TY - JOUR A1 - Liebig, Ferenc A1 - Henning, Ricky A1 - Sarhan, Radwan Mohamed A1 - Prietzel, Claudia Christina A1 - Bargheer, Matias A1 - Koetz, Joachim T1 - A new route to gold nanoflowers JF - Nanotechnology N2 - Catanionic vesicles spontaneously formed by mixing the anionic surfactant bis(2-ethylhexyl)sulfosuccinate sodium salt with the cationic surfactant cetyltrimethylammonium bromide were used as a reducing medium to produce gold clusters, which are embedded and well-ordered into the template phase. The gold clusters can be used as seeds in the growth process that follows by adding ascorbic acid as a mild reducing component. When the ascorbic acid was added very slowly in an ice bath round-edged gold nanoflowers were produced. When the same experiments were performed at room temperature in the presence of Ag+ ions, sharp-edged nanoflowers could be synthesized. The mechanism of nanoparticle formation can be understood to be a non-diffusion-limited Ostwald ripening process of preordered gold nanoparticles embedded in catanionic vesicle fragments. Surface-enhanced Raman scattering experiments show an excellent enhancement factor of 1.7 . 10(5) for the nanoflowers deposited on a silicon wafer. KW - catanionic vesicles KW - gold cluster KW - gold nanoflowers KW - crystal growth KW - HRTEM KW - SEM Y1 - 2018 U6 - https://doi.org/10.1088/1361-6528/aaaffd SN - 0957-4484 SN - 1361-6528 VL - 29 IS - 18 PB - IOP Publ. Ltd. CY - Bristol ER - TY - JOUR A1 - Liebig, Ferenc A1 - Henning, Ricky A1 - Sarhan, Radwan Mohamed A1 - Prietzel, Claudia Christina A1 - Schmitt, Clemens Nikolaus Zeno A1 - Bargheer, Matias A1 - Koetz, Joachim T1 - A simple one-step procedure to synthesise gold nanostars in concentrated aqueous surfactant solutions JF - RSC Advances N2 - Due to the enhanced electromagnetic field at the tips of metal nanoparticles, the spiked structure of gold nanostars (AuNSs) is promising for surface-enhanced Raman scattering (SERS). Therefore, the challenge is the synthesis of well designed particles with sharp tips. The influence of different surfactants, i.e., dioctyl sodium sulfosuccinate (AOT), sodium dodecyl sulfate (SDS), and benzylhexadecyldimethylammonium chloride (BDAC), as well as the combination of surfactant mixtures on the formation of nanostars in the presence of Ag⁺ ions and ascorbic acid was investigated. By varying the amount of BDAC in mixed micelles the core/spike-shell morphology of the resulting AuNSs can be tuned from small cores to large ones with sharp and large spikes. The concomitant red-shift in the absorption toward the NIR region without losing the SERS enhancement enables their use for biological applications and for time-resolved spectroscopic studies of chemical reactions, which require a permanent supply with a fresh and homogeneous solution. HRTEM micrographs and energy-dispersive X-ray (EDX) experiments allow us to verify the mechanism of nanostar formation according to the silver underpotential deposition on the spike surface in combination with micelle adsorption. KW - optical-properties KW - nanoparticles KW - sers KW - ultrafast KW - size KW - nanotriangles KW - nanoflowers KW - wavelength Y1 - 2019 U6 - https://doi.org/10.1039/C9RA02384D SN - 2046-2069 VL - 9 SP - 23633 EP - 23641 PB - RSC Publishing CY - London ER - TY - JOUR A1 - Mattern, Maximilian A1 - Pudell, Jan-Etienne A1 - Laskin, Gennadii A1 - Reppert, Alexander von A1 - Bargheer, Matias T1 - Analysis of the temperature- and fluence-dependent magnetic stress in laser-excited SrRuO3 JF - Structural dynamics 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. 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 - 2020 U6 - https://doi.org/10.1063/4.0000072 SN - 2329-7778 VL - 8 IS - 2 PB - AIP Publishing LLC CY - Melville, NY 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 - Pavlenko, Elena S. A1 - Sander, Mathias A1 - Mitzscherling, S. A1 - Pudell, Jan-Etienne A1 - Zamponi, Flavio A1 - Roessle, M. A1 - Bojahr, Andre A1 - Bargheer, Matias T1 - Azobenzene - functionalized polyelectrolyte nanolayers as ultrafast optoacoustic transducers JF - Nanoscale N2 - We introduce azobenzene-functionalized polyelectrolyte multilayers as efficient, inexpensive optoacoustic transducers for hyper-sound strain waves in the GHz range. By picosecond transient reflectivity measurements we study the creation of nanoscale strain waves, their reflection from interfaces, damping by scattering from nanoparticles and propagation in soft and hard adjacent materials like polymer layers, quartz and mica. The amplitude of the generated