TY - GEN A1 - Ye, Fangyuan A1 - Zhang, Shuo A1 - Warby, Jonathan A1 - Wu, Jiawei A1 - Gutierrez-Partida, Emilio A1 - Lang, Felix A1 - Shah, Sahil A1 - Saglamkaya, Elifnaz A1 - Sun, Bowen A1 - Zu, Fengshuo A1 - Shoaee, Safa A1 - Wang, Haifeng A1 - Stiller, Burkhard A1 - Neher, Dieter A1 - Zhu, Wei-Hong A1 - Stolterfoht, Martin A1 - Wu, Yongzhen T1 - Overcoming C₆₀-induced interfacial recombination in inverted perovskite solar cells by electron-transporting carborane T2 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe N2 - Inverted perovskite solar cells still suffer from significant non-radiative recombination losses at the perovskite surface and across the perovskite/C₆₀ interface, limiting the future development of perovskite-based single- and multi-junction photovoltaics. Therefore, more effective inter- or transport layers are urgently required. To tackle these recombination losses, we introduce ortho-carborane as an interlayer material that has a spherical molecular structure and a three-dimensional aromaticity. Based on a variety of experimental techniques, we show that ortho-carborane decorated with phenylamino groups effectively passivates the perovskite surface and essentially eliminates the non-radiative recombination loss across the perovskite/C₆₀ interface with high thermal stability. We further demonstrate the potential of carborane as an electron transport material, facilitating electron extraction while blocking holes from the interface. The resulting inverted perovskite solar cells deliver a power conversion efficiency of over 23% with a low non-radiative voltage loss of 110 mV, and retain >97% of the initial efficiency after 400 h of maximum power point tracking. Overall, the designed carborane based interlayer simultaneously enables passivation, electron-transport and hole-blocking and paves the way toward more efficient and stable perovskite solar cells. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1317 Y1 - 2022 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-587705 SN - 1866-8372 IS - 1317 ER - TY - JOUR A1 - Ye, Fangyuan A1 - Zhang, Shuo A1 - Warby, Jonathan A1 - Wu, Jiawei A1 - Gutierrez-Partida, Emilio A1 - Lang, Felix A1 - Shah, Sahil A1 - Saglamkaya, Elifnaz A1 - Sun, Bowen A1 - Zu, Fengshuo A1 - Shoai, Safa A1 - Wang, Haifeng A1 - Stiller, Burkhard A1 - Neher, Dieter A1 - Zhu, Wei-Hong A1 - Stolterfoht, Martin A1 - Wu, Yongzhen T1 - Overcoming C₆₀-induced interfacial recombination in inverted perovskite solar cells by electron-transporting carborane JF - Nature Communications N2 - Inverted perovskite solar cells still suffer from significant non-radiative recombination losses at the perovskite surface and across the perovskite/C₆₀ interface, limiting the future development of perovskite-based single- and multi-junction photovoltaics. Therefore, more effective inter- or transport layers are urgently required. To tackle these recombination losses, we introduce ortho-carborane as an interlayer material that has a spherical molecular structure and a three-dimensional aromaticity. Based on a variety of experimental techniques, we show that ortho-carborane decorated with phenylamino groups effectively passivates the perovskite surface and essentially eliminates the non-radiative recombination loss across the perovskite/C₆₀ interface with high thermal stability. We further demonstrate the potential of carborane as an electron transport material, facilitating electron extraction while blocking holes from the interface. The resulting inverted perovskite solar cells deliver a power conversion efficiency of over 23% with a low non-radiative voltage loss of 110 mV, and retain >97% of the initial efficiency after 400 h of maximum power point tracking. Overall, the designed carborane based interlayer simultaneously enables passivation, electron-transport and hole-blocking and paves the way toward more efficient and stable perovskite solar cells. Y1 - 2022 U6 - https://doi.org/10.1038/s41467-022-34203-x SN - 2041-1723 VL - 13 IS - 1 PB - Springer Nature CY - London ER - TY - JOUR A1 - López de Guereñu Kurganova, Anna A1 - Klier, Dennis Tobias A1 - Haubitz, Toni A1 - Kumke, Michael Uwe T1 - Influence of Gd3+ doping concentration on the properties of Na(Y,Gd)F-4 BT - Yb3+, Tm3+ upconverting nanoparticles and their long-term aging behavior JF - Photochemical & photobiological sciences / European Society for Photobiology N2 - We present a systematic study on the properties of Na(Y,Gd)F-4-based upconverting nanoparticles (UCNP) doped with 18% Yb3+, 2% Tm3+, and the influence of Gd3+ (10-50 mol% Gd3+). UCNP were synthesized via the solvothermal method and had a range of diameters within 13 and 50 nm. Structural and photophysical changes were monitored for the UCNP samples after a 24-month incubation period in dry phase and further redispersion. Structural characterization was performed by means of X-ray diffraction (XRD), transmission electron microscopy (TEM) as well as dynamic light scattering (DLS), and the upconversion luminescence (UCL) studies were executed at various temperatures (from 4 to 295 K) using time-resolved and steady-state spectroscopy. An increase in the hexagonal lattice phase with the increase of Gd3+ content was found, although the cubic phase was prevalent in most samples. The Tm3+-luminescence intensity