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This paper reports on the absolute response of a Fuji BAS-TR image plate to relatively low energy protons (< 0.2 MeV) and carbon ions (< 1 MeV) accelerated by a 10-TW-class compact high-intensity laser system. A Thomson parabola spectrometer was used to discriminate between different ion species while dispersing the ions according to their kinetic energy. Ion parabolic traces were recorded by an image plate detector overlaid with a slotted CR-39 solid-state detector. The obtained response function for the protons was reasonably extrapolated from previously reported higher-ion-energy response functions. Conversely, the obtained response function for carbon ions was one order of magnitude higher than the value extrapolated from previously reported higher-ion-energy response functions. In a previous study, it was determined that if the stopping range of carbon ions is comparable to or smaller than the grain size of the phosphor, then some ions will provide all their energy to the binder resin rather than the phosphor. As a result, it is believed that the imaging plate (IP) response will be reduced. Our results show good agreement with the empirical formula of Lelasseux et al., which does not consider photo-stimulated luminescence (PSL) reduction due to the urethane resin. It was shown that the PSL reduction due to the deactivation of the urethane resin is smaller than previously predicted., source:https://aip.scitation.org/doi/10.1063/5.0035618

This paper reports on the absolute response of a Fuji BAS-TR image plate to relatively low energy protons (< 0.2 MeV) and carbon ions (< 1 MeV) accelerated by a 10-TW-class compact high-intensity laser system. A Thomson parabola spectrometer was used to discriminate between different ion species while dispersing the ions according to their kinetic energy. Ion parabolic traces were recorded by an image plate detector overlaid with a slotted CR-39 solid-state detector. The obtained response function for the protons was reasonably extrapolated from previously reported higher-ion-energy response functions. Conversely, the obtained response function for carbon ions was one order of magnitude higher than the value extrapolated from previously reported higher-ion-energy response functions. In a previous study, it was determined that if the stopping range of carbon ions is comparable to or smaller than the grain size of the phosphor, then some ions will provide all their energy to the binder resin rather than the phosphor. As a result, it is believed that the imaging plate (IP) response will be reduced. Our results show good agreement with the empirical formula of Lelasseux et al., which does not consider photo-stimulated luminescence (PSL) reduction due to the urethane resin. It was shown that the PSL reduction due to the deactivation of the urethane resin is smaller than previously predicted.

We developed an optically synchronized highly stable frequency-doubled Nd:YAG laser with sub-nanosecond pulse duration. The 1064 nm seed pulses generated by soliton self-frequency shift in a photonic crystal fiber from Ti:sapphire oscillator pulses were stabilized by controlling input pulse polarization. The seed pulses were amplified to 200 mJ by diode-pumped amplifiers with a high stability of only <0.2% (rms). With an external LBO doubler, the system generated 330 ps green pulse energy of 130 mJ at 532 nm with a conversion efficiency of 65%. The pulse duration was further extended to 490 ps by adjusting Nd:YAG crystal temperature. To the best of our knowledge, these results present a longer pulse duration with higher stability than previous Nd:YAG lasers with sub-nanosecond optical synchronization.