TY - JOUR A1 - Bojahr, Andre A1 - Herzog, Marc A1 - Mitzscherling, Steffen A1 - Maerten, Lena A1 - Schick, Daniel A1 - Goldshteyn, J. A1 - Leitenberger, Wolfram A1 - Shayduk, R. A1 - Gaal, P. A1 - Bargheer, Matias T1 - Brillouin scattering of visible and hard X-ray photons from optically synthesized phonon wavepackets JF - Optics express : the international electronic journal of optics N2 - We monitor how destructive interference of undesired phonon frequency components shapes a quasi-monochromatic hypersound wavepacket spectrum during its local real-time preparation by a nanometric transducer and follow the subsequent decay by nonlinear coupling. We prove each frequency component of an optical supercontinuum probe to be sensitive to one particular phonon wavevector in bulk material and cross-check this by ultrafast x-ray diffraction experiments with direct access to the lattice dynamics. Establishing reliable experimental techniques with direct access to the transient spectrum of the excitation is crucial for the interpretation in strongly nonlinear regimes, such as soliton formation. Y1 - 2013 U6 - https://doi.org/10.1364/OE.21.021188 SN - 1094-4087 VL - 21 IS - 18 SP - 21188 EP - 21197 PB - Optical Society of America CY - Washington ER - TY - JOUR A1 - Bojahr, Andre A1 - Herzog, Marc A1 - Schick, Daniel A1 - Vrejoiu, Ionela A1 - Bargheer, Matias T1 - Calibrated real-time detection of nonlinearly propagating strain waves JF - Physical review : B, Condensed matter and materials physics N2 - Epitaxially grown metallic oxide transducers support the generation of ultrashort strain pulses in SrTiO3 (STO) with high amplitudes up to 0.5%. The strain amplitudes are calibrated by real-time measurements of the lattice deformation using ultrafast x-ray diffraction. We determine the speed at which the strain fronts propagate by broadband picosecond ultrasonics and conclude that, above a strain level of approx. 0.2%, the compressive and tensile strain components travel at considerably different sound velocities, indicating nonlinear wave behavior. Simulations based on an anharmonic linear-chain model are in excellent accord with the experimental findings and show how the spectrum of coherent phonon modes changes with time. Y1 - 2012 U6 - https://doi.org/10.1103/PhysRevB.86.144306 SN - 1098-0121 VL - 86 IS - 14 PB - American Physical Society CY - College Park ER - TY - JOUR A1 - Bojahr, Andre A1 - Schick, Daniel A1 - Märten, Lena A1 - Herzog, Marc A1 - Vrejoiu, Ionela A1 - von Korff Schmising, Clemens A1 - Milne, Chris A1 - Johnson, Steven Lee A1 - Bargheer, Matias T1 - Comparing the oscillation phase in optical pump-probe spectra to ultrafast x-ray diffraction in the metal-dielectric SrRuO3/SrTiO3 superlattice JF - Physical review : B, Condensed matter and materials physics N2 - We measured the ultrafast optical response of metal-dielectric superlattices by broadband all-optical pump-probe spectroscopy. The observed phase of the superlattice mode depends on the probe wavelength, making assignments of the excitation mechanism difficult. Ultrafast x-ray diffraction data reveal the true oscillation phase of the lattice which changes as a function of the excitation fluence. This result is confirmed by the fluence dependence of optical transients. We set up a linear chain model of the lattice dynamics and successfully simulated the broadband optical reflection by unit-cell resolved calculation of the strain-dependent dielectric functions of the constituting materials. Y1 - 2012 U6 - https://doi.org/10.1103/PhysRevB.85.224302 SN - 1098-0121 VL - 85 IS - 22 PB - American Physical Society CY - College Park ER - TY - JOUR A1 - Enquist, Henrik A1 - Navirian, Hengameh A1 - Nueske, Ralf A1 - von Korff Schmising, Clemens A1 - Jurgilaitis, Andrius A1 - Herzog, Marc A1 - Bargheer, Matias A1 - Sondhauss, Peter A1 - Larsson, Joergen T1 - Subpicosecond hard x-ray streak camera using single-photon counting N2 - We have developed and characterized a hard x-ray accumulating streak camera that achieves subpicosecond time resolution by using single-photon counting. A high repetition rate of 2 kHz was achieved by use of a readout camera with built-in image processing capabilities. The effects of sweep jitter were removed by using a UV timing reference. The use of single-photon counting allows the camera to reach a high quantum efficiency by