as well as the Tm3+-luminescence decay times peaked at the Gd3+ concentration of 30 mol%. Although the general upconverting luminescence properties of the nanoparticles were preserved, the 24-month incubation period lead to irreversible agglomeration of the UCNP and changes in luminescence band ratios and lifetimes. KW - Upconversion luminescence KW - Lanthanides KW - Near infra-red KW - Ultra-low KW - temperature KW - Time-resolved spectroscopy Y1 - 2022 U6 - https://doi.org/10.1007/s43630-021-00161-4 SN - 1474-905X SN - 1474-9092 VL - 21 IS - 2 SP - 235 EP - 245 PB - Springer CY - Heidelberg ER - TY - GEN A1 - Seckler, Henrik A1 - Metzler, Ralf T1 - Bayesian deep learning for error estimation in the analysis of anomalous diffusion T2 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe N2 - Sprache Englisch Modern single-particle-tracking techniques produce extensive time-series of diffusive motion in a wide variety of systems, from single-molecule motion in living-cells to movement ecology. The quest is to decipher the physical mechanisms encoded in the data and thus to better understand the probed systems. We here augment recently proposed machine-learning techniques for decoding anomalous-diffusion data to include an uncertainty estimate in addition to the predicted output. To avoid the Black-Box-Problem a Bayesian-Deep-Learning technique named Stochastic-Weight-Averaging-Gaussian is used to train models for both the classification of the diffusionmodel and the regression of the anomalous diffusion exponent of single-particle-trajectories. Evaluating their performance, we find that these models can achieve a wellcalibrated error estimate while maintaining high prediction accuracies. In the analysis of the output uncertainty predictions we relate these to properties of the underlying diffusion models, thus providing insights into the learning process of the machine and the relevance of the output. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1314 KW - random-walk KW - models Y1 - 2022 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-586025 SN - 1866-8372 IS - 1314 ER - TY - JOUR A1 - Seckler, Henrik A1 - Metzler, Ralf T1 - Bayesian deep learning for error estimation in the analysis of anomalous diffusion JF - Nature Communnications N2 - Modern single-particle-tracking techniques produce extensive time-series of diffusive motion in a wide variety of systems, from single-molecule motion in living-cells to movement ecology. The quest is to decipher the physical mechanisms encoded in the data and thus to better understand the probed systems. We here augment recently proposed machine-learning techniques for decoding anomalous-diffusion data to include an uncertainty estimate in addition to the predicted output. To avoid the Black-Box-Problem a Bayesian-Deep-Learning technique named Stochastic-Weight-Averaging-Gaussian is used to train models for both the classification of the diffusionmodel and the regression of the anomalous diffusion exponent of single-particle-trajectories. Evaluating their performance, we find that these models can achieve a wellcalibrated error estimate while maintaining high prediction accuracies. In the analysis of the output uncertainty predictions we relate these to properties of the underlying diffusion models, thus providing insights into the learning process of the machine and the relevance of the output. KW - random-walk KW - models Y1 - 2022 U6 - https://doi.org/10.1038/s41467-022-34305-6 SN - 2041-1723 VL - 13 PB - Nature Publishing Group UK CY - London ER - TY - JOUR A1 - Fritsch, Daniel T1 - Revisiting the Cu-Zn disorder in kesterite type Cu2ZnSnSe4 employing a novel approach to hybrid functional calculations JF - Applied Sciences : open access journal N2 - In recent years, the search for more efficient and environmentally friendly materials to be employed in the next generation of thin film solar cell devices has seen a shift towards hybrid halide perovskites and chalcogenide materials crystallising in the kesterite crystal structure. Prime examples for the latter are Cu2ZnSnS4, Cu2ZnSnSe4, and their solid solution Cu2ZnSn(SxSe1-x)(4), where actual devices already demonstrated power conversion efficiencies of about 13 %. However, in their naturally occurring kesterite crystal structure, the so-called Cu-Zn disorder plays an important role and impacts the structural, electronic, and optical properties. To understand the influence of Cu-Zn disorder, we perform first-principles calculations based on density functional theory combined with special quasirandom structures to accurately model the cation disorder. Since the electronic band gaps and derived optical properties are severely underestimated by (semi)local exchange and correlation functionals, supplementary hybrid functional calculations have been performed. Concerning the latter, we additionally employ a recently devised technique to speed up structural relaxations for hybrid functional calculations. Our calculations show that the Cu-Zn disorder leads to a slight increase in the unit cell volume compared to the conventional kesterite structure showing full cation order, and that the band gap gets reduced by about 0.2 eV, which is in very good agreement with earlier experimental and theoretical findings. Our detailed results on