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Marco Cammarata

Publications and source records attributed to Marco Cammarata.

7 recordsLinked to original sources

Break-down of the relationship between {\alpha}-relaxation and equilibration in hydrostatically compressed metallic glasses

Glasses encode the memory of any thermo-mechanical treatment applied to them. This ability is associated to the existence of a myriad of metastable amorphous states which can be probed through different experimental pathways. It is usually assumed that this memory can be erased in the supercooled liquid, and that this process occurs on a time scale controlled by the {\alpha}-relaxation. We find that this assumption does not apply for hydrostatically compressed glasses. Annealing under pressure a prototypical metallic glass can irreversibly modify its dynamics, thermodynamics and structure, reduce the atomic mobility and lead to structural modifications of the first coordination shells which reduce the thermal stability with respect to a glass annealed in absence of pressure. When heated above their glass transition temperature, these compressed glasses do not convert into the pristine supercooled liquid, implying the existence of an additional process, beyond the {\alpha}-relaxation, contributing to the equilibrium recovery of the material. These results establish pressure as a powerful tool for engineering non-equilibrium glassy materials with tailored properties, while deepening our understanding of relaxation dynamics in disordered systems under extreme conditions.

cond-mat.mtrl-sci

High-pressure X-ray photon correlation spectroscopy at fourth-generation synchrotron sources

A new experimental setup combining X-Ray Photon Correlation Spectroscopy (XPCS) in the hard x-ray regime and a high-pressure sample environment is developed to monitor the pressure dependence of the internal motion of complex systems down to the atomic scale in the multi-gigapascal range, from room temperature to 600K. The high flux of coherent high energy x-rays at 4th generation synchrotron source solves the problems caused by the absorption of the Diamond Anvil Cells used to generate the high pressure, enabling the measurement of the intermediate scattering function over 6 orders of magnitude in time, from $10^{-3}$ s to $10^{3}$s. The constraints posed by the high-pressure generation such as the preservation of X-ray coherence, as well as the sample, pressure and temperature stability, are discussed, and the feasibility of high-pressure XPCS is demonstrated through results obtained on metallic glasses.

physics.app-ph

Beam focus modifications by cropping partially coherent X-ray beams

We simulate the focusing of a partially-coherent X-ray beam emitted by an undulator in a fourth-generation storage ring performing coherent mode decomposition and wave optics propagation. The focus position is shifted, and its size is enlarged when an entrance slit crops the beam. This is the usual case when a slit is used to select the coherent fraction. The pairing of two focusing elements (mirrors, lenses or transfocators) to ensure a fixed focal position is also analyzed. Our results show that the image of a partially coherent source, such an undulator in a low-emittance storage ring, is a non-trivial function of the aperture used to control the coherence fraction.

physics.optics

Tilting refractive x-ray lenses for fine-tuning their focal length

In this work, we measure and model tilted x-ray refractive lenses to investigate their effects on an x-ray beam. The modelling is benchmarked against at-wavelength metrology obtained with x-ray speckle vector tracking experiments (XSVT) at the BM05 beamline at the ESRF-EBS light source, showing very good agreement. This validation permits us to explore possible applications of tilted x-ray lenses in optical design: we demonstrate that tilting 1D lenses around their focusing direction can be used for fine-tuning their focal length with possible applications in beamline optical design.

physics.optics

A fast and light tool for partially-coherent beamline simulations in fourth generation storage rings based on coherent mode decomposition

A new algorithm to perform coherent mode decomposition of the undulator radiation is proposed. It is based in separating the horizontal and vertical directions, reducing the problem by working with one-dimension wavefronts. The validity conditions of this approximation are discussed. Simulations require low computer resources, and run interactively in a laptop. We study the focusing with lenses of the radiation emitted by an undulator in a fourth-generation storage ring (EBS-ESRF). Results are compared against multiple optics packages implementing a variety of methods for dealing with partial coherence: full 2D coherent mode decomposition, Monte-Carlo combination of wavefronts from electrons entering the undulator with different initial conditions, and hybrid ray-tracing correcting geometrical optics with wave optics.

physics.acc-ph

Lattice phonon modes of the spin crossover crystal [Fe(phen)2(NCS)2] studied by THz, IR, Raman spectroscopies and DFT calculations

[Fe(phen)2(NCS)2] is a prototype transition metal complex material, which undergoes a phase transition between low-spin (LS) and high-spin (HS) phases, induced by temperature, pressure or light. Vibrational modes play a key role for spin-state switching both in thermal and photo-induced cases, by contributing to vibrational entropy for thermal equilibrium transitions or driving the fast structural trapping of the photoinduced high spin state. Here we study the crystal phonon modes of [Fe(phen)2(NCS)2], by combining THz, IR, and Raman spectroscopies sensitive to modes in different frequency ranges and different symmetries. We compare the experimental results to DFT calculations performed in a periodic 3D crystal for understanding the phonon modes in the crystal, compared to molecular vibrations. Indeed, each vibrational mode of the isolated molecule combines into several modes of different symmetry and frequency in the crystal, as the unit cell contains four molecules. We focus our attention on the HS symmetric and anti-symmetric breathing modes in the crystal as well as on the N-CS stretching modes.

cond-mat.mtrl-sci

Watching coherent molecular structural dynamics during photoreaction: beyond kinetic description

A deep understanding of molecular photo-transformations is challenging because of the complex interaction between the configurations of electrons and nuclei. An initial optical excitation dissipates energy into electronic and structural degrees of freedom, often in less than one trillionth (10^-12) of a second. Molecular dynamics induced by photoexcitation have been very successfully studied with femtosecond optical spectroscopies, but electronic and nuclear dynamics are often very difficult to disentangle. X-ray based spectroscopies can reduce the ambiguity between theoretical models and experimental data, but it is only with the recent development of bright ultrafast X-ray sources, that key information during transient molecular processes can be obtained on their intrinsic timescale. In this letter, Free Electron Laser (FEL) radiation is used to measure ultrafast changes in the X-ray Absorption Near Edge Structure (XANES) during the prototypical photoreaction of a spin crossover compound. We reveal its transformation from the ligand-located electronic photoexcitation to the structural trapping of the high spin state. The results require a description beyond a kinetic model and provide a direct observation of a dynamic breathing of the main structural change. The coherent structural oscillations (period of ~265 fs) in the photoproduct potential lose synchrony within ~330 fs, whereas incoherent motions reveal the energy redistribution and vibrational cooling within ~1.6 ps. We foresee that ultrafast X-ray spectroscopies will provide invaluable insight to understand the complex physics of fundamental light induced phenomena, which are of prime interest in a multitude of chemical, physical and biological processes.

physics.chem-ph