Nowadays powerful X-ray sources like synchrotrons and free-electron lasers are considered as ultimate tools for probing microscopic properties in materials. However, the correct interpretation of such experiments requires a good understanding on how the beam affects the properties of the sample, knowledge that is currently lacking for intense X-rays. Here we use X-ray photon correlation spectroscopy to probe static and dynamic properties of oxide and metallic glasses. We find that although the structure does not depend on the flux, strong fluxes do induce a non-trivial microscopic motion in oxide glasses, whereas no such dependence is found for metallic glasses. These results show that high fluxes can alter dynamical properties in hard materials, an effect that needs to be considered in the analysis of X-ray data but which also gives novel possibilities to study materials properties since the beam can not only be used to probe the dynamics but also to pump it.

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 Xray 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.

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Hard x rays induce atomic dynamics in oxide glasses at doses low enough that the average structure is unchanged. X-ray photon correlation spectroscopy is used here to study this effect in a series of alkali borate glasses characterized by different network connectivity. The product of the x-ray dose rate per atom and the decay time of the density correlation function is a sample-dependent parameter with the dimensions of an energy: It varies between a fraction of eV and few tens of eV and is sensitive to the network connectivity of the glass. It can then be used to access some bonding information also in cases where the x rays perturb the material, a regime of great interest in modern x-ray-based experiments.