structural, electronic, and optical properties will be discussed with respect to available experimental data, and will provide further insights into the atomistic origin of the disorder-induced band gap lowering in these promising kesterite type materials. KW - Cu2ZnSnSe4 KW - CZTSe KW - chalcogenide KW - kesterite KW - Cu-Zn disorder KW - density KW - functional theory KW - hybrid functional KW - special quasirandom structure Y1 - 2022 U6 - https://doi.org/10.3390/app12052576 SN - 2076-3417 VL - 12 IS - 5 PB - MDPI CY - Basel ER - TY - GEN A1 - Sposini, Vittoria A1 - Krapf, Diego A1 - Marinari, Enzo A1 - Sunyer, Raimon A1 - Ritort, Felix A1 - Taheri, Fereydoon A1 - Selhuber-Unkel, Christine A1 - Benelli, Rebecca A1 - Weiss, Matthias A1 - Metzler, Ralf A1 - Oshanin, Gleb T1 - Towards a robust criterion of anomalous diffusion T2 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe N2 - Anomalous-diffusion, the departure of the spreading dynamics of diffusing particles from the traditional law of Brownian-motion, is a signature feature of a large number of complex soft-matter and biological systems. Anomalous-diffusion emerges due to a variety of physical mechanisms, e.g., trapping interactions or the viscoelasticity of the environment. However, sometimes systems dynamics are erroneously claimed to be anomalous, despite the fact that the true motion is Brownian—or vice versa. This ambiguity in establishing whether the dynamics as normal or anomalous can have far-reaching consequences, e.g., in predictions for reaction- or relaxation-laws. Demonstrating that a system exhibits normal- or anomalous-diffusion is highly desirable for a vast host of applications. Here, we present a criterion for anomalous-diffusion based on the method of power-spectral analysis of single trajectories. The robustness of this criterion is studied for trajectories of fractional-Brownian-motion, a ubiquitous stochastic process for the description of anomalous-diffusion, in the presence of two types of measurement errors. In particular, we find that our criterion is very robust for subdiffusion. Various tests on surrogate data in absence or presence of additional positional noise demonstrate the efficacy of this method in practical contexts. Finally, we provide a proof-of-concept based on diverse experiments exhibiting both normal and anomalous-diffusion. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1313 Y1 - 2023 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-585967 SN - 1866-8372 IS - 1313 ER - TY - JOUR A1 - Sposini, Vittoria A1 - Krapf, Diego A1 - Marinari, Enzo A1 - Sunyer, Raimon A1 - Ritort, Felix A1 - Taheri, Fereydoon A1 - Selhuber-Unkel, Christine A1 - Benelli, Rebecca A1 - Weiss, Matthias A1 - Metzler, Ralf A1 - Oshanin, Gleb T1 - Towards a robust criterion of anomalous diffusion JF - Communications Physics N2 - Anomalous-diffusion, the departure of the spreading dynamics of diffusing particles from the traditional law of Brownian-motion, is a signature feature of a large number of complex soft-matter and biological systems. Anomalous-diffusion emerges due to a variety of physical mechanisms, e.g., trapping interactions or the viscoelasticity of the environment. However, sometimes systems dynamics are erroneously claimed to be anomalous, despite the fact that the true motion is Brownian—or vice versa. This ambiguity in establishing whether the dynamics as normal or anomalous can have far-reaching consequences, e.g., in predictions for reaction- or relaxation-laws. Demonstrating that a system exhibits normal- or anomalous-diffusion is highly desirable for a vast host of applications. Here, we present a criterion for anomalous-diffusion based on the method of power-spectral analysis of single trajectories. The robustness of this criterion is studied for trajectories of fractional-Brownian-motion, a ubiquitous stochastic process for the description of anomalous-diffusion, in the presence of two types of measurement errors. In particular, we find that our criterion is very robust for subdiffusion. Various tests on surrogate data in absence or presence of additional positional noise demonstrate the efficacy of this method in practical contexts. Finally, we provide a proof-of-concept based on diverse experiments exhibiting both normal and anomalous-diffusion. Y1 - 2022 U6 - https://doi.org/10.1038/s42005-022-01079-8 SN - 2399-3650 VL - 5 PB - Springer Nature CY - London ER - TY - GEN A1 - Mayer, Dennis A1 - Lever, Fabiano A1 - Picconi, David A1 - Metje, Jan A1 - Ališauskas, Skirmantas A1 - Calegari, Francesca A1 - Düsterer, Stefan A1 - Ehlert, Christopher A1 - Feifel, Raimund A1 - Niebuhr, Mario A1 - Manschwetus, Bastian A1 - Kuhlmann, Marion A1 - Mazza, Tommaso A1 - Robinson, Matthew Scott A1 - Squibb, Richard James A1 - Trabattoni, Andrea A1 - Wallner, Måns A1 - Saalfrank, Peter A1 - Wolf, Thomas J. A. A1 - Gühr, Markus T1 - Following excited-state chemical shifts in molecular ultrafast x-ray photoelectron spectroscopy T2 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe N2 - The conversion of photon energy into other energetic forms in molecules is accompanied by charge moving on ultrafast timescales. We directly observe the charge motion at a specific site in an electronically excited molecule using time-resolved x-ray photoelectron spectroscopy (TR-XPS). We extend the concept of static chemical shift from conventional XPS by the excited-state chemical shift (ESCS), which is connected to the charge in the framework of a potential model. This allows us to invert TR-XPS spectra to the dynamic charge at a specific atom. We demonstrate the power of TR-XPS by using sulphur 2p-core-electron-emission probing to study the UV-excited dynamics of 2-thiouracil. The method allows us to discover that a major part of the population relaxes to the molecular ground state within 220–250 fs. In addition, a 250-fs oscillation, visible in the kinetic energy of the TR-XPS, reveals a coherent exchange of population among electronic states. