TY - JOUR A1 - Navirian, Hengameh A. A1 - Schick, Daniel A1 - Gaal, Peter A1 - Leitenberger, Wolfram A1 - Shayduk, Roman A1 - Bargheer, Matias T1 - Thermoelastic study of nanolayered structures using time-resolved X-ray diffraction at high repetition rate JF - Applied physics letters N2 - We investigate the thermoelastic response of a nanolayered sample composed of a metallic SrRuO3 electrode sandwiched between a ferroelectric Pb(Zr0.2Ti0.8)O-3 film with negative thermal expansion and a SrTiO3 substrate. SrRuO3 is rapidly heated by fs-laser pulses with 208 kHz repetition rate. Diffraction of X-ray pulses derived from a synchrotron measures the transient out-of-plane lattice constant c of all three materials simultaneously from 120 ps to 5 mu s with a relative accuracy up to Delta c/c = 10(-6). The in-plane propagation of sound is essential for understanding the delayed out-of-plane compression of Pb(Zr0.2Ti0.8)O-3. Y1 - 2014 U6 - https://doi.org/10.1063/1.4861873 SN - 0003-6951 SN - 1077-3118 VL - 104 IS - 2 PB - American Institute of Physics CY - Melville ER - TY - JOUR A1 - Schick, Daniel A1 - Bojahr, Andre A1 - Herzog, Marc A1 - Shayduk, Roman A1 - von Korff Schmising, Clemens A1 - Bargheer, Matias T1 - Udkm1Dsim-A simulation toolkit for 1D ultrafast dynamics in condensed matter JF - Computer physics communications : an international journal devoted to computational physics and computer programs in physics N2 - The UDKM1DSIM toolbox is a collection of MATLAB (MathWorks Inc.) classes and routines to simulate the structural dynamics and the according X-ray diffraction response in one-dimensional crystalline sample structures upon an arbitrary time-dependent external stimulus, e.g. an ultrashort laser pulse. The toolbox provides the capabilities to define arbitrary layered structures on the atomic level including a rich database of corresponding element-specific physical properties. The excitation of ultrafast dynamics is represented by an N-temperature model which is commonly applied for ultrafast optical excitations. Structural dynamics due to thermal stress are calculated by a linear-chain model of masses and springs. The resulting X-ray diffraction response is computed by dynamical X-ray theory. The UDKM1DSIM toolbox is highly modular and allows for introducing user-defined results at any step in the simulation procedure. Program summary Program title: udkm1Dsim Catalogue identifier: AERH_v1_0 Program summary URL: http://cpc.cs.qub.ac.uk/summaries/AERH_v1_0.html Licensing provisions: BSD No. of lines in distributed program, including test data, etc.: 130221 No. of bytes in distributed program, including test data, etc.: 2746036 Distribution format: tar.gz Programming language: Matlab (MathWorks Inc.). Computer: PC/Workstation. Operating system: Running Matlab installation required (tested on MS Win XP -7, Ubuntu Linux 11.04-13.04). Has the code been vectorized or parallelized?: Parallelization for dynamical XRD computations. Number of processors used: 1-12 for Matlab Parallel Computing Toolbox; 1 - infinity for Matlab Distributed Computing Toolbox External routines: Optional: Matlab Parallel Computing Toolbox, Matlab Distributed Computing Toolbox Required (included in the package): mtimesx Fast Matrix Multiply for Matlab by James Tursa, xml io tools by Jaroslaw Tuszynski, textprogressbar by Paul Proteus Nature of problem: Simulate the lattice dynamics of 1D crystalline sample structures due to an ultrafast excitation including thermal transport and compute the corresponding transient X-ray diffraction pattern. Solution method: Restrictions: The program is restricted to 1D sample structures and is further limited to longitudinal acoustic phonon modes and symmetrical X-ray diffraction geometries. Unusual features: The program is highly modular and allows the inclusion of user-defined inputs at any time of the simulation procedure. Running time: The running time is highly dependent on the number of unit cells in the sample structure and other simulation parameters such as time span or angular grid for X-ray diffraction computations. However, the example files are computed in approx. 1-5 min each on a 8 Core Processor with 16 GB RAM available. KW - Ultrafast dynamics KW - Heat diffusion KW - N-temperature model KW - Coherent phonons KW - Incoherent phonons KW - Thermoelasticity KW - Dynamical X-ray theory Y1 - 2014 U6 - https://doi.org/10.1016/j.cpc.2013.10.009 SN - 0010-4655 SN - 1879-2944 VL - 185 IS - 2 SP - 651 EP - 660 PB - Elsevier CY - Amsterdam ER - TY - JOUR A1 - Cui, Qianling A1 - Yashchenok, Alexey A1 - Zhang, Lu A1 - Li, Lidong A1 - Masic, Admir A1 - Wienskol, Gabriele A1 - Moehwald, Helmuth A1 - Bargheer, Matias T1 - Fabrication of Bifunctional Gold/Gelatin Hybrid Nanocomposites and Their Application JF - ACS applied materials & interfaces N2 - Herein, a facile method is presented to integrate large gold nanoflowers (similar to 80 nm) and small gold nanoparticles (2-4 nm) into a single entity, exhibiting both surface-enhanced Raman scattering (SERS) and catalytic activity. The as-prepared gold nanoflowers were coated by a gelatin layer, in which the gold precursor was adsorbed and in situ reduced into small gold nanoparticles. The thickness of the gelatin shell is controlled to less than 10 nm, ensuring that the small gold nanoparticles are still in a SERS-active range of the inner Au core. Therefore, the reaction catalyzed