not limiting the divergence of the photoelectrons. Y1 - 2010 UR - http://www.opticsinfobase.org/ U6 - https://doi.org/10.1364/OL.35.003219 SN - 0146-9592 ER - TY - JOUR A1 - Gaal, P. A1 - Schick, Daniel A1 - Herzog, Marc A1 - Bojahr, Andre A1 - Shayduk, Roman A1 - Goldshteyn, J. A1 - Navirian, Hengameh A. A1 - Leitenberger, Wolfram A1 - Vrejoiu, Ionela A1 - Khakhulin, D. A1 - Wulff, M. A1 - Bargheer, Matias T1 - Time-domain sampling of x-ray pulses using an ultrafast sample response JF - Applied physics letters N2 - We employ the ultrafast response of a 15.4 nm thin SrRuO3 layer grown epitaxially on a SrTiO3 substrate to perform time-domain sampling of an x-ray pulse emitted from a synchrotron storage ring. Excitation of the sample with an ultrashort laser pulse triggers coherent expansion and compression waves in the thin layer, which turn the diffraction efficiency on and off at a fixed Bragg angle during 5 ps. This is significantly shorter than the duration of the synchrotron x-ray pulse of 100 ps. Cross-correlation measurements of the ultrafast sample response and the synchrotron x-ray pulse allow to reconstruct the x-ray pulse shape. Y1 - 2012 U6 - https://doi.org/10.1063/1.4769828 SN - 0003-6951 VL - 101 IS - 24 PB - American Institute of Physics CY - Melville ER - TY - JOUR A1 - Gaal, Peter A1 - Schick, Daniel A1 - Herzog, Marc A1 - Bojahr, Andre A1 - Shayduk, Roman A1 - Goldshteyn, Jevgeni A1 - Leitenberger, Wolfram A1 - Vrejoiu, Ionela A1 - Khakhulin, Dmitry A1 - Wulff, Michael A1 - Bargheer, Matias T1 - Ultrafast switching of hard X-rays JF - Journal of synchrotron radiation N2 - A new concept for shortening hard X-ray pulses emitted from a third-generation synchrotron source down to few picoseconds is presented. The device, called the PicoSwitch, exploits the dynamics of coherent acoustic phonons in a photo-excited thin film. A characterization of the structure demonstrates switching times of <= 5 ps and a peak reflectivity of similar to 10(-3). The device is tested in a real synchrotron-based pump-probe experiment and reveals features of coherent phonon propagation in a second thin film sample, thus demonstrating the potential to significantly improve the temporal resolution at existing synchrotron facilities. KW - ultrafast X-ray diffraction KW - thin film KW - coherent phonons KW - X-ray switching KW - pulse shortening KW - optical pump X-ray probe KW - time-resolved Y1 - 2014 U6 - https://doi.org/10.1107/S1600577513031949 SN - 0909-0495 SN - 1600-5775 VL - 21 SP - 380 EP - 385 PB - Wiley-Blackwell CY - Hoboken ER - TY - THES A1 - Herzog, Marc T1 - Structural dynamics of photoexcited nanolayered perovskites studied by ultrafast x-ray diffraction T1 - Untersuchung der Strukturdynamik photoangeregter Nanoschicht-Perowskite mittels ultraschneller Röntgenbeugung N2 - This publication-based thesis represents a contribution to the active research field of ultrafast structural dynamics in laser-excited nanostructures. The investigation of such dynamics is mandatory for the understanding of the various physical processes on microscopic scales in complex materials which have great potentials for advances in many technological applications. I theoretically and experimentally examine the coherent, incoherent and anharmonic lattice dynamics of epitaxial metal-insulator heterostructures on timescales ranging from femtoseconds up to nanoseconds. To infer information on the transient dynamics in the photoexcited crystal lattices experimental techniques using ultrashort optical and x-ray pulses are employed. The experimental setups include table-top sources as well as large-scale facilities such as synchrotron sources. At the core of my work lies the development of a linear-chain model to simulate and analyze the photoexcited atomic-scale dynamics. The calculated strain fields are then used to simulate the optical and x-ray response of the considered thin films and multilayers in order to relate the experimental signatures to particular structural processes. This way one obtains insight into the rich lattice dynamics exhibiting coherent transport of vibrational energy from local excitations via delocalized phonon modes of the samples. The complex deformations in tailored multilayers are identified to give rise to highly nonlinear x-ray diffraction responses due to transient interference effects. The