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1301 Y1 - 2022 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-577442 SN - 1866-8372 IS - 1301 ER - TY - JOUR A1 - Mayer, Dennis A1 - Lever, Fabiano A1 - Picconi, David A1 - Metje, Jan A1 - Ališauskas, Skirmantas A1 - Calegari, Francesca A1 - Düsterer, Stefan A1 - Ehlert, Christopher A1 - Feifel, Raimund A1 - Niebuhr, Mario A1 - Manschwetus, Bastian A1 - Kuhlmann, Marion A1 - Mazza, Tommaso A1 - Robinson, Matthew Scott A1 - Squibb, Richard James A1 - Trabattoni, Andrea A1 - Wallner, Måns A1 - Saalfrank, Peter A1 - Wolf, Thomas J. A. A1 - Gühr, Markus T1 - Following excited-state chemical shifts in molecular ultrafast x-ray photoelectron spectroscopy JF - Nature Communications N2 - The conversion of photon energy into other energetic forms in molecules is accompanied by charge moving on ultrafast timescales. We directly observe the charge motion at a specific site in an electronically excited molecule using time-resolved x-ray photoelectron spectroscopy (TR-XPS). We extend the concept of static chemical shift from conventional XPS by the excited-state chemical shift (ESCS), which is connected to the charge in the framework of a potential model. This allows us to invert TR-XPS spectra to the dynamic charge at a specific atom. We demonstrate the power of TR-XPS by using sulphur 2p-core-electron-emission probing to study the UV-excited dynamics of 2-thiouracil. The method allows us to discover that a major part of the population relaxes to the molecular ground state within 220–250 fs. In addition, a 250-fs oscillation, visible in the kinetic energy of the TR-XPS, reveals a coherent exchange of population among electronic states. Y1 - 2022 U6 - https://doi.org/10.1038/s41467-021-27908-y SN - 2041-1723 VL - 13 PB - Springer Nature CY - Berlin ER - TY - THES A1 - Piankova, Diana T1 - Electron pair distribution function (ePDF) analysis and advanced transmission electron microscopy (TEM) techniques BT - a perfect tandem to study the evolution of short-range order in materials Y1 - 2022 ER - TY - THES A1 - Stoll, Andreas T1 - Advanced spectroscopic instruments enabled by integrated optics N2 - The aim of this work is the study of silica Arrayed Waveguide Gratings (AWGs) in the context of applications in astronomy. The specific focus lies on the investigation of the feasibility and technology limits of customized silica AWG devices for high resolution near-infrared spectroscopy. In a series of theoretical and experimental studies, AWG devices of varying geometry, foot-print and spectral resolution are constructed, simulated using a combination of a numerical beam propagation method and Fraunhofer diffraction and fabricated devices are characterized with respect to transmission efficiency, spectral resolution and polarization sensitivity. The impact of effective index non-uniformities on the performance of high-resolution AWG devices is studied numerically. Characterization results of fabricated devices are used to extrapolate the technology limits of the silica platform. The important issues of waveguide birefringence and defocus aberration are discussed theoretically and addressed experimentally by selection of an appropriate aberration-minimizing anastigmatic AWG layout structure. The drawbacks of the anastigmatic AWG geometry are discussed theoretically. From the results of the experimental studies, it is concluded that fabrication-related phase errors and waveguide birefringence are the primary limiting factors for the growth of AWG spectral resolution. It is shown that, without post-processing, the spectral resolving power is phase-error-limited to R < 40, 000 and, in the case of unpolarized light, birefringence-limited to R < 30, 000 in the AWG devices presented in this work. Necessary measures, such as special waveguide geometries and post-fabrication phase error correction are proposed for future designs. The elimination of defocus aberration using an anastigmatic AWG geometry is successfully demonstrated in experiment. Finally, a novel, non-planar dispersive in-fibre waveguide structure is proposed, discussed and studied theoretically. N2 - Das Ziel der vorliegenden Arbeit ist die Untersuchung von Arrayed Waveguide Gratings (AWGs) auf SiO2-Basis im Kontext von Anwendungen in der Astronomie. Der besondere Fokus liegt auf der Untersuchung der Machbarkeit und der technologischen Grenzen von spezialisierten AWGs für die hochauflösende Nahinfrarot-Spektroskopie. In einer Reihe von theoretischen und experimentellen Studien werden AWGs unterschiedlicher Geometrie, Größe und spektraler Auflösung konstruiert, unter Verwendung einer numerischen