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 - Herzog, Marc A1 - von Reppert, Alexander A1 - Pudell, Jan-Etienne A1 - Henkel, Carsten A1 - Kronseder, Matthias A1 - Back, Christian H. A1 - Maznev, Alexei A. A1 - Bargheer, Matias T1 - Phonon-dominated energy transport in purely metallic heterostructures JF - Advanced functional materials N2 - Ultrafast X-ray diffraction is used to quantify the transport of energy in laser-excited nanoscale gold-nickel (Au-Ni) bilayers. Electron transport and efficient electron-phonon coupling in Ni convert the laser-deposited energy in the conduction electrons within a few picoseconds into a strong non-equilibrium between hot Ni and cold Au phonons at the bilayer interface. Modeling of the subsequent equilibration dynamics within various two-temperature models confirms that for ultrathin Au films, the thermal transport is dominated by phonons instead of conduction electrons because of the weak electron-phonon coupling in Au. KW - heterostructures KW - nanoscale energy transports KW - non-equilibrium KW - thermal KW - transports KW - ultrafast phenomena Y1 - 2022 U6 - https://doi.org/10.1002/adfm.202206179 SN - 1616-301X SN - 1616-3028 VL - 32 IS - 41 PB - Wiley-VCH CY - Weinheim ER - TY - JOUR A1 - Shayduk, Roman A1 - Hallmann, Jörg A1 - Rodriguez-Fernandez, Angel A1 - Scholz, Markus A1 - Lu, Wei A1 - Bösenberg, Ulrike A1 - Möller, Johannes A1 - Zozulya, Alexey A1 - Jiang, Man A1 - Wegner, Ulrike A1 - Secareanu, Radu-Costin A1 - Palmer, Guido A1 - Emons, Moritz A1 - Lederer, Max A1 - Volkov, Sergey A1 - Lindfors-Vrejoiu, Ionela A1 - Schick, Daniel A1 - Herzog, Marc A1 - Bargheer, Matias A1 - Madsen, Anders T1 - Femtosecond x-ray diffraction study of multi-THz coherent phonons in SrTiO3 JF - Applied physics letters N2 - We report generation of ultra-broadband longitudinal acoustic coherent phonon wavepackets in SrTiO3 (STO) with frequency components extending throughout the first Brillouin zone. The wavepackets are efficiently generated in STO using femtosecond infrared laser excitation of an atomically flat 1.6 nm-thick epitaxial SrRuO3 film. We use femtosecond x-ray diffraction at the European X-Ray Free Electron Laser Facility to study the dispersion and damping of phonon wavepackets. The experimentally determined damping constants for multi-THz frequency phonons compare favorably to the extrapolation of a simple ultrasound damping model over several orders of magnitude. Y1 - 2022 U6 - https://doi.org/10.1063/5.0083256 SN - 0003-6951 SN - 1077-3118 VL - 120 IS - 20 PB - AIP Publishing CY - Melville 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 - Mor, Selene A1 - Herzog, Marc A1 - Noack, Johannes A1 - Katayama, Naoyuki A1 - Nohara, Minoru A1 - Takagi, Hide A1 - Trunschke, Annette A1 - Mizokawa, Takashi A1 - Monney, Claude A1 - Stähler, Julia T1 - Inhibition of the photoinduced structural phase transition in the excitonic insulator Ta2NiSe5 JF - Physical review : B, Condensed matter and materials physics N2 - Femtosecond time-resolved midinfrared reflectivity is used to investigate the electron and phonon dynamics occurring at the direct band gap of the excitonic insulator Ta2NiSe5 below the critical temperature of its structural phase transition. We find that the phonon dynamics show a strong coupling to the excitation of free carriers at the Gamma point of the Brillouin zone. The optical response saturates at a critical excitation fluence F-C = 0.30 +/- 0.08 mJ/cm(2) due to optical absorption saturation. This limits the optical excitation density in Ta2NiSe5 so that the system cannot be pumped sufficiently strongly to undergo the structural change to the high-temperature phase. We thereby demonstrate that Ta2NiSe5 exhibits a blocking mechanism when pumped in the near-infrared regime, preventing a nonthermal structural phase transition. Y1 - 2018 U6 - https://doi.org/10.1103/PhysRevB.97.115154 SN - 2469-9950 SN - 2469-9969 VL - 97 IS - 11 PB - American Physical Society CY - College Park 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 - JOUR A1 - von Reppert, Alexander A1 - Willig, Lisa A1 - Pudell, Jan-Etienne A1 - Roessle, M. A1 - Leitenberger, Wolfram A1 - Herzog, Marc A1 - Ganss, F. A1 - Hellwig, O. A1 - Bargheer, Matias T1 - Ultrafast laser generated strain in granular and continuous FePt thin films JF - Applied physics letters N2 - We employ ultrafast X-ray diffraction to compare the lattice dynamics of laser-excited continuous and granular FePt films on MgO (100) substrates. Contrary to recent results on free-standing granular films, we observe in both cases a pronounced and long-lasting out-of-plane expansion. We attribute this discrepancy to the in-plane expansion, which is suppressed by symmetry in continuous films. Granular films on substrates are less constrained and already show a reduced out-of-plane contraction. Via the Poisson effect, out-of-plane contractions drive in-plane expansion and vice versa. Consistently, the granular film exhibits a short-lived out-of-plane contraction driven