by these nanocomposites can be monitored in situ using label-free SERS spectroscopy. In addition, these bifunctional nanocomposites are also attractive candidates for application in SERS monitoring of bioreactions because of their excellent biocompatibility. KW - core-shell nanostructure KW - gold KW - hybrid material KW - gelatin KW - nanoparticles KW - surface-enhanced Raman scattering Y1 - 2014 U6 - https://doi.org/10.1021/am5000068 SN - 1944-8244 VL - 6 IS - 3 SP - 1999 EP - 2002 PB - American Chemical Society CY - Washington 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 - JOUR A1 - Schick, Daniel A1 - Herzog, Marc A1 - Wen, Haidan A1 - Chen, Pice A1 - Adamo, Carolina A1 - Gaal, Peter A1 - Schlom, Darrell G. A1 - Evans, Paul G. A1 - Li, Yuelin A1 - Bargheer, Matias T1 - Localized excited charge carriers generate ultrafast inhomogeneous strain in the multiferroic BiFeO3 JF - Physical review letters N2 - We apply ultrafast x-ray diffraction with femtosecond temporal resolution to monitor the lattice dynamics in a thin film of multiferroic BiFeO3 after above-band-gap photoexcitation. The sound-velocity limited evolution of the observed lattice strains indicates a quasi-instantaneous photoinduced stress which decays on a nanosecond time scale. This stress exhibits an inhomogeneous spatial profile evidenced by the broadening of the Bragg peak. These new data require substantial modification of existing models of photogenerated stresses in BiFeO3: the relevant excited charge carriers must remain localized to be consistent with the data. Y1 - 2014 U6 - https://doi.org/10.1103/PhysRevLett.112.097602 SN - 0031-9007 SN - 1079-7114 VL - 112 IS - 9 PB - American Physical Society CY - College Park ER - TY - JOUR A1 - Goldshteyn, Jevgeni A1 - Bojahr, Andre A1 - Gaal, Peter A1 - Schick, Daniel A1 - Bargheer, Matias T1 - Selective preparation and detection of phonon polariton wavepackets by stimulated Raman scattering JF - Physica status solidi : Physica status solidi N2 - Wavevector-selective impulsive excitation of phonon-polaritons by a spectrally broad femtosecond transient grating produces wavepackets propagating in opposite directions. The photons in spectrally narrow probe pulses are scattered from these elementary excitations in lithium niobate (LiNbO3). Both elastically and inelastically scattered photons are simultaneously detected in a spectrometer. The Stokes- and anti-Stokes shifted probe pulses uniquely determine the propagation direction of the detected polariton wavepacket components and correspond to creation or annihilation of phonon-polaritons. Our experiments with spectrally broad pump and spectrally narrow probe pulses allows dissecting the four-wave-mixing process into two sequential stimulated Raman scattering events. Y1 - 2014 U6 - https://doi.org/10.1002/pssb.201350114 SN - 0370-1972 SN - 1521-3951 VL - 251 IS - 4 SP - 821 EP - 828 PB - Wiley-VCH CY - Weinheim ER - TY - JOUR A1 - Cui, Qianling A1 - Shen, Guizhi A1 - Yan, Xuehai A1 - Li, Lidong A1 - Moehwald, Helmuth A1 - Bargheer, Matias T1 - Fabrication of Au@Pt multibranched nanoparticles and their application to in situ SERS monitoring JF - ACS applied materials & interfaces N2 - Here, we present an Au@Pt core-shell multibranched nanoparticle as a new substrate capable of in situ surface-enhanced Raman scattering (SERS), thereby enabling monitoring of the catalytic reaction on the active surface. By careful control of the amount of Pt deposited bimetallic Au@Pt, nanoparticles with moderate performance both for SERS and catalytic activity were obtained. The Pt-catalyzed reduction of 4-nitrothiophenol by borohydride was chosen as the model reaction. The intermediate during the reaction was captured and clearly identified via SERS spectroscopy. We established in situ SERS spectroscopy as a promising and powerful technique to investigate in situ reactions taking place in heterogeneous catalysis. KW - nanoparticles KW - gold KW - core-shell nanostructure KW - surface-enhanced Raman scattering KW - heterogeneous catalysis KW - bimetallic nanoparticles Y1 - 2014 U6 - https://doi.org/10.1021/am504709a SN - 1944-8244 VL - 6 IS - 19 SP - 17075 EP - 17081 PB - American Chemical Society CY - Washington ER - TY - JOUR A1 - Schick, Daniel A1 - Herzog, Marc A1 - Bojahr, Andre A1 - Leitenberger, Wolfram A1 - Hertwig, Andreas A1 - Shayduk, Roman A1 - Bargheer, Matias T1 - Ultrafast lattice response of photoexcited thin films studied by X-ray diffraction JF - Structural dynamics N2 - Using ultrafast X-ray diffraction, we study the coherent picosecond lattice dynamics of photoexcited thin films in the two limiting cases, where the photoinduced stress profile decays on a length scale larger and smaller than the film thickness. We solve a unifying analytical model of the strain propagation for acoustic impedance-matched opaque films on a semi-infinite transparent substrate, showing that the lattice dynamics essentially depend on two parameters: One for the spatial profile and one for the amplitude of the strain. We illustrate the results by comparison with high-quality ultrafast X-ray diffraction data of SrRuO3 films on SrTiO3 substrates. (C) 2014 Author(s). All article content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 Unported License. Y1 - 2014 U6 - https://doi.org/10.1063/1.4901228 SN - 2329-7778 VL - 1 IS - 6 PB - American Institute of Physics CY - Melville ER -