Beam-Propagation-Methode (BPM) und Fraunhofer-Beugung simuliert und hinsichtlich Effizienz, spektraler Auflösung und Polarisationsempfindlichkeit charakterisiert. Der Einfluss von Variationen des effektiven Brechungsindex auf die Leistung von hochauflösenden AWGs wird numerisch untersucht. Mit hergestellten AWGs gewonnene Messergebnisse werden verwendet, um die technologischen Grenzen der SiO2-Plattform zu extrapolieren. Die relevanten Probleme der Polarisationsempfindlichkeit und der in kanonischen Rowland-Geometrien auftretenden Defokusaberration werden theoretisch diskutiert und experimentell durch die Auswahl einer geeigneten aberrationsminimierenden AWG-Struktur angegangen. Die Nachteile anastigmatischer AWGs werden theoretisch diskutiert. Aus den Ergebnissen der experimentellen Studien wird geschlossen, dass herstellungsbedingte Phasenfehler und Wellenleiter-Doppelbrechung die primären begrenzenden Faktoren für die Erhöhung der AWG-Spektralauflösung sind. Es wird gezeigt, dass das spektrale Auflösungsvermögen der in dieser Arbeit präsentierten AWGs ohne Phasenfehlerkorrektur auf R < 40, 000 und durch Doppelbrechung auf R < 30, 000 im Fall unpolarisierten Lichtes begrenzt ist. Notwendige Maßnahmen wie spezielle Wellenleitergeometrien und Phasenfehlerkorrektur nach der Herstellung werden für zukünftige AWG-Designs empfohlen. Die Eliminierung von Defokussierungsfehlern unter Verwendung einer anastigmatischen AWG-Geometrie wird erfolgreich im Experiment demonstriert. Schließlich wird eine neuartige, in eine optische Faser eingebettete, nicht-planare dispersive Wellenleiterstruktur vorgeschlagen, diskutiert und theoretisch untersucht. KW - Astrophotonics KW - Integrated spectrograph KW - planar lightwave circuit KW - arrayed waveguide grating KW - silica-on-silicon KW - Astrophotonik KW - integrierter Spektrograph KW - planare Lichtwellenleiter KW - Siliziumdioxid-auf-Silizium Y1 - 2022 ER - TY - THES A1 - Mayer, Dennis T1 - Time-resolved x-ray spectroscopy of 2-thiouracil T1 - Zeitaufgelöste Röntgenspektroskopie an 2-Thiouracil N2 - In this thesis, I present my contributions to the field of ultrafast molecular spectroscopy. Using the molecule 2-thiouracil as an example, I use ultrashort x-ray pulses from free- electron lasers to study the relaxation dynamics of gas-phase molecular samples. Taking advantage of the x-ray typical element- and site-selectivity, I investigate the charge flow and geometrical changes in the excited states of 2-thiouracil. In order to understand the photoinduced dynamics of molecules, knowledge about the ground-state structure and the relaxation after photoexcitation is crucial. Therefore, a part of this thesis covers the electronic ground-state spectroscopy of mainly 2-thiouracil to provide the basis for the time-resolved experiments. Many of the previously published studies that focused on the gas-phase time-resolved dynamics of thionated uracils after UV excitation relied on information from solution phase spectroscopy to determine the excitation energies. This is not an optimal strategy as solvents alter the absorption spec- trum and, hence, there is no guarantee that liquid-phase spectra resemble the gas-phase spectra. Therefore, I measured the UV-absorption spectra of all three thionated uracils to provide a gas-phase reference and, in combination with calculations, we determined the excited states involved in the transitions. In contrast to the UV absorption, the literature on the x-ray spectroscopy of thionated uracil is sparse. Thus, we measured static photoelectron, Auger-Meitner and x-ray absorption spectra on the sulfur L edge before or parallel to the time-resolved experiments we performed at FLASH (DESY, Hamburg). In addition, (so far unpublished) measurements were performed at the synchrotron SOLEIL (France) which have been included in this thesis and show the spin-orbit splitting of the S 2p photoline and its satellite which was not observed at the free-electron laser. The relaxation of 2-thiouracil has been studied extensively in recent years with ultrafast visible and ultraviolet methods showing the ultrafast nature of the molecular process after photoexcitation. Ultrafast spectroscopy probing the core-level electrons provides a complementary approach to common optical ultrafast techniques. The method inherits its local sensitivity from the strongly localised core electrons. The core energies and core-valence transitions are strongly affected by local valence charge and geometry changes, and past studies have utilised this sensitivity to investigate the molecular process reflected by the ultrafast dynamics. We have built an apparatus that provides the requirements to perform time-resolved x-ray spectroscopy on molecules in the gas phase. With the apparatus, we performed UV-pump x-ray-probe electron spectroscopy on the S 2p edge of 2-thiouracil using the free-electron laser FLASH2. While the UV triggers the relaxation dynamics, the x-ray probes the single sulfur atom inside the molecule. I implemented photoline self-referencing for the photoelectron spectral analysis. This minimises the spectral jitter of the FEL, which is due to the underlying self-amplified spontaneous emission (SASE) process. With this approach, we were not only able to study dynamical changes in the binding energy of the electrons