understanding of such effects and the ability to precisely calculate those are exploited for the design of novel ultrafast x-ray optics. In particular, I present several Phonon Bragg Switch concepts to efficiently generate ultrashort x-ray pulses for time-resolved structural investigations. By extension of the numerical models to include incoherent phonon propagation and anharmonic lattice potentials I present a new view on the fundamental research topics of nanoscale thermal transport and anharmonic phonon-phonon interactions such as nonlinear sound propagation and phonon damping. The former issue is exemplified by the time-resolved heat conduction from thin SrRuO3 films into a SrTiO3 substrate which exhibits an unexpectedly slow heat conductivity. Furthermore, I discuss various experiments which can be well reproduced by the versatile numerical models and thus evidence strong lattice anharmonicities in the perovskite oxide SrTiO3. The thesis also presents several advances of experimental techniques such as time-resolved phonon spectroscopy with optical and x-ray photons as well as concepts for the implementation of x-ray diffraction setups at standard synchrotron beamlines with largely improved time-resolution for investigations of ultrafast structural processes. This work forms the basis for ongoing research topics in complex oxide materials including electronic correlations and phase transitions related to the elastic, magnetic and polarization degrees of freedom. N2 - Diese publikationsbasierte Dissertation ist ein Beitrag zu dem aktuellen Forschungsgebiet der ultraschnellen Strukturdynamik in laserangeregten Nanostrukturen. Die Erforschung solcher Vorgänge ist unabdingbar für ein Verständnis der vielseitigen physikalischen Prozesse auf mikroskopischen Längenskalen in komplexen Materialien, welche enorme Weiterentwicklungen für technologische Anwendungen versprechen. Meine theoretischen und experimentellen Untersuchungen betrachten kohärente, inkohärente und anharmonische Gitterdynamiken in epitaktischen Metal-Isolator-Heterostrukturen auf Zeitskalen von Femtosekunden bis Nanosekunden. Um Einsichten in solche transienten Prozesse in laserangeregten Kristallen zu erhalten, werden experimentelle Techniken herangezogen, die ultrakurze Pulse von sichtbarem Licht und Röntgenstrahlung verwenden. Ein zentraler Bestandteil meiner Arbeit ist die Entwicklung eines Linearkettenmodells zur Simulation und Analyse der laserinitiierten Atombewegungen. Die damit errechneten Verzerrungsfelder werden anschließend verwendet, um die Änderung der optischen und Röntgeneigenschaften der betrachteten Dünnfilm- und Vielschichtsysteme zu simulieren. Diese Rechnungen werden dann mit den experimentellen Daten verglichen, um die experimentellen Signaturen mit errechneten strukturellen Prozessen zu identifizieren. Dadurch erhält man Einsicht in die vielseitige Gitterdynamiken, was z.B. einen kohärenten Transport der Vibrationsenergie von lokal angeregten Bereichen durch delokalisierte Phononenmoden offenbart. Es wird gezeigt, dass die komplexen Deformationen in maßgeschneiderten Vielschichtsystemen hochgradig nichtlineare Röntgenbeugungseffekte auf Grund von transienten Interferenzerscheinungen verursachen. Das Verständnis dieser Prozesse und die Möglichkeit, diese präzise zu simulieren, werden dazu verwendet, neuartige ultraschnelle Röntgenoptiken zu entwerfen. Insbesondere erläutere ich mehrere Phonon-Bragg-Schalter-Konzepte für die effiziente Erzeugung ultrakurzer Röntgenpulse, die in zeitaufgelösten Strukturanalysen Anwendung finden. Auf Grund der Erweiterung der numerischen Modelle zur Beschreibung von inkohärenter Phononenausbreitung und anharmonischer Gitterpotentiale decken diese ebenfalls die aktuellen Themengebiete von Wärmetransport auf Nanoskalen und anharmonischer Phonon-Phonon-Wechselwirkung (z.B. nichtlineare Schallausbreitung und Phononendämpfung) ab. Die erstere Thematik wird am Beispiel der zeitaufgelösten Wärmeleitung von einem dünnen SrRuO3-Film in ein SrTiO3-Substrat behandelt, wobei ein unerwartet langsamer Wärmetransport zu Tage tritt. Außerdem diskutiere ich mehrere Experimente, die auf Grund der sehr guten Reproduzierbarkeit durch die numerischen Modelle starke Gitteranharmonizitäten in dem oxidischen Perowskit SrTiO3 bezeugen. Diese Dissertation erarbeitet zusätzlich verschiedene Weiterentwicklungen von