction schemes for biased RQA statistics, which are based on diagonal lines, we propose a simple method for dealing with border effects of an RP in RQA and a skeletonization algorithm for RPs. This results in less biased (diagonal line based) RQA statistics for flow-like data. Third, a novel type of RQA characteristic is developed, which can be viewed as a generalized non-linear powerspectrum of high dimensional systems. The spike powerspectrum transforms a spike-train like signal into its frequency domain. When transforming the diagonal line-dependent recurrence rate (τ-RR) of a RP in this way, characteristic periods, which can be seen in the state space representation of the system can be unraveled. This is not the case, when Fourier transforming τ-RR. Finally, RA and RQA are applied to climate science in the third part and neuroscience in the fourth part. To the best of our knowledge, this is the first time RPs and RQA have been used to analyze lake sediment data in a paleoclimate context. Therefore, we first elaborate on the basic formalism and the interpretation of visually visible patterns in RPs in relation to the underlying proxy data. We show that these patterns can be used to classify certain types of variability and transitions in the Potassium record from six short (< 17m) sediment cores collected during the Chew Bahir Drilling Project. Building on this, the long core (∼ m composite) from the same site is analyzed and two types of variability and transitions are identified and compared with ODP Site  wetness index from the eastern Mediterranean. Type  variability likely reflects the influence of precessional forcing in the lower latitudes at times of maximum values of the long eccentricity cycle ( kyr) of the earth's orbit around the sun, with a tendency towards extreme events. Type  variability appears to be related to the minimum values of this cycle and corresponds to fairly rapid transitions between relatively dry and relatively wet conditions. In contrast, RQA has been applied in the neuroscientific context for almost two decades. In the final part, RQA statistics are used to quantify the complexity in a specific frequency band of multivariate EEG (electroencephalography) data. By analyzing experimental data, it can be shown that the complexity of the signal measured in this way across the sensorimotor cortex decreases as motor tasks are performed. The results are consistent with and comple- ment the well known concepts of motor-related brain processes. We assume that the thus discovered features of neuronal dynamics in the sensorimotor cortex together with the robust RQA methods for identifying and classifying these contribute to the non-invasive EEG-based development of brain-computer interfaces (BCI) for motor control and rehabilitation. The present work is an important step towards a robust analysis of complex systems based on recurrence.},
  language  = {en}
}
@phdthesis{Riedl2021,
  author    = {Riedl, Simon},
  title     = {Active tectonics in the Kenya Rift},
  doi       = {10.25932/publishup-53855},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-538552},
  school      = {Universit{\"a}t Potsdam},
  pages     = {xi, 207},
  year      = {2021},
  abstract  = {Magmatische und tektonisch aktive Grabenzonen (Rifts) stellen die Vorstufen entstehender Plattengrenzen dar. Diese sich spreizenden tektonischen Provinzen zeichnen sich durch allgegenw{\"a}rtige Abschiebungen aus, und die r{\"a}umliche Verteilung, die Geometrie, und das Alter dieser Abschiebungen l{\"a}sst R{\"u}ckschl{\"u}sse auf die r{\"a}umlichen und zeitlichen Zusammenh{\"a}nge zwischen tektonischer Deformation, Magmatismus und langwelliger Krustendeformation in Rifts zu. Diese Arbeit konzentriert sich auf die St{\"o}rungsaktivit{\"a}t im Kenia-Rift des k{\"a}nozoischen Ostafrikanischen Grabensystems im Zeitraum zwischen dem mittleren Pleistoz{\"a}n und dem Holoz{\"a}n. Um die fr{\"u}hen Stadien der Entstehung kontinentaler Plattengrenzen zu untersuchen, wird in dieser Arbeit eine zeitlich gemittelte minimale Extensionsrate f{\"u}r den inneren Graben des N{\"o}rdlichen Kenia-Rifts (NKR) f{\"u}r die letzten 0,5 Mio Jahre