but also to detect an oscillatory behaviour in the shift of the observed photoline, which we associate with non-adiabatic dynamics involving several electronic states. Moreover, we were able to link the UV-induced shift in binding energy to the local charge flow at the sulfur which is directly connected to the electronic state. Furthermore, the analysis of the Auger-Meitner electrons shows that energy shifts observed at early stages of the photoinduced relaxation are related to the geometry change in the molecule. More specifically, the observed increase in kinetic energy of the Auger-Meitner electrons correlates with a previously predicted C=S bond stretch. N2 - In dieser Arbeit präsentiere ich meine Beiträge zum Gebiet der ultraschnellen Molekülspektroskopie. Am Beispiel des Moleküls 2-Thiouracil verwende ich ultrakurze Röntgenpulse von Freie-Elektronen-Lasern, um die Relaxationsdynamik von Molekülproben in der Gasphase zu untersuchen. Unter Ausnutzung der für Röntgenstrahlung typischen Element- und Ortsselektivität untersuche ich den Ladungsfluss und die geometrischen Veränderungen in den angeregten Zuständen von 2-Thiouracil. Um die photoinduzierte Dynamik von Molekülen zu verstehen, ist das Wissen über die Grundzustandsstruktur und die Relaxation nach Photoanregung entscheidend. Daher befasst sich ein Teil dieser Arbeit mit der elektronischen Grundzustandsspektroskopie von 2-Thiouracil, um die Grundlage für die zeitaufgelösten Experimente zu schaffen. Viele der bisher veröffentlichten Studien, die sich mit der zeitaufgelösten Dynamik von Thiouracilen in der Gasphase nach UV-Anregung befassten, stützten sich zur Bestimmung der Anregungsenergien auf Informationen aus der Spektroskopie in Lösung. Dies ist nicht optimal, da Lösungsmittel das Absorptionsspektrum verändern und es daher keine Garantie dafür gibt, dass die Spektren in Lösung den Spektren der Gasphase ähneln. Daher habe ich die UV-Absorptionsspektren aller drei Thiouracile gemessen, um eine Referenz für die Gasphase zu erhalten, und in Kombination mit Berechnungen die an den Übergängen beteiligten angeregten Zustände bestimmt. Im Gegensatz zur UV-Absorption ist die Literatur zur Röntgenspektroskopie von thioniertem Uracil spärlich. Daher haben wir statische Photoelektronen-, Auger-Meitner- und Röntgenabsorptionsspektren an der Schwefel-L-Kante vor oder parallel zu den zeitaufgelösten Experimenten an FLASH (DESY, Hamburg) gemessen. Darüber hinaus wurden (bisher unveröffentlichte) Messungen am Synchrotron SOLEIL (Frankreich) durchgeführt, die in diese Arbeit eingeflossen sind und die Spin-Orbit-Aufspaltung der S 2p-Photolinie und ihres Satelliten zeigen, die am Freie-Elektronen-Laser nicht beobachtet wurde. Die Relaxation von 2-Thiouracil wurde in den letzten Jahren ausgiebig mit ultraschnellen Methoden im sichtbaren und ultravioletten Spektralbereich untersucht, die die ultraschnelle Natur des molekularen Prozesses nach der Photoanregung zeigen. Die ultraschnelle Spektroskopie, bei der die Elektronen des Kernniveaus untersucht werden, bietet einen ergänzenden Ansatz zu den üblichen optischen Techniken. Die Methode erhält ihre lokale Empfindlichkeit durch die stark lokalisierten Kernelektronen. Die Kernenergien und Kern-Valenz-Übergänge werden stark von lokalen Valenzladungs- und Geometrieänderungen beeinflusst, und frühere Studien haben diese Empfindlichkeit genutzt, um den molekularen Prozess zu untersuchen, der sich in der ultraschnellen Dynamik widerspiegelt. Wir haben eine Apparatur gebaut, die die Voraussetzungen für die Durchführung zeitaufgelöster Röntgenspektroskopie an Molekülen in der Gasphase bietet. Mit dieser Apparatur haben wir Anregungs-Abfrage-Elektronenspektroskopie an der S 2p-Kante von 2-Thiouracil an dem Freie-Elektronen-Laser FLASH2 durchgeführt. Zuerst triggert ein UV-Puls die Relaxationsdynamik und anschließend tastet ein Röntgenpuls das einzelne Schwefelatom im Inneren des Moleküls ab. Für die Analyse der Photoelektronenspektren habe ich eine Selbstrefernzierung der Photolinie implementiert, mit deren Hilfe der spektrale Jitter des FEL minimiert werden konnte. Dieser ist auf den zugrunde liegenden Prozess der selbstverstärkten spontanen Emission (SASE) zurückzuführen. Mit diesem Ansatz konnten wir nicht nur dynamische Veränderungen in der Bindungsenergie der Elektronen untersuchen, sondern auch ein oszillierendes Verhalten in der Verschiebung der beobachteten Photolinie feststellen, das wir mit einer nicht-adiabatischen Dynamik in Verbindung bringen, an der mehrere elektronische Zustände beteiligt sind. Außerdem konnten wir die UV-induzierte Verschiebung der Bindungsenergie mit dem lokalen Ladungsfluss am Schwefel in Verbindung bringen, der direkt mit dem elektronischen Zustand verbunden ist. Darüber hinaus zeigt die Analyse der Auger-Meitner-Elektronen, dass die in frühen Stadien der photoinduzierten Relaxation beobachteten Energieverschiebungen mit der Geometrieänderung des Moleküls zusammenhängen. Genauer gesagt korreliert der beobachtete Anstieg der kinetischen Energie der Auger-Meitner-Elektronen mit einer zuvor vorhergesagten Dehnung der C=S-Bindung. KW - thiouracil KW - ultrafast molecular dynamics KW - x-ray spectroscopy KW - Auger-Meitner electron spectroscopy KW - photoelectron spectroscopy KW - free-electron laser KW - FLASH KW - excited-state