首页> 外文会议>Conference on optical trapping and optical micromanipulation XIV >Photoionization of water molecules by a train of attosecond pulses assisted by a near-infrared laser: delay and polarization control
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Photoionization of water molecules by a train of attosecond pulses assisted by a near-infrared laser: delay and polarization control

机译:通过近红外激光器辅助的Attosecond脉冲火车的水分子光离子:延迟和极化控制

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Basic reactions involving water molecules are essential to understand the interaction between radiation and the biological tissue because living cells are composed mostly by water. Therefore, the knowledge of ionization of the latter is crucial in many domains of Biology and Physics. So, we study theoretically the photoionization of water molecules by extreme ultraviolet attopulse trains assisted by lasers in the near-infrared range. We use a separable Coulomb-Volkov model in which the temporal evolution of the system can be divided into three stages allowing spatial and temporal separation for the Coulomb and Volkov final state wavefunctions. First, we analyze photoelectron angular distributions for different delays between the attopulse train and the assistant laser field. We compare our results for water and Ne atoms as they belong to the same isoelectronic series. Moreover, we contrast our calculations with previous theoretical and experimental work for Ar atoms due to the similarities of the orbitals involved in the reaction. Second, we study the effect of varying the relative orientations of the attopulse and laser field polarizations and we compare our predictions with other theories and experiments. We expect these studies contribute to the improvement of polarization experiments and the development of the attopulse trains and assistant laser fields technologies. Finally, we hope our work promote progress on the control of the chemical reactivity of water molecules since this could be useful in different fields such as radiobiology and medical physics.
机译:涉及水分子基本反应是必须理解辐射与生物组织,因为活细胞被水主要由之间的相互作用。因此,后者的电离的知识是在生物和物理的许多领域是至关重要的。因此,我们通过在近红外范围内的激光器辅​​助极紫外attopulse列车理论上研究水分子的光电离。我们用一个可分离的库仑 - 沃尔科夫模式,即系统的时间演变可分为三个阶段,允许库仑和沃尔科夫最终状态的波函数的空间和时间间隔。首先,我们分析光电子的attopulse火车和助手激光场之间不同的延迟角分布。我们比较我们对水和氖原子结果,因为它们属于同一系列等电子。此外,我们对比我们与氩原子前人的理论和实验工作的计算由于参与反应的轨道的相似性。其次,我们研究改变attopulse和激光场极化的相对取向的影响,我们比较我们的预测与其他理论和实验。我们希望这些研究有助于偏振实验的改进和attopulse火车和助理激光领域的技术发展。最后,我们希望我们的工作促进水分子的化学反应的控制进度,因为这可能是在不同的领域,如放射生物学和医学物理学是有用的。

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