abgeleitet. Die Analyse beruht auf Messungen mit Hilfe des digitalen TanDEM-X-H{\"o}henmodells, um die Abschiebungen entlang der vulkanisch-tektonischen Achse des inneren Grabens des NKR zu kartieren und deren Versatzbetr{\"a}ge zu bestimmen. Mithilfe von vorhandenen Geochronologiedaten der deformierten vulkanischen Einheiten sowie in dieser Arbeit erstellten ⁴⁰Ar/³⁹Ar-Datierungen werden zeitlich gemittelte Extensionsraten berechnet. Die Auswertungen zeigen, dass im inneren Graben des NKR die langfristige Extensionsrate f{\"u}r mittelpleistoz{\"a}ne bis rezente St{\"o}rungen Mindestwerte von 1,0 bis 1,6 mm yr⁻¹ aufweist und lokal allerdings auch Werte bis zu 2,0 mm yr⁻¹ existieren. In Anbetracht der nahezu inaktiven Randst{\"o}rungen des NKR zeigt sich somit, dass sich die Extension auf die Region der aktiven vulkanisch-tektonischen Achse im inneren Graben konzentriert und somit ein fortgeschrittenes Stadium kontinentaler Extensionsprozesse im NKR vorliegt. In dieser Arbeit wird diese r{\"a}umlich fokussierte Extension zudem im Rahmen einer St{\"o}rungsanalyse der j{\"u}ngsten vulkanischen Erscheinungen des Kenia-Rifts betrachtet. Die Arbeit analysiert mithilfe von Gel{\"a}ndekartierungen und eines auf Luftbildern basierenden Gel{\"a}ndemodells die St{\"o}rungscharakteristika der etwa 36 tausend Jahre alten Menengai-Kaldera und der umliegenden Gebiete im zentralen Kenia-Rift. Im Allgemeinen sind die holoz{\"a}nen St{\"o}rungen innerhalb des Rifts reine, NNO-streichende Abschiebungen, die somit das gegenw{\"a}rtige tektonische Spannungsfeld wiederspiegeln; innerhalb der Menengai-Kaldera sind die jungen Strukturen jedoch von andauernder magmatischer Aktivit{\"a}t und von Aufdomung {\"u}berpr{\"a}gt. Die Kaldera befindet sich im Zentrum eines sich aktiv dehnenden Riftsegments und zusammen mit den anderen quart{\"a}ren Vulkanen des Kenia-Rifts lassen sich diese Bereiche als Kernpunkte der extensionalen St{\"o}rungsaktivit{\"a}t verstehen, die letztlich zu einer weiter entwickelten Phase magmengest{\"u}tzter Kontinentalseparation f{\"u}hren werden. Die bereits seit dem Terti{\"a}r andauernde St{\"o}rungsaktivit{\"a}t im Kenia-Rift f{\"u}hrt zur Zergliederung der gr{\"o}ßeren Rift-Senken in kleinere Segmente und beeinflusst die Sedimentologie und die Hydrologie dieser Riftbecken. Gegenw{\"a}rtig sind die meisten, durch St{\"o}rungen begrenzten Becken des Kenia-Rifts hydrologisch isoliert, sie waren aber w{\"a}hrend feuchter Klimaphasen hydrologisch miteinander verbunden; in dieser Arbeit untersuche ich deshalb auch diese hydrologische Verbindung der Rift-Becken f{\"u}r die Zeit der Afrikanischen Feuchteperiode des fr{\"u}hen Holoz{\"a}ns. Mithilfe der Analyse von digitalen Gel{\"a}ndemodellen, unter Ber{\"u}cksichtigung von geomorphologischen Anzeigern f{\"u}r Seespiegelhochst{\"a}nde, Radiokarbondatierungen und einer {\"U}bersicht {\"u}ber Fossiliendaten konnten zwei kaskadierende Flusssysteme aus diesen Daten abgeleitet werden: eine Flusskaskade in Richtung S{\"u}den und eine in Richtung Norden. Beide Kaskaden haben die derzeit isolierten Becken w{\"a}hrend des fr{\"u}hen Holoz{\"a}ns durch {\"u}berlaufende Seen und eingeschnittene Schluchten miteinander verbunden. Diese hydrologische Verbindung f{\"u}hrte zu der Ausbreitung aquatischer Fauna entlang des Rifts, und gleichzeitig stellte die Wasserscheide zwischen den beiden Flusssystemen den einzigen terrestrischen Ausbreitungskorridor dar, der eine {\"U}berquerung des Kenia-Rifts erm{\"o}glichte. Diese tektonisch-geomorphologische Rekonstruktion erkl{\"a}rt die heute isolierten Vorkommen nilotischer Fischarten in den Riftseen Kenias sowie die isolierten Vorkommen Guineo-Congolischer S{\"a}ugetiere in W{\"a}ldern {\"o}stlich des Kenia-Rifts, die sich {\"u}ber die Wasserscheide im Kenia-Rift ausbreiten konnten. Auf l{\"a}ngeren Zeitskalen sind solche Phasen hydrologischer Verbindung und Phasen der Isolation wiederholt aufgetreten und zeigen sich in wechselnden pal{\"a}o{\"o}kologischen Indikatoren in Sedimentbohrkernen. Hier stelle ich einen Sedimentbohrkern aus dem Koora-Becken des S{\"u}dlichen Kenia-Rifts vor, der einen Datensatz der Pal{\"a}o-Umweltbedingungen der