by ultrafast demagnetization which is followed by a reduced and delayed expansion. From the acoustic reflections of the observed strain waves at the film-substrate interface, we extract a 13% reduction of the elastic constants in thin 10 nm FePt films compared to bulk-like samples. (C) 2018 Author(s). Y1 - 2018 U6 - https://doi.org/10.1063/1.5050234 SN - 0003-6951 SN - 1077-3118 VL - 113 IS - 12 PB - American Institute of Physics CY - Melville ER - TY - GEN A1 - Zeuschner, Steffen Peer A1 - Mattern, Maximilian A1 - Pudell, Jan-Etienne A1 - von Reppert, Alexander A1 - Rössle, M. A1 - Leitenberger, Wolfram A1 - Schwarzkopf, J. A1 - Boschker, J. E. A1 - Herzog, Marc A1 - Bargheer, Matias T1 - Reciprocal space slicing BT - a time-efficient approach to femtosecond x-ray diffraction T2 - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe N2 - An experimental technique that allows faster assessment of out-of-plane strain dynamics of thin film heterostructures via x-ray diffraction is presented. In contrast to conventional high-speed reciprocal space-mapping setups, our approach reduces the measurement time drastically due to a fixed measurement geometry with a position-sensitive detector. This means that neither the incident (ω) nor the exit (2θ) diffraction angle is scanned during the strain assessment via x-ray diffraction. Shifts of diffraction peaks on the fixed x-ray area detector originate from an out-of-plane strain within the sample. Quantitative strain assessment requires the determination of a factor relating the observed shift to the change in the reciprocal lattice vector. The factor depends only on the widths of the peak along certain directions in reciprocal space, the diffraction angle of the studied reflection, and the resolution of the instrumental setup. We provide a full theoretical explanation and exemplify the concept with picosecond strain dynamics of a thin layer of NbO2. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1137 Y1 - 2021 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-499761 SN - 1866-8372 IS - 1137 ER - TY - JOUR A1 - Zeuschner, Steffen Peer A1 - Mattern, Maximilian A1 - Pudell, Jan-Etienne A1 - von Reppert, Alexander A1 - Rössle, M. A1 - Leitenberger, Wolfram A1 - Schwarzkopf, J. A1 - Boschker, J. E. A1 - Herzog, Marc A1 - Bargheer, Matias T1 - Reciprocal space slicing BT - a time-efficient approach to femtosecond x-ray diffraction JF - Structural Dynamics N2 - An experimental technique that allows faster assessment of out-of-plane strain dynamics of thin film heterostructures via x-ray diffraction is presented. In contrast to conventional high-speed reciprocal space-mapping setups, our approach reduces the measurement time drastically due to a fixed measurement geometry with a position-sensitive detector. This means that neither the incident (ω) nor the exit (2θ) diffraction angle is scanned during the strain assessment via x-ray diffraction. Shifts of diffraction peaks on the fixed x-ray area detector originate from an out-of-plane strain within the sample. Quantitative strain assessment requires the determination of a factor relating the observed shift to the change in the reciprocal lattice vector. The factor depends only on the widths of the peak along certain directions in reciprocal space, the diffraction angle of the studied reflection, and the resolution of the instrumental setup. We provide a full theoretical explanation and exemplify the concept with picosecond strain dynamics of a thin layer of NbO2. Y1 - 0202 U6 - https://doi.org/10.1063/4.0000040 SN - 2329-7778 VL - 8 PB - AIP Publishing LLC CY - Melville, NY ER - TY - JOUR A1 - Pudell, Jan-Etienne A1 - von Reppert, Alexander A1 - Schick, D. A1 - Zamponi, F. A1 - Rössle, Matthias A1 - Herzog, Marc A1 - Zabel, Hartmut A1 - Bargheer, Matias T1 - Ultrafast negative thermal expansion driven by spin disorder JF - Physical review : B, Condensed matter and materials physics N2 - We measure the transient strain profile in a nanoscale multilayer system composed of yttrium, holmium, and niobium after laser excitation using ultrafast x-ray diffraction. The strain propagation through each layer is determined by transient changes in the material-specific Bragg angles. We experimentally derive the exponentially decreasing stress profile driving the strain wave and show that it closely matches the optical penetration depth. Below the Neel temperature of Ho, the optical excitation triggers negative thermal expansion, which is induced by a quasi-instantaneous contractive stress and a second contractive stress contribution increasing on a 12-ps timescale. These two timescales were recently measured for the spin disordering in Ho [Rettig et al., Phys. Rev. Lett. 116, 257202 (2016)]. As a consequence, we observe an unconventional bipolar strain pulse with an inverted sign traveling through the heterostructure. Y1 - 2019 U6 - https://doi.org/10.1103/PhysRevB.99.094304 SN - 2469-9950 SN - 2469-9969 VL - 99 IS - 9 PB - American Physical Society CY - College Park ER -