strain epsilon similar to 5 x 10(-4) is calibrated by ultrafast X-ray diffraction. Y1 - 2016 U6 - https://doi.org/10.1039/c6nr01448h SN - 2040-3364 SN - 2040-3372 VL - 8 SP - 13297 EP - 13302 PB - Royal Society of Chemistry CY - Cambridge ER - 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 - Kiel, Mareike A1 - Möhwald, Helmuth A1 - Bargheer, Matias T1 - Broadband measurements of the transient optical complex dielectric function of a nanoparticle/polymer composite upon ultrafast excitation JF - Physical review : B, Condensed matter and materials physics N2 - We determined experimentally the complex transient optical dielectric function of a well-characterized polyelectrolyte/gold-nanoparticle composite system over a broad spectral range upon short pulse laser excitation by simultaneously measuring the time-dependent reflectance and transmittance of white light pulses with femtosecond pump-probe spectroscopy. We extracted directly the ultrafast changes in the real and imaginary parts of the effective dielectric function, epsilon(eff)(r) (omega,t)and epsilon(eff)(i) (omega,t), from the experiment. This complete experimental set of information on the time-dependent complex dielectric function challenges theories modeling the transient dielectric function of gold particles and the effective medium. Y1 - 2011 U6 - https://doi.org/10.1103/PhysRevB.84.165121 SN - 1098-0121 VL - 84 IS - 16 PB - American Physical Society CY - College Park 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 - 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 - 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 - 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 - Deb, Marwan A1 - Popova, Elena A1 - Jaffrès, Henri-Yves A1 - Keller, Niels A1 - Bargheer, Matias T1 - Controlling high-frequency spin-wave dynamics using double-pulse laser excitation JF - Physical review applied N2 - Manipulating spin waves is highly required for the development of innovative data transport and processing technologies. Recently, the possibility of triggering high-frequency standing spin waves in magnetic insulators using femtosecond laser pulses was discovered, raising the question about how one can manipulate their dynamics. Here we explore this question by investigating the ultrafast magnetiza-tion and spin-wave dynamics induced by double-pulse laser excitation. We demonstrate a suppression or enhancement of the amplitudes of the standing spin waves by precisely tuning the time delay between the two pulses. The results can be understood as the constructive or destructive interference of the spin waves induced by the first and second laser pulses. Our findings open exciting perspectives towards generating single-mode standing spin waves that combine high frequency with large amplitude and low magnetic damping. Y1 - 2022 U6 - https://doi.org/10.1103/PhysRevApplied.18.044001 SN - 2331-7019 VL - 18 IS - 4 PB - American Physical Society CY - College Park ER - TY - JOUR A1 - Maerten, Lena A1 - Bojahr, Andre A1 - Gohlke, Mathias A1 - Rössle, Matthias A1 - Bargheer, Matias T1 - Coupling of GHz Phonons to Ferroelastic Domain Walls in SrTiO3 JF - Physical review letters N2 - We study the linear and nonlinear acoustic response of SrTiO3 across its ferroelastic transition at T-a = 105 K by time domain Brillouin scattering. Above T-a we observe that for a strain amplitude of similar to 0.18% the sound velocity for compressive strain exceeds the tensile strain velocity by 3%. Below T-a we find a giant slowing down of the sound velocity by 12% and attribute this to the coupling of GHz phonons to ferroelastic twin domain walls. We propose a new mechanism for this coupling on the ultrafast time scale, providing an important new test ground for theories used to simulate atomic motion in domain forming crystals. Y1 - 2015 U6 - https://doi.org/10.1103/PhysRevLett.114.047401 SN - 0031-9007 SN - 1079-7114 VL - 114 IS - 4 PB - American Physical Society CY - College Park ER - TY - JOUR A1 - Deb, Marwan A1 - Popova, Elena A1 - Hehn, Michel A1 - Keller, Niels A1 - Petit-Watelot, Sebastien A1 - Bargheer, Matias A1 - Mangin, Stephane A1 - Malinowski, Gregory T1 - Damping of Standing Spin Waves in Bismuth-Substituted Yttrium Iron Garnet as Seen via the Time-Resolved Magneto-Optical Kerr Effect JF - Physical review applied N2 - We investigate spin-wave resonance modes and their damping in insulating thin films of bismuth-substituted yttrium iron garnet by performing femtosecond magneto-optical pump-probe experiments. For large magnetic fields in the range below the