Spectroscopic characterization of ultrashort laser driven targets incorporating both Boltzmann and particle-in-cell models

M. Sherrill, J. Abdallah, G. Csanak, E. Dodd, Y. Fukuda, Y. Akahane, M. Aoyama, N. Inoue, H. Ueda, K. Yamakawa, A. Faenov, A. Magunov, T. Pikuz, I. Skobelev
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引用次数: 1

Abstract

A model that solves simultaneously both the electron and atomic kinetics was used to generate synthetic X-ray spectra to characterize high intensity ultrashort-laser-driven target experiments. A particle-in-cell simulation was used to model the laser interaction for both cluster and foil targets and provided the initial electron energy distribution function (EEDF) for a Boltzmann solver. Previously reported success in the spectroscopic characterization of an irradiated Ar cluster target has motivated the authors to apply this technique in a feasibility study to assess the possibility of recording time resolved spectra of a 10 micron Ti foil target irradiated by a 500 fs, I= 1.0 × 1018W/cm2 short-pulse laser. Though this model suggests that both Ar cluster and Ti foil plasmas are held in a highly non-equilibrium state for both the EEDF and the ion level populations for several picoseconds, the spectral line features of the foil experiment was shown to evolve too quickly to be seen by current ultrafast time resolved spectrometers.
结合玻尔兹曼和细胞内粒子模型的超短激光驱动目标的光谱表征
利用一个同时解决电子动力学和原子动力学的模型来生成合成x射线光谱,以表征高强度超短激光驱动的靶实验。采用粒子池模拟方法对簇靶和箔靶的激光相互作用进行了模拟,并给出了玻尔兹曼解算器的初始电子能量分布函数。先前报道的辐照Ar簇目标光谱表征的成功,促使作者将该技术应用于可行性研究,以评估在500 fs, I= 1.0 × 1018W/cm2短脉冲激光照射下记录10微米Ti箔目标时间分辨光谱的可能性。虽然该模型表明Ar团簇和Ti箔等离子体在几皮秒内都处于高度非平衡状态,但箔实验的谱线特征演变得太快,目前的超快时间分辨光谱仪无法观察到。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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