Tracking primary radiation-induced processes in matter requires ultrafast sources and high precision timing. While compact laser-driven ion accelerators are seeding the development of novel high instantaneous flux applications, combining the ultrashort ion and laser pulse durations with their inherent synchronicity to trace the real-time evolution of initial damage events has yet to be realized. Here we report on the absolute measurement of proton bursts as short as 3.5±0.7 ps from laser solid target interactions for this purpose. Our results verify that laser-driven ion acceleration can deliver interaction times over a factor of hundred shorter than those of state-of-the-art accelerators optimized for high instantaneous flux. Furthermore, these observations draw ion interaction physics into the field of ultrafast science, opening the opportunity for quantitative comparison with both numerical modelling and the adjacent fields of ultrafast electron and photon interactions in matter.
Here we show that the determining factor for physical radiation enhancement effects for a clinically realistic cluster of heavy-atom bearing nanoparticles is the total number of heavy atoms packed into the cluster. We do this through a multiscale Monte Carlo approach which permits the consideration of radiation transport through clusters of millions of nanoparticles. The finding is in contrast to that predicted when isolated nanoparticles are considered and is a direct consequence of the Auger electrons playing less of a role for clusters compared to isolate nanoparticles. We further show that this result is agnostic to selection of the subcellular region considered to be sensitive to the effects of radiation, provided the inside the cluster of nanoparticles is not considered to be biologically active.
Recently, measurements of few-picosecond (ps, 10−12 s) pulses of laser-driven protons were realised by the observation of transient opacity in SiO2. This ultrafast response could be understood by the formation of self-trapped excitonic states in the material, creating a rapid de-excitation channel for conduction band electrons. Here we extend this work to examine the onset and evolution of an ion-induced opacity in transparent dielectrics, namely multicomponent variants of SiO2. The fast recovery observed in SiO2 is in sharp contrast to borosilicate (BK7) and soda-lime glasses. We find that the opacity decay timescales for BK7 and soda-lime glass are orders of magnitude greater than the 3.5 ps proton pump pulse duration and discuss the underlying processes which may be affecting the extended recovery of the material. Simultaneous probing with 2nd harmonic radiation allows estimates of ultrafast electron dynamics due to proton interactions in matter to be investigated, this indicates that a rapid evolution of an initially unstructured ion-induced dose distribution seeds the longer term recovery pathways in the irradiated dielectrics. When combined, these results demonstrate the efficacy of utilising ultrafast laser-driven ionising radiation along with highly synchronised probe pulses to enable the study of ion-induced damage in matter on ultrafast timescales in real time.
Vector soliton propagation in circularly birefringent fibers was studied by perturbation analysis and numerically. The results show that in presence of both Raman self-frequency shift and group velocity difference between circularly polarized components the Raman cross-polarization term causes an energy transfer from the slower to the faster circular component of vector solitons. This effect leads to polarization stabilization of circularly polarized vector solitons.
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