TY - GEN A1 - Mattern, Maximilian A1 - Pudell, Jan-Etienne A1 - Laskin, G. A1 - von Reppert, Alexander A1 - Bargheer, Matias T1 - Analysis of the temperature- and fluence-dependent magnetic stress in laser-excited SrRuO3 T2 - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe N2 - We use ultrafast x-ray diffraction to investigate the effect of expansive phononic and contractive magnetic stress driving the picosecond strain response of a metallic perovskite SrRuO3 thin film upon femtosecond laser excitation. We exemplify how the anisotropic bulk equilibrium thermal expansion can be used to predict the response of the thin film to ultrafast deposition of energy. It is key to consider that the laterally homogeneous laser excitation changes the strain response compared to the near-equilibrium thermal expansion because the balanced in-plane stresses suppress the Poisson stress on the picosecond timescale. We find a very large negative Grüneisen constant describing the large contractive stress imposed by a small amount of energy in the spin system. The temperature and fluence dependence of the strain response for a double-pulse excitation scheme demonstrates the saturation of the magnetic stress in the high-fluence regime. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1144 KW - Thin films KW - Thermodynamic properties KW - Bragg peak KW - Ultrafast X-ray diffraction KW - Thermal effects KW - Phonons KW - Magnetism KW - Lattice dynamics KW - Lasers KW - Perovskites Y1 - 2021 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-515718 SN - 1866-8372 ER - TY - JOUR A1 - Sander, Mathias A1 - Koc, A. A1 - Kwamen, C. T. A1 - Michaels, H. A1 - von Reppert, Alexander A1 - Pudell, Jan-Etienne A1 - Zamponi, Flavio A1 - Bargheer, Matias A1 - Sellmann, J. A1 - Schwarzkopf, J. A1 - Gaal, P. T1 - Characterization of an ultrafast Bragg-Switch for shortening hard x-ray pulses JF - Journal of applied physics N2 - We present a nanostructured device that functions as photoacoustic hard x-ray switch. The device is triggered by femtosecond laser pulses and allows for temporal gating of hard x-rays on picosecond (ps) timescales. It may be used for pulse picking or even pulse shortening in 3rd generation synchrotron sources. Previous approaches mainly suffered from insufficient switching contrasts due to excitation-induced thermal distortions. We present a new approach where thermal distortions are spatially separated from the functional switching layers in the structure. Our measurements yield a switching contrast of 14, which is sufficient for efficient hard x-ray pulse shortening. The optimized structure also allows for utilizing the switch at high repetition rates of up to 208 kHz. Published by AIP Publishing. Y1 - 2016 U6 - https://doi.org/10.1063/1.4967835 SN - 0021-8979 SN - 1089-7550 VL - 120 PB - American Institute of Physics CY - Melville ER - TY - JOUR A1 - Mattern, Maximilian A1 - von Reppert, Alexander A1 - Zeuschner, Steffen Peer A1 - Herzog, Marc A1 - Pudell, Jan-Etienne A1 - Bargheer, Matias T1 - Concepts and use cases for picosecond ultrasonics with x-rays JF - Photoacoustics N2 - This review discusses picosecond ultrasonics experiments using ultrashort hard x-ray probe pulses to extract the transient strain response of laser-excited nanoscopic structures from Bragg-peak shifts. This method provides direct, layer-specific, and quantitative information on the picosecond strain response for structures down to few-nm thickness. We model the transient strain using the elastic wave equation and express the driving stress using Gruneisen parameters stating that the laser-induced stress is proportional to energy density changes in the microscopic subsystems of the solid, i.e., electrons, phonons and spins. The laser-driven strain response can thus serve as an ultrafast proxy for local energy-density and temperature changes, but we emphasize the importance of the nanoscale morphology for an accurate interpretation due to the Poisson effect. The presented experimental use cases encompass ultrathin and opaque metal-heterostructures, continuous and granular nanolayers as well as negative thermal expansion materials, that each pose a challenge to established all-optical techniques. KW - Picosecond ultrasonics KW - Ultrafast x-ray diffraction KW - Ultrafast x-ray KW - scattering KW - Ultrafast photoacoustics KW - Nanoscale heat transfer KW - Negative KW - thermal expansion Y1 - 2023 U6 - https://doi.org/10.1016/j.pacs.2023.100503 SN - 2213-5979 