experimentellen Methoden, wie z.B. die zeitaufgelöste Phononenspektroskopie mittels optischer Photonen und Röntgenphotonen, sowie Konzepte für die Umsetzung von Röntgenbeugungsexperimenten an Standard-Synchrotronquellen mit stark verbesserter Zeitauflösung für weitere Studien von ultraschnellen Strukturvorgängen. KW - ultraschnelle Röntgenbeugung KW - Phononen KW - epitaktisch KW - ultrafast x-ray diffraction KW - phonons KW - epitaxial Y1 - 2012 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-62632 ER - TY - JOUR A1 - Herzog, Marc A1 - Bojahr, Andre A1 - Goldshteyn, J. A1 - Leitenberger, Wolfram A1 - Vrejoiu, I. A1 - Khakhulin, D. A1 - Wulff, M. A1 - Shayduk, Roman A1 - Gaal, P. A1 - Bargheer, Matias T1 - Detecting optically synthesized quasi-monochromatic sub-terahertz phonon wavepackets by ultrafast x-ray diffraction JF - Applied physics letters N2 - We excite an epitaxial SrRuO3 thin film transducer by a pulse train of ultrashort laser pulses, launching coherent sound waves into the underlying SrTiO3 substrate. Synchrotron-based x-ray diffraction (XRD) data exhibiting separated sidebands to the substrate peak evidence the excitation of a quasi-monochromatic phonon wavepacket with sub-THz central frequency. The frequency and bandwidth of this sound pulse can be controlled by the optical pulse train. We compare the experimental data to combined lattice dynamics and dynamical XRD simulations to verify the coherent phonon dynamics. In addition, we observe a lifetime of 130 ps of such sub-THz phonons in accordance with the theory. KW - acoustic waves KW - epitaxial layers KW - phonon dispersion relations KW - terahertz waves KW - thin film devices KW - X-ray diffraction Y1 - 2012 U6 - https://doi.org/10.1063/1.3688492 SN - 0003-6951 VL - 100 IS - 9 PB - American Institute of Physics CY - Melville ER - TY - JOUR A1 - Herzog, Marc A1 - Leitenberger, Wolfram A1 - Shayduk, Roman A1 - van der Veen, Renske Marjan A1 - Milne, Chris J. A1 - Johnson, Steven Lee A1 - Vrejoiu, Ionela A1 - Alexe, Marin A1 - Hesse, Dietrich A1 - Bargheer, Matias T1 - Ultrafast manipulation of hard x-rays by efficient Bragg switches N2 - We experimentally demonstrate efficient switching of the hard x-ray Bragg reflectivity of a SrRuO3 /SrTiO3 superlattice by optical excitation of large-amplitude coherent acoustic superlattice phonons. The rocking curve changes drastically on a 1 ps timescale. The (0 0 116) reflection is almost extinguished (Delta R/R-0=-0.91), while the (0 0 118) reflection increases by more than an order of magnitude (Delta R/R-0=24.1). The change of the x-ray structure factor depends nonlinearly on the phonon amplitude, allowing manipulation of the x-ray response on a timescale considerably shorter than the phonon period. Numerical simulations for a superlattice with slightly changed geometry and realistic parameters predict a switching-contrast ratio Delta R/R-0 of 700 with high reflectivity. Y1 - 2010 UR - http://apl.aip.org/ U6 - https://doi.org/10.1063/1.3402773 SN - 0003-6951 ER - TY - JOUR A1 - Herzog, Marc A1 - Reppert, Alexander von 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 - Herzog, Marc A1 - Schick, Daniel A1 - Gaal, P. A1 - Shayduk, Roman A1 - von Korff Schmising, Clemens A1 - Bargheer, Matias T1 - Analysis of ultrafast X-ray diffraction data in a linear-chain model of the lattice dynamics JF - Applied physics : A, Materials science & processing N2 - We present ultrafast X-ray diffraction (UXRD) experiments which sensitively probe impulsively excited acoustic phonons propagating in a SrRuO3/SrTiO3 superlattice and further into the substrate. These findings are discussed together with previous UXRD results (Herzog et al. in Appl. Phys. Lett. 96, 161906, 2010; Woerner et al. in Appl. Phys. A 96, 83, 2009; v. Korff Schmising in Phys. Rev. B 78, 060404(R), 2008 and in Appl. Phys. B 88, 1, 2007) using a normal-mode analysis of a linear-chain model of masses and springs, thus identifying them as linear-response phenomena. We point out the direct correspondence of calculated observables with X-ray signals. In this framework the complex lattice motion turns out to result from an interference of vibrational eigenmodes of the coupled system of nanolayers and substrate. UXRD in principle selectively measures the lattice motion occurring with a specific wavevector, however, each Bragg reflection only measures