chemical shift KW - Thiouracil KW - ultraschnelle Moleküldynamik KW - Röntgenspektroskopie KW - Photoelektronenspektroskopie KW - pump-probe spectroscopy KW - Freie-Elektronen-Laser KW - Anregungs-Abfrage-Spektroskopie Y1 - 2022 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-571636 ER - TY - JOUR A1 - Vilk, Ohad A1 - Aghion, Erez A1 - Avgar, Tal A1 - Beta, Carsten A1 - Nagel, Oliver A1 - Sabri, Adal A1 - Sarfati, Raphael A1 - Schwartz, Daniel K. A1 - Weiß, Matthias A1 - Krapf, Diego A1 - Nathan, Ran A1 - Metzler, Ralf A1 - Assaf, Michael T1 - Unravelling the origins of anomalous diffusion BT - from molecules to migrating storks JF - Physical review research / American Physical Society N2 - Anomalous diffusion or, more generally, anomalous transport, with nonlinear dependence of the mean-squared displacement on the measurement time, is ubiquitous in nature. It has been observed in processes ranging from microscopic movement of molecules to macroscopic, large-scale paths of migrating birds. Using data from multiple empirical systems, spanning 12 orders of magnitude in length and 8 orders of magnitude in time, we employ a method to detect the individual underlying origins of anomalous diffusion and transport in the data. This method decomposes anomalous transport into three primary effects: long-range correlations (“Joseph effect”), fat-tailed probability density of increments (“Noah effect”), and nonstationarity (“Moses effect”). We show that such a decomposition of real-life data allows us to infer nontrivial behavioral predictions and to resolve open questions in the fields of single-particle tracking in living cells and movement ecology. Y1 - 2022 U6 - https://doi.org/10.1103/PhysRevResearch.4.033055 SN - 2643-1564 VL - 4 IS - 3 PB - American Physical Society CY - College Park, MD ER - TY - GEN A1 - Vilk, Ohad A1 - Aghion, Erez A1 - Avgar, Tal A1 - Beta, Carsten A1 - Nagel, Oliver A1 - Sabri, Adal A1 - Sarfati, Raphael A1 - Schwartz, Daniel K. A1 - Weiß, Matthias A1 - Krapf, Diego A1 - Nathan, Ran A1 - Metzler, Ralf A1 - Assaf, Michael T1 - Unravelling the origins of anomalous diffusion BT - from molecules to migrating storks T2 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe N2 - Anomalous diffusion or, more generally, anomalous transport, with nonlinear dependence of the mean-squared displacement on the measurement time, is ubiquitous in nature. It has been observed in processes ranging from microscopic movement of molecules to macroscopic, large-scale paths of migrating birds. Using data from multiple empirical systems, spanning 12 orders of magnitude in length and 8 orders of magnitude in time, we employ a method to detect the individual underlying origins of anomalous diffusion and transport in the data. This method decomposes anomalous transport into three primary effects: long-range correlations (“Joseph effect”), fat-tailed probability density of increments (“Noah effect”), and nonstationarity (“Moses effect”). We show that such a decomposition of real-life data allows us to infer nontrivial behavioral predictions and to resolve open questions in the fields of single-particle tracking in living cells and movement ecology. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1303 Y1 - 2022 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-577643 SN - 1866-8372 IS - 1303 ER - TY - JOUR A1 - Bekir, Marek A1 - Sharma, Anjali A1 - Umlandt, Maren A1 - Lomadze, Nino A1 - Santer, Svetlana T1 - How to make a surface act as a micropump JF - Advanced materials interfaces N2 - In this paper, the phenomenon of light-driven diffusioosmotic (DO) long-range attractive and repulsive interactions between micro-sized objects trapped near a solid wall is investigated. The range of the DO flow extends several times the size of microparticles and can be adjusted to point towards or away from the particle by varying irradiation parameters such as intensity or wavelength of light. The "fuel" of the light-driven DO flow is a photosensitive surfactant which can be photo-isomerized between trans and cis-states. The trans-isomer tends to accumulate at the interface, while the cis-isomer prefers to stay in solution. In combination with a dissimilar photo-isomerization rate at the interface and in bulk, this yields a concentration gradient of the isomers around single particles resulting in local light-driven diffusioosmotic (l-LDDO) flow. Here, the extended analysis of the l-LDDO flow as a function of irradiation parameters by introducing time-dependent development of the concentration excess of isomers near the particle surface is presented. It is also demonstrated that the l-LDDO can be generated at any solid/liquid interface being more pronounced in the case of strongly absorbing material. This phenomenon has plenty of potential applications since it makes any type of surface act as a micropump. KW - azobenzene containing surfactant KW - light-driven diffusioosmosis KW - rate of KW - photo-isomerization Y1 - 2022 U6 - https://doi.org/10.1002/admi.202102395 SN - 2196-7350 VL - 9 IS - 12 PB - Wiley-VCH CY - Weinheim ER - TY - JOUR A1 - Mayer, Dennis A1 - Lever, Fabiano A1 - Gühr, Markus T1 - Data analysis procedures for time-resolved x-ray photoelectron spectroscopy at a SASE free-electron-laser JF - Journal of physics : B, Atomic, molecular and optical