Résumé
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.