letzten 1 Million Jahre beinhaltet. Dieser Datensatz zeigt, dass etwa vor 400 tausend Jahren die zuvor relativ stabilen Umweltbedingungen zum Erliegen kamen und tektonische, hydrologische und {\"o}kologische Ver{\"a}nderungen dazu f{\"u}hrten, dass die Wasserverf{\"u}gbarkeit, die Grasland-Vergesellschaftungen und die Bedeckung durch Baumvegetation zunehmend st{\"a}rkeren und h{\"a}ufigeren Schwankungen unterlagen. Diese großen Ver{\"a}nderungen fallen zeitlich mit Phasen zusammen, in denen das s{\"u}dliche Becken des Kenia-Rifts von vulkanischer und tektonischer Aktivit{\"a}t besonders betroffen war. Die vorliegende Arbeit zeigt deshalb deutlich, inwiefern die tektonischen und geomorphologischen Gegebenheiten im Zuge einer zeitlich langanhaltenden Extension die Hydrologie, die Pal{\"a}o-Umweltbedingungen sowie die Biodiversit{\"a}t einer Riftzone beeinflussen k{\"o}nnen.},
  language  = {en}
}
@phdthesis{Lin2021,
  author    = {Lin, Chiao-I},
  title     = {The survey of the prevalence of chronic ankle instability in elite Taiwanese basketball athletes},
  doi       = {10.25932/publishup-53553},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-535534},
  school      = {Universit{\"a}t Potsdam},
  pages     = {xi, 128},
  year      = {2021},
  abstract  = {BACKGROUND: Ankle sprains are common in basketball. It could develop into Chronic Ankle Instability (CAI) causing decreased quality of life, functional performance, early osteoarthritis, and increased risk of other injuries. To develop a strategy of CAI prevention, localized epidemiology data and a valid/reliable tool are essential. However, the epidemiological data of CAI is not conclusive from previous studies and the prevalence of CAI in Taiwanese basketball athletes are not clear. In addition, a valid and reliable tool among the Taiwan-Chinese version to evaluate ankle instability is missing. PURPOSE: The aims were to have an overview of the prevalence of CAI in sports population using a systematic review, to develop a valid and reliable cross-cultural adapted Cumberland Ankle Instability Tool Questionnaire (CAIT) in Taiwan-Chinese (CAIT-TW), and to survey the prevalence of CAI in elite basketball athletes in Taiwan using CAIT-TW. METHODS: Firstly, a systematic search was conducted. Research articles applying CAI related questionnaires in order to survey the prevalence of CAI were included in the review. Second, the English version of CAIT was translated and cross-culturally adapted into the CAIT-TW. The construct validity, test-retest reliability, internal consistency, and cutoff score of CAIT-TW were evaluated in an athletic population (N=135). Finally, the cross-sectional data of CAI prevalence in 388 elite Taiwanese basketball athletes were presented. Demographics, presence of CAI, and difference of prevalence between gender, different competitive levels and play positions were evaluated. RESULTS: The prevalence of CAI was 25\%, ranging between 7\% and 53\%. The prevalence of CAI among participants with a history of ankle sprains was 46\%, ranging between 9\% and 76\%. In addition, the cross-cultural adapted CAIT-TW showed a moderate to strong construct validity, an excellent test-retest reliability, a good internal consistency, and a cutoff score of 21.5 for the Taiwanese athletic population. Finally, 26\% of Taiwanese basketball athletes had unilateral CAI while 50\% of them had bilateral CAI. In addition, women athletes in the investigated cohort had a higher prevalence of CAI than men. There was no difference in prevalence between competitive levels and among play positions. CONCLUSION: The systematic review shows that the prevalence of CAI has a wide range among included studies. This could be due to the different exclusion criteria, age, sports discipline, or other factors among the included studies. For future studies, standardized criteria to investigate the epidemiology of CAI are required. The CAI epidemiological study should be prospective. Factors affecting the prevalence of CAI ability should be investigated and described. The translated CAIT-TW is a valid and reliable tool to differentiate between stable and unstable ankles in athletes and may further apply for research or daily practice in Taiwan. In the Taiwanese basketball population, CAI is highly prevalent. This might relate to the research method, preexisting ankle instability, and training-related issues. Women showed a higher prevalence of CAI than men. When applying the preventive measure, gender should be taken into consideration.},