VL - 31 PB - Elsevier CY - Amsterdam ER - TY - JOUR A1 - Mattern, Maximilian A1 - von Reppert, Alexander A1 - Zeuschner, Steffen Peer A1 - Pudell, Jan-Etienne A1 - Kühne, F. A1 - Diesing, Detlef A1 - Herzog, Marc A1 - Bargheer, Matias T1 - Electronic energy transport in nanoscale Au/Fe hetero-structures in the perspective of ultrafast lattice dynamics JF - Applied physics letters N2 - We study the ultrafast electronic transport of energy in a photoexcited nanoscale Au/Fe hetero-structure by modeling the spatiotemporal profile of energy densities that drives transient strain, which we quantify by femtosecond x-ray diffraction. This flow of energy is relevant for intrinsic demagnetization and ultrafast spin transport. We measured lattice strain for different Fe layer thicknesses ranging from few atomic layers to several nanometers and modeled the spatiotemporal flow of energy densities. The combination of a high electron-phonon coupling coefficient and a large Sommerfeld constant in Fe is found to yield electronic transfer of nearly all energy from Au to Fe within the first hundreds of femtoseconds. Y1 - 2022 U6 - https://doi.org/10.1063/5.0080378 SN - 0003-6951 SN - 1077-3118 VL - 120 IS - 9 PB - AIP Publishing CY - Melville ER - TY - JOUR A1 - Willig, Lisa A1 - von Reppert, Alexander A1 - Deb, Marwan A1 - Ganss, F. A1 - Hellwig, O. A1 - Bargheer, Matias T1 - Finite-size effects in ultrafast remagnetization dynamics of FePt JF - Physical review : B, Condensed matter and materials physics N2 - We investigate the ultrafast magnetization dynamics of FePt in the L1(0) phase after an optical heating pulse, as used in heat-assisted magnetic recording. We compare continuous and nano-granular thin films and emphasize the impact of the finite size on the remagnetization dynamics. The remagnetization speeds up significantly with increasing external magnetic field only for the continuous film, where domain-wall motion governs the dynamics. The ultrafast remagnetization dynamics in the continuous film are only dominated by heat transport in the regime of high magnetic fields, whereas the timescale required for cooling is prevalent in the granular film for all magnetic field strengths. These findings highlight the necessary conditions for studying the intrinsic heat transport properties in magnetic materials. Y1 - 2019 U6 - https://doi.org/10.1103/PhysRevB.100.224408 SN - 2469-9950 SN - 2469-9969 VL - 100 IS - 22 PB - American Physical Society CY - College Park ER - TY - JOUR A1 - Koc, A. A1 - Reinhardt, M. A1 - von Reppert, Alexander A1 - Rössle, Matthias A1 - Leitenberger, Wolfram A1 - Gleich, M. A1 - Weinelt, M. A1 - Zamponi, Flavio A1 - Bargheer, Matias T1 - Grueneisen-approach for the experimental determination of transient spin and phonon energies from ultrafast x-ray diffraction data: gadolinium JF - Journal of physics : Condensed matter N2 - We study gadolinium thin films as a model system for ferromagnets with negative thermal expansion. Ultrashort laser pulses heat up the electronic subsystem and we follow the transient strain via ultrafast x-ray diffraction. In terms of a simple Grueneisen approach, the strain is decomposed into two contributions proportional to the thermal energy of spin and phonon subsystems. Our analysis reveals that upon femtosecond laser excitation, phonons and spins can be driven out of thermal equilibrium for several nanoseconds. KW - ultrafast KW - x-ray diffraction KW - magnetostriction KW - nonequilibrium KW - spin KW - phonon KW - rare earth Y1 - 2017 U6 - https://doi.org/10.1088/1361-648X/aa7187 SN - 0953-8984 SN - 1361-648X VL - 29 SP - 5884 EP - 5891 PB - IOP Publ. Ltd. CY - Bristol ER - TY - GEN A1 - Pudell, Jan-Etienne A1 - Maznev, Alexei A1 - Herzog, Marc A1 - Kronseder, M. A1 - Back, Christian A1 - Malinowski, Gregory A1 - von Reppert, Alexander A1 - Bargheer, Matias T1 - Layer specific observation of slow thermal equilibration in ultrathin metallic nanostructures by femtosecond X-ray diffraction T2 - Postprints der Universität Potsdam Mathematisch-Naturwissenschaftliche Reihe N2 - Ultrafast heat transport in nanoscale metal multilayers is of great interest in the context of optically induced demagnetization, remagnetization and switching. If the penetration depth of light exceeds the bilayer thickness, layer-specific information is unavailable from optical probes. Femtosecond diffraction experiments provide unique experimental access to heat transport over single digit nanometer distances. Here, we investigate the structural response and the energy flow in the ultrathin double-layer system: gold on ferromagnetic nickel. Even though the excitation pulse is incident from the Au side, we observe a very rapid heating of the Ni lattice, whereas the Au lattice initially remains cold. The subsequent heat transfer from Ni to the Au lattice is found to be two orders of magnitude slower than predicted by the conventional heat equation and much slower than electron-phonon coupling times in Au. We present a simplified model calculation highlighting the relevant thermophysical quantities. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 797 KW - thin magnetic layers KW - optical-excitation KW - heat-capacity KW - electron KW - gold KW - dynamics Y1 - 2019 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-426233 SN - 1866-8372 IS - 797 ER - TY - JOUR A1 - Pudell, Jan-Etienne A1 - Maznev, A. A. A1 - Herzog, Marc A1 - Kronseder, M. A1 - Back, Christian H. A1 - Malinowski, Gregory A1 - von Reppert, Alexander A1 - Bargheer, Matias T1 - Layer specific observation of slow thermal equilibration in ultrathin metallic nanostructures by femtosecond X-ray diffraction JF - Nature Communications N2 - Ultrafast heat transport in nanoscale metal multilayers is of great interest in the context of optically induced demagnetization, remagnetization and switching. If the penetration depth of light exceeds the bilayer thickness, layer-specific information is unavailable from optical probes. Femtosecond diffraction experiments provide unique experimental access to heat transport over single digit nanometer distances. Here, we investigate the structural response and the energy flow in the ultrathin double-layer system: gold on ferromagnetic nickel. Even though the excitation pulse is incident from the Au side, we observe a very rapid heating of the Ni lattice, whereas the Au lattice initially remains cold. The subsequent heat transfer from Ni to the Au lattice is found to be two orders of magnitude slower than predicted by the conventional heat equation and much slower than electron-phonon coupling times in Au. We present a simplified model calculation highlighting the relevant thermophysical quantities. Y1 - 2018 U6 - https://doi.org/10.1038/s41467-018-05693-5 SN - 2041-1723 VL - 9 PB - Nature Publ. Group CY - London ER - TY - THES A1 - von Reppert, Alexander T1 - Magnetic strain contributions in laser-excited metals studied by time-resolved X-ray diffraction T1 - Untersuchung magnetischer Beiträge zur Ausdehnung laserangeregter Metalle mittels zeitaufgelöster Röntgenbeugungsexperimente N2 - In this work I explore the impact of magnetic order on the laser-induced ultrafast strain response of metals. Few experiments with femto- or picosecond time-resolution have so far investigated magnetic stresses. This is contrasted by the industrial usage of magnetic invar materials or magnetostrictive transducers for ultrasound generation, which already utilize magnetostrictive stresses in the low frequency regime. In the reported experiments I investigate how the energy deposition by the absorption of femtosecond laser pulses in thin metal films leads to an ultrafast stress generation. I utilize that this stress drives an expansion that emits nanoscopic strain pulses, so called hypersound, into adjacent layers. Both the expansion and the strain pulses change the average inter-atomic distance in the sample, which can be tracked with sub-picosecond time resolution using an X-ray diffraction setup at a laser-driven Plasma X-ray source. Ultrafast X-ray diffraction can also be applied to buried layers within heterostructures that cannot be accessed by optical methods, which exhibit a limited penetration into metals. The reconstruction of the initial energy transfer processes from the shape of the strain pulse in buried detection layers represents a contribution of this work to the field of picosecond ultrasonics. A central point for the analysis of the experiments is the direct link between the deposited energy density in the nano-structures and the resulting stress on the crystal lattice. The underlying thermodynamical concept of a Grüneisen parameter provides the theoretical framework for my work. I demonstrate how the Grüneisen principle can be used for the interpretation of the strain response on ultrafast timescales in various materials and that it can be extended to describe magnetic stresses. The class of heavy rare-earth elements exhibits especially large