physics N2 - The random nature of self-amplified spontaneous emission (SASE) is a well-known challenge for x-ray core level spectroscopy at SASE free-electron lasers (FELs). Especially in time-resolved experiments that require a combination of good temporal and spectral resolution the jitter and drifts in the spectral characteristics, relative arrival time as well as power fluctuations can smear out spectral-temporal features. We present a combination of methods for the analysis of time-resolved photoelectron spectra based on power and time corrections as well as self-referencing of a strong photoelectron line. Based on sulfur 2p photoelectron spectra of 2-thiouracil taken at the SASE FEL FLASH2, we show that it is possible to correct for some of the photon energy drift and jitter even when reliable shot-to-shot photon energy data is not available. The quality of pump-probe difference spectra improves as random jumps in energy between delay points reduce significantly. The data analysis allows to identify coherent oscillations of 1 eV shift on the mean photoelectron line of 4 eV width with an error of less than 0.1 eV. KW - free-electron laser KW - photoelectron spectroscopy KW - FLASH Y1 - 2022 U6 - https://doi.org/10.1088/1361-6455/ac3c91 SN - 0953-4075 SN - 1361-6455 VL - 55 IS - 5 PB - IOP Publ. CY - Bristol ER - TY - GEN A1 - Sarabadani, Jalal A1 - Metzler, Ralf A1 - Ala-Nissila, Tapio T1 - Driven polymer translocation into a channel: Isoflux tension propagation theory and Langevin dynamics simulations T2 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe N2 - Isoflux tension propagation (IFTP) theory and Langevin dynamics (LD) simulations are employed to study the dynamics of channel-driven polymer translocation in which a polymer translocates into a narrow channel and the monomers in the channel experience a driving force fc. In the high driving force limit, regardless of the channel width, IFTP theory predicts τ ∝ f βc for the translocation time, where β = −1 is the force scaling exponent. Moreover, LD data show that for a very narrow channel fitting only a single file of monomers, the entropic force due to the subchain inside the channel does not play a significant role in the translocation dynamics and the force exponent β = −1 regardless of the force magnitude. As the channel width increases the number of possible spatial configurations of the subchain inside the channel becomes significant and the resulting entropic force causes the force exponent to drop below unity. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1292 Y1 - 2023 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-574387 SN - 1866-8372 IS - 1292 SP - 033003-1 EP - 033003-14 ER - TY - JOUR A1 - Sarabadani, Jalal A1 - Metzler, Ralf A1 - Ala-Nissila, Tapio T1 - Driven polymer translocation into a channel: Isoflux tension propagation theory and Langevin dynamics simulations JF - Physical Review Research N2 - Isoflux tension propagation (IFTP) theory and Langevin dynamics (LD) simulations are employed to study the dynamics of channel-driven polymer translocation in which a polymer translocates into a narrow channel and the monomers in the channel experience a driving force fc. In the high driving force limit, regardless of the channel width, IFTP theory predicts τ ∝ f βc for the translocation time, where β = −1 is the force scaling exponent. Moreover, LD data show that for a very narrow channel fitting only a single file of monomers, the entropic force due to the subchain inside the channel does not play a significant role in the translocation dynamics and the force exponent β = −1 regardless of the force magnitude. As the channel width increases the number of possible spatial configurations of the subchain inside the channel becomes significant and the resulting entropic force causes the force exponent to drop below unity. Y1 - 2022 U6 - https://doi.org/10.1103/PhysRevResearch.4.033003 SN - 2643-1564 VL - 4 SP - 033003-1 EP - 033003-14 PB - American Physical Society CY - College Park, Maryland, USA ET - 3 ER - TY - JOUR A1 - Smirnov, Lev A. A1 - Bolotov, Maxim A1 - Bolotov, Dmitri A1 - Osipov, Grigory V. A1 - Pikovsky, Arkady T1 - Finite-density-induced motility and turbulence of chimera solitons JF - New Journal of Physics N2 - We consider a one-dimensional oscillatory medium with a coupling through a diffusive linear field. In the limit of fast diffusion this setup reduces to the classical Kuramoto–Battogtokh model. We demonstrate that for a finite diffusion stable chimera solitons, namely localized synchronous domain in an infinite asynchronous environment, are possible. The solitons are stable also for finite density of oscillators, but in this case they sway with a nearly constant speed. This finite-density-induced motility disappears in the continuum limit, as the velocity of the solitons is inverse proportional to the density. A long-wave instability of the homogeneous asynchronous state causes soliton turbulence, which appears as a sequence of soliton mergings and creations. As the instability of the asynchronous state becomes stronger, this turbulence develops into a spatio-temporal intermittency. KW - chimera KW - soliton KW - finite-size effects Y1 - 2022 U6 - https://doi.org/10.1088/1367-2630/ac63d9 SN - 1367-2630 VL - 24 PB - IOP CY - London ER -