  language  = {en}
}
@phdthesis{Sand2021,
  author    = {Sand, Patrick},
  title     = {{\"U}bergangsmetallkatalysierte Funktionalisierungsreaktionen an Vinylsulfonylverbindungen},
  doi       = {10.25932/publishup-53687},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-536879},
  school      = {Universit{\"a}t Potsdam},
  pages     = {ix, 169},
  year      = {2021},
  abstract  = {Innerhalb dieser Arbeit erfolgte die erstmalige systematische Untersuchung von Vinylsulfons{\"a}ureethylester (1a), Phenylvinylsulfon (1b), N-Benzyl-N-methylethensulfonamid (1c) in der FUJIWARA-MORITANI Reaktion (alternativ als DHR bezeichnet). Bei dieser {\"u}bergangsmetallkatalysierten Reaktion erfolgt der Aufbau einer neuen C-C-Bindung unter der doppelten Aktivierung einer C-H-Bindung. Somit kann ein atom{\"o}konomischer Aufbau von Molek{\"u}len realisiert werden, da keine Beiprodukte in Form von Salzen entstehen. Als aromatischer Reaktant wurden Acetanilide (2) verwendet, damit eine regiospezifische Kupplung durch die katalysatordirigierende Acetamid-Gruppe (CDG) erfolgt. F{\"u}r die Pd-katalysierte DHR wurde eine umfangreiche Optimierung durchgef{\"u}hrt und anschließend konnten neun verschieden, substituierte 2 mit 1a und sieben verschieden, substituierte 2 mit 1b funktionalisiert werden. Da eine Reaktion mit 1c ausblieb, erfolgte ein Wechsel auf eine Ru-katalysierte Methode f{\"u}r die DHR. Mit dieser Methode konnte 1c mit Acetaniliden funktionalisiert werden und das Spektrum der verwendeten 2, in Form von deaktivierenden Substituenten erweitert werden. Im Anschluss wurden die sulfalkenylierten Acetanilide in weiterf{\"u}hrenden Reaktionen untersucht. Hierf{\"u}r wurde eine Reaktionssequenz bestehend aus einer DeacetylierungDiazotierung-Kupplungsreaktion verwendet, um die Acetamid-Gruppe in eine Abgangsgruppe zu {\"u}berf{\"u}hren und danach in einer MATSUDA-HECK Reaktion zu kuppeln. Mit dieser Methode konnten mehrere 1,2-Dialkenylbenzole erhalten werden und die CDG ein weiteres Mal genutzt werden. Neben der {\"U}berf{\"u}hrung der CDG in eine Abgangsgruppe konnte diese auch in die Synthese verschiedener Heterozyklen integriert werden. Daf{\"u}r erfolgte zun{\"a}chst eine 1,3-Zykloaddition durch deprotonierten Tosylmethylisocanid an der elektronenarmen Sulfalkenylgruppe zur Synthese von Pyrrolen. Anschließend erfolgte eine Kupplung der PyrrolFunktion und der CDG durch Zyklokondensation, wodurch Quinoline dargestellt wurden. Durch diese Synthesen konnten Schwefelanaloga des Naturstoffes Marinoquionolin A erhalten werden. Ein weitere {\"u}bergangsmetallkatalysierte C-H-Aktivierungsreaktion, die MATSUDA-HECK Reaktion, wurde genutzt, um 1b zu mit verschieden, subtituierten Diazoniumsalzen zu arylieren. Hier konnten zahlreichen Styrenylsulfone erhalten werden. Der erfolgreiche Einsatz der Vinylsulfonylverbindungen in der Kreuzmetathese konnte innerhalb dieser Arbeit nicht erreicht werden. Daher erfolgte die Synthese verschiedener dialkenylierter Sulfonamide. Hierf{\"u}r wurde die Kettenl{\"a}nge der Alkenyl-Gruppe am Schwefel zwischen 2-3 und am Stickstoff zwischen 3-4 variiert. Der Einsatz der dialkenylierten Sulfonamide erfolgte in den zuvor untersuchten C-H-Aktivierungsmethoden. N-Allyl-N-phenylethensulfonamid (3) konnte erfolgreich in der DHR und HECK Reaktion funktionalisiert werden. Hierbei erfolgte eine methodenspezifische Kupplung in Abh{\"a}ngigkeit von der Elektronendichte der entsprechenden Alkenyl-Gruppe. Die DHR f{\"u}hrte zur selektiven Arylierung der Vinyl-Gruppe und die HECK Reaktion zur Arylierung an der Allyl-Gruppe. Gemischte Produkte wurden nicht erhalten. F{\"u}r die weiteren Diolefine wurde komplexe Produktgemische erhalten. Des Weiteren wurden die Diolefine in der Ringschlussmetathese untersucht und die entsprechenden Sultame in sehr guten