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Giacomo Baldi

Publications and source records attributed to Giacomo Baldi.

4 recordsLinked to original sources

X-ray photo-induced atomic motion in Phase Change Materials and conventional covalent chalcogenide glasses

X-ray Photon Correlation Spectroscopy (XPCS) enables direct access to atomic-scale dynamics in disordered materials, revealing both spontaneous and X-ray-induced relaxation processes. Here, we study two compositionally similar alloy glasses near their glass transition temperatures: the phase change material (PCM) Ge15Sb85 and the non-PCM alloy Ge15Te85. Both exhibit X-ray induced atomic motion, yet with markedly different responses. Ge15Sb85 undergoes an immediate transition to a photo-induced yielding state, characterised by stationary dynamics governed solely by the absorbed dose. In contrast, Ge15Te85 shows a progressive slowing-down of the relaxation process, accompanied by a crossover from compressed to stretched exponential decay in the density autocorrelation functions. This behaviour is consistent with the emergence of liquid-like collective motion as supported by de Gennes narrowing in the wave-vector dependence of the dynamics at length scales comparable with the first sharp diffraction peak. Unlike Ge15Sb85, this alloy does not reach a stationary regime within experimental timescales, implying that the yielding transition occurs only after thousands of seconds with the available dose rate. Its response is also temperature dependent: at lower temperatures, the dynamics reflects intrinsic stress relaxation processes, whereas at higher temperatures becomes dose-controlled. These findings demonstrate that the dynamical response to X-ray excitation is not determined solely by chemical composition or bonding character, but results from the interplay between irradiation effects and structural relaxation pathways.

cond-mat.mtrl-sci

Boson peak in covalent network glasses: Isostaticity and marginal stability

The boson peak (BP) stands as a key feature in understanding glasses and amorphous materials. It directly underlies their anomalous material properties, including thermal behaviors such as excess specific heat and low thermal conductivity, as well as mechanical characteristics such as nonaffine elasticity and fragile plasticity. Despite its importance, understanding of the BP remains limited in covalent network glasses. The most promising concepts are isostaticity and marginal stability, which have been established in theories of rigidity percolation and the jamming transition. While these concepts, supported by comprehensive data, account for the BP in packing-based glasses, comparable explanations have not yet been demonstrated for covalent network glasses. Here we study silica glass, a prototypical covalent network glass, using molecular dynamics simulations. We show that the BP in silica glass is governed by near-isostatic constraints and marginal stability, supporting their universality across diverse glassy systems. Furthermore, we reveal that these principles manifest as a wavenumber-independent band in the dynamical structure factor, and we demonstrate consistency with inelastic X-ray scattering data on silica glass. Our results provide a unified, experimentally testable framework for deciphering the BP and for refining the interpretation of scattering data in amorphous materials.

cond-mat.dis-nn

Vibrational dynamics of non-crystalline solids

The boson peak (BP) is an excess of vibrational states over the Debye law appearing at terahertz frequencies. It is found in all glasses and marks the crossover between the long-wavelength behavior, where the solid can be considered as an isotropic continuum, and the region where the wavelength of the sound wave starts to experience the microscopic details of the structure. This chapter is devoted to a review of the main experimental observations regarding the vibrational dynamics of amorphous solids, as detected by neutron and X-ray scattering techniques. A first part of the chapter is devoted to the measurements of the BP and its evolution as a function of external parameters, such as temperature, pressure, or density. The second part of the chapter reviews the wavevector evolution of the dynamic structure factor, which provides evidence of a pseudo-acoustic propagating mode up to frequencies comparable to those of the BP. This longitudinal mode has a sound attenuation which follows the Rayleigh scattering law and a negative dispersion that can partially explain the deviation from the Debye law. At higher frequencies, the inelastic spectrum presents a complex pattern of vibrations, with evidences of two peaks in various systems. To conclude, we will highlight the information that can be gained on the nature of the glass vibrational modes from a comparison with the dynamics of the corresponding polycrystal.

cond-mat.dis-nn

Relaxation dynamics induced in glasses by the absorption of hard X-ray photons

X-ray photon correlation is used to probe the slow dynamics of the glass-former B2O3 across the glass transition. In the undercooled liquid phase the decay times of the measured correlation functions are consistent with visible light scattering results and independent of the incoming flux; in the glass they are instead temperature independent and show a definite dependence on the X-ray flux. This dependence can be exploited to obtain information on the volume occupied by the atoms that move in the glass following an absorption event. The length scale derived in this way, of the order of the nanometer, is consistent with that reported for the dynamical heterogeneities, suggesting the existence of a new scheme to get access to this fundamental quantity.

cond-mat.dis-nn