magnetostriction effects, which can even lead to an unconventional contraction of the laser-excited transducer material. Such a dominant contribution of the magnetic stress to the motion of atoms has not been demonstrated previously. The observed rise time of the magnetic stress contribution in Dysprosium is identical to the decrease in the helical spin-order, that has been found previously using time-resolved resonant X-ray diffraction. This indicates that the strength of the magnetic stress can be used as a proxy of the underlying magnetic order. Such magnetostriction measurements are applicable even in case of antiparallel or non-collinear alignment of the magnetic moments and a vanishing magnetization. The strain response of metal films is usually determined by the pressure of electrons and lattice vibrations. I have developed a versatile two-pulse excitation routine that can be used to extract the magnetic contribution to the strain response even if systematic measurements above and below the magnetic ordering temperature are not feasible. A first laser pulse leads to a partial ultrafast demagnetization so that the amplitude and shape of the strain response triggered by the second pulse depends on the remaining magnetic order. With this method I could identify a strongly anisotropic magnetic stress contribution in the magnetic data storage material iron-platinum and identify the recovery of the magnetic order by the variation of the pulse-to-pulse delay. The stark contrast of the expansion of iron-platinum nanograins and thin films shows that the different constraints for the in-plane expansion have a strong influence on the out-of-plane expansion, due to the Poisson effect. I show how such transverse strain contributions need to be accounted for when interpreting the ultrafast out-of-plane strain response using thermal expansion coefficients obtained in near equilibrium conditions. This work contributes an investigation of magnetostriction on ultrafast timescales to the literature of magnetic effects in materials. It develops a method to extract spatial and temporal varying stress contributions based on a model for the amplitude and shape of the emitted strain pulses. Energy transfer processes result in a change of the stress profile with respect to the initial absorption of the laser pulses. One interesting example occurs in nanoscopic gold-nickel heterostructures, where excited electrons rapidly transport energy into a distant nickel layer, that takes up much more energy and expands faster and stronger than the laser-excited gold capping layer. Magnetic excitations in rare earth materials represent a large energy reservoir that delays the energy transfer into adjacent layers. Such magneto-caloric effects are known in thermodynamics but not extensively covered on ultrafast timescales. The combination of ultrafast X-ray diffraction and time-resolved techniques with direct access to the magnetization has a large potential to uncover and quantify such energy transfer processes. N2 - In dieser Arbeit untersuche ich den Einfluss magnetischer Ordnung auf die laser-induzierte, ultraschnelle Ausdehnung von Metallen. In Experimenten mit Femto- oder Pikosekunden Zeitauflösung sind magnetische Drücke bisher kaum erforscht. Dies steht im Kontrast zur industriellen Verwendung von magnetischen Invar Materialien oder magnetostriktiven Ultraschallgebern, in denen magnetische Drücke bereits in niedrigeren Frequenzbereichen Anwendung finden. In meinen Experimenten untersuche ich, wie der Energieeintrag durch die Absorption von Femtosekunden-Laserpulsen in dünnen Metallschichten zu einem ultraschnellen Druckanstieg führt. Dabei nutze ich, dass der Druckanstieg zu einer Ausdehnung führt, welche Deformationswellen auf der Nanometerskala, sogenannte Hyperschallpulse, in angrenzende Schichten aussendet. Sowohl die Ausdehnung als auch die Deformationspulse ändern den mittleren Abstand zwischen den Atomen in der Probe, welcher mittels Röntgenbeugung an einer Laser-getriebenen Plasma-Röntgenquelle mit einer Subpikosekunden-Zeitauflösung detektiert wird. Das Verfahren der ultraschnellen Röntgenbeugung gelingt auch in Heterostrukturen mit vergrabenen Detektionsschichten, zu denen optische Methoden aufgrund ihrer limitierter Eindringtiefe in Metallen keinen Zugang haben. Ein Beitrag dieser Arbeit zum Feld der Pikosekunden-Akustik ist es, aus der Ausdehnung einer solchen Detektionsschicht Rückschlüsse auf die initialen Energietransferprozesse zu