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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Orientation and Alignment dynamics of polar molecule driven by shaped laser pulses
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Orientation and Alignment dynamics of polar molecule driven by shaped laser pulses

机译:由成形激光脉冲驱动的极性分子的定向和对准动态

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摘要

We review the theoretical status of intense laser induced orientation and alignment-a field of study which lies at the interface of intense laser physics and chemical dynamics and having potential applications such as high harmonic generation, nano-scale processing and control of chemical reactions. The evolution of the rotational wave packet and its dynamics leading to orientation and alignment is the topic of the present discussion. The major part of this article primarily presents an overview of recent theoretical progress in controlling the orientation and alignment dynamics of a molecule by means of shaped laser pulses. The various theoretical approaches that lead to orientation and alignment such as static electrostatic field in combination with laser field(s), combination of orienting and aligning field, combination of aligning fields, combination of orienting fields, application of train of pulses etc. are discussed. It is observed that the train of pulses is quite an efficient tool for increasing the orientation or alignment of a molecule without causing the molecule to ionize. The orientation and alignment both can occur in adiabatic and non-adiabatic conditions with the rotational period of the molecule taken under consideration. The discussion is mostly limited to non-adiabatic rotational excitation (NAREX) i.e. cases in which the pulse duration is shorter than the rotational period of the molecule. We have emphasised on the so called half-cycle pulse (HCP) and square pulse (SQP). The effect of ramped pulses and of collision on the various laser parameters is also studied. We summarize the current discussion by presenting a consistent theoretical approach for describing the action of such pulses on movement of molecules. The impact of a particular pulse shape on the post-pulse dynamics is also calculated and analysed. In addition to this, the roles played by various laser parameters including the laser frequency, the pulse duration and the system temperature etc. are illustrated and discussed. The concept of alignment is extended from one-dimensional alignment to three-dimensional alignment with the proper choice of molecule and the polarised light. We conclude the article by discussing the potential applications of intense laser orientation and alignment.
机译:本文综述了强激光诱导取向和对准的理论研究现状,该领域位于强激光物理和化学动力学的界面,在高次谐波产生、纳米尺度处理和化学反应控制等方面具有潜在的应用。旋转波包的演化及其导致定向和对准的动力学是本讨论的主题。本文的主要部分主要介绍了利用整形激光脉冲控制分子取向和取向动力学的最新理论进展。讨论了导致定向和对准的各种理论方法,如静电场与激光场的组合、定向和对准场的组合、对准场的组合、定向场的组合、脉冲序列的应用等。据观察,脉冲序列是在不引起分子电离的情况下增加分子取向或排列的有效工具。考虑到分子的旋转周期,取向和排列都可以在绝热和非绝热条件下发生。讨论主要局限于非绝热旋转激发(NAREX),即脉冲持续时间短于分子旋转周期的情况。我们强调了所谓的半周期脉冲(HCP)和方脉冲(SQP)。还研究了倾斜脉冲和碰撞对各种激光参数的影响。我们总结了当前的讨论,提出了一个一致的理论方法来描述这种脉冲对分子运动的作用。还计算和分析了特定脉冲形状对脉冲后动力学的影响。此外,还对激光频率、脉冲宽度和系统温度等各种激光参数所起的作用进行了说明和讨论。通过选择合适的分子和偏振光,排列的概念从一维排列扩展到三维排列。最后,我们讨论了强激光定向和对准的潜在应用。

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