magnetization saturation, we find that the damping of high-order standing spin-wave (SSW) modes is about 40 times lower than that for the fundamental one. The observed phenomenon can be explained by considering different features of magnetic anisotropy and exchange fields that, respectively, define the precession frequency for fundamental and high-order SSWs. These results provide further insight into SSWs in iron garnets and may be exploited in many new photomagnonic devices. Y1 - 2019 U6 - https://doi.org/10.1103/PhysRevApplied.12.044006 SN - 2331-7019 VL - 12 IS - 4 PB - American Physical Society CY - College Park ER - TY - JOUR A1 - Liebig, Ferenc A1 - Sarhan, Radwan Mohamed A1 - Sander, Mathias A1 - Koopman, Wouter-Willem Adriaan A1 - Schuetz, Roman A1 - Bargheer, Matias A1 - Koetz, Joachim T1 - Deposition of Gold Nanotriangles in Large Scale Close-Packed Monolayers for X-ray-Based Temperature Calibration and SERS Monitoring of Plasmon-Driven Catalytic Reactions JF - ACS applied materials & interfaces KW - gold nanotriangles KW - monolayer formation KW - SERS KW - dimerization KW - heat measurement Y1 - 2017 U6 - https://doi.org/10.1021/acsami.7b07231 SN - 1944-8244 VL - 9 SP - 20247 EP - 20253 PB - American Chemical Society CY - Washington 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 - Mitzscherling, Steffen A1 - Cui, Q. A1 - Koopman, Wouter-Willem Adriaan A1 - Bargheer, Matias T1 - Dielectric function of two-phase colloid-polymer nanocomposite JF - Physical chemistry, chemical physics : a journal of European Chemical Societies N2 - The plasmon resonance of metal nanoparticles determines their optical response in the visible spectral range. Many details such as the electronic properties of gold near the particle surface and the local environment of the particles influence the spectra. We show how the cheap but highly precise fabrication of composite nanolayers by spin-assisted layer-by-layer deposition of polyelectrolytes can be used to investigate the spectral response of gold nanospheres (GNS) and gold nanorods (GNR) in a self-consistent way, using the established Maxwell-Garnett effective medium (MGEM) theory beyond the limit of homogeneous media. We show that the dielectric function of gold nanoparticles differs from the bulk value and experimentally characterize the shape and the surrounding of the particles thoroughly by SEM, AFM and ellipsometry. Averaging the dielectric functions of the layered surrounding by an appropriate weighting with the electric field intensity yields excellent agreement for the spectra of several nanoparticles and nanorods with various cover-layer thicknesses. Y1 - 2015 U6 - https://doi.org/10.1039/c5cp04326c SN - 1463-9076 SN - 1463-9084 VL - 17 IS - 44 SP - 29465 EP - 29474 PB - Royal Society of Chemistry CY - Cambridge ER - TY - JOUR A1 - Shayduk, Roman A1 - Herzog, Marc A1 - Bojahr, Andre A1 - Schick, Daniel A1 - Gaal, Peter A1 - Leitenberger, Wolfram A1 - Navirian, Hengameh A1 - Sander, Mathias A1 - Goldshteyn, Jevgenij A1 - Vrejoiu, Ionela A1 - Bargheer, Matias T1 - Direct time-domain sampling of subterahertz coherent acoustic phonon spectra in SrTiO3 using ultrafast x-ray diffraction JF - Physical review : B, Condensed matter and materials physics N2 - We synthesize sub-THz longitudinal quasimonochromatic acoustic phonons in a SrTiO3 single crystal using a SrRuO3/SrTiO3 superlattice as an optical-acoustic transducer. The generated acoustic phonon spectrum is determined using ultrafast x-ray diffraction. The analysis of the generated phonon spectrum in the time domain reveals a k-vector dependent phonon lifetime. It is observed that even at sub-THz frequencies the phonon lifetime agrees with the 1/omega(2) power law known from Akhiezer's model for hyper sound attenuation. The observed shift of the synthesized spectrum to the higher q is discussed in the framework of nonlinear effects appearing due to the high amplitude of the synthesized phonons. Y1 - 2013 U6 - https://doi.org/10.1103/PhysRevB.87.184301 SN - 1098-0121 VL - 87 IS - 18 PB - American Physical Society CY - College Park ER - TY - JOUR A1 - El-Nagar, Gumaa A. A1 - Sarhan, Radwan Mohamed A1 - Abouserie, Ahed A1 - Maticiuc, Natalia A1 - Bargheer, Matias A1 - Lauermann, Iver A1 - Roth, Christina T1 - Efficient 3D-Silver Flower-like Microstructures for Non-Enzymatic Hydrogen Peroxide (H2O2) Amperometric Detection JF - Scientific reports Y1 - 2017 U6 - https://doi.org/10.1038/s41598-017-11965-9 SN - 2045-2322 VL - 7 PB - Nature Publ. Group CY - London 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 -