Ausbeuten erhalten. Die Verwendung der Sultame in der C-H-Aktivierung war erfolglos. Es wird vermutet, dass f{\"u}r diese zweifachsubstituierten Sulfonamide die vorhandenen Reaktionsbedingungen optimiert werden m{\"u}ssen. Abschließend wurden verschiedene, enantiomerenreine Olefine ausgehend von Levoglucosenon dargestellt. Hierf{\"u}r wurde Levoglucosenon zun{\"a}chst mit einem Allyl- und 3-Butenylgrignard Reagenz umgesetzt. Die entsprechenden Produkte wurden in moderaten Ausbeuten erhalten. Eine weitere Methode begann mit der Reduktion von Levoglucosenon zum Levoglucosenol. Dieser Alkohol wurde mit Allylbromid erfolgreich verethert. Neben der Untersuchungen zur Ethersynthese, erfolgte die Veresterung von Levoglucosenol mit verschiedenen Sulfonylchloriden zu den entsprechenden Sulfons{\"a}ureestern. Diese Olefine wurden in einer Dominometathesereaktion untersucht. Ausgehend vom Allyllevoglucosenylether erfolgte die Darstellung eines Dihydrofurans.},
  language  = {de}
}
@phdthesis{Kossmann2021,
  author    = {Kossmann, Janina},
  title     = {Controlled condensation to functional materials - synergetic effect of nitrogen content and pore structure},
  doi       = {10.25932/publishup-53693},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-536935},
  school      = {Universit{\"a}t Potsdam},
  pages     = {vi, 148},
  year      = {2021},
  abstract  = {The development and optimization of carbonaceous materials is of great interest for several applications including gas sorption, electrochemical storage and conversion, or heterogeneous catalysis. In this thesis, the exploration and optimization of nitrogen containing carbonaceous materials by direct condensation of smart chosen, molecular precursors will be presented. As suggested with the concept of noble carbons, the choice of a stable, nitrogen-containing precursor will lead to an even more stable, nitrogen doped carbonaceous material with a controlled structure and electronic properties. Molecules fulfilling this requirement are for example nucleobases. The direct condensation of nucleobases leads to highly nitrogen containing carbonaceous materials without any further post or pretreatment. By using salt melt templating, pore structure adjustment is possible without the use of hazardous or toxic reagents and the template can be reused. Using these simple tools, the synergetic effect of the pore structure and nitrogen content of the materials can be explored. Within this thesis, the influence of the condensation parameters will be correlated to the structure and performance of the materials. First, the influence of the condensation temperature to the porosity and nitrogen content of guanine will be discussed and the exploration of highly CO2 selective structural pores in C1N1 materials will be shown. Further tuning the pore structure of the materials by salt melt templating will be then explored, the potential of the prepared materials as heterogeneous catalysts and their basic catalytic strength will be correlated to their nitrogen content and pore morphology. A similar approach is used to explore the water sorption behavior of uric acid derived carbonaceous materials as potential sorbents for heat transformation applications. Changes in maximum water uptake and hydrophilicity of the prepared materials will be correlated to the nitrogen content and pore architecture. Due to the high thermal stability, porosity, and nitrogen content of ionic liquid derived nitrogen doped carbonaceous materials, a simple impregnation and calcination route can be conducted to obtain copper nano cluster decorated nitrogen-doped carbonaceous materials. The activity as catalyst for the oxygen reduction reaction of the obtained materials will be shown and structure performance relations are discussed. In conclusion, the versatility of nitrogen doped carbonaceous materials with a nitrogen to carbon ratio of up to one will be shown. The possibility to tune the pore structure as well as the nitrogen content by using a simple procedure including salt melt templating as well as the use of molecular precursors and their effect on the performance will be discussed.},
  language  = {en}
}