the amplitude of a delocalized phonon mode in a spatially localized region, determined by the nanocomposition of the sample or the extinction depth of X-rays. This leads to a decay of experimental signals although the excited modes survive. Y1 - 2012 U6 - https://doi.org/10.1007/s00339-011-6719-z SN - 0947-8396 VL - 106 IS - 3 SP - 489 EP - 499 PB - Springer CY - New York ER - TY - JOUR A1 - Herzog, Marc A1 - Schick, Daniel A1 - Leitenberger, Wolfram A1 - Shayduk, Roman A1 - van der Veen, Renske M. A1 - Milne, Christopher J. A1 - Johnson, Steven Lee A1 - Vrejoiu, Ionela A1 - Bargheer, Matias T1 - Tailoring interference and nonlinear manipulation of femtosecond x-rays JF - New journal of physics : the open-access journal for physics N2 - We present ultrafast x-ray diffraction (UXRD) experiments on different photoexcited oxide superlattices. All data are successfully simulated by dynamical x-ray diffraction calculations based on a microscopic model, that accounts for the linear response of phonons to the excitation laser pulse. Some Bragg reflections display a highly nonlinear strain dependence. The origin of linear and two distinct nonlinear response phenomena is discussed in a conceptually simpler model using the interference of envelope functions that describe the diffraction efficiency of the average constituent nanolayers. The combination of both models facilitates rapid and accurate simulations of UXRD experiments. Y1 - 2012 U6 - https://doi.org/10.1088/1367-2630/14/1/013004 SN - 1367-2630 VL - 14 IS - 1 PB - IOP Publ. Ltd. CY - Bristol ER - TY - JOUR A1 - Mattern, Maximilian A1 - Reppert, Alexander von 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 - Reppert, Alexander von 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 - Golez, Denis A1 - Werner, Philipp A1 - Eckstein, Martin A1 - Katayama, Naoyuki A1 - Nohara, Minoru A1 - Takagi, Hide A1 - Mizokawa, Takashi A1 - Monney, Claude A1 - Staehler, Julia T1 - Ultrafast Electronic Band Gap Control in an Excitonic Insulator JF - Physical review letters N2 - We report on the nonequilibrium dynamics of the electronic structure of the layered semiconductor Ta2NiSe5 investigated by time-and angle-resolved photoelectron spectroscopy. We show that below the critical excitation density of F-C = 0.2 mJ cm(-2), the band gap narrows transiently, while it is enhanced above FC. Hartree-Fock calculations reveal that this effect can be explained by the presence of the low-temperature excitonic insulator phase of Ta2NiSe5, whose order parameter is connected to the gap size. This work demonstrates the ability to manipulate the band gap of Ta2NiSe5 with light on the femtosecond time scale. Y1 - 2017 U6 - https://doi.org/10.1103/PhysRevLett.119.086401 SN - 0031-9007 SN - 1079-7114 VL - 119 SP - 11559 EP - 11567 PB - American Physical Society CY - College Park 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 - Navirian, Hengameh A. A1 - Herzog, Marc A1 - Goldshteyn, J. A1 - Leitenberger, Wolfram A1 - Vrejoiu, Ionella A1 - Khakhulin, D. A1 - Wulff, M. A1 - Shayduk, Roman A1 - Gaal, P. A1 - Bargheer, Matias T1 - Shortening x-ray pulses for pump-probe experiments at synchrotrons JF - Journal of applied physics N2 - We implemented an experimental scheme for ultrafast x-ray diffraction at storage rings based on a laser-driven Bragg-switch that shortens the x-ray pulses emitted from an undulator. The increased time-resolution is demonstrated by observing changes of intensity, position and width of the diffraction peaks of a La(0.7)Sr(0.3)MnO(3)/SrTiO(3) superlattice sample after optical excitation, i.e., by quantitatively measuring the propagation of an expansion wave through the sample. These experimental transients with timescales of 35 to 60 ps evidence a reduction of the x-ray pulse duration by a factor of two. Y1 - 2011 U6 - https://doi.org/10.1063/1.3601057 SN - 0021-8979 VL - 109 IS - 12 PB - American Institute of Physics CY - Melville 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 - Reppert, Alexander von 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 - GEN A1 - Pudell, Jan-Etienne A1 - Maznev, Alexei A1 - Herzog, Marc A1 - Kronseder, M. A1 - Back, Christian A1 - Malinowski, Gregory A1 - Reppert, Alexander von 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 - Reppert, Alexander von 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 -