ziehen. Der direkte Zusammenhang zwischen der eingebrachten Energiedichte in die Nanostrukturen und dem resultierenden Druck auf das Atomgitter ist ein zentraler Punkt in meiner Analyse der Experimente. Das zu Grunde liegende thermodynamische Konzept des Grüneisen-Parameters bildet den theoretischen Kontext meiner Publikationen. Anhand verschiedener Materialien demonstriere ich, wie dieses Prinzip auch zur Analyse der Ausdehnung auf ultraschnellen Zeitskalen verwendet werden kann und sich auch auf magnetische Drücke übertragen lässt. Insbesondere in der Materialklasse der schweren, seltenen Erdelemente sind Magnetostriktionseffekte sehr groß und führen dort sogar zu einem ungewöhnlichen Zusammenziehen des Materials nach der Laseranregung. Solch ein bestimmender Einfluss des magnetischen Drucks auf die Atombewegung ist bisher nicht gezeigt worden. Die Zeitskala des magnetischen Druckanstiegs entspricht dabei der beobachteten Abnahme der helikalen Spin-Ordnung, welche zuvor mittels zeitaufgelöster, resonanter Röntgenbeugung ermittelt wurde. Dies zeigt, dass die Stärke des magnetischen Drucks als Maß für magnetische Ordnung dienen kann, insbesondere auch im Fall von antiparalleler oder nicht-kollinearer Ordnung der magnetischen Momente in Proben mit verschwindender Magnetisierung. In Metallfilmen ist die Dehnung des Atomgitters in der Regel durch Druck von Elektronen und Gitterschwingungen geprägt. Um den magnetischen Druckbeitrag auch in solchen Fällen zu extrahieren, in denen systematische Experimente oberhalb und unterhalb der magnetischen Ordnungstemperatur nicht praktikabel sind, habe ich ein neuartiges Doppelpuls-Anregungsverfahren entwickelt, welches allgemein für die Untersuchung von Phasenübergängen nützlich ist. Der Energieeintrag durch den ersten Laserpuls führt dabei zu einer partiellen, ultraschnellen Demagnetisierung, sodass die Amplitude und Form der Gitterausdehnung nach dem zweiten Puls von der Stärke des verbliebenen magnetischen Drucks und somit von der verbliebenen magnetischen Ordnung abhängt. Mit dieser Methode ist es möglich geworden, einen stark richtungsabhängigen, magnetischen Druckbeitrag im Speichermedium Eisen-Platin zu identifizieren und mittels Variation des Puls-zu-Puls Abstands auch die Rückkehr der magnetischen Ordnung zu zeigen. Die unterschiedliche Ausdehnung von Eisen-Platin Nanopartikeln und dünnen Filmen zeigt dabei, dass die verschiedenen Zwangsbedingungen für die Ausdehnung entlang der Probenoberfläche aufgrund des Poisson-Effekts einen entscheidenden Einfluss auf die ultraschnelle Ausdehnung senkrecht zur Probenoberfläche hat. Ich analysiere, wie die zugrunde liegende Querkontraktion bei der Interpretation der ultraschnellen Ausdehnung auf der Basis von thermischen Ausdehnungskoeffizienten im Quasi-Gleichgewicht berücksichtigt werden kann. Meine Arbeit erweitert die Literatur um einen Beitrag zur ultraschnellen Magnetostriktion und entwickelt eine Methodik mittels derer räumlich und zeitlich variierende Druckbeiträge anhand einer Modellierung der Form der Deformationswellen extrahiert werden können. Energietransferprozesse spiegeln sich dabei durch eine Änderung des Druckprofils gegenüber dem Absorptionsprofil der Laserpulse wider. KW - lattice dynamics KW - magnetism KW - ultrafast KW - X-ray diffraction KW - Gitterdynamik KW - Magnetismus KW - ultraschnell KW - Röntgenbeugung Y1 - 2021 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-535582 ER - TY - GEN A1 - von Reppert, Alexander A1 - Puddell, J. A1 - Koc, A. A1 - Reinhardt, M. A1 - Leitenberger, Wolfram A1 - Dumesnil, K. A1 - Zamponi, Flavio A1 - Bargheer, Matias T1 - Persistent nonequilibrium dynamics of the thermal energies in the spin and phonon systems of an antiferromagnet N2 - We present a temperature and fluence dependent Ultrafast X-Ray Diffraction study of a laser-heated antiferromagnetic dysprosium thin film. The loss of antiferromagnetic order is evidenced by a pronounced lattice contraction. We devise a method to determine the energy flow between the phonon and spin system from calibrated Bragg peak positions in thermal equilibrium. Reestablishing the magnetic order is much slower than the cooling of the lattice, especially around the Néel temperature. Despite the pronounced magnetostriction, the transfer of energy from the spin system to the phonons in Dy is slow after the spin-order is lost. